geneid | 5664 |
---|---|
ensemblid | ENSG00000143801.18 |
hgncid | 9509 |
symbol | PSEN2 |
name | presenilin 2 |
refseq_nuc | NM_000447.3 |
refseq_prot | NP_000438.2 |
ensembl_nuc | ENST00000366783.8 |
ensembl_prot | ENSP00000355747.3 |
mane_status | MANE Select |
chr | chr1 |
start | 226870616 |
end | 226896098 |
strand | + |
ver | v1.2 |
region | chr1:226870616-226896098 |
region5000 | chr1:226865616-226901098 |
regionname0 | PSEN2_chr1_226870616_226896098 |
regionname5000 | PSEN2_chr1_226865616_226901098 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 448 | 410 | 88 | 70 | 192 | 18 | 40 | 153 | PSEN2_chr1_226865616_226901098 | PSEN2 | copy fasta | chr1 | 226865616 | 226901098 |
a0002 | 0/0 | 448 | 2 | 1 | 0 | 0 | 0 | 1 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | copy fasta | chr1 | 226865616 | 226901098 |
a0003 | 0/0 | 448 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | PSEN2_chr1_226865616_226901098 | PSEN2 | copy fasta | chr1 | 226865616 | 226901098 |
a0004 | 0/0 | 448 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | copy fasta | chr1 | 226865616 | 226901098 |
a0005 | 0/0 | 448 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | copy fasta | chr1 | 226865616 | 226901098 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 1347 | 175 | 31 | 34 | 85 | 8 | 16 | PSEN2_chr1_226865616_226901098 | PSEN2 | copy fasta | chr1 | 226865616 | 226901098 |
c0002 | 1/0 | 1347 | 96 | 8 | 22 | 52 | 5 | 8 | PSEN2_chr1_226865616_226901098 | PSEN2 | copy fasta | chr1 | 226865616 | 226901098 |
c0003 | 0/0 | 1347 | 72 | 18 | 7 | 34 | 2 | 11 | PSEN2_chr1_226865616_226901098 | PSEN2 | copy fasta | chr1 | 226865616 | 226901098 |
c0004 | 0/0 | 1347 | 20 | 0 | 4 | 13 | 0 | 3 | PSEN2_chr1_226865616_226901098 | PSEN2 | copy fasta | chr1 | 226865616 | 226901098 |
c0005 | 0/0 | 1347 | 14 | 12 | 2 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | copy fasta | chr1 | 226865616 | 226901098 |
c0006 | 0/0 | 1347 | 9 | 8 | 0 | 0 | 0 | 1 | PSEN2_chr1_226865616_226901098 | PSEN2 | copy fasta | chr1 | 226865616 | 226901098 |
c0007 | 0/0 | 1347 | 5 | 5 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | copy fasta | chr1 | 226865616 | 226901098 |
c0008 | 0/0 | 1347 | 5 | 0 | 0 | 5 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | copy fasta | chr1 | 226865616 | 226901098 |
c0009 | 0/0 | 1347 | 3 | 3 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | copy fasta | chr1 | 226865616 | 226901098 |
c0010 | 0/0 | 1347 | 2 | 0 | 0 | 2 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | copy fasta | chr1 | 226865616 | 226901098 |
c0011 | 0/0 | 1347 | 2 | 1 | 0 | 0 | 0 | 1 | PSEN2_chr1_226865616_226901098 | PSEN2 | copy fasta | chr1 | 226865616 | 226901098 |
c0012 | 0/0 | 1347 | 2 | 0 | 0 | 2 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | copy fasta | chr1 | 226865616 | 226901098 |
c0013 | 0/0 | 1347 | 2 | 0 | 0 | 0 | 2 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | copy fasta | chr1 | 226865616 | 226901098 |
c0014 | 0/0 | 1347 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | copy fasta | chr1 | 226865616 | 226901098 |
c0015 | 0/0 | 1347 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | copy fasta | chr1 | 226865616 | 226901098 |
c0016 | 0/0 | 1347 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | copy fasta | chr1 | 226865616 | 226901098 |
c0017 | 0/0 | 1347 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | copy fasta | chr1 | 226865616 | 226901098 |
c0018 | 0/0 | 1347 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | copy fasta | chr1 | 226865616 | 226901098 |
c0019 | 0/0 | 1347 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | copy fasta | chr1 | 226865616 | 226901098 |
c0020 | 0/0 | 1347 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN2_chr1_226865616_226901098 | PSEN2 | copy fasta | chr1 | 226865616 | 226901098 |
c0021 | 0/0 | 1347 | 1 | 0 | 0 | 0 | 1 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | copy fasta | chr1 | 226865616 | 226901098 |
c0022 | 0/0 | 1347 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN2_chr1_226865616_226901098 | PSEN2 | copy fasta | chr1 | 226865616 | 226901098 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 903 | 180 | 30 | 35 | 87 | 10 | 17 | PSEN2_chr1_226865616_226901098 | PSEN2 | copy fasta | chr1 | 226865616 | 226901098 |
t0002 | 0/0 | 903 | 106 | 26 | 12 | 54 | 2 | 12 | PSEN2_chr1_226865616_226901098 | PSEN2 | copy fasta | chr1 | 226865616 | 226901098 |
t0003 | 0/0 | 903 | 62 | 0 | 16 | 35 | 5 | 6 | PSEN2_chr1_226865616_226901098 | PSEN2 | copy fasta | chr1 | 226865616 | 226901098 |
t0004 | 0/0 | 903 | 40 | 18 | 5 | 14 | 0 | 3 | PSEN2_chr1_226865616_226901098 | PSEN2 | copy fasta | chr1 | 226865616 | 226901098 |
t0005 | 0/0 | 903 | 7 | 5 | 2 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | copy fasta | chr1 | 226865616 | 226901098 |
t0006 | 0/0 | 903 | 5 | 5 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | copy fasta | chr1 | 226865616 | 226901098 |
t0007 | 1/0 | 903 | 3 | 1 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | copy fasta | chr1 | 226865616 | 226901098 |
t0008 | 0/0 | 903 | 3 | 0 | 0 | 0 | 0 | 3 | PSEN2_chr1_226865616_226901098 | PSEN2 | copy fasta | chr1 | 226865616 | 226901098 |
t0009 | 0/0 | 903 | 2 | 2 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | copy fasta | chr1 | 226865616 | 226901098 |
t0010 | 0/0 | 903 | 1 | 0 | 0 | 0 | 1 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | copy fasta | chr1 | 226865616 | 226901098 |
t0011 | 0/0 | 903 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | copy fasta | chr1 | 226865616 | 226901098 |
t0012 | 0/0 | 903 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | copy fasta | chr1 | 226865616 | 226901098 |
t0013 | 0/0 | 903 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | copy fasta | chr1 | 226865616 | 226901098 |
t0014 | 0/0 | 903 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | copy fasta | chr1 | 226865616 | 226901098 |
t0015 | 0/0 | 903 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | copy fasta | chr1 | 226865616 | 226901098 |
t0016 | 0/0 | 903 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN2_chr1_226865616_226901098 | PSEN2 | copy fasta | chr1 | 226865616 | 226901098 |
t0017 | 0/0 | 903 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | copy fasta | chr1 | 226865616 | 226901098 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 44 | 2 | 7 | 32 | 1 | 2 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0002 | 0/0 | 28 | 0 | 5 | 18 | 1 | 4 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0003 | 0/0 | 23 | 0 | 2 | 14 | 0 | 7 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0004 | 0/0 | 16 | 0 | 3 | 13 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0005 | 0/0 | 12 | 0 | 0 | 12 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0006 | 0/0 | 10 | 0 | 4 | 6 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0007 | 0/0 | 10 | 0 | 0 | 7 | 0 | 3 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0008 | 0/0 | 10 | 0 | 7 | 0 | 3 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0009 | 0/0 | 8 | 7 | 1 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0010 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0011 | 0/0 | 7 | 1 | 1 | 0 | 0 | 5 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0012 | 0/0 | 7 | 0 | 5 | 2 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0013 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0014 | 0/0 | 6 | 4 | 2 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0015 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0016 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0017 | 0/0 | 5 | 0 | 1 | 0 | 2 | 2 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0018 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0019 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0020 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0021 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0022 | 0/0 | 3 | 0 | 0 | 2 | 1 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0025 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0026 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0027 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0030 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0031 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0033 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0034 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0043 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0080 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0088 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 1347 | 175 | 31 | 34 | 85 | 8 | 16 | PSEN2_chr1_226865616_226901098 | PSEN2 | copy fasta | chr1 | 226865616 | 226901098 |
a0001c0002 | 1/0 | 1347 | 96 | 8 | 22 | 52 | 5 | 8 | PSEN2_chr1_226865616_226901098 | PSEN2 | copy fasta | chr1 | 226865616 | 226901098 |
a0001c0003 | 0/0 | 1347 | 72 | 18 | 7 | 34 | 2 | 11 | PSEN2_chr1_226865616_226901098 | PSEN2 | copy fasta | chr1 | 226865616 | 226901098 |
a0001c0004 | 0/0 | 1347 | 20 | 0 | 4 | 13 | 0 | 3 | PSEN2_chr1_226865616_226901098 | PSEN2 | copy fasta | chr1 | 226865616 | 226901098 |
a0001c0005 | 0/0 | 1347 | 14 | 12 | 2 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | copy fasta | chr1 | 226865616 | 226901098 |
a0001c0006 | 0/0 | 1347 | 9 | 8 | 0 | 0 | 0 | 1 | PSEN2_chr1_226865616_226901098 | PSEN2 | copy fasta | chr1 | 226865616 | 226901098 |
a0001c0007 | 0/0 | 1347 | 5 | 5 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | copy fasta | chr1 | 226865616 | 226901098 |
a0001c0008 | 0/0 | 1347 | 5 | 0 | 0 | 5 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | copy fasta | chr1 | 226865616 | 226901098 |
a0001c0009 | 0/0 | 1347 | 3 | 3 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | copy fasta | chr1 | 226865616 | 226901098 |
a0001c0012 | 0/0 | 1347 | 2 | 0 | 0 | 2 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | copy fasta | chr1 | 226865616 | 226901098 |
a0001c0013 | 0/0 | 1347 | 2 | 0 | 0 | 0 | 2 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | copy fasta | chr1 | 226865616 | 226901098 |
a0001c0015 | 0/0 | 1347 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | copy fasta | chr1 | 226865616 | 226901098 |
a0001c0016 | 0/0 | 1347 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | copy fasta | chr1 | 226865616 | 226901098 |
a0001c0017 | 0/0 | 1347 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | copy fasta | chr1 | 226865616 | 226901098 |
a0001c0018 | 0/0 | 1347 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | copy fasta | chr1 | 226865616 | 226901098 |
a0001c0019 | 0/0 | 1347 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | copy fasta | chr1 | 226865616 | 226901098 |
a0001c0021 | 0/0 | 1347 | 1 | 0 | 0 | 0 | 1 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | copy fasta | chr1 | 226865616 | 226901098 |
a0001c0022 | 0/0 | 1347 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN2_chr1_226865616_226901098 | PSEN2 | copy fasta | chr1 | 226865616 | 226901098 |
a0002c0011 | 0/0 | 1347 | 2 | 1 | 0 | 0 | 0 | 1 | PSEN2_chr1_226865616_226901098 | PSEN2 | copy fasta | chr1 | 226865616 | 226901098 |
a0003c0010 | 0/0 | 1347 | 2 | 0 | 0 | 2 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | copy fasta | chr1 | 226865616 | 226901098 |
a0004c0014 | 0/0 | 1347 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | copy fasta | chr1 | 226865616 | 226901098 |
a0005c0020 | 0/0 | 1347 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN2_chr1_226865616_226901098 | PSEN2 | copy fasta | chr1 | 226865616 | 226901098 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 2249 | 172 | 30 | 34 | 84 | 7 | 16 | PSEN2_chr1_226865616_226901098 | PSEN2 | copy fasta | chr1 | 226865616 | 226901098 |
a0001c0001t0010 | 0/0 | 2249 | 1 | 0 | 0 | 0 | 1 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | copy fasta | chr1 | 226865616 | 226901098 |
a0001c0001t0012 | 0/0 | 2249 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | copy fasta | chr1 | 226865616 | 226901098 |
a0001c0001t0014 | 0/0 | 2249 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | copy fasta | chr1 | 226865616 | 226901098 |
a0001c0002t0002 | 0/0 | 2249 | 30 | 7 | 6 | 15 | 0 | 2 | PSEN2_chr1_226865616_226901098 | PSEN2 | copy fasta | chr1 | 226865616 | 226901098 |
a0001c0002t0003 | 0/0 | 2249 | 62 | 0 | 16 | 35 | 5 | 6 | PSEN2_chr1_226865616_226901098 | PSEN2 | copy fasta | chr1 | 226865616 | 226901098 |
a0001c0002t0007 | 1/0 | 2249 | 2 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | copy fasta | chr1 | 226865616 | 226901098 |
a0001c0002t0011 | 0/0 | 2249 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | copy fasta | chr1 | 226865616 | 226901098 |
a0001c0002t0017 | 0/0 | 2249 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | copy fasta | chr1 | 226865616 | 226901098 |
a0001c0003t0002 | 0/0 | 2249 | 56 | 8 | 6 | 32 | 2 | 8 | PSEN2_chr1_226865616_226901098 | PSEN2 | copy fasta | chr1 | 226865616 | 226901098 |
a0001c0003t0004 | 0/0 | 2249 | 11 | 9 | 1 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | copy fasta | chr1 | 226865616 | 226901098 |
a0001c0003t0007 | 0/0 | 2249 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | copy fasta | chr1 | 226865616 | 226901098 |
a0001c0003t0008 | 0/0 | 2249 | 3 | 0 | 0 | 0 | 0 | 3 | PSEN2_chr1_226865616_226901098 | PSEN2 | copy fasta | chr1 | 226865616 | 226901098 |
a0001c0003t0015 | 0/0 | 2249 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | copy fasta | chr1 | 226865616 | 226901098 |
a0001c0004t0004 | 0/0 | 2249 | 19 | 0 | 4 | 13 | 0 | 2 | PSEN2_chr1_226865616_226901098 | PSEN2 | copy fasta | chr1 | 226865616 | 226901098 |
a0001c0004t0016 | 0/0 | 2249 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN2_chr1_226865616_226901098 | PSEN2 | copy fasta | chr1 | 226865616 | 226901098 |
a0001c0005t0004 | 0/0 | 2249 | 7 | 7 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | copy fasta | chr1 | 226865616 | 226901098 |
a0001c0005t0005 | 0/0 | 2249 | 7 | 5 | 2 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | copy fasta | chr1 | 226865616 | 226901098 |
a0001c0006t0002 | 0/0 | 2249 | 9 | 8 | 0 | 0 | 0 | 1 | PSEN2_chr1_226865616_226901098 | PSEN2 | copy fasta | chr1 | 226865616 | 226901098 |
a0001c0007t0006 | 0/0 | 2249 | 5 | 5 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | copy fasta | chr1 | 226865616 | 226901098 |
a0001c0008t0002 | 0/0 | 2249 | 5 | 0 | 0 | 5 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | copy fasta | chr1 | 226865616 | 226901098 |
a0001c0009t0002 | 0/0 | 2249 | 3 | 3 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | copy fasta | chr1 | 226865616 | 226901098 |
a0001c0012t0002 | 0/0 | 2249 | 2 | 0 | 0 | 2 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | copy fasta | chr1 | 226865616 | 226901098 |
a0001c0013t0001 | 0/0 | 2249 | 2 | 0 | 0 | 0 | 2 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | copy fasta | chr1 | 226865616 | 226901098 |
a0001c0015t0004 | 0/0 | 2249 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | copy fasta | chr1 | 226865616 | 226901098 |
a0001c0016t0009 | 0/0 | 2249 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | copy fasta | chr1 | 226865616 | 226901098 |
a0001c0017t0009 | 0/0 | 2249 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | copy fasta | chr1 | 226865616 | 226901098 |
a0001c0018t0001 | 0/0 | 2249 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | copy fasta | chr1 | 226865616 | 226901098 |
a0001c0019t0001 | 0/0 | 2249 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | copy fasta | chr1 | 226865616 | 226901098 |
a0001c0021t0001 | 0/0 | 2249 | 1 | 0 | 0 | 0 | 1 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | copy fasta | chr1 | 226865616 | 226901098 |
a0001c0022t0002 | 0/0 | 2249 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN2_chr1_226865616_226901098 | PSEN2 | copy fasta | chr1 | 226865616 | 226901098 |
a0002c0011t0004 | 0/0 | 2249 | 2 | 1 | 0 | 0 | 0 | 1 | PSEN2_chr1_226865616_226901098 | PSEN2 | copy fasta | chr1 | 226865616 | 226901098 |
a0003c0010t0001 | 0/0 | 2249 | 2 | 0 | 0 | 2 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | copy fasta | chr1 | 226865616 | 226901098 |
a0004c0014t0013 | 0/0 | 2249 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | copy fasta | chr1 | 226865616 | 226901098 |
a0005c0020t0001 | 0/0 | 2249 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN2_chr1_226865616_226901098 | PSEN2 | copy fasta | chr1 | 226865616 | 226901098 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 42 | 2 | 7 | 30 | 1 | 2 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0001t0001g0004 | 0/0 | 16 | 0 | 3 | 13 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0001t0001g0006 | 0/0 | 10 | 0 | 4 | 6 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0001t0001g0009 | 0/0 | 8 | 7 | 1 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0001t0001g0010 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0001t0001g0011 | 0/0 | 7 | 1 | 1 | 0 | 0 | 5 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0001t0001g0016 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0001t0001g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0001t0001g0026 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0001t0001g0031 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0001t0001g0080 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0001t0010g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0001t0012g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0001t0014g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0002t0002g0007 | 0/0 | 9 | 0 | 0 | 7 | 0 | 2 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0002t0002g0012 | 0/0 | 7 | 0 | 5 | 2 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0002t0002g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0002t0002g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0002t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0002t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0002t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0002t0002g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0002t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0002t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0002t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0002t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0002t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0002t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0002t0003g0002 | 0/0 | 27 | 0 | 5 | 17 | 1 | 4 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0002t0003g0008 | 0/0 | 10 | 0 | 7 | 0 | 3 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0002t0003g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0002t0003g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0002t0003g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0002t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0002t0003g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0002t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0002t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0002t0003g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0002t0003g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0002t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0002t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0002t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0002t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0002t0003g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0002t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0002t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0002t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0002t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0002t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0002t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0002t0003g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0002t0003g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0002t0007g0088 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0002t0007g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0002t0011g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0002t0017g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0003t0002g0003 | 0/0 | 20 | 0 | 2 | 13 | 0 | 5 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0003t0002g0005 | 0/0 | 12 | 0 | 0 | 12 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0003t0002g0018 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0003t0002g0022 | 0/0 | 3 | 0 | 0 | 2 | 1 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0003t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0003t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0003t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0003t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0003t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0003t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0003t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0003t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0003t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0003t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0003t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0003t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0003t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0003t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0003t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0003t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0003t0004g0027 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0003t0004g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0003t0004g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0003t0004g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0003t0004g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0003t0004g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0003t0004g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0003t0004g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0003t0007g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0003t0008g0003 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0003t0008g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0003t0015g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0004t0004g0013 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0004t0004g0025 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0004t0004g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0004t0004g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0004t0004g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0004t0004g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0004t0004g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0004t0004g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0004t0004g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0004t0004g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0004t0004g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0004t0016g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0005t0004g0021 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0005t0004g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0005t0004g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0005t0005g0014 | 0/0 | 6 | 4 | 2 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0005t0005g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0006t0002g0015 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0006t0002g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0006t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0006t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0007t0006g0019 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0007t0006g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0008t0002g0020 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0008t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0009t0002g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0009t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0012t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0012t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0013t0001g0030 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0015t0004g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0016t0009g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0017t0009g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0018t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0019t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0021t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0001c0022t0002g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0002c0011t0004g0043 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0003c0010t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0003c0010t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0004c0014t0013g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
a0005c0020t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0003 | t0002 | g0022 | EUR | GBR | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0017 | EUR | GBR | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0113 | EUR | GBR | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG00280 | hp1 | a0001 | c0002 | t0003 | g0150 | EUR | FIN | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0085 | EUR | FIN | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0110 | EUR | FIN | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG00323 | hp2 | a0001 | c0001 | t0010 | g0120 | EUR | FIN | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG00423 | hp1 | a0001 | c0008 | t0002 | g0020 | EAS | CHS | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | CHS | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | CHS | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG00558 | hp1 | a0001 | c0002 | t0002 | g0012 | EAS | CHS | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG00558 | hp2 | a0001 | c0004 | t0004 | g0013 | EAS | CHS | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG00597 | hp1 | a0001 | c0003 | t0002 | g0003 | EAS | CHS | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | CHS | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG00621 | hp1 | a0001 | c0002 | t0003 | g0002 | EAS | CHS | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG00733 | hp2 | a0001 | c0003 | t0002 | g0059 | AMR | PUR | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG00738 | hp2 | a0001 | c0002 | t0003 | g0008 | AMR | PUR | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG00741 | hp2 | a0001 | c0002 | t0003 | g0002 | AMR | PUR | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG01071 | hp1 | a0001 | c0002 | t0003 | g0008 | AMR | PUR | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG01071 | hp2 | a0001 | c0002 | t0003 | g0041 | AMR | PUR | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG01074 | hp2 | a0001 | c0004 | t0004 | g0163 | AMR | PUR | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG01081 | hp1 | a0001 | c0002 | t0003 | g0002 | AMR | PUR | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG01099 | hp2 | a0001 | c0002 | t0002 | g0012 | AMR | PUR | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG01106 | hp1 | a0001 | c0003 | t0002 | g0018 | AMR | PUR | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG01106 | hp2 | a0001 | c0002 | t0003 | g0008 | AMR | PUR | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG01109 | hp2 | a0001 | c0003 | t0004 | g0027 | AMR | PUR | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG01168 | hp2 | a0001 | c0005 | t0005 | g0014 | AMR | PUR | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG01169 | hp1 | a0001 | c0005 | t0005 | g0014 | AMR | PUR | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG01175 | hp1 | a0001 | c0002 | t0003 | g0002 | AMR | PUR | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG01175 | hp2 | a0001 | c0002 | t0003 | g0041 | AMR | PUR | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG01243 | hp2 | a0001 | c0002 | t0003 | g0008 | AMR | PUR | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG01257 | hp1 | a0001 | c0002 | t0003 | g0137 | AMR | CLM | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | CLM | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | CLM | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG01346 | hp2 | a0001 | c0003 | t0002 | g0003 | AMR | CLM | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG01358 | hp1 | a0001 | c0004 | t0004 | g0025 | AMR | CLM | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | CLM | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG01361 | hp1 | a0001 | c0002 | t0003 | g0008 | AMR | CLM | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG01361 | hp2 | a0001 | c0003 | t0002 | g0003 | AMR | CLM | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG01433 | hp1 | a0001 | c0002 | t0003 | g0143 | AMR | CLM | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG01496 | hp1 | a0001 | c0002 | t0003 | g0002 | AMR | CLM | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | CLM | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG01515 | hp1 | a0001 | c0003 | t0002 | g0055 | EUR | IBS | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG01515 | hp2 | a0001 | c0002 | t0003 | g0008 | EUR | IBS | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG01516 | hp1 | a0001 | c0013 | t0001 | g0030 | EUR | IBS | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG01516 | hp2 | a0001 | c0002 | t0003 | g0002 | EUR | IBS | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG01517 | hp1 | a0001 | c0002 | t0003 | g0008 | EUR | IBS | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG01517 | hp2 | a0001 | c0013 | t0001 | g0030 | EUR | IBS | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG01884 | hp1 | a0001 | c0002 | t0002 | g0068 | AFR | ACB | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG01891 | hp1 | a0001 | c0006 | t0002 | g0024 | AFR | ACB | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG01891 | hp2 | a0001 | c0006 | t0002 | g0015 | AFR | ACB | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG01928 | hp1 | a0001 | c0003 | t0002 | g0054 | AMR | PEL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG01928 | hp2 | a0001 | c0002 | t0002 | g0012 | AMR | PEL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG01934 | hp2 | a0001 | c0004 | t0004 | g0025 | AMR | PEL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG01943 | hp1 | a0001 | c0002 | t0002 | g0012 | AMR | PEL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PEL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG01952 | hp1 | a0001 | c0004 | t0004 | g0025 | AMR | PEL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG01952 | hp2 | a0001 | c0002 | t0002 | g0012 | AMR | PEL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG01975 | hp1 | a0001 | c0002 | t0003 | g0002 | AMR | PEL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | PEL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG01978 | hp1 | a0001 | c0002 | t0002 | g0012 | AMR | PEL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG01981 | hp1 | a0001 | c0002 | t0003 | g0008 | AMR | PEL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | PEL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG01993 | hp1 | a0001 | c0002 | t0003 | g0008 | AMR | PEL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG01993 | hp2 | a0001 | c0018 | t0001 | g0017 | AMR | PEL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PEL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG02004 | hp2 | a0001 | c0003 | t0002 | g0058 | AMR | PEL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG02027 | hp1 | a0001 | c0004 | t0004 | g0162 | EAS | KHV | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG02027 | hp2 | a0003 | c0010 | t0001 | g0166 | EAS | KHV | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG02040 | hp1 | a0001 | c0002 | t0003 | g0144 | EAS | KHV | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG02040 | hp2 | a0001 | c0002 | t0003 | g0134 | EAS | KHV | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG02055 | hp1 | a0001 | c0007 | t0006 | g0019 | AFR | ACB | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | ACB | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | KHV | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG02056 | hp2 | a0001 | c0002 | t0003 | g0040 | EAS | KHV | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG02071 | hp2 | a0001 | c0004 | t0004 | g0013 | EAS | KHV | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG02074 | hp1 | a0001 | c0002 | t0002 | g0012 | EAS | KHV | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG02074 | hp2 | a0001 | c0002 | t0003 | g0124 | EAS | KHV | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG02083 | hp1 | a0001 | c0002 | t0003 | g0002 | EAS | KHV | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG02083 | hp2 | a0001 | c0003 | t0015 | g0003 | EAS | KHV | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG02129 | hp1 | a0001 | c0002 | t0003 | g0002 | EAS | KHV | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | KHV | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG02135 | hp1 | a0001 | c0002 | t0003 | g0142 | EAS | KHV | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG02145 | hp1 | a0001 | c0003 | t0004 | g0176 | AFR | ACB | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG02145 | hp2 | a0001 | c0009 | t0002 | g0130 | AFR | ACB | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | CDX | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | CDX | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG02165 | hp2 | a0001 | c0002 | t0003 | g0002 | EAS | CDX | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | ACB | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG02257 | hp2 | a0001 | c0005 | t0005 | g0070 | AFR | ACB | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG02280 | hp1 | a0001 | c0007 | t0006 | g0019 | AFR | ACB | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG02280 | hp2 | a0001 | c0002 | t0002 | g0131 | AFR | ACB | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PEL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG02451 | hp2 | a0001 | c0005 | t0004 | g0171 | AFR | ACB | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG02572 | hp2 | a0001 | c0003 | t0007 | g0075 | AFR | GWD | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG02602 | hp1 | a0001 | c0002 | t0003 | g0002 | SAS | PJL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG02602 | hp2 | a0001 | c0003 | t0002 | g0003 | SAS | PJL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | GWD | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG02615 | hp2 | a0001 | c0016 | t0009 | g0048 | AFR | GWD | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG02622 | hp1 | a0001 | c0005 | t0004 | g0021 | AFR | GWD | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG02622 | hp2 | a0001 | c0006 | t0002 | g0015 | AFR | GWD | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG02630 | hp1 | a0001 | c0006 | t0002 | g0015 | AFR | GWD | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG02647 | hp1 | a0001 | c0003 | t0004 | g0027 | AFR | GWD | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG02647 | hp2 | a0001 | c0003 | t0002 | g0018 | AFR | GWD | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG02698 | hp1 | a0001 | c0004 | t0004 | g0156 | SAS | PJL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG02717 | hp1 | a0001 | c0005 | t0004 | g0021 | AFR | GWD | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG02723 | hp1 | a0001 | c0005 | t0004 | g0044 | AFR | GWD | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG02723 | hp2 | a0001 | c0003 | t0002 | g0018 | AFR | GWD | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG02735 | hp2 | a0001 | c0004 | t0004 | g0157 | SAS | PJL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG02738 | hp2 | a0001 | c0006 | t0002 | g0129 | SAS | PJL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG02809 | hp1 | a0001 | c0005 | t0004 | g0021 | AFR | GWD | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG02818 | hp2 | a0001 | c0003 | t0002 | g0169 | AFR | GWD | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG02886 | hp1 | a0001 | c0003 | t0004 | g0172 | AFR | GWD | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG02886 | hp2 | a0001 | c0005 | t0005 | g0014 | AFR | GWD | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | GWD | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG02896 | hp2 | a0002 | c0011 | t0004 | g0043 | AFR | GWD | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG02922 | hp1 | a0001 | c0002 | t0002 | g0039 | AFR | ESN | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG02922 | hp2 | a0001 | c0006 | t0002 | g0133 | AFR | ESN | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG02965 | hp1 | a0001 | c0002 | t0002 | g0067 | AFR | ESN | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG02965 | hp2 | a0001 | c0009 | t0002 | g0015 | AFR | ESN | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG02970 | hp1 | a0001 | c0009 | t0002 | g0015 | AFR | ESN | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG02976 | hp1 | a0001 | c0003 | t0004 | g0045 | AFR | ESN | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG02976 | hp2 | a0001 | c0002 | t0002 | g0066 | AFR | ESN | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG03017 | hp1 | a0001 | c0003 | t0002 | g0003 | SAS | PJL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG03017 | hp2 | a0001 | c0002 | t0003 | g0138 | SAS | PJL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | GWD | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG03098 | hp1 | a0001 | c0006 | t0002 | g0024 | AFR | MSL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG03098 | hp2 | a0004 | c0014 | t0013 | g0049 | AFR | MSL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG03130 | hp1 | a0001 | c0007 | t0006 | g0019 | AFR | ESN | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG03130 | hp2 | a0001 | c0003 | t0002 | g0018 | AFR | ESN | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | ESN | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG03139 | hp2 | a0001 | c0005 | t0005 | g0014 | AFR | ESN | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG03195 | hp1 | a0001 | c0003 | t0004 | g0173 | AFR | ESN | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG03195 | hp2 | a0001 | c0001 | t0014 | g0071 | AFR | ESN | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | MSL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG03225 | hp1 | a0001 | c0003 | t0004 | g0027 | AFR | MSL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG03225 | hp2 | a0001 | c0003 | t0004 | g0045 | AFR | MSL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG03453 | hp1 | a0001 | c0003 | t0004 | g0170 | AFR | MSL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG03453 | hp2 | a0001 | c0007 | t0006 | g0106 | AFR | MSL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG03486 | hp1 | a0001 | c0003 | t0002 | g0018 | AFR | MSL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG03490 | hp1 | a0001 | c0003 | t0008 | g0003 | SAS | PJL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG03491 | hp2 | a0001 | c0003 | t0002 | g0063 | SAS | PJL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG03516 | hp1 | a0001 | c0002 | t0002 | g0039 | AFR | ESN | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG03516 | hp2 | a0001 | c0005 | t0005 | g0014 | AFR | ESN | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG03540 | hp1 | a0001 | c0002 | t0017 | g0132 | AFR | GWD | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG03540 | hp2 | a0001 | c0003 | t0002 | g0168 | AFR | GWD | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG03579 | hp2 | a0001 | c0006 | t0002 | g0024 | AFR | MSL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG03654 | hp1 | a0002 | c0011 | t0004 | g0043 | SAS | PJL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG03654 | hp2 | a0001 | c0003 | t0002 | g0053 | SAS | PJL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG03669 | hp1 | a0001 | c0002 | t0003 | g0151 | SAS | PJL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | STU | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG03688 | hp2 | a0001 | c0002 | t0003 | g0002 | SAS | STU | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG03704 | hp1 | a0001 | c0003 | t0002 | g0003 | SAS | PJL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG03831 | hp1 | a0005 | c0020 | t0001 | g0017 | SAS | BEB | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG03831 | hp2 | a0001 | c0002 | t0002 | g0007 | SAS | BEB | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG03834 | hp1 | a0001 | c0003 | t0002 | g0003 | SAS | BEB | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG03834 | hp2 | a0001 | c0004 | t0016 | g0123 | SAS | BEB | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG03927 | hp1 | a0001 | c0002 | t0002 | g0007 | SAS | BEB | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG03927 | hp2 | a0001 | c0002 | t0003 | g0002 | SAS | BEB | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | BEB | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG03942 | hp2 | a0001 | c0003 | t0002 | g0003 | SAS | BEB | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG04115 | hp1 | a0001 | c0003 | t0002 | g0178 | SAS | STU | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG04184 | hp1 | a0001 | c0003 | t0008 | g0060 | SAS | BEB | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG04184 | hp2 | a0001 | c0022 | t0002 | g0007 | SAS | BEB | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG04204 | hp1 | a0001 | c0002 | t0003 | g0002 | SAS | STU | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG04204 | hp2 | a0001 | c0003 | t0008 | g0003 | SAS | STU | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0031 | SAS | STU | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0114 | SAS | STU | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA18522 | hp1 | a0001 | c0005 | t0004 | g0044 | AFR | YRI | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA18522 | hp2 | a0001 | c0003 | t0002 | g0167 | AFR | YRI | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA18612 | hp1 | a0001 | c0002 | t0002 | g0007 | EAS | CHB | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA18612 | hp2 | a0001 | c0002 | t0003 | g0002 | EAS | CHB | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA18747 | hp2 | a0001 | c0004 | t0004 | g0159 | EAS | CHB | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | YRI | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA18906 | hp2 | a0001 | c0005 | t0005 | g0014 | AFR | YRI | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA18941 | hp1 | a0001 | c0003 | t0002 | g0003 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA18942 | hp1 | a0001 | c0003 | t0002 | g0057 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA18942 | hp2 | a0001 | c0003 | t0002 | g0003 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA18943 | hp1 | a0001 | c0004 | t0004 | g0013 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA18944 | hp1 | a0001 | c0012 | t0002 | g0061 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA18944 | hp2 | a0001 | c0003 | t0002 | g0003 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA18946 | hp1 | a0001 | c0003 | t0002 | g0005 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA18947 | hp2 | a0001 | c0002 | t0002 | g0152 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA18948 | hp1 | a0001 | c0002 | t0003 | g0136 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA18948 | hp2 | a0001 | c0002 | t0002 | g0177 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA18949 | hp1 | a0001 | c0003 | t0002 | g0005 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA18950 | hp1 | a0001 | c0002 | t0003 | g0042 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA18952 | hp1 | a0001 | c0002 | t0003 | g0002 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA18957 | hp2 | a0001 | c0002 | t0003 | g0149 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA18959 | hp1 | a0001 | c0003 | t0002 | g0022 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA18959 | hp2 | a0003 | c0010 | t0001 | g0165 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA18960 | hp2 | a0001 | c0002 | t0003 | g0002 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA18962 | hp1 | a0001 | c0002 | t0007 | g0121 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA18962 | hp2 | a0001 | c0002 | t0003 | g0002 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA18963 | hp1 | a0001 | c0002 | t0002 | g0038 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA18963 | hp2 | a0001 | c0003 | t0004 | g0161 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA18965 | hp2 | a0001 | c0002 | t0003 | g0140 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA18966 | hp1 | a0001 | c0003 | t0002 | g0050 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA18966 | hp2 | a0001 | c0008 | t0002 | g0020 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA18969 | hp2 | a0001 | c0003 | t0002 | g0005 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA18971 | hp1 | a0001 | c0008 | t0002 | g0020 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA18971 | hp2 | a0001 | c0003 | t0002 | g0005 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA18972 | hp1 | a0001 | c0004 | t0004 | g0154 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA18973 | hp1 | a0001 | c0003 | t0002 | g0005 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA18974 | hp1 | a0001 | c0002 | t0003 | g0148 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA18975 | hp1 | a0001 | c0003 | t0002 | g0005 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA18975 | hp2 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA18976 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA18976 | hp2 | a0001 | c0002 | t0003 | g0146 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA18977 | hp1 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA18977 | hp2 | a0001 | c0002 | t0003 | g0002 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA18979 | hp1 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA18981 | hp1 | a0001 | c0002 | t0002 | g0128 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA18982 | hp1 | a0001 | c0002 | t0003 | g0145 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA18982 | hp2 | a0001 | c0002 | t0003 | g0002 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA18983 | hp1 | a0001 | c0003 | t0002 | g0005 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA18983 | hp2 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA18985 | hp2 | a0001 | c0003 | t0002 | g0003 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA18987 | hp1 | a0001 | c0002 | t0003 | g0002 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA18988 | hp2 | a0001 | c0002 | t0003 | g0042 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA18992 | hp1 | a0001 | c0008 | t0002 | g0126 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA18992 | hp2 | a0001 | c0019 | t0001 | g0001 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA18993 | hp1 | a0001 | c0002 | t0003 | g0139 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA18993 | hp2 | a0001 | c0002 | t0002 | g0127 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA18995 | hp2 | a0001 | c0004 | t0004 | g0155 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA18997 | hp1 | a0001 | c0002 | t0003 | g0040 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA18998 | hp2 | a0001 | c0003 | t0002 | g0005 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA19002 | hp1 | a0001 | c0004 | t0004 | g0158 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA19003 | hp2 | a0001 | c0002 | t0003 | g0141 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA19004 | hp2 | a0001 | c0003 | t0002 | g0003 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA19005 | hp1 | a0001 | c0002 | t0003 | g0002 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA19007 | hp1 | a0001 | c0002 | t0011 | g0002 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA19007 | hp2 | a0001 | c0004 | t0004 | g0013 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA19009 | hp1 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA19009 | hp2 | a0001 | c0003 | t0002 | g0005 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA19010 | hp1 | a0001 | c0002 | t0003 | g0135 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA19011 | hp2 | a0001 | c0003 | t0002 | g0005 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA19012 | hp2 | a0001 | c0004 | t0004 | g0160 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | LWK | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | LWK | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA19043 | hp1 | a0001 | c0003 | t0004 | g0174 | AFR | LWK | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | LWK | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA19056 | hp1 | a0001 | c0003 | t0002 | g0005 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA19057 | hp2 | a0001 | c0004 | t0004 | g0013 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA19060 | hp2 | a0001 | c0003 | t0002 | g0003 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA19062 | hp1 | a0001 | c0004 | t0004 | g0013 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA19062 | hp2 | a0001 | c0003 | t0002 | g0005 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA19064 | hp2 | a0001 | c0003 | t0002 | g0003 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA19067 | hp1 | a0001 | c0001 | t0012 | g0001 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA19067 | hp2 | a0001 | c0003 | t0002 | g0003 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA19068 | hp1 | a0001 | c0002 | t0003 | g0002 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA19070 | hp2 | a0001 | c0003 | t0002 | g0003 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA19072 | hp1 | a0001 | c0003 | t0002 | g0022 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA19078 | hp1 | a0001 | c0002 | t0003 | g0002 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA19078 | hp2 | a0001 | c0003 | t0002 | g0003 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA19079 | hp1 | a0001 | c0002 | t0003 | g0147 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA19080 | hp2 | a0001 | c0004 | t0004 | g0013 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA19081 | hp1 | a0001 | c0003 | t0002 | g0003 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA19082 | hp2 | a0001 | c0002 | t0003 | g0002 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA19083 | hp1 | a0001 | c0003 | t0002 | g0003 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA19083 | hp2 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA19084 | hp1 | a0001 | c0008 | t0002 | g0020 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA19088 | hp1 | a0001 | c0003 | t0002 | g0052 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA19089 | hp1 | a0001 | c0002 | t0003 | g0002 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA19090 | hp1 | a0001 | c0003 | t0002 | g0051 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA19090 | hp2 | a0001 | c0003 | t0002 | g0056 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA19091 | hp1 | a0001 | c0002 | t0003 | g0002 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA19091 | hp2 | a0001 | c0012 | t0002 | g0062 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA20752 | hp1 | a0001 | c0002 | t0003 | g0008 | EUR | TSI | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA20752 | hp2 | a0001 | c0021 | t0001 | g0017 | EUR | TSI | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0078 | EUR | TSI | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0107 | EUR | TSI | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG01123 | hp2 | a0001 | c0002 | t0002 | g0125 | AMR | CLM | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG02109 | hp1 | a0001 | c0015 | t0004 | g0175 | AFR | ACB | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | ACB | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG02486 | hp1 | a0001 | c0005 | t0004 | g0021 | AFR | ACB | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG02486 | hp2 | a0001 | c0003 | t0002 | g0064 | AFR | ACB | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG03471 | hp1 | a0001 | c0006 | t0002 | g0015 | AFR | MSL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | MSL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG06807 | hp1 | a0001 | c0007 | t0006 | g0019 | AFR | USA | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | USA | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA18955 | hp2 | a0001 | c0002 | t0002 | g0038 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA20300 | hp1 | a0001 | c0017 | t0009 | g0047 | AFR | USA | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA20300 | hp2 | a0001 | c0002 | t0002 | g0153 | AFR | USA | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | LWK | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | LWK | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0080 | REF | REF | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
homoSapiens_grch38 | hp1 | a0001 | c0002 | t0007 | g0088 | REF | REF | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:226882007
|
G | A | 1 | a0003 | 2 | HG02027.hp2 NA18959.hp2 |
missense_variant | MODERATE | c.100G>A | p.Gly34Ser | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 4/13 | 483/2249 | 100/1347 | 34/448 | chr1 | 226882007 | ||
chr1:226883725
|
G | C | 1 | a0004 | 1 | HG03098.hp2 | missense_variant | MODERATE | c.162G>C | p.Glu54Asp | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 5/13 | 545/2249 | 162/1347 | 54/448 | chr1 | 226883725 | ||
chr1:226883748
|
G | A | 1 | a0002 | 2 | HG02896.hp2 HG03654.hp1 |
missense_variant | MODERATE | c.185G>A | p.Arg62His | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 5/13 | 568/2249 | 185/1347 | 62/448 | chr1 | 226883748 | ||
chr1:226888112
|
A | G | 1 | a0005 | 1 | HG03831.hp1 | missense_variant | MODERATE | c.520A>G | p.Met174Val | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 7/13 | 903/2249 | 520/1347 | 174/448 | chr1 | 226888112 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:226881976
|
T | C | 17 | a0001c0001a0001c0003a0001c0004others(14): Show | 302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
synonymous_variant | LOW | c.69T>C | p.Ala23Ala | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 4/13 | 452/2249 | 69/1347 | 23/448 | chr1 | 226881976 | ||
chr1:226882036
|
C | T | 8 | a0001c0001a0001c0007a0001c0013others(5): Show | 188 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(185): Show |
synonymous_variant | LOW | c.129C>T | p.Asn43Asn | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 4/13 | 512/2249 | 129/1347 | 43/448 | chr1 | 226882036 | ||
chr1:226882039
|
T | A | 1 | a0001c0009 | 3 | HG02145.hp2 HG02965.hp2 HG02970.hp1 |
synonymous_variant | LOW | c.132T>A | p.Thr44Thr | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 4/13 | 515/2249 | 132/1347 | 44/448 | chr1 | 226882039 | ||
chr1:226883824
|
C | T | 8 | a0001c0001a0001c0007a0001c0013others(5): Show | 188 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(185): Show |
synonymous_variant | LOW | c.261C>T | p.His87His | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 5/13 | 644/2249 | 261/1347 | 87/448 | chr1 | 226883824 | ||
chr1:226883863
|
C | T | 1 | a0001c0021 | 1 | NA20752.hp2 | synonymous_variant | LOW | c.300C>T | p.Ile100Ile | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 5/13 | 683/2249 | 300/1347 | 100/448 | chr1 | 226883863 | ||
chr1:226885622
|
C | T | 2 | a0001c0016a0001c0017 | 2 | HG02615.hp2 NA20300.hp1 |
synonymous_variant | LOW | c.441C>T | p.Ser147Ser | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 6/13 | 824/2249 | 441/1347 | 147/448 | chr1 | 226885622 | ||
chr1:226888901
|
A | G | 1 | a0001c0022 | 1 | HG04184.hp2 | synonymous_variant | LOW | c.639A>G | p.Ala213Ala | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 8/13 | 1022/2249 | 639/1347 | 213/448 | chr1 | 226888901 | ||
chr1:226888970
|
T | C | 5 | a0001c0006a0001c0009a0001c0015others(2): Show | 15 | HG01891.hp1 HG01891.hp2 HG01993.hp2 others(12): Show |
synonymous_variant | LOW | c.708T>C | p.Ser236Ser | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 8/13 | 1091/2249 | 708/1347 | 236/448 | chr1 | 226888970 | ||
chr1:226889018
|
G | C | 1 | a0001c0013 | 2 | HG01516.hp1 HG01517.hp2 |
synonymous_variant | LOW | c.756G>C | p.Ala252Ala | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 8/13 | 1139/2249 | 756/1347 | 252/448 | chr1 | 226889018 | ||
chr1:226890039
|
C | G | 1 | a0001c0012 | 2 | NA18944.hp1 NA19091.hp2 |
synonymous_variant | LOW | c.792C>G | p.Leu264Leu | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 9/13 | 1175/2249 | 792/1347 | 264/448 | chr1 | 226890039 | ||
chr1:226890108
|
C | T | 2 | a0001c0004a0001c0008 | 25 | HG00423.hp1 HG00558.hp2 HG01074.hp2 others(22): Show |
synonymous_variant | LOW | c.861C>T | p.Pro287Pro | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 9/13 | 1244/2249 | 861/1347 | 287/448 | chr1 | 226890108 | ||
chr1:226891294
|
G | T | 2 | a0001c0005a0001c0017 | 15 | HG01168.hp2 HG01169.hp1 HG02257.hp2 others(12): Show |
synonymous_variant | LOW | c.903G>T | p.Thr301Thr | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 10/13 | 1286/2249 | 903/1347 | 301/448 | chr1 | 226891294 | ||
chr1:226894110
|
C | T | 2 | a0001c0007a0004c0014 | 6 | HG02055.hp1 HG02280.hp1 HG03098.hp2 others(3): Show |
synonymous_variant | LOW | c.1176C>T | p.Phe392Phe | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 12/13 | 1559/2249 | 1176/1347 | 392/448 | chr1 | 226894110 | ||
chr1:226895549
|
C | T | 1 | a0001c0019 | 1 | NA18992.hp2 | synonymous_variant | LOW | c.1317C>T | p.Asp439Asp | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 13/13 | 1700/2249 | 1317/1347 | 439/448 | chr1 | 226895549 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:226870643
|
A | G | 21 | a0001c0001t0014a0001c0002t0002a0001c0002t0003others(18): Show | 218 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(215): Show |
5_prime_UTR_variant | MODIFIER | c.-356A>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 1/13 | 11265 | chr1 | 226870643 | |||||
chr1:226871273
|
A | G | 2 | a0001c0016t0009a0001c0017t0009 | 2 | HG02615.hp2 NA20300.hp1 |
5_prime_UTR_variant | MODIFIER | c.-338A>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/13 | 10635 | chr1 | 226871273 | |||||
chr1:226871283
|
C | G | 1 | a0001c0001t0012 | 1 | NA19067.hp1 | 5_prime_UTR_variant | MODIFIER | c.-328C>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/13 | 10625 | chr1 | 226871283 | |||||
chr1:226871314
|
A | C | 1 | a0001c0002t0017 | 1 | HG03540.hp1 | 5_prime_UTR_variant | MODIFIER | c.-297A>C | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/13 | 10594 | chr1 | 226871314 | |||||
chr1:226871336
|
C | T | 3 | a0001c0002t0003a0001c0002t0011a0001c0004t0016 | 64 | HG00280.hp1 HG00621.hp1 HG00738.hp2 others(61): Show |
5_prime_UTR_variant | MODIFIER | c.-275C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/13 | 10572 | chr1 | 226871336 | |||||
chr1:226875489
|
T | C | 1 | a0001c0001t0010 | 1 | HG00323.hp2 | 5_prime_UTR_variant | MODIFIER | c.-82T>C | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/13 | 6419 | chr1 | 226875489 | |||||
chr1:226875507
|
A | G | 1 | a0001c0003t0015 | 1 | HG02083.hp2 | 5_prime_UTR_variant | MODIFIER | c.-64A>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/13 | 6401 | chr1 | 226875507 | |||||
chr1:226875528
|
C | T | 7 | a0001c0003t0004a0001c0004t0004a0001c0004t0016others(4): Show | 48 | HG00558.hp2 HG01074.hp2 HG01109.hp2 others(45): Show |
5_prime_UTR_variant | MODIFIER | c.-43C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/13 | 6380 | chr1 | 226875528 | |||||
chr1:226895849
|
C | T | 10 | a0001c0001t0001a0001c0001t0010a0001c0001t0012others(7): Show | 183 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(180): Show |
3_prime_UTR_variant | MODIFIER | c.*270C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 13/13 | 270 | chr1 | 226895849 | |||||
chr1:226895984
|
G | T | 2 | a0001c0007t0006a0004c0014t0013 | 6 | HG02055.hp1 HG02280.hp1 HG03098.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*405G>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 13/13 | 405 | chr1 | 226895984 | |||||
chr1:226896066
|
G | C | 1 | a0001c0003t0008 | 3 | HG03490.hp1 HG04184.hp1 HG04204.hp2 |
3_prime_UTR_variant | MODIFIER | c.*487G>C | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 13/13 | 487 | chr1 | 226896066 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:226870697
|
G | T | 1 | a0001c0003t0002g0178 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-350+48G>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 1/12 | chr1 | 226870697 | ||||||
chr1:226870717
|
T | A | 1 | a0001c0001t0001g0046 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-350+68T>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 1/12 | chr1 | 226870717 | ||||||
chr1:226870739
|
T | G | 24 | a0001c0003t0002g0003a0001c0003t0002g0005a0001c0003t0002g0022others(21): Show | 57 | HG00099.hp1 HG00597.hp1 HG00733.hp2 others(54): Show |
intron_variant | MODIFIER | c.-350+90T>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 1/12 | chr1 | 226870739 | ||||||
chr1:226870945
|
C | T | 1 | a0001c0002t0002g0177 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-350+296C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 1/12 | chr1 | 226870945 | ||||||
chr1:226871055
|
T | A | 1 | a0001c0001t0001g0065 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-349-207T>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 1/12 | chr1 | 226871055 | ||||||
chr1:226871112
|
C | G | 12 | a0001c0003t0002g0169a0001c0003t0004g0027a0001c0003t0004g0045others(9): Show | 19 | HG01109.hp2 HG02109.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.-349-150C>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 1/12 | chr1 | 226871112 | ||||||
chr1:226871125
|
C | T | 3 | a0001c0003t0002g0018a0001c0003t0002g0167a0001c0003t0002g0168 | 7 | HG01106.hp1 HG02647.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.-349-137C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 1/12 | chr1 | 226871125 | ||||||
chr1:226871176
|
G | A | 3 | a0001c0002t0002g0066a0001c0002t0002g0067a0001c0002t0002g0068 | 3 | HG01884.hp1 HG02965.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-349-86G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 1/12 | chr1 | 226871176 | ||||||
chr1:226871664
|
T | G | 1 | a0001c0001t0001g0069 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.-207+260T>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/12 | chr1 | 226871664 | ||||||
chr1:226871702
|
G | A | 2 | a0001c0005t0005g0014a0001c0005t0005g0070 | 7 | HG01168.hp2 HG01169.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.-207+298G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/12 | chr1 | 226871702 | ||||||
chr1:226871905
|
C | G | 108 | a0001c0001t0001g0026a0001c0001t0001g0164a0001c0002t0002g0007others(105): Show | 231 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(228): Show |
intron_variant | MODIFIER | c.-207+501C>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/12 | chr1 | 226871905 | ||||||
chr1:226872034
|
C | T | 1 | a0001c0001t0001g0122 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.-207+630C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/12 | chr1 | 226872034 | ||||||
chr1:226872038
|
G | C | 51 | a0001c0001t0014g0071a0001c0002t0002g0007a0001c0002t0002g0012others(48): Show | 114 | HG00280.hp1 HG00423.hp1 HG00558.hp1 others(111): Show |
intron_variant | MODIFIER | c.-207+634G>C | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/12 | chr1 | 226872038 | ||||||
chr1:226872082
|
G | A | 13 | a0001c0003t0004g0161a0001c0004t0004g0013a0001c0004t0004g0025others(10): Show | 22 | HG00558.hp2 HG01074.hp2 HG01358.hp1 others(19): Show |
intron_variant | MODIFIER | c.-207+678G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/12 | chr1 | 226872082 | ||||||
chr1:226872083
|
G | A | 1 | a0001c0001t0001g0072 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-207+679G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/12 | chr1 | 226872083 | ||||||
chr1:226872092
|
T | C | 1 | a0001c0001t0001g0073 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-207+688T>C | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/12 | chr1 | 226872092 | ||||||
chr1:226872227
|
G | A | 1 | a0001c0001t0001g0074 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-207+823G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/12 | chr1 | 226872227 | ||||||
chr1:226872329
|
A | G | 3 | a0001c0002t0002g0066a0001c0002t0002g0067a0001c0002t0002g0068 | 3 | HG01884.hp1 HG02965.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-207+925A>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/12 | chr1 | 226872329 | ||||||
chr1:226872641
|
C | T | 50 | a0001c0002t0002g0007a0001c0002t0002g0012a0001c0002t0002g0038others(47): Show | 113 | HG00280.hp1 HG00423.hp1 HG00558.hp1 others(110): Show |
intron_variant | MODIFIER | c.-207+1237C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/12 | chr1 | 226872641 | ||||||
chr1:226872730
|
A | T | 1 | a0001c0003t0002g0064 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-207+1326A>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/12 | chr1 | 226872730 | ||||||
chr1:226872789
|
A | C | 27 | a0001c0003t0004g0027a0001c0003t0004g0045a0001c0003t0004g0161others(24): Show | 48 | HG00558.hp2 HG01074.hp2 HG01109.hp2 others(45): Show |
intron_variant | MODIFIER | c.-207+1385A>C | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/12 | chr1 | 226872789 | ||||||
chr1:226872811
|
C | A | 1 | a0001c0001t0001g0069 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.-207+1407C>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/12 | chr1 | 226872811 | ||||||
chr1:226872842
|
A | G | 1 | a0001c0001t0010g0120 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-207+1438A>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/12 | chr1 | 226872842 | ||||||
chr1:226872943
|
C | T | 1 | a0001c0001t0001g0119 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-207+1539C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/12 | chr1 | 226872943 | ||||||
chr1:226872975
|
T | C | 106 | a0001c0002t0002g0007a0001c0002t0002g0012a0001c0002t0002g0038others(103): Show | 227 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(224): Show |
intron_variant | MODIFIER | c.-207+1571T>C | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/12 | chr1 | 226872975 | ||||||
chr1:226873016
|
A | T | 1 | a0001c0002t0002g0153 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-207+1612A>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/12 | chr1 | 226873016 | ||||||
chr1:226873107
|
G | A | 1 | a0001c0002t0003g0124 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-207+1703G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/12 | chr1 | 226873107 | ||||||
chr1:226873164
|
C | G | 1 | a0001c0002t0002g0152 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-207+1760C>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/12 | chr1 | 226873164 | ||||||
chr1:226873177
|
C | CA | 14 | a0001c0001t0001g0076a0001c0002t0002g0007a0001c0002t0002g0012others(11): Show | 32 | HG00423.hp1 HG00558.hp1 HG01099.hp2 others(29): Show |
intron_variant | MODIFIER | c.-207+1786dupA | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr1 | 226873177 | |||||
chr1:226873177
|
CA | C | 14 | a0001c0001t0001g0118a0001c0003t0004g0027a0001c0003t0004g0045others(11): Show | 26 | HG01109.hp2 HG01168.hp2 HG01169.hp1 others(23): Show |
intron_variant | MODIFIER | c.-207+1786delA | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr1 | 226873177 | |||||
chr1:226873425
|
T | A | 13 | a0001c0003t0004g0161a0001c0004t0004g0013a0001c0004t0004g0025others(10): Show | 21 | HG00558.hp2 HG01074.hp2 HG01358.hp1 others(18): Show |
intron_variant | MODIFIER | c.-206-1940T>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/12 | chr1 | 226873425 | ||||||
chr1:226873465
|
G | A | 2 | a0001c0004t0004g0154a0001c0004t0004g0155 | 2 | NA18972.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.-206-1900G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/12 | chr1 | 226873465 | ||||||
chr1:226873513
|
T | C | 1 | a0001c0001t0001g0077 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-206-1852T>C | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/12 | chr1 | 226873513 | ||||||
chr1:226873604
|
C | T | 26 | a0001c0002t0003g0002a0001c0002t0003g0008a0001c0002t0003g0040others(23): Show | 64 | HG00280.hp1 HG00621.hp1 HG00738.hp2 others(61): Show |
intron_variant | MODIFIER | c.-206-1761C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/12 | chr1 | 226873604 | ||||||
chr1:226873721
|
A | G | 11 | a0001c0001t0001g0006a0001c0001t0001g0046a0001c0001t0001g0109others(8): Show | 20 | HG00140.hp1 HG00323.hp1 HG00597.hp2 others(17): Show |
intron_variant | MODIFIER | c.-206-1644A>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/12 | chr1 | 226873721 | ||||||
chr1:226873784
|
A | G | 25 | a0001c0003t0002g0003a0001c0003t0002g0005a0001c0003t0002g0018others(22): Show | 62 | HG00099.hp1 HG00597.hp1 HG00733.hp2 others(59): Show |
intron_variant | MODIFIER | c.-206-1581A>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/12 | chr1 | 226873784 | ||||||
chr1:226873888
|
C | G | 27 | a0001c0003t0004g0027a0001c0003t0004g0045a0001c0003t0004g0161others(24): Show | 48 | HG00558.hp2 HG01074.hp2 HG01109.hp2 others(45): Show |
intron_variant | MODIFIER | c.-206-1477C>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/12 | chr1 | 226873888 | ||||||
chr1:226873954
|
T | A | 50 | a0001c0002t0002g0007a0001c0002t0002g0012a0001c0002t0002g0038others(47): Show | 113 | HG00280.hp1 HG00423.hp1 HG00558.hp1 others(110): Show |
intron_variant | MODIFIER | c.-206-1411T>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/12 | chr1 | 226873954 | ||||||
chr1:226874007
|
C | G | 1 | a0004c0014t0013g0049 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-206-1358C>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/12 | chr1 | 226874007 | ||||||
chr1:226874011
|
A | C | 17 | a0001c0002t0002g0007a0001c0002t0002g0012a0001c0002t0002g0038others(14): Show | 38 | HG00423.hp1 HG00558.hp1 HG01099.hp2 others(35): Show |
intron_variant | MODIFIER | c.-206-1354A>C | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/12 | chr1 | 226874011 | ||||||
chr1:226874062
|
C | A | 14 | a0001c0003t0004g0161a0001c0004t0004g0013a0001c0004t0004g0025others(11): Show | 23 | HG00558.hp2 HG01074.hp2 HG01358.hp1 others(20): Show |
intron_variant | MODIFIER | c.-206-1303C>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/12 | chr1 | 226874062 | ||||||
chr1:226874145
|
A | T | 1 | a0001c0006t0002g0024 | 3 | HG01891.hp1 HG03098.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-206-1220A>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/12 | chr1 | 226874145 | ||||||
chr1:226874246
|
G | A | 12 | a0001c0002t0002g0007a0001c0002t0002g0012a0001c0002t0002g0038others(9): Show | 30 | HG00423.hp1 HG00558.hp1 HG01099.hp2 others(27): Show |
intron_variant | MODIFIER | c.-206-1119G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/12 | chr1 | 226874246 | ||||||
chr1:226874272
|
G | A | 1 | a0001c0003t0004g0170 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-206-1093G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/12 | chr1 | 226874272 | ||||||
chr1:226874349
|
G | A | 5 | a0001c0005t0004g0021a0001c0005t0004g0044a0001c0005t0004g0171others(2): Show | 14 | HG01168.hp2 HG01169.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.-206-1016G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/12 | chr1 | 226874349 | ||||||
chr1:226874428
|
C | A | 106 | a0001c0002t0002g0007a0001c0002t0002g0012a0001c0002t0002g0038others(103): Show | 227 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(224): Show |
intron_variant | MODIFIER | c.-206-937C>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/12 | chr1 | 226874428 | ||||||
chr1:226874436
|
G | A | 1 | a0001c0001t0001g0078 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-206-929G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/12 | chr1 | 226874436 | ||||||
chr1:226874456
|
A | G | 27 | a0001c0003t0004g0027a0001c0003t0004g0045a0001c0003t0004g0161others(24): Show | 48 | HG00558.hp2 HG01074.hp2 HG01109.hp2 others(45): Show |
intron_variant | MODIFIER | c.-206-909A>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/12 | chr1 | 226874456 | ||||||
chr1:226874462
|
A | G | 1 | a0001c0001t0001g0108 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-206-903A>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/12 | chr1 | 226874462 | ||||||
chr1:226874627
|
T | C | 27 | a0001c0003t0004g0027a0001c0003t0004g0045a0001c0003t0004g0161others(24): Show | 48 | HG00558.hp2 HG01074.hp2 HG01109.hp2 others(45): Show |
intron_variant | MODIFIER | c.-206-738T>C | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/12 | chr1 | 226874627 | ||||||
chr1:226874688
|
T | C | 27 | a0001c0003t0004g0027a0001c0003t0004g0045a0001c0003t0004g0161others(24): Show | 48 | HG00558.hp2 HG01074.hp2 HG01109.hp2 others(45): Show |
intron_variant | MODIFIER | c.-206-677T>C | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/12 | chr1 | 226874688 | ||||||
chr1:226874727
|
G | A | 1 | a0001c0001t0001g0109 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-206-638G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/12 | chr1 | 226874727 | ||||||
chr1:226874784
|
C | G | 27 | a0001c0003t0004g0027a0001c0003t0004g0045a0001c0003t0004g0161others(24): Show | 48 | HG00558.hp2 HG01074.hp2 HG01109.hp2 others(45): Show |
intron_variant | MODIFIER | c.-206-581C>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/12 | chr1 | 226874784 | ||||||
chr1:226874834
|
A | T | 1 | a0001c0003t0002g0063 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-206-531A>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/12 | chr1 | 226874834 | ||||||
chr1:226874901
|
G | A | 3 | a0001c0001t0001g0028a0001c0001t0001g0079a0001c0001t0001g0080 | 4 | HG01167.hp1 HG01169.hp2 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.-206-464G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/12 | chr1 | 226874901 | ||||||
chr1:226874905
|
G | T | 20 | a0001c0003t0002g0003a0001c0003t0002g0005a0001c0003t0002g0022others(17): Show | 53 | HG00099.hp1 HG00597.hp1 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.-206-460G>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/12 | chr1 | 226874905 | ||||||
chr1:226874947
|
G | A | 1 | a0001c0001t0001g0023 | 3 | NA18906.hp1 NA19030.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-206-418G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/12 | chr1 | 226874947 | ||||||
chr1:226875101
|
C | T | 1 | a0002c0011t0004g0043 | 2 | HG02896.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.-206-264C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/12 | chr1 | 226875101 | ||||||
chr1:226875130
|
G | A | 50 | a0001c0002t0002g0007a0001c0002t0002g0012a0001c0002t0002g0038others(47): Show | 113 | HG00280.hp1 HG00423.hp1 HG00558.hp1 others(110): Show |
intron_variant | MODIFIER | c.-206-235G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/12 | chr1 | 226875130 | ||||||
chr1:226875217
|
A | G | 2 | a0001c0002t0002g0127a0001c0002t0002g0128 | 2 | NA18981.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.-206-148A>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/12 | chr1 | 226875217 | ||||||
chr1:226875308
|
G | A | 5 | a0001c0003t0004g0045a0001c0003t0004g0170a0001c0003t0004g0172others(2): Show | 6 | HG02886.hp1 HG02976.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.-206-57G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/12 | chr1 | 226875308 | ||||||
chr1:226875671
|
C | T | 1 | a0004c0014t0013g0049 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-21+121C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226875671 | ||||||
chr1:226875699
|
C | T | 50 | a0001c0002t0002g0007a0001c0002t0002g0012a0001c0002t0002g0038others(47): Show | 113 | HG00280.hp1 HG00423.hp1 HG00558.hp1 others(110): Show |
intron_variant | MODIFIER | c.-21+149C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226875699 | ||||||
chr1:226875786
|
A | G | 1 | a0001c0001t0001g0107 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-21+236A>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226875786 | ||||||
chr1:226875970
|
T | C | 118 | a0001c0001t0001g0011a0001c0001t0001g0016a0001c0001t0001g0029others(115): Show | 250 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(247): Show |
intron_variant | MODIFIER | c.-21+420T>C | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226875970 | ||||||
chr1:226876031
|
G | T | 13 | a0001c0003t0004g0161a0001c0004t0004g0013a0001c0004t0004g0025others(10): Show | 21 | HG00558.hp2 HG01074.hp2 HG01358.hp1 others(18): Show |
intron_variant | MODIFIER | c.-21+481G>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226876031 | ||||||
chr1:226876098
|
C | T | 1 | a0001c0002t0003g0151 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-21+548C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226876098 | ||||||
chr1:226876105
|
C | T | 1 | a0001c0001t0001g0087 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-21+555C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226876105 | ||||||
chr1:226876143
|
C | T | 1 | a0001c0007t0006g0106 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-21+593C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226876143 | ||||||
chr1:226876172
|
A | G | 1 | a0001c0002t0003g0150 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-21+622A>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226876172 | ||||||
chr1:226876250
|
AC | A | 4 | a0001c0006t0002g0015a0001c0006t0002g0129a0001c0009t0002g0015others(1): Show | 8 | HG01891.hp2 HG02145.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-21+701delC | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226876250 | ||||||
chr1:226876306
|
C | A | 2 | a0001c0004t0004g0156a0001c0004t0004g0157 | 2 | HG02698.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.-21+756C>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226876306 | ||||||
chr1:226876348
|
G | A | 2 | a0001c0004t0004g0158a0001c0004t0004g0159 | 2 | NA18747.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.-21+798G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226876348 | ||||||
chr1:226876483
|
G | T | 2 | a0001c0006t0002g0024a0001c0006t0002g0133 | 4 | HG01891.hp1 HG02922.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-21+933G>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226876483 | ||||||
chr1:226876560
|
C | A | 27 | a0001c0003t0004g0027a0001c0003t0004g0045a0001c0003t0004g0161others(24): Show | 48 | HG00558.hp2 HG01074.hp2 HG01109.hp2 others(45): Show |
intron_variant | MODIFIER | c.-21+1010C>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226876560 | ||||||
chr1:226876606
|
T | C | 27 | a0001c0003t0004g0027a0001c0003t0004g0045a0001c0003t0004g0161others(24): Show | 48 | HG00558.hp2 HG01074.hp2 HG01109.hp2 others(45): Show |
intron_variant | MODIFIER | c.-21+1056T>C | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226876606 | ||||||
chr1:226876629
|
C | T | 2 | a0001c0012t0002g0061a0001c0012t0002g0062 | 2 | NA18944.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.-21+1079C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226876629 | ||||||
chr1:226876679
|
G | A | 1 | a0001c0003t0002g0050 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-21+1129G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226876679 | ||||||
chr1:226876694
|
C | T | 1 | a0001c0001t0001g0117 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-21+1144C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226876694 | ||||||
chr1:226876926
|
T | C | 5 | a0001c0003t0002g0018a0001c0003t0002g0167a0001c0003t0002g0168others(2): Show | 9 | HG01106.hp1 HG02572.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.-21+1376T>C | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226876926 | ||||||
chr1:226877019
|
G | A | 14 | a0001c0003t0004g0161a0001c0004t0004g0013a0001c0004t0004g0025others(11): Show | 23 | HG00558.hp2 HG01074.hp2 HG01358.hp1 others(20): Show |
intron_variant | MODIFIER | c.-21+1469G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226877019 | ||||||
chr1:226877167
|
C | G | 1 | a0001c0003t0002g0064 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-21+1617C>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226877167 | ||||||
chr1:226877180
|
AG | A | 5 | a0001c0005t0004g0021a0001c0005t0004g0044a0001c0005t0004g0171others(2): Show | 14 | HG01168.hp2 HG01169.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.-21+1631delG | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226877180 | ||||||
chr1:226877205
|
C | T | 1 | a0001c0002t0002g0128 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-21+1655C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226877205 | ||||||
chr1:226877272
|
G | T | 27 | a0001c0003t0004g0027a0001c0003t0004g0045a0001c0003t0004g0161others(24): Show | 48 | HG00558.hp2 HG01074.hp2 HG01109.hp2 others(45): Show |
intron_variant | MODIFIER | c.-21+1722G>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226877272 | ||||||
chr1:226877384
|
G | A | 1 | a0001c0003t0002g0051 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.-21+1834G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226877384 | ||||||
chr1:226877565
|
G | T | 3 | a0001c0001t0001g0010a0001c0001t0001g0074a0001c0001t0001g0105 | 10 | HG00673.hp2 NA18941.hp2 NA18954.hp1 others(7): Show |
intron_variant | MODIFIER | c.-21+2015G>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226877565 | ||||||
chr1:226877673
|
G | A | 1 | a0001c0005t0004g0044 | 2 | HG02723.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-21+2123G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226877673 | ||||||
chr1:226877777
|
G | A | 19 | a0001c0003t0002g0003a0001c0003t0002g0005a0001c0003t0002g0022others(16): Show | 52 | HG00099.hp1 HG00597.hp1 HG00733.hp2 others(49): Show |
intron_variant | MODIFIER | c.-21+2227G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226877777 | ||||||
chr1:226878040
|
A | G | 1 | a0001c0003t0002g0059 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-21+2490A>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226878040 | ||||||
chr1:226878153
|
C | T | 17 | a0001c0002t0002g0007a0001c0002t0002g0012a0001c0002t0002g0038others(14): Show | 38 | HG00423.hp1 HG00558.hp1 HG01099.hp2 others(35): Show |
intron_variant | MODIFIER | c.-21+2603C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226878153 | ||||||
chr1:226878154
|
A | G | 1 | a0001c0001t0001g0037 | 2 | NA19002.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.-21+2604A>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226878154 | ||||||
chr1:226878211
|
C | A | 1 | a0001c0003t0004g0172 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-21+2661C>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226878211 | ||||||
chr1:226878241
|
A | C | 2 | a0001c0004t0004g0025a0001c0004t0004g0163 | 4 | HG01074.hp2 HG01358.hp1 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.-21+2691A>C | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226878241 | ||||||
chr1:226878328
|
C | T | 2 | a0001c0002t0003g0042a0001c0002t0003g0149 | 3 | NA18950.hp1 NA18957.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.-21+2778C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226878328 | ||||||
chr1:226878355
|
A | T | 1 | a0003c0010t0001g0166 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-21+2805A>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226878355 | ||||||
chr1:226878440
|
C | T | 1 | a0001c0001t0001g0036 | 2 | HG02056.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.-21+2890C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226878440 | ||||||
chr1:226878509
|
T | G | 1 | a0001c0001t0001g0073 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-21+2959T>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226878509 | ||||||
chr1:226878546
|
A | C | 1 | a0001c0001t0001g0116 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-21+2996A>C | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226878546 | ||||||
chr1:226878673
|
A | T | 1 | a0001c0002t0003g0148 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-21+3123A>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226878673 | ||||||
chr1:226878675
|
A | G | 1 | a0003c0010t0001g0165 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-21+3125A>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226878675 | ||||||
chr1:226878881
|
T | C | 4 | a0001c0002t0002g0153a0001c0003t0004g0027a0001c0003t0004g0176others(1): Show | 6 | HG01109.hp2 HG02109.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.-20-3007T>C | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226878881 | ||||||
chr1:226879172
|
C | T | 4 | a0001c0002t0003g0145a0001c0002t0003g0146a0001c0002t0003g0147others(1): Show | 4 | HG02145.hp2 NA18976.hp2 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20-2716C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226879172 | ||||||
chr1:226879195
|
C | G | 7 | a0001c0001t0001g0004a0001c0001t0001g0035a0001c0001t0001g0076others(4): Show | 23 | HG00408.hp1 HG00438.hp1 HG01081.hp2 others(20): Show |
intron_variant | MODIFIER | c.-20-2693C>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226879195 | ||||||
chr1:226879288
|
T | A | 1 | a0001c0002t0002g0125 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-20-2600T>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226879288 | ||||||
chr1:226879289
|
C | T | 1 | a0001c0002t0002g0125 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-20-2599C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226879289 | ||||||
chr1:226879571
|
C | G | 2 | a0001c0001t0001g0085a0001c0001t0001g0086 | 2 | HG00280.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.-20-2317C>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226879571 | ||||||
chr1:226879641
|
C | G | 2 | a0001c0001t0001g0101a0001c0001t0001g0108 | 2 | HG03471.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-20-2247C>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226879641 | ||||||
chr1:226879758
|
C | T | 14 | a0001c0003t0004g0161a0001c0004t0004g0013a0001c0004t0004g0025others(11): Show | 23 | HG00558.hp2 HG01074.hp2 HG01358.hp1 others(20): Show |
intron_variant | MODIFIER | c.-20-2130C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226879758 | ||||||
chr1:226879955
|
G | A | 9 | a0001c0001t0001g0017a0001c0001t0001g0028a0001c0001t0001g0073others(6): Show | 12 | HG00099.hp2 HG01167.hp1 HG01168.hp1 others(9): Show |
intron_variant | MODIFIER | c.-20-1933G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226879955 | ||||||
chr1:226880000
|
A | G | 1 | a0001c0001t0001g0100 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-20-1888A>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226880000 | ||||||
chr1:226880042
|
T | C | 1 | a0001c0001t0001g0081 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-20-1846T>C | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226880042 | ||||||
chr1:226880074
|
T | G | 1 | a0001c0002t0003g0148 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-20-1814T>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226880074 | ||||||
chr1:226880075
|
G | T | 1 | a0001c0002t0003g0148 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-20-1813G>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226880075 | ||||||
chr1:226880076
|
T | G | 1 | a0001c0002t0003g0148 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-20-1812T>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226880076 | ||||||
chr1:226880213
|
A | G | 13 | a0001c0003t0004g0027a0001c0003t0004g0045a0001c0003t0004g0170others(10): Show | 25 | HG01109.hp2 HG01168.hp2 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.-20-1675A>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226880213 | ||||||
chr1:226880245
|
C | T | 1 | a0001c0001t0001g0119 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-20-1643C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226880245 | ||||||
chr1:226880348
|
A | G | 27 | a0001c0003t0004g0027a0001c0003t0004g0045a0001c0003t0004g0161others(24): Show | 48 | HG00558.hp2 HG01074.hp2 HG01109.hp2 others(45): Show |
intron_variant | MODIFIER | c.-20-1540A>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226880348 | ||||||
chr1:226880350
|
G | A | 1 | a0001c0003t0002g0052 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-20-1538G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226880350 | ||||||
chr1:226880526
|
G | A | 13 | a0001c0003t0004g0161a0001c0004t0004g0013a0001c0004t0004g0025others(10): Show | 21 | HG00558.hp2 HG01074.hp2 HG01358.hp1 others(18): Show |
intron_variant | MODIFIER | c.-20-1362G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226880526 | ||||||
chr1:226880545
|
A | AGACAGCG others(15): Show |
122 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(119): Show | 283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.-20-1289_-20-1268d others(24): Show |
PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr1 | 226880545 | |||||
chr1:226880545
|
A | AGACAGCG others(37): Show |
1 | a0001c0001t0001g0084 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-20-1311_-20-1268d others(46): Show |
PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr1 | 226880545 | |||||
chr1:226880545
|
AGACAGCG others(15): Show |
A | 13 | a0001c0003t0004g0027a0001c0003t0004g0045a0001c0003t0004g0170others(10): Show | 25 | HG01109.hp2 HG01168.hp2 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.-20-1289_-20-1268d others(24): Show |
PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr1 | 226880545 | |||||
chr1:226880621
|
A | C | 2 | a0001c0001t0001g0034a0001c0003t0002g0058 | 3 | HG02004.hp2 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-20-1267A>C | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226880621 | ||||||
chr1:226880633
|
G | T | 1 | a0001c0002t0003g0041 | 2 | HG01071.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.-20-1255G>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226880633 | ||||||
chr1:226880697
|
G | T | 27 | a0001c0003t0004g0027a0001c0003t0004g0045a0001c0003t0004g0161others(24): Show | 48 | HG00558.hp2 HG01074.hp2 HG01109.hp2 others(45): Show |
intron_variant | MODIFIER | c.-20-1191G>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226880697 | ||||||
chr1:226880771
|
G | A | 13 | a0001c0003t0004g0027a0001c0003t0004g0045a0001c0003t0004g0170others(10): Show | 25 | HG01109.hp2 HG01168.hp2 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.-20-1117G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226880771 | ||||||
chr1:226881169
|
A | G | 1 | a0002c0011t0004g0043 | 2 | HG02896.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.-20-719A>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226881169 | ||||||
chr1:226881293
|
C | T | 1 | a0001c0002t0003g0144 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-20-595C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226881293 | ||||||
chr1:226881544
|
C | G | 7 | a0001c0002t0002g0066a0001c0002t0002g0067a0001c0002t0002g0068others(4): Show | 11 | HG01884.hp1 HG01891.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.-20-344C>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226881544 | ||||||
chr1:226881566
|
A | G | 81 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(78): Show | 188 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.-20-322A>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226881566 | ||||||
chr1:226881636
|
C | T | 2 | a0001c0001t0001g0099a0001c0001t0001g0100 | 2 | HG02109.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.-20-252C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226881636 | ||||||
chr1:226881656
|
C | T | 2 | a0001c0006t0002g0024a0001c0006t0002g0133 | 4 | HG01891.hp1 HG02922.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20-232C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226881656 | ||||||
chr1:226881658
|
T | A | 1 | a0001c0002t0003g0148 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-20-230T>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226881658 | ||||||
chr1:226881714
|
A | G | 1 | a0001c0001t0001g0073 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-20-174A>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226881714 | ||||||
chr1:226882078
|
A | G | 5 | a0001c0003t0004g0045a0001c0003t0004g0170a0001c0003t0004g0172others(2): Show | 6 | HG02886.hp1 HG02976.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.141+30A>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 4/12 | chr1 | 226882078 | ||||||
chr1:226882102
|
C | G | 1 | a0001c0004t0004g0159 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.141+54C>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 4/12 | chr1 | 226882102 | ||||||
chr1:226882106
|
A | G | 4 | a0001c0006t0002g0015a0001c0006t0002g0129a0001c0009t0002g0015others(1): Show | 8 | HG01891.hp2 HG02145.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.141+58A>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 4/12 | chr1 | 226882106 | ||||||
chr1:226882173
|
C | G | 13 | a0001c0003t0004g0027a0001c0003t0004g0045a0001c0003t0004g0170others(10): Show | 25 | HG01109.hp2 HG01168.hp2 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.141+125C>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 4/12 | chr1 | 226882173 | ||||||
chr1:226882238
|
A | G | 1 | a0001c0001t0001g0098 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.141+190A>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 4/12 | chr1 | 226882238 | ||||||
chr1:226882417
|
G | C | 5 | a0001c0002t0003g0040a0001c0002t0003g0134a0001c0002t0003g0135others(2): Show | 6 | HG02040.hp2 HG02056.hp2 NA18948.hp1 others(3): Show |
intron_variant | MODIFIER | c.141+369G>C | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 4/12 | chr1 | 226882417 | ||||||
chr1:226882446
|
G | C | 1 | a0001c0001t0001g0082 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.141+398G>C | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 4/12 | chr1 | 226882446 | ||||||
chr1:226882502
|
C | G | 5 | a0001c0003t0002g0018a0001c0003t0002g0167a0001c0003t0002g0168others(2): Show | 9 | HG01106.hp1 HG02572.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.141+454C>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 4/12 | chr1 | 226882502 | ||||||
chr1:226882531
|
C | T | 1 | a0001c0003t0004g0176 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.141+483C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 4/12 | chr1 | 226882531 | ||||||
chr1:226882551
|
C | T | 2 | a0001c0003t0002g0005a0001c0003t0002g0057 | 13 | NA18942.hp1 NA18946.hp1 NA18949.hp1 others(10): Show |
intron_variant | MODIFIER | c.141+503C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 4/12 | chr1 | 226882551 | ||||||
chr1:226882677
|
C | T | 81 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(78): Show | 188 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.141+629C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 4/12 | chr1 | 226882677 | ||||||
chr1:226882899
|
G | A | 5 | a0001c0003t0004g0045a0001c0003t0004g0170a0001c0003t0004g0172others(2): Show | 6 | HG02886.hp1 HG02976.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.142-806G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 4/12 | chr1 | 226882899 | ||||||
chr1:226882994
|
C | T | 81 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(78): Show | 188 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.142-711C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 4/12 | chr1 | 226882994 | ||||||
chr1:226883099
|
ACCT | A | 4 | a0001c0006t0002g0015a0001c0006t0002g0129a0001c0009t0002g0015others(1): Show | 8 | HG01891.hp2 HG02145.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.142-601_142-599del others(3): Show |
PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr1 | 226883099 | |||||
chr1:226883253
|
T | C | 3 | a0001c0002t0002g0039a0001c0002t0002g0131a0001c0002t0017g0132 | 4 | HG02280.hp2 HG02922.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.142-452T>C | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 4/12 | chr1 | 226883253 | ||||||
chr1:226883307
|
G | A | 1 | a0002c0011t0004g0043 | 2 | HG02896.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.142-398G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 4/12 | chr1 | 226883307 | ||||||
chr1:226883335
|
C | T | 4 | a0001c0006t0002g0015a0001c0006t0002g0129a0001c0009t0002g0015others(1): Show | 8 | HG01891.hp2 HG02145.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.142-370C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 4/12 | chr1 | 226883335 | ||||||
chr1:226883347
|
T | C | 154 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(151): Show | 340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.142-358T>C | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 4/12 | chr1 | 226883347 | ||||||
chr1:226883423
|
C | A | 5 | a0001c0003t0004g0045a0001c0003t0004g0170a0001c0003t0004g0172others(2): Show | 6 | HG02886.hp1 HG02976.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.142-282C>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 4/12 | chr1 | 226883423 | ||||||
chr1:226883483
|
A | C | 1 | a0001c0002t0003g0143 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.142-222A>C | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 4/12 | chr1 | 226883483 | ||||||
chr1:226883493
|
T | C | 1 | a0001c0003t0002g0054 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.142-212T>C | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 4/12 | chr1 | 226883493 | ||||||
chr1:226883570
|
G | T | 1 | a0001c0002t0002g0068 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.142-135G>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 4/12 | chr1 | 226883570 | ||||||
chr1:226883584
|
G | A | 13 | a0001c0003t0004g0161a0001c0004t0004g0013a0001c0004t0004g0025others(10): Show | 21 | HG00558.hp2 HG01074.hp2 HG01358.hp1 others(18): Show |
intron_variant | MODIFIER | c.142-121G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 4/12 | chr1 | 226883584 | ||||||
chr1:226883585
|
C | T | 1 | a0001c0004t0004g0157 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.142-120C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 4/12 | chr1 | 226883585 | ||||||
chr1:226883663
|
G | A | 81 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(78): Show | 188 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.142-42G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 4/12 | chr1 | 226883663 | ||||||
chr1:226883676
|
T | C | 110 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(107): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.142-29T>C | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 4/12 | chr1 | 226883676 | ||||||
chr1:226883678
|
C | T | 2 | a0001c0001t0001g0035a0001c0001t0001g0104 | 3 | HG02132.hp2 HG02155.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.142-27C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 4/12 | chr1 | 226883678 | ||||||
chr1:226883682
|
C | T | 1 | a0002c0011t0004g0043 | 2 | HG02896.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.142-23C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 4/12 | chr1 | 226883682 | ||||||
chr1:226883683
|
C | T | 1 | a0001c0001t0001g0083 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.142-22C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 4/12 | chr1 | 226883683 | ||||||
chr1:226883983
|
G | A | 1 | a0001c0001t0001g0046 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.356+64G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 5/12 | chr1 | 226883983 | ||||||
chr1:226884002
|
A | C | 13 | a0001c0003t0004g0027a0001c0003t0004g0045a0001c0003t0004g0170others(10): Show | 25 | HG01109.hp2 HG01168.hp2 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.356+83A>C | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 5/12 | chr1 | 226884002 | ||||||
chr1:226884065
|
T | C | 27 | a0001c0003t0002g0003a0001c0003t0002g0005a0001c0003t0002g0018others(24): Show | 64 | HG00099.hp1 HG00597.hp1 HG00733.hp2 others(61): Show |
intron_variant | MODIFIER | c.356+146T>C | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 5/12 | chr1 | 226884065 | ||||||
chr1:226884300
|
C | T | 27 | a0001c0003t0002g0003a0001c0003t0002g0005a0001c0003t0002g0018others(24): Show | 64 | HG00099.hp1 HG00597.hp1 HG00733.hp2 others(61): Show |
intron_variant | MODIFIER | c.356+381C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 5/12 | chr1 | 226884300 | ||||||
chr1:226884447
|
G | A | 2 | a0001c0016t0009g0048a0001c0017t0009g0047 | 2 | HG02615.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.356+528G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 5/12 | chr1 | 226884447 | ||||||
chr1:226884538
|
C | CT | 22 | a0001c0001t0001g0115a0001c0003t0002g0003a0001c0003t0002g0005others(19): Show | 57 | HG00597.hp1 HG00733.hp2 HG01106.hp1 others(54): Show |
intron_variant | MODIFIER | c.356+635dupT | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr1 | 226884538 | |||||
chr1:226884538
|
CT | C | 29 | a0001c0001t0001g0081a0001c0001t0001g0089a0001c0001t0001g0090others(26): Show | 41 | HG01109.hp2 HG01167.hp2 HG01168.hp2 others(38): Show |
intron_variant | MODIFIER | c.356+635delT | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr1 | 226884538 | |||||
chr1:226884554
|
T | A | 3 | a0001c0002t0002g0066a0001c0002t0002g0067a0001c0002t0002g0068 | 3 | HG01884.hp1 HG02965.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.356+635T>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 5/12 | chr1 | 226884554 | ||||||
chr1:226884566
|
T | C | 137 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(134): Show | 302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.356+647T>C | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 5/12 | chr1 | 226884566 | ||||||
chr1:226884600
|
G | T | 2 | a0001c0001t0001g0114a0001c0002t0003g0142 | 2 | HG02135.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.356+681G>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 5/12 | chr1 | 226884600 | ||||||
chr1:226884610
|
T | C | 17 | a0001c0002t0002g0007a0001c0002t0002g0012a0001c0002t0002g0038others(14): Show | 38 | HG00423.hp1 HG00558.hp1 HG01099.hp2 others(35): Show |
intron_variant | MODIFIER | c.356+691T>C | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 5/12 | chr1 | 226884610 | ||||||
chr1:226884700
|
G | A | 1 | a0001c0002t0002g0177 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.356+781G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 5/12 | chr1 | 226884700 | ||||||
chr1:226884787
|
G | A | 1 | a0001c0002t0003g0134 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.357-751G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 5/12 | chr1 | 226884787 | ||||||
chr1:226884923
|
A | T | 1 | a0001c0001t0001g0097 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.357-615A>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 5/12 | chr1 | 226884923 | ||||||
chr1:226884985
|
C | T | 1 | a0004c0014t0013g0049 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.357-553C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 5/12 | chr1 | 226884985 | ||||||
chr1:226885130
|
A | G | 137 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(134): Show | 302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.357-408A>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 5/12 | chr1 | 226885130 | ||||||
chr1:226885139
|
G | A | 5 | a0001c0001t0001g0009a0001c0001t0001g0089a0001c0001t0001g0091others(2): Show | 15 | HG01261.hp2 HG01884.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.357-399G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 5/12 | chr1 | 226885139 | ||||||
chr1:226885239
|
G | A | 13 | a0001c0003t0004g0027a0001c0003t0004g0045a0001c0003t0004g0170others(10): Show | 25 | HG01109.hp2 HG01168.hp2 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.357-299G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 5/12 | chr1 | 226885239 | ||||||
chr1:226885287
|
A | C | 2 | a0001c0016t0009g0048a0001c0017t0009g0047 | 2 | HG02615.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.357-251A>C | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 5/12 | chr1 | 226885287 | ||||||
chr1:226885408
|
C | T | 1 | a0001c0001t0001g0164 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.357-130C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 5/12 | chr1 | 226885408 | ||||||
chr1:226885410
|
A | T | 1 | a0001c0001t0001g0164 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.357-128A>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 5/12 | chr1 | 226885410 | ||||||
chr1:226885504
|
G | C | 1 | a0001c0002t0003g0146 | 1 | NA18976.hp2 | intron_variant | MODIFIER | c.357-34G>C | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 5/12 | chr1 | 226885504 | ||||||
chr1:226885694
|
C | T | 1 | a0001c0002t0003g0136 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.498+15C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 6/12 | chr1 | 226885694 | ||||||
chr1:226885709
|
G | C | 137 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(134): Show | 302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.498+30G>C | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 6/12 | chr1 | 226885709 | ||||||
chr1:226885747
|
C | G | 1 | a0001c0001t0001g0082 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.498+68C>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 6/12 | chr1 | 226885747 | ||||||
chr1:226885824
|
C | T | 1 | a0001c0002t0003g0142 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.498+145C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 6/12 | chr1 | 226885824 | ||||||
chr1:226885958
|
C | T | 1 | a0001c0004t0004g0156 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.498+279C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 6/12 | chr1 | 226885958 | ||||||
chr1:226885964
|
G | A | 2 | a0001c0001t0001g0026a0001c0001t0001g0164 | 4 | NA18945.hp2 NA18984.hp2 NA18997.hp2 others(1): Show |
intron_variant | MODIFIER | c.498+285G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 6/12 | chr1 | 226885964 | ||||||
chr1:226885968
|
C | CAAG | 109 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(106): Show | 237 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.498+290_498+292dup others(3): Show |
PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr1 | 226885968 | |||||
chr1:226885976
|
C | T | 1 | a0001c0001t0001g0113 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.498+297C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 6/12 | chr1 | 226885976 | ||||||
chr1:226886011
|
T | G | 109 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(106): Show | 237 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.498+332T>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 6/12 | chr1 | 226886011 | ||||||
chr1:226886040
|
A | T | 56 | a0001c0003t0002g0003a0001c0003t0002g0005a0001c0003t0002g0018others(53): Show | 114 | HG00099.hp1 HG00558.hp2 HG00597.hp1 others(111): Show |
intron_variant | MODIFIER | c.498+361A>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 6/12 | chr1 | 226886040 | ||||||
chr1:226886210
|
A | G | 1 | a0001c0005t0004g0044 | 2 | HG02723.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.498+531A>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 6/12 | chr1 | 226886210 | ||||||
chr1:226886246
|
A | T | 1 | a0001c0002t0003g0146 | 1 | NA18976.hp2 | intron_variant | MODIFIER | c.498+567A>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 6/12 | chr1 | 226886246 | ||||||
chr1:226886301
|
C | T | 25 | a0001c0003t0004g0027a0001c0003t0004g0045a0001c0003t0004g0161others(22): Show | 45 | HG00558.hp2 HG01074.hp2 HG01109.hp2 others(42): Show |
intron_variant | MODIFIER | c.498+622C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 6/12 | chr1 | 226886301 | ||||||
chr1:226886346
|
C | T | 1 | a0001c0005t0004g0171 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.498+667C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 6/12 | chr1 | 226886346 | ||||||
chr1:226886424
|
G | A | 108 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(105): Show | 252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.498+745G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 6/12 | chr1 | 226886424 | ||||||
chr1:226886451
|
C | G | 13 | a0001c0003t0004g0161a0001c0004t0004g0013a0001c0004t0004g0025others(10): Show | 21 | HG00558.hp2 HG01074.hp2 HG01358.hp1 others(18): Show |
intron_variant | MODIFIER | c.498+772C>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 6/12 | chr1 | 226886451 | ||||||
chr1:226886539
|
G | T | 1 | a0001c0005t0005g0070 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.498+860G>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 6/12 | chr1 | 226886539 | ||||||
chr1:226886559
|
C | T | 1 | a0001c0003t0002g0053 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.498+880C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 6/12 | chr1 | 226886559 | ||||||
chr1:226886642
|
G | A | 13 | a0001c0003t0004g0161a0001c0004t0004g0013a0001c0004t0004g0025others(10): Show | 21 | HG00558.hp2 HG01074.hp2 HG01358.hp1 others(18): Show |
intron_variant | MODIFIER | c.498+963G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 6/12 | chr1 | 226886642 | ||||||
chr1:226886739
|
C | T | 2 | a0001c0001t0001g0016a0001c0001t0001g0087 | 6 | HG02572.hp1 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.498+1060C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 6/12 | chr1 | 226886739 | ||||||
chr1:226886837
|
C | T | 1 | a0001c0002t0003g0141 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.498+1158C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 6/12 | chr1 | 226886837 | ||||||
chr1:226886909
|
C | T | 1 | a0001c0002t0003g0146 | 1 | NA18976.hp2 | intron_variant | MODIFIER | c.499-1182C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 6/12 | chr1 | 226886909 | ||||||
chr1:226886910
|
T | G | 1 | a0001c0002t0003g0146 | 1 | NA18976.hp2 | intron_variant | MODIFIER | c.499-1181T>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 6/12 | chr1 | 226886910 | ||||||
chr1:226886924
|
C | A | 5 | a0001c0003t0004g0045a0001c0003t0004g0170a0001c0003t0004g0172others(2): Show | 6 | HG02886.hp1 HG02976.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.499-1167C>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 6/12 | chr1 | 226886924 | ||||||
chr1:226886972
|
A | G | 1 | a0001c0004t0004g0162 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.499-1119A>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 6/12 | chr1 | 226886972 | ||||||
chr1:226886981
|
G | C | 1 | a0001c0003t0002g0055 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.499-1110G>C | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 6/12 | chr1 | 226886981 | ||||||
chr1:226887125
|
G | A | 1 | a0001c0001t0001g0110 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.499-966G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 6/12 | chr1 | 226887125 | ||||||
chr1:226887210
|
C | T | 1 | a0001c0001t0001g0104 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.499-881C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 6/12 | chr1 | 226887210 | ||||||
chr1:226887318
|
G | A | 1 | a0001c0001t0001g0092 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.499-773G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 6/12 | chr1 | 226887318 | ||||||
chr1:226887663
|
C | A | 1 | a0001c0002t0002g0038 | 2 | NA18955.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.499-428C>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 6/12 | chr1 | 226887663 | ||||||
chr1:226887681
|
T | C | 1 | a0001c0001t0001g0023 | 3 | NA18906.hp1 NA19030.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.499-410T>C | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 6/12 | chr1 | 226887681 | ||||||
chr1:226887701
|
G | A | 82 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(79): Show | 191 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(188): Show |
intron_variant | MODIFIER | c.499-390G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 6/12 | chr1 | 226887701 | ||||||
chr1:226887757
|
C | A | 1 | a0001c0001t0001g0093 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.499-334C>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 6/12 | chr1 | 226887757 | ||||||
chr1:226887970
|
G | A | 1 | a0001c0003t0002g0064 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.499-121G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 6/12 | chr1 | 226887970 | ||||||
chr1:226888215
|
G | A | 5 | a0001c0003t0002g0055a0001c0006t0002g0015a0001c0006t0002g0129others(2): Show | 9 | HG01515.hp1 HG01891.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.566+57G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 7/12 | chr1 | 226888215 | ||||||
chr1:226888238
|
C | T | 2 | a0001c0001t0001g0029a0001c0001t0001g0086 | 3 | HG01109.hp1 HG01243.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.566+80C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 7/12 | chr1 | 226888238 | ||||||
chr1:226888283
|
G | A | 10 | a0001c0001t0001g0017a0001c0001t0001g0028a0001c0001t0001g0073others(7): Show | 13 | HG00099.hp2 HG01167.hp1 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.566+125G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 7/12 | chr1 | 226888283 | ||||||
chr1:226888359
|
A | G | 15 | a0001c0002t0002g0007a0001c0002t0002g0012a0001c0002t0002g0038others(12): Show | 31 | HG00558.hp1 HG01099.hp2 HG01123.hp2 others(28): Show |
intron_variant | MODIFIER | c.566+201A>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 7/12 | chr1 | 226888359 | ||||||
chr1:226888447
|
A | G | 1 | a0001c0003t0002g0064 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.566+289A>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 7/12 | chr1 | 226888447 | ||||||
chr1:226888448
|
A | G | 1 | a0001c0003t0004g0174 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.566+290A>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 7/12 | chr1 | 226888448 | ||||||
chr1:226888522
|
C | G | 32 | a0001c0002t0002g0066a0001c0002t0002g0067a0001c0002t0002g0068others(29): Show | 72 | HG00099.hp1 HG00597.hp1 HG00733.hp2 others(69): Show |
intron_variant | MODIFIER | c.567-307C>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 7/12 | chr1 | 226888522 | ||||||
chr1:226888579
|
A | G | 3 | a0001c0003t0004g0170a0001c0003t0004g0172a0001c0003t0004g0173 | 3 | HG02886.hp1 HG03195.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.567-250A>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 7/12 | chr1 | 226888579 | ||||||
chr1:226888608
|
C | T | 2 | a0001c0002t0003g0139a0001c0002t0003g0140 | 2 | NA18965.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.567-221C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 7/12 | chr1 | 226888608 | ||||||
chr1:226889073
|
G | C | 1 | a0001c0007t0006g0106 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.787+24G>C | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 8/12 | chr1 | 226889073 | ||||||
chr1:226889115
|
C | A | 8 | a0001c0003t0004g0027a0001c0003t0004g0176a0001c0005t0004g0021others(5): Show | 19 | HG01109.hp2 HG01168.hp2 HG01169.hp1 others(16): Show |
intron_variant | MODIFIER | c.787+66C>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 8/12 | chr1 | 226889115 | ||||||
chr1:226889164
|
G | A | 1 | a0002c0011t0004g0043 | 2 | HG02896.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.787+115G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 8/12 | chr1 | 226889164 | ||||||
chr1:226889254
|
C | T | 13 | a0001c0003t0004g0027a0001c0003t0004g0045a0001c0003t0004g0170others(10): Show | 25 | HG01109.hp2 HG01168.hp2 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.787+205C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 8/12 | chr1 | 226889254 | ||||||
chr1:226889338
|
G | A | 1 | a0001c0003t0002g0168 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.787+289G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 8/12 | chr1 | 226889338 | ||||||
chr1:226889629
|
G | A | 1 | a0001c0002t0002g0153 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.788-406G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 8/12 | chr1 | 226889629 | ||||||
chr1:226889841
|
T | G | 1 | a0001c0003t0002g0056 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.788-194T>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 8/12 | chr1 | 226889841 | ||||||
chr1:226889931
|
G | A | 1 | a0001c0001t0001g0118 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.788-104G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 8/12 | chr1 | 226889931 | ||||||
chr1:226889945
|
G | C | 7 | a0001c0006t0002g0015a0001c0006t0002g0024a0001c0006t0002g0129others(4): Show | 13 | HG01891.hp1 HG01891.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.788-90G>C | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 8/12 | chr1 | 226889945 | ||||||
chr1:226890148
|
C | T | 1 | a0001c0002t0003g0135 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.886+15C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 9/12 | chr1 | 226890148 | ||||||
chr1:226890366
|
C | T | 4 | a0001c0001t0001g0009a0001c0001t0001g0089a0001c0001t0001g0091others(1): Show | 11 | HG01261.hp2 HG01884.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.886+233C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 9/12 | chr1 | 226890366 | ||||||
chr1:226890417
|
G | A | 1 | a0002c0011t0004g0043 | 2 | HG02896.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.886+284G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 9/12 | chr1 | 226890417 | ||||||
chr1:226890677
|
G | T | 13 | a0001c0003t0004g0027a0001c0003t0004g0045a0001c0003t0004g0170others(10): Show | 25 | HG01109.hp2 HG01168.hp2 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.886+544G>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 9/12 | chr1 | 226890677 | ||||||
chr1:226890798
|
G | A | 1 | a0001c0003t0004g0174 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.887-480G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 9/12 | chr1 | 226890798 | ||||||
chr1:226890808
|
T | G | 1 | a0001c0001t0001g0073 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.887-470T>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 9/12 | chr1 | 226890808 | ||||||
chr1:226890873
|
G | A | 3 | a0001c0002t0002g0066a0001c0002t0002g0067a0001c0002t0002g0068 | 3 | HG01884.hp1 HG02965.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.887-405G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 9/12 | chr1 | 226890873 | ||||||
chr1:226890891
|
C | T | 111 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(108): Show | 255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.887-387C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 9/12 | chr1 | 226890891 | ||||||
chr1:226890900
|
C | T | 1 | a0001c0002t0002g0152 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.887-378C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 9/12 | chr1 | 226890900 | ||||||
chr1:226890936
|
C | T | 1 | a0001c0001t0001g0122 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.887-342C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 9/12 | chr1 | 226890936 | ||||||
chr1:226890982
|
C | T | 1 | a0001c0006t0002g0129 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.887-296C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 9/12 | chr1 | 226890982 | ||||||
chr1:226891020
|
T | A | 79 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(76): Show | 183 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.887-258T>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 9/12 | chr1 | 226891020 | ||||||
chr1:226891127
|
A | G | 1 | a0001c0006t0002g0133 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.887-151A>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 9/12 | chr1 | 226891127 | ||||||
chr1:226891174
|
G | A | 1 | a0001c0001t0001g0080 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.887-104G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 9/12 | chr1 | 226891174 | ||||||
chr1:226891254
|
T | C | 137 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(134): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.887-24T>C | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 9/12 | chr1 | 226891254 | ||||||
chr1:226891254
|
T | G | 2 | a0001c0003t0004g0027a0001c0003t0004g0176 | 4 | HG01109.hp2 HG02145.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.887-24T>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 9/12 | chr1 | 226891254 | ||||||
chr1:226891521
|
C | G | 79 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(76): Show | 183 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.970+160C>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 10/12 | chr1 | 226891521 | ||||||
chr1:226891600
|
G | C | 13 | a0001c0003t0004g0027a0001c0003t0004g0045a0001c0003t0004g0170others(10): Show | 25 | HG01109.hp2 HG01168.hp2 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.971-143G>C | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 10/12 | chr1 | 226891600 | ||||||
chr1:226891942
|
G | A | 4 | a0001c0006t0002g0015a0001c0006t0002g0129a0001c0009t0002g0015others(1): Show | 8 | HG01891.hp2 HG02145.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.1072+98G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 11/12 | chr1 | 226891942 | ||||||
chr1:226891972
|
C | T | 1 | a0002c0011t0004g0043 | 2 | HG02896.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.1072+128C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 11/12 | chr1 | 226891972 | ||||||
chr1:226891980
|
A | G | 1 | a0001c0004t0004g0163 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1072+136A>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 11/12 | chr1 | 226891980 | ||||||
chr1:226891999
|
C | T | 25 | a0001c0003t0002g0003a0001c0003t0002g0005a0001c0003t0002g0018others(22): Show | 62 | HG00099.hp1 HG00597.hp1 HG00733.hp2 others(59): Show |
intron_variant | MODIFIER | c.1072+155C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 11/12 | chr1 | 226891999 | ||||||
chr1:226892013
|
C | G | 13 | a0001c0003t0004g0027a0001c0003t0004g0045a0001c0003t0004g0170others(10): Show | 25 | HG01109.hp2 HG01168.hp2 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.1072+169C>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 11/12 | chr1 | 226892013 | ||||||
chr1:226892058
|
C | T | 1 | a0001c0001t0001g0112 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1072+214C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 11/12 | chr1 | 226892058 | ||||||
chr1:226892077
|
G | T | 1 | a0001c0001t0001g0095 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1072+233G>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 11/12 | chr1 | 226892077 | ||||||
chr1:226892103
|
C | T | 15 | a0001c0004t0004g0013a0001c0004t0004g0025a0001c0004t0004g0154others(12): Show | 27 | HG00423.hp1 HG00558.hp2 HG01074.hp2 others(24): Show |
intron_variant | MODIFIER | c.1072+259C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 11/12 | chr1 | 226892103 | ||||||
chr1:226892118
|
C | T | 1 | a0001c0003t0002g0064 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1072+274C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 11/12 | chr1 | 226892118 | ||||||
chr1:226892120
|
G | A | 32 | a0001c0002t0002g0066a0001c0002t0002g0067a0001c0002t0002g0068others(29): Show | 72 | HG00099.hp1 HG00597.hp1 HG00733.hp2 others(69): Show |
intron_variant | MODIFIER | c.1072+276G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 11/12 | chr1 | 226892120 | ||||||
chr1:226892465
|
C | T | 139 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(136): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.1072+621C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 11/12 | chr1 | 226892465 | ||||||
chr1:226892561
|
G | A | 1 | a0001c0002t0002g0039 | 2 | HG02922.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1072+717G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 11/12 | chr1 | 226892561 | ||||||
chr1:226892584
|
T | C | 161 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(158): Show | 351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.1072+740T>C | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 11/12 | chr1 | 226892584 | ||||||
chr1:226892606
|
C | T | 1 | a0002c0011t0004g0043 | 2 | HG02896.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.1072+762C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 11/12 | chr1 | 226892606 | ||||||
chr1:226892751
|
G | A | 32 | a0001c0002t0002g0066a0001c0002t0002g0067a0001c0002t0002g0068others(29): Show | 72 | HG00099.hp1 HG00597.hp1 HG00733.hp2 others(69): Show |
intron_variant | MODIFIER | c.1072+907G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 11/12 | chr1 | 226892751 | ||||||
chr1:226892758
|
G | A | 79 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(76): Show | 183 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.1072+914G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 11/12 | chr1 | 226892758 | ||||||
chr1:226892808
|
A | T | 1 | a0001c0001t0001g0033 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1072+964A>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 11/12 | chr1 | 226892808 | ||||||
chr1:226892860
|
T | C | 5 | a0001c0003t0004g0045a0001c0003t0004g0170a0001c0003t0004g0172others(2): Show | 6 | HG02886.hp1 HG02976.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.1072+1016T>C | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 11/12 | chr1 | 226892860 | ||||||
chr1:226892868
|
A | G | 3 | a0001c0002t0002g0066a0001c0002t0002g0067a0001c0002t0002g0068 | 3 | HG01884.hp1 HG02965.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1072+1024A>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 11/12 | chr1 | 226892868 | ||||||
chr1:226892889
|
C | A | 1 | a0001c0002t0003g0135 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1072+1045C>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 11/12 | chr1 | 226892889 | ||||||
chr1:226892964
|
G | T | 1 | a0001c0002t0017g0132 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1073-1043G>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 11/12 | chr1 | 226892964 | ||||||
chr1:226893099
|
A | ATT | 13 | a0001c0003t0004g0027a0001c0003t0004g0045a0001c0003t0004g0170others(10): Show | 25 | HG01109.hp2 HG01168.hp2 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.1073-906_1073-905d others(4): Show |
PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr1 | 226893099 | |||||
chr1:226893140
|
G | T | 1 | a0002c0011t0004g0043 | 2 | HG02896.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.1073-867G>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 11/12 | chr1 | 226893140 | ||||||
chr1:226893226
|
C | T | 126 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(123): Show | 282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.1073-781C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 11/12 | chr1 | 226893226 | ||||||
chr1:226893281
|
G | C | 1 | a0001c0002t0003g0139 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1073-726G>C | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 11/12 | chr1 | 226893281 | ||||||
chr1:226893283
|
C | G | 1 | a0001c0001t0001g0103 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1073-724C>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 11/12 | chr1 | 226893283 | ||||||
chr1:226893312
|
C | T | 1 | a0001c0003t0002g0051 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1073-695C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 11/12 | chr1 | 226893312 | ||||||
chr1:226893327
|
A | C | 79 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(76): Show | 183 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.1073-680A>C | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 11/12 | chr1 | 226893327 | ||||||
chr1:226893491
|
C | T | 183 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(180): Show | 402 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(399): Show |
intron_variant | MODIFIER | c.1073-516C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 11/12 | chr1 | 226893491 | ||||||
chr1:226893576
|
T | G | 4 | a0001c0007t0006g0019a0001c0007t0006g0106a0002c0011t0004g0043others(1): Show | 8 | HG02055.hp1 HG02280.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1073-431T>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 11/12 | chr1 | 226893576 | ||||||
chr1:226893604
|
A | G | 29 | a0001c0002t0002g0066a0001c0002t0002g0067a0001c0002t0002g0068others(26): Show | 66 | HG00099.hp1 HG00597.hp1 HG00733.hp2 others(63): Show |
intron_variant | MODIFIER | c.1073-403A>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 11/12 | chr1 | 226893604 | ||||||
chr1:226893660
|
T | G | 1 | a0001c0001t0001g0094 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1073-347T>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 11/12 | chr1 | 226893660 | ||||||
chr1:226893840
|
T | A | 14 | a0001c0004t0004g0013a0001c0004t0004g0025a0001c0004t0004g0154others(11): Show | 25 | HG00423.hp1 HG00558.hp2 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.1073-167T>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 11/12 | chr1 | 226893840 | ||||||
chr1:226893866
|
A | C | 1 | a0001c0003t0002g0056 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1073-141A>C | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 11/12 | chr1 | 226893866 | ||||||
chr1:226893921
|
A | G | 125 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(122): Show | 282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.1073-86A>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 11/12 | chr1 | 226893921 | ||||||
chr1:226893969
|
C | T | 1 | a0001c0001t0001g0032 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1073-38C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 11/12 | chr1 | 226893969 | ||||||
chr1:226894149
|
G | A | 110 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(107): Show | 244 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.1191+24G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 12/12 | chr1 | 226894149 | ||||||
chr1:226894229
|
C | T | 4 | a0001c0006t0002g0015a0001c0006t0002g0129a0001c0009t0002g0015others(1): Show | 8 | HG01891.hp2 HG02145.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.1191+104C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 12/12 | chr1 | 226894229 | ||||||
chr1:226894308
|
G | A | 5 | a0001c0003t0002g0018a0001c0003t0002g0167a0001c0003t0002g0168others(2): Show | 9 | HG01106.hp1 HG02572.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.1191+183G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 12/12 | chr1 | 226894308 | ||||||
chr1:226894366
|
G | T | 14 | a0001c0004t0004g0013a0001c0004t0004g0025a0001c0004t0004g0154others(11): Show | 25 | HG00423.hp1 HG00558.hp2 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.1191+241G>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 12/12 | chr1 | 226894366 | ||||||
chr1:226894404
|
G | C | 29 | a0001c0002t0002g0066a0001c0002t0002g0067a0001c0002t0002g0068others(26): Show | 66 | HG00099.hp1 HG00597.hp1 HG00733.hp2 others(63): Show |
intron_variant | MODIFIER | c.1191+279G>C | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 12/12 | chr1 | 226894404 | ||||||
chr1:226894490
|
G | A | 14 | a0001c0004t0004g0013a0001c0004t0004g0025a0001c0004t0004g0154others(11): Show | 25 | HG00423.hp1 HG00558.hp2 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.1191+365G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 12/12 | chr1 | 226894490 | ||||||
chr1:226894499
|
A | G | 1 | a0001c0007t0006g0106 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1191+374A>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 12/12 | chr1 | 226894499 | ||||||
chr1:226894633
|
T | C | 2 | a0001c0002t0003g0145a0001c0002t0003g0147 | 2 | NA18982.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.1191+508T>C | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 12/12 | chr1 | 226894633 | ||||||
chr1:226894645
|
A | G | 161 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(158): Show | 351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.1191+520A>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 12/12 | chr1 | 226894645 | ||||||
chr1:226894733
|
G | A | 1 | a0001c0002t0003g0041 | 2 | HG01071.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.1191+608G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 12/12 | chr1 | 226894733 | ||||||
chr1:226894737
|
G | A | 11 | a0001c0002t0002g0007a0001c0002t0002g0012a0001c0002t0002g0038others(8): Show | 26 | HG00558.hp1 HG01099.hp2 HG01123.hp2 others(23): Show |
intron_variant | MODIFIER | c.1191+612G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 12/12 | chr1 | 226894737 | ||||||
chr1:226894744
|
A | G | 43 | a0001c0002t0002g0066a0001c0002t0002g0067a0001c0002t0002g0068others(40): Show | 93 | HG00099.hp1 HG00597.hp1 HG00733.hp2 others(90): Show |
intron_variant | MODIFIER | c.1191+619A>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 12/12 | chr1 | 226894744 | ||||||
chr1:226894751
|
C | T | 1 | a0001c0001t0001g0108 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1191+626C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 12/12 | chr1 | 226894751 | ||||||
chr1:226894858
|
T | C | 14 | a0001c0004t0004g0013a0001c0004t0004g0025a0001c0004t0004g0154others(11): Show | 25 | HG00423.hp1 HG00558.hp2 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.1192-566T>C | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 12/12 | chr1 | 226894858 | ||||||
chr1:226894882
|
C | A | 6 | a0001c0005t0004g0021a0001c0005t0004g0044a0001c0005t0004g0171others(3): Show | 15 | HG01168.hp2 HG01169.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.1192-542C>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 12/12 | chr1 | 226894882 | ||||||
chr1:226894984
|
C | A | 1 | a0002c0011t0004g0043 | 2 | HG02896.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.1192-440C>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 12/12 | chr1 | 226894984 | ||||||
chr1:226894992
|
C | G | 8 | a0001c0003t0004g0027a0001c0003t0004g0176a0001c0005t0004g0021others(5): Show | 19 | HG01109.hp2 HG01168.hp2 HG01169.hp1 others(16): Show |
intron_variant | MODIFIER | c.1192-432C>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 12/12 | chr1 | 226894992 | ||||||
chr1:226895025
|
T | A | 79 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(76): Show | 183 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.1192-399T>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 12/12 | chr1 | 226895025 | ||||||
chr1:226895156
|
A | G | 1 | a0001c0001t0001g0100 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1192-268A>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 12/12 | chr1 | 226895156 | ||||||
chr1:226895266
|
C | A | 1 | a0001c0001t0001g0102 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1192-158C>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 12/12 | chr1 | 226895266 |