geneid | 25940 |
---|---|
ensemblid | ENSG00000119812.20 |
hgncid | 24520 |
symbol | FAM98A |
name | family with sequence similarity 98 member A |
refseq_nuc | NM_015475.5 |
refseq_prot | NP_056290.3 |
ensembl_nuc | ENST00000238823.13 |
ensembl_prot | ENSP00000238823.8 |
mane_status | MANE Select |
chr | chr2 |
start | 33583660 |
end | 33599299 |
strand | - |
ver | v1.2 |
region | chr2:33583660-33599299 |
region5000 | chr2:33578660-33604299 |
regionname0 | FAM98A_chr2_33583660_33599299 |
regionname5000 | FAM98A_chr2_33578660_33604299 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 518 | 399 | 91 | 75 | 173 | 14 | 44 | 142 | FAM98A_chr2_33578660_33604299 | FAM98A | copy fasta | chr2 | 33578660 | 33604299 |
a0002 | 0/0 | 518 | 2 | 0 | 1 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | copy fasta | chr2 | 33578660 | 33604299 |
a0003 | 0/0 | 518 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | copy fasta | chr2 | 33578660 | 33604299 |
a0004 | 0/0 | 518 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | copy fasta | chr2 | 33578660 | 33604299 |
a0005 | 0/0 | 518 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | copy fasta | chr2 | 33578660 | 33604299 |
a0006 | 0/0 | 518 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAM98A_chr2_33578660_33604299 | FAM98A | copy fasta | chr2 | 33578660 | 33604299 |
a0007 | 0/0 | 518 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAM98A_chr2_33578660_33604299 | FAM98A | copy fasta | chr2 | 33578660 | 33604299 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1557 | 385 | 79 | 75 | 172 | 13 | 44 | FAM98A_chr2_33578660_33604299 | FAM98A | copy fasta | chr2 | 33578660 | 33604299 |
c0002 | 0/0 | 1557 | 10 | 10 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | copy fasta | chr2 | 33578660 | 33604299 |
c0003 | 0/0 | 1557 | 2 | 2 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | copy fasta | chr2 | 33578660 | 33604299 |
c0004 | 0/0 | 1557 | 2 | 0 | 1 | 0 | 1 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | copy fasta | chr2 | 33578660 | 33604299 |
c0005 | 0/0 | 1557 | 1 | 0 | 0 | 0 | 1 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | copy fasta | chr2 | 33578660 | 33604299 |
c0006 | 0/0 | 1557 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | copy fasta | chr2 | 33578660 | 33604299 |
c0007 | 0/0 | 1557 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | copy fasta | chr2 | 33578660 | 33604299 |
c0008 | 0/0 | 1557 | 1 | 0 | 0 | 0 | 1 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | copy fasta | chr2 | 33578660 | 33604299 |
c0009 | 0/0 | 1557 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | copy fasta | chr2 | 33578660 | 33604299 |
c0010 | 0/0 | 1557 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | copy fasta | chr2 | 33578660 | 33604299 |
c0011 | 0/0 | 1557 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | copy fasta | chr2 | 33578660 | 33604299 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 1195 | 232 | 49 | 54 | 89 | 7 | 32 | FAM98A_chr2_33578660_33604299 | FAM98A | copy fasta | chr2 | 33578660 | 33604299 |
t0002 | 1/0 | 1195 | 123 | 8 | 17 | 80 | 6 | 11 | FAM98A_chr2_33578660_33604299 | FAM98A | copy fasta | chr2 | 33578660 | 33604299 |
t0003 | 0/0 | 1195 | 22 | 16 | 2 | 0 | 3 | 1 | FAM98A_chr2_33578660_33604299 | FAM98A | copy fasta | chr2 | 33578660 | 33604299 |
t0004 | 0/0 | 1195 | 15 | 15 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | copy fasta | chr2 | 33578660 | 33604299 |
t0005 | 0/0 | 1195 | 3 | 3 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | copy fasta | chr2 | 33578660 | 33604299 |
t0006 | 0/0 | 1195 | 3 | 0 | 0 | 3 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | copy fasta | chr2 | 33578660 | 33604299 |
t0007 | 0/0 | 1195 | 2 | 0 | 2 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | copy fasta | chr2 | 33578660 | 33604299 |
t0008 | 0/0 | 1195 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | copy fasta | chr2 | 33578660 | 33604299 |
t0009 | 0/0 | 1195 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | copy fasta | chr2 | 33578660 | 33604299 |
t0010 | 0/0 | 1195 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | copy fasta | chr2 | 33578660 | 33604299 |
t0011 | 0/0 | 1195 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | copy fasta | chr2 | 33578660 | 33604299 |
t0012 | 0/0 | 1195 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | copy fasta | chr2 | 33578660 | 33604299 |
t0013 | 0/0 | 1195 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | copy fasta | chr2 | 33578660 | 33604299 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 1/0 | 54 | 4 | 10 | 31 | 3 | 5 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0002 | 0/0 | 51 | 3 | 14 | 26 | 2 | 6 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0003 | 0/0 | 19 | 8 | 4 | 5 | 0 | 2 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0004 | 0/0 | 17 | 0 | 7 | 9 | 0 | 1 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0005 | 0/0 | 12 | 0 | 10 | 0 | 0 | 2 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0006 | 0/0 | 10 | 2 | 3 | 3 | 0 | 2 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0007 | 0/0 | 10 | 0 | 0 | 10 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0008 | 0/0 | 8 | 1 | 0 | 7 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0009 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0010 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0011 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0012 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0013 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0014 | 0/0 | 5 | 0 | 1 | 2 | 0 | 2 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0015 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0016 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0017 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0018 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0019 | 0/1 | 4 | 0 | 0 | 0 | 2 | 1 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0020 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0021 | 0/0 | 4 | 1 | 1 | 0 | 1 | 1 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0022 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0023 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0026 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0027 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0028 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0030 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0037 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0040 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0042 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0043 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0044 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1557 | 385 | 79 | 75 | 172 | 13 | 44 | FAM98A_chr2_33578660_33604299 | FAM98A | copy fasta | chr2 | 33578660 | 33604299 |
a0001c0002 | 0/0 | 1557 | 10 | 10 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | copy fasta | chr2 | 33578660 | 33604299 |
a0001c0003 | 0/0 | 1557 | 2 | 2 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | copy fasta | chr2 | 33578660 | 33604299 |
a0001c0005 | 0/0 | 1557 | 1 | 0 | 0 | 0 | 1 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | copy fasta | chr2 | 33578660 | 33604299 |
a0001c0006 | 0/0 | 1557 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | copy fasta | chr2 | 33578660 | 33604299 |
a0002c0004 | 0/0 | 1557 | 2 | 0 | 1 | 0 | 1 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | copy fasta | chr2 | 33578660 | 33604299 |
a0003c0010 | 0/0 | 1557 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | copy fasta | chr2 | 33578660 | 33604299 |
a0004c0007 | 0/0 | 1557 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | copy fasta | chr2 | 33578660 | 33604299 |
a0005c0008 | 0/0 | 1557 | 1 | 0 | 0 | 0 | 1 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | copy fasta | chr2 | 33578660 | 33604299 |
a0006c0009 | 0/0 | 1557 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | copy fasta | chr2 | 33578660 | 33604299 |
a0007c0011 | 0/0 | 1557 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | copy fasta | chr2 | 33578660 | 33604299 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 2751 | 223 | 46 | 53 | 87 | 4 | 32 | FAM98A_chr2_33578660_33604299 | FAM98A | copy fasta | chr2 | 33578660 | 33604299 |
a0001c0001t0002 | 1/0 | 2751 | 121 | 8 | 17 | 78 | 6 | 11 | FAM98A_chr2_33578660_33604299 | FAM98A | copy fasta | chr2 | 33578660 | 33604299 |
a0001c0001t0003 | 0/0 | 2751 | 22 | 16 | 2 | 0 | 3 | 1 | FAM98A_chr2_33578660_33604299 | FAM98A | copy fasta | chr2 | 33578660 | 33604299 |
a0001c0001t0004 | 0/0 | 2751 | 5 | 5 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | copy fasta | chr2 | 33578660 | 33604299 |
a0001c0001t0005 | 0/0 | 2751 | 3 | 3 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | copy fasta | chr2 | 33578660 | 33604299 |
a0001c0001t0006 | 0/0 | 2751 | 3 | 0 | 0 | 3 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | copy fasta | chr2 | 33578660 | 33604299 |
a0001c0001t0007 | 0/0 | 2751 | 2 | 0 | 2 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | copy fasta | chr2 | 33578660 | 33604299 |
a0001c0001t0008 | 0/0 | 2751 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | copy fasta | chr2 | 33578660 | 33604299 |
a0001c0001t0009 | 0/0 | 2751 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | copy fasta | chr2 | 33578660 | 33604299 |
a0001c0001t0010 | 0/0 | 2751 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | copy fasta | chr2 | 33578660 | 33604299 |
a0001c0001t0011 | 0/0 | 2751 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | copy fasta | chr2 | 33578660 | 33604299 |
a0001c0001t0012 | 0/0 | 2751 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | copy fasta | chr2 | 33578660 | 33604299 |
a0001c0001t0013 | 0/0 | 2751 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | copy fasta | chr2 | 33578660 | 33604299 |
a0001c0002t0004 | 0/0 | 2751 | 10 | 10 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | copy fasta | chr2 | 33578660 | 33604299 |
a0001c0003t0001 | 0/0 | 2751 | 2 | 2 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | copy fasta | chr2 | 33578660 | 33604299 |
a0001c0005t0001 | 0/0 | 2751 | 1 | 0 | 0 | 0 | 1 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | copy fasta | chr2 | 33578660 | 33604299 |
a0001c0006t0002 | 0/0 | 2751 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | copy fasta | chr2 | 33578660 | 33604299 |
a0002c0004t0001 | 0/0 | 2751 | 2 | 0 | 1 | 0 | 1 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | copy fasta | chr2 | 33578660 | 33604299 |
a0003c0010t0001 | 0/0 | 2751 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | copy fasta | chr2 | 33578660 | 33604299 |
a0004c0007t0002 | 0/0 | 2751 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | copy fasta | chr2 | 33578660 | 33604299 |
a0005c0008t0001 | 0/0 | 2751 | 1 | 0 | 0 | 0 | 1 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | copy fasta | chr2 | 33578660 | 33604299 |
a0006c0009t0001 | 0/0 | 2751 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | copy fasta | chr2 | 33578660 | 33604299 |
a0007c0011t0001 | 0/0 | 2751 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | copy fasta | chr2 | 33578660 | 33604299 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 51 | 3 | 14 | 26 | 2 | 6 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0001g0003 | 0/0 | 19 | 8 | 4 | 5 | 0 | 2 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0001g0004 | 0/0 | 17 | 0 | 7 | 9 | 0 | 1 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0001g0005 | 0/0 | 12 | 0 | 10 | 0 | 0 | 2 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0001g0006 | 0/0 | 10 | 2 | 3 | 3 | 0 | 2 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0001g0007 | 0/0 | 10 | 0 | 0 | 10 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0001g0010 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0001g0014 | 0/0 | 5 | 0 | 1 | 2 | 0 | 2 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0001g0018 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0001g0019 | 0/1 | 4 | 0 | 0 | 0 | 2 | 1 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0001g0020 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0001g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0001g0028 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0001g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0002g0001 | 1/0 | 54 | 4 | 10 | 31 | 3 | 5 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0002g0008 | 0/0 | 8 | 1 | 0 | 7 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0002g0009 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0002g0012 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0002g0022 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0002g0023 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0002g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0002g0026 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0002g0027 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0002g0040 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0002g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0002g0042 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0002g0043 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0003g0013 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0003g0015 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0003g0016 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0003g0021 | 0/0 | 4 | 1 | 1 | 0 | 1 | 1 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0003g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0003g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0003g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0004g0017 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0004g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0005g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0005g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0005g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0006g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0006g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0007g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0007g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0008g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0009g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0010g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0011g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0012g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0001t0013g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0002t0004g0011 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0002t0004g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0002t0004g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0002t0004g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0003t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0005t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0001c0006t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0002c0004t0001g0037 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0003c0010t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0004c0007t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0005c0008t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0006c0009t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
a0007c0011t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0002 | g0001 | EUR | GBR | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG00140 | hp2 | a0002 | c0004 | t0001 | g0037 | EUR | GBR | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG00280 | hp2 | a0001 | c0001 | t0002 | g0001 | EUR | FIN | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG00323 | hp1 | a0001 | c0005 | t0001 | g0054 | EUR | FIN | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG00323 | hp2 | a0005 | c0008 | t0001 | g0087 | EUR | FIN | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | CHS | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG00423 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | CHS | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | CHS | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG00544 | hp1 | a0001 | c0001 | t0002 | g0124 | EAS | CHS | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG00544 | hp2 | a0001 | c0001 | t0002 | g0135 | EAS | CHS | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | CHS | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | CHS | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | CHS | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG00735 | hp2 | a0001 | c0001 | t0007 | g0140 | AMR | PUR | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG00738 | hp2 | a0001 | c0001 | t0012 | g0074 | AMR | PUR | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG01074 | hp1 | a0001 | c0001 | t0003 | g0021 | AMR | PUR | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0145 | AMR | PUR | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG01081 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG01106 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG01106 | hp2 | a0002 | c0004 | t0001 | g0037 | AMR | PUR | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG01109 | hp1 | a0001 | c0001 | t0003 | g0013 | AMR | PUR | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG01167 | hp1 | a0001 | c0001 | t0002 | g0125 | AMR | PUR | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0026 | AMR | PUR | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG01175 | hp2 | a0001 | c0001 | t0002 | g0130 | AMR | PUR | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG01192 | hp2 | a0001 | c0001 | t0007 | g0139 | AMR | PUR | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG01256 | hp2 | a0001 | c0001 | t0002 | g0137 | AMR | CLM | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | CLM | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | CLM | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG01515 | hp1 | a0001 | c0001 | t0002 | g0040 | EUR | IBS | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG01515 | hp2 | a0001 | c0001 | t0003 | g0058 | EUR | IBS | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0019 | EUR | IBS | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG01516 | hp2 | a0001 | c0001 | t0002 | g0043 | EUR | IBS | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0019 | EUR | IBS | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG01517 | hp2 | a0001 | c0001 | t0003 | g0057 | EUR | IBS | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | ACB | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | ACB | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | ACB | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG01975 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0141 | AMR | PEL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PEL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PEL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG02015 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | KHV | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG02015 | hp2 | a0001 | c0001 | t0002 | g0068 | EAS | KHV | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | KHV | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG02040 | hp2 | a0001 | c0001 | t0002 | g0131 | EAS | KHV | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG02055 | hp1 | a0003 | c0010 | t0001 | g0085 | AFR | ACB | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG02055 | hp2 | a0001 | c0001 | t0003 | g0052 | AFR | ACB | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | KHV | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | KHV | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG02132 | hp2 | a0001 | c0001 | t0009 | g0128 | EAS | KHV | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | ACB | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG02145 | hp2 | a0001 | c0001 | t0002 | g0138 | AFR | ACB | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CDX | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | CDX | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CDX | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | CDX | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG02257 | hp2 | a0001 | c0003 | t0001 | g0031 | AFR | ACB | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG02258 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | ACB | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | ACB | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PEL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG02280 | hp1 | a0001 | c0001 | t0004 | g0017 | AFR | ACB | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG02293 | hp1 | a0001 | c0001 | t0002 | g0023 | AMR | PEL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PEL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG02451 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | ACB | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG02451 | hp2 | a0001 | c0001 | t0003 | g0015 | AFR | ACB | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG02523 | hp1 | a0004 | c0007 | t0002 | g0127 | EAS | KHV | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG02523 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG02572 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | GWD | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0042 | SAS | PJL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG02615 | hp1 | a0001 | c0001 | t0002 | g0136 | AFR | GWD | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG02622 | hp1 | a0001 | c0002 | t0004 | g0063 | AFR | GWD | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG02630 | hp1 | a0001 | c0002 | t0004 | g0011 | AFR | GWD | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG02630 | hp2 | a0001 | c0001 | t0005 | g0077 | AFR | GWD | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0055 | SAS | PJL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG02698 | hp1 | a0001 | c0001 | t0003 | g0021 | SAS | PJL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0044 | SAS | PJL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | GWD | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG02717 | hp2 | a0001 | c0002 | t0004 | g0011 | AFR | GWD | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG02723 | hp2 | a0001 | c0001 | t0004 | g0061 | AFR | GWD | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0088 | SAS | PJL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG02809 | hp2 | a0001 | c0001 | t0003 | g0015 | AFR | GWD | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG02818 | hp1 | a0001 | c0002 | t0004 | g0029 | AFR | GWD | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG02886 | hp1 | a0001 | c0003 | t0001 | g0031 | AFR | GWD | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG02886 | hp2 | a0001 | c0002 | t0004 | g0071 | AFR | GWD | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG02895 | hp2 | a0001 | c0001 | t0003 | g0015 | AFR | GWD | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG02896 | hp1 | a0001 | c0002 | t0004 | g0011 | AFR | GWD | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | GWD | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG02897 | hp1 | a0001 | c0001 | t0003 | g0015 | AFR | GWD | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | GWD | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG02922 | hp1 | a0001 | c0002 | t0004 | g0011 | AFR | ESN | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG02922 | hp2 | a0001 | c0001 | t0003 | g0056 | AFR | ESN | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | ESN | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG02970 | hp2 | a0001 | c0001 | t0003 | g0016 | AFR | ESN | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG02976 | hp1 | a0001 | c0001 | t0003 | g0016 | AFR | ESN | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | ESN | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0106 | SAS | PJL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG03041 | hp2 | a0001 | c0001 | t0003 | g0051 | AFR | GWD | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | MSL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | MSL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | ESN | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG03139 | hp2 | a0001 | c0001 | t0008 | g0081 | AFR | ESN | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | ESN | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | ESN | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | MSL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG03225 | hp2 | a0001 | c0001 | t0003 | g0013 | AFR | MSL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0043 | SAS | PJL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG03453 | hp2 | a0001 | c0001 | t0004 | g0017 | AFR | MSL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG03486 | hp1 | a0001 | c0001 | t0003 | g0016 | AFR | MSL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | MSL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | ESN | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG03516 | hp2 | a0001 | c0001 | t0003 | g0013 | AFR | ESN | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG03540 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | GWD | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG03579 | hp1 | a0001 | c0001 | t0005 | g0122 | AFR | MSL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | MSL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0030 | SAS | PJL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | STU | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0099 | SAS | STU | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0026 | SAS | PJL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0053 | SAS | PJL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | BEB | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0059 | SAS | BEB | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0078 | SAS | BEB | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | BEB | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0143 | SAS | BEB | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0144 | SAS | BEB | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | BEB | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | BEB | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0050 | SAS | STU | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0092 | SAS | STU | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | STU | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0044 | SAS | STU | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0126 | SAS | STU | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | YRI | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA18522 | hp2 | a0001 | c0001 | t0003 | g0013 | AFR | YRI | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHB | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0048 | EAS | CHB | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | YRI | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA18906 | hp2 | a0001 | c0001 | t0004 | g0017 | AFR | YRI | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA18939 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA18947 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA18948 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA18950 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA18952 | hp1 | a0001 | c0001 | t0013 | g0149 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA18952 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA18954 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA18956 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA18957 | hp2 | a0001 | c0001 | t0010 | g0100 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA18960 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA18966 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA18966 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA18968 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA18968 | hp2 | a0001 | c0001 | t0006 | g0117 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA18969 | hp1 | a0006 | c0009 | t0001 | g0101 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA18969 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA18972 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA18977 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA18978 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA18980 | hp1 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA18981 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA18983 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA18986 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA18987 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA18988 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA18989 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA18990 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA18991 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA18994 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA18995 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA18997 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA18998 | hp2 | a0007 | c0011 | t0001 | g0115 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA18999 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA19001 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA19002 | hp1 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA19004 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA19005 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA19006 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA19009 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA19010 | hp2 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA19043 | hp1 | a0001 | c0001 | t0004 | g0017 | AFR | LWK | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | LWK | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA19054 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA19055 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA19056 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA19057 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA19059 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA19059 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA19060 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA19068 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA19068 | hp2 | a0001 | c0001 | t0011 | g0148 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA19070 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA19075 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA19076 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA19078 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA19078 | hp2 | a0001 | c0001 | t0006 | g0039 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA19081 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA19083 | hp2 | a0001 | c0006 | t0002 | g0123 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA19086 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA19087 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA19087 | hp2 | a0001 | c0001 | t0006 | g0039 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA19088 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA19089 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA19091 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0026 | EUR | TSI | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA20805 | hp1 | a0001 | c0001 | t0003 | g0021 | EUR | TSI | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0001 | EUR | TSI | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0042 | SAS | GIH | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | GIH | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | CLM | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG02109 | hp1 | a0001 | c0001 | t0003 | g0021 | AFR | ACB | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG02109 | hp2 | a0001 | c0002 | t0004 | g0011 | AFR | ACB | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG02486 | hp2 | a0001 | c0001 | t0003 | g0013 | AFR | ACB | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG02559 | hp1 | a0001 | c0002 | t0004 | g0029 | AFR | ACB | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG02559 | hp2 | a0001 | c0001 | t0003 | g0016 | AFR | ACB | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG03471 | hp1 | a0001 | c0001 | t0005 | g0120 | AFR | MSL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG03471 | hp2 | a0001 | c0001 | t0002 | g0027 | AFR | MSL | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | USA | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
HG06807 | hp2 | a0001 | c0002 | t0004 | g0011 | AFR | USA | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA20300 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | USA | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | USA | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | LWK | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | LWK | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0019 | REF | REF | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0001 | REF | REF | FAM98A_chr2_33578660_33604299 | FAM98A | chr2 | 33578660 | 33604299 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:33584927
|
C | A | 1 | a0005 | 1 | HG00323.hp2 | missense_variant | MODERATE | c.1406G>T | p.Gly469Val | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 8/8 | 1484/2751 | 1406/1557 | 469/518 | chr2 | 33584927 | ||
chr2:33584933
|
C | T | 1 | a0004 | 1 | HG02523.hp1 | missense_variant | MODERATE | c.1400G>A | p.Arg467His | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 8/8 | 1478/2751 | 1400/1557 | 467/518 | chr2 | 33584933 | ||
chr2:33585113
|
C | A | 1 | a0006 | 1 | NA18969.hp1 | missense_variant | MODERATE | c.1220G>T | p.Gly407Val | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 8/8 | 1298/2751 | 1220/1557 | 407/518 | chr2 | 33585113 | ||
chr2:33585571
|
T | C | 1 | a0002 | 2 | HG00140.hp2 HG01106.hp2 |
missense_variant | MODERATE | c.847A>G | p.Ser283Gly | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 7/8 | 925/2751 | 847/1557 | 283/518 | chr2 | 33585571 | ||
chr2:33586638
|
T | A | 1 | a0003 | 1 | HG02055.hp1 | missense_variant | MODERATE | c.644A>T | p.Tyr215Phe | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 6/8 | 722/2751 | 644/1557 | 215/518 | chr2 | 33586638 | ||
chr2:33588412
|
T | C | 1 | a0007 | 1 | NA18998.hp2 | missense_variant | MODERATE | c.445A>G | p.Ile149Val | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 4/8 | 523/2751 | 445/1557 | 149/518 | chr2 | 33588412 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:33584917
|
A | G | 1 | a0001c0002 | 10 | HG02109.hp2 HG02559.hp1 HG02622.hp1 others(7): Show |
synonymous_variant | LOW | c.1416T>C | p.Gly472Gly | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 8/8 | 1494/2751 | 1416/1557 | 472/518 | chr2 | 33584917 | ||
chr2:33592150
|
C | T | 1 | a0001c0006 | 1 | NA19083.hp2 | synonymous_variant | LOW | c.267G>A | p.Pro89Pro | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 3/8 | 345/2751 | 267/1557 | 89/518 | chr2 | 33592150 | ||
chr2:33595568
|
C | T | 1 | a0001c0005 | 1 | HG00323.hp1 | synonymous_variant | LOW | c.123G>A | p.Glu41Glu | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/8 | 201/2751 | 123/1557 | 41/518 | chr2 | 33595568 | ||
chr2:33595622
|
C | T | 1 | a0001c0003 | 2 | HG02257.hp2 HG02886.hp1 |
synonymous_variant | LOW | c.69G>A | p.Leu23Leu | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/8 | 147/2751 | 69/1557 | 23/518 | chr2 | 33595622 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:33583745
|
T | C | 1 | a0001c0001t0011 | 1 | NA19068.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1031A>G | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 8/8 | 1031 | chr2 | 33583745 | |||||
chr2:33584204
|
G | A | 1 | a0001c0001t0010 | 1 | NA18957.hp2 | 3_prime_UTR_variant | MODIFIER | c.*572C>T | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 8/8 | 572 | chr2 | 33584204 | |||||
chr2:33584227
|
A | G | 16 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(13): Show | 278 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(275): Show |
3_prime_UTR_variant | MODIFIER | c.*549T>C | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 8/8 | 549 | chr2 | 33584227 | |||||
chr2:33584297
|
G | C | 1 | a0001c0001t0012 | 1 | HG00738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*479C>G | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 8/8 | 479 | chr2 | 33584297 | |||||
chr2:33584323
|
G | C | 1 | a0001c0001t0007 | 2 | HG00735.hp2 HG01192.hp2 |
3_prime_UTR_variant | MODIFIER | c.*453C>G | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 8/8 | 453 | chr2 | 33584323 | |||||
chr2:33584381
|
C | G | 1 | a0001c0001t0009 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*395G>C | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 8/8 | 395 | chr2 | 33584381 | |||||
chr2:33584385
|
G | T | 1 | a0001c0001t0006 | 3 | NA18968.hp2 NA19078.hp2 NA19087.hp2 |
3_prime_UTR_variant | MODIFIER | c.*391C>A | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 8/8 | 391 | chr2 | 33584385 | |||||
chr2:33584404
|
C | G | 1 | a0001c0001t0003 | 22 | HG01074.hp1 HG01109.hp1 HG01515.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*372G>C | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 8/8 | 372 | chr2 | 33584404 | |||||
chr2:33584548
|
A | C | 1 | a0001c0001t0008 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*228T>G | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 8/8 | 228 | chr2 | 33584548 | |||||
chr2:33584627
|
A | G | 1 | a0001c0001t0005 | 3 | HG02630.hp2 HG03471.hp1 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*149T>C | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 8/8 | 149 | chr2 | 33584627 | |||||
chr2:33584759
|
T | G | 2 | a0001c0001t0004a0001c0002t0004 | 15 | HG02109.hp2 HG02280.hp1 HG02559.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*17A>C | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 8/8 | 17 | chr2 | 33584759 | |||||
chr2:33599247
|
G | C | 1 | a0001c0001t0013 | 1 | NA18952.hp1 | 5_prime_UTR_variant | MODIFIER | c.-26C>G | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 1/8 | 26 | chr2 | 33599247 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:33585460
|
G | T | 1 | a0001c0001t0001g0119 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.889-16C>A | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 7/7 | chr2 | 33585460 | ||||||
chr2:33585890
|
T | C | 1 | a0001c0001t0001g0146 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.721-193A>G | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 6/7 | chr2 | 33585890 | ||||||
chr2:33585946
|
G | C | 1 | a0001c0001t0002g0041 | 2 | HG02015.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.721-249C>G | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 6/7 | chr2 | 33585946 | ||||||
chr2:33585989
|
C | T | 1 | a0007c0011t0001g0115 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.721-292G>A | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 6/7 | chr2 | 33585989 | ||||||
chr2:33586405
|
A | G | 1 | a0001c0001t0001g0036 | 2 | NA19000.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.720+157T>C | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 6/7 | chr2 | 33586405 | ||||||
chr2:33586409
|
T | C | 1 | a0001c0001t0005g0120 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.720+153A>G | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 6/7 | chr2 | 33586409 | ||||||
chr2:33586428
|
A | G | 1 | a0001c0001t0001g0142 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.720+134T>C | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 6/7 | chr2 | 33586428 | ||||||
chr2:33586449
|
C | G | 54 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(51): Show | 152 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.720+113G>C | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 6/7 | chr2 | 33586449 | ||||||
chr2:33586740
|
G | T | 1 | a0001c0001t0001g0103 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.604-62C>A | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 5/7 | chr2 | 33586740 | ||||||
chr2:33586770
|
T | G | 1 | a0001c0001t0001g0146 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.604-92A>C | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 5/7 | chr2 | 33586770 | ||||||
chr2:33586869
|
A | T | 34 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0018others(31): Show | 84 | HG00323.hp1 HG00423.hp1 HG00738.hp2 others(81): Show |
intron_variant | MODIFIER | c.604-191T>A | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 5/7 | chr2 | 33586869 | ||||||
chr2:33586929
|
C | T | 1 | a0001c0001t0001g0142 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.604-251G>A | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 5/7 | chr2 | 33586929 | ||||||
chr2:33587046
|
A | G | 6 | a0001c0001t0001g0014a0001c0001t0001g0028a0001c0001t0001g0044others(3): Show | 13 | HG01070.hp2 HG01361.hp2 HG02056.hp1 others(10): Show |
intron_variant | MODIFIER | c.603+194T>C | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 5/7 | chr2 | 33587046 | ||||||
chr2:33587138
|
A | T | 1 | a0001c0001t0001g0075 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.603+102T>A | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 5/7 | chr2 | 33587138 | ||||||
chr2:33587161
|
C | A | 1 | a0001c0001t0001g0146 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.603+79G>T | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 5/7 | chr2 | 33587161 | ||||||
chr2:33587624
|
C | T | 1 | a0001c0001t0002g0137 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.523-304G>A | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 4/7 | chr2 | 33587624 | ||||||
chr2:33587675
|
A | G | 1 | a0001c0001t0001g0142 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.523-355T>C | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 4/7 | chr2 | 33587675 | ||||||
chr2:33587735
|
T | A | 96 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(93): Show | 255 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(252): Show |
intron_variant | MODIFIER | c.523-415A>T | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 4/7 | chr2 | 33587735 | ||||||
chr2:33587735
|
T | G | 1 | a0001c0001t0001g0045 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.523-415A>C | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 4/7 | chr2 | 33587735 | ||||||
chr2:33587746
|
C | T | 1 | a0001c0001t0001g0144 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.523-426G>A | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 4/7 | chr2 | 33587746 | ||||||
chr2:33587747
|
G | A | 10 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0032others(7): Show | 18 | HG00738.hp2 HG01255.hp1 HG01516.hp1 others(15): Show |
intron_variant | MODIFIER | c.523-427C>T | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 4/7 | chr2 | 33587747 | ||||||
chr2:33587804
|
T | C | 3 | a0001c0001t0001g0079a0001c0001t0001g0118a0001c0001t0001g0119 | 3 | HG01243.hp1 HG03209.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.523-484A>G | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 4/7 | chr2 | 33587804 | ||||||
chr2:33587901
|
T | C | 3 | a0001c0001t0001g0083a0001c0001t0001g0084a0003c0010t0001g0085 | 3 | HG01884.hp1 HG02055.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.522+434A>G | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 4/7 | chr2 | 33587901 | ||||||
chr2:33587960
|
A | G | 1 | a0001c0001t0002g0126 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.522+375T>C | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 4/7 | chr2 | 33587960 | ||||||
chr2:33587964
|
G | A | 1 | a0001c0001t0001g0098 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.522+371C>T | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 4/7 | chr2 | 33587964 | ||||||
chr2:33588051
|
T | C | 4 | a0001c0001t0001g0121a0001c0001t0005g0077a0001c0001t0005g0120others(1): Show | 4 | HG02630.hp2 HG03195.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.522+284A>G | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 4/7 | chr2 | 33588051 | ||||||
chr2:33588071
|
T | C | 1 | a0001c0001t0001g0114 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.522+264A>G | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 4/7 | chr2 | 33588071 | ||||||
chr2:33588196
|
C | A | 1 | a0001c0001t0001g0143 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.522+139G>T | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 4/7 | chr2 | 33588196 | ||||||
chr2:33588900
|
A | AT | 63 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(60): Show | 169 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.338-382dupA | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 3/7 | chr2 | 33588900 | ||||||
chr2:33588941
|
A | C | 1 | a0001c0001t0001g0106 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.338-422T>G | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 3/7 | chr2 | 33588941 | ||||||
chr2:33589116
|
C | G | 1 | a0001c0001t0001g0099 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.338-597G>C | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 3/7 | chr2 | 33589116 | ||||||
chr2:33589180
|
A | C | 1 | a0001c0001t0001g0045 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.338-661T>G | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 3/7 | chr2 | 33589180 | ||||||
chr2:33589264
|
G | C | 43 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0018others(40): Show | 107 | HG00323.hp1 HG00423.hp1 HG00738.hp2 others(104): Show |
intron_variant | MODIFIER | c.338-745C>G | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 3/7 | chr2 | 33589264 | ||||||
chr2:33589415
|
T | C | 1 | a0001c0001t0001g0102 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.338-896A>G | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 3/7 | chr2 | 33589415 | ||||||
chr2:33589523
|
A | G | 54 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(51): Show | 152 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.338-1004T>C | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 3/7 | chr2 | 33589523 | ||||||
chr2:33589525
|
A | G | 2 | a0001c0001t0001g0066a0001c0001t0001g0067 | 2 | NA18954.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.338-1006T>C | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 3/7 | chr2 | 33589525 | ||||||
chr2:33589622
|
G | T | 1 | a0001c0001t0001g0073 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.338-1103C>A | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 3/7 | chr2 | 33589622 | ||||||
chr2:33589823
|
T | C | 1 | a0001c0001t0001g0103 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.338-1304A>G | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 3/7 | chr2 | 33589823 | ||||||
chr2:33590104
|
G | A | 1 | a0001c0001t0001g0045 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.338-1585C>T | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 3/7 | chr2 | 33590104 | ||||||
chr2:33590222
|
C | T | 1 | a0002c0004t0001g0037 | 2 | HG00140.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.338-1703G>A | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 3/7 | chr2 | 33590222 | ||||||
chr2:33590317
|
T | G | 109 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(106): Show | 279 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(276): Show |
intron_variant | MODIFIER | c.337+1763A>C | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 3/7 | chr2 | 33590317 | ||||||
chr2:33590348
|
C | T | 1 | a0001c0001t0011g0148 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.337+1732G>A | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 3/7 | chr2 | 33590348 | ||||||
chr2:33590404
|
A | G | 47 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(44): Show | 144 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.337+1676T>C | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 3/7 | chr2 | 33590404 | ||||||
chr2:33590584
|
G | A | 4 | a0001c0001t0001g0121a0001c0001t0005g0077a0001c0001t0005g0120others(1): Show | 4 | HG02630.hp2 HG03195.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.337+1496C>T | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 3/7 | chr2 | 33590584 | ||||||
chr2:33590746
|
T | C | 1 | a0001c0001t0001g0104 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.337+1334A>G | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 3/7 | chr2 | 33590746 | ||||||
chr2:33590881
|
T | C | 42 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0018others(39): Show | 105 | HG00323.hp1 HG00423.hp1 HG00738.hp2 others(102): Show |
intron_variant | MODIFIER | c.337+1199A>G | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 3/7 | chr2 | 33590881 | ||||||
chr2:33591133
|
A | C | 3 | a0001c0001t0001g0095a0001c0001t0001g0097a0001c0001t0001g0098 | 3 | HG01123.hp1 HG01358.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.337+947T>G | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 3/7 | chr2 | 33591133 | ||||||
chr2:33591195
|
C | CT | 50 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(47): Show | 149 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.337+884dupA | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 3/7 | chr2 | 33591195 | ||||||
chr2:33591482
|
G | A | 1 | a0001c0001t0002g0132 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.337+598C>T | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 3/7 | chr2 | 33591482 | ||||||
chr2:33591518
|
C | T | 98 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(95): Show | 261 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(258): Show |
intron_variant | MODIFIER | c.337+562G>A | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 3/7 | chr2 | 33591518 | ||||||
chr2:33591674
|
G | A | 4 | a0001c0001t0001g0121a0001c0001t0005g0077a0001c0001t0005g0120others(1): Show | 4 | HG02630.hp2 HG03195.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.337+406C>T | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 3/7 | chr2 | 33591674 | ||||||
chr2:33591714
|
C | T | 9 | a0001c0001t0001g0064a0001c0001t0003g0013a0001c0001t0003g0015others(6): Show | 22 | HG01074.hp1 HG01109.hp1 HG01515.hp2 others(19): Show |
intron_variant | MODIFIER | c.337+366G>A | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 3/7 | chr2 | 33591714 | ||||||
chr2:33591739
|
A | G | 102 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(99): Show | 265 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(262): Show |
intron_variant | MODIFIER | c.337+341T>C | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 3/7 | chr2 | 33591739 | ||||||
chr2:33591827
|
A | C | 1 | a0001c0001t0008g0081 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.337+253T>G | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 3/7 | chr2 | 33591827 | ||||||
chr2:33591841
|
G | A | 1 | a0001c0001t0001g0110 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.337+239C>T | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 3/7 | chr2 | 33591841 | ||||||
chr2:33591848
|
G | A | 1 | a0001c0001t0004g0061 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.337+232C>T | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 3/7 | chr2 | 33591848 | ||||||
chr2:33591877
|
T | C | 1 | a0001c0001t0001g0046 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.337+203A>G | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 3/7 | chr2 | 33591877 | ||||||
chr2:33591950
|
G | A | 6 | a0001c0001t0001g0062a0001c0001t0004g0017a0001c0001t0004g0061others(3): Show | 15 | HG02109.hp2 HG02280.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.337+130C>T | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 3/7 | chr2 | 33591950 | ||||||
chr2:33592071
|
T | G | 1 | a0001c0001t0002g0129 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.337+9A>C | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 3/7 | chr2 | 33592071 | ||||||
chr2:33592302
|
T | C | 19 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0032others(16): Show | 36 | HG00738.hp2 HG01255.hp1 HG01516.hp1 others(33): Show |
intron_variant | MODIFIER | c.203-88A>G | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33592302 | ||||||
chr2:33592442
|
T | G | 1 | a0001c0001t0001g0045 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.203-228A>C | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33592442 | ||||||
chr2:33592492
|
A | G | 47 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(44): Show | 144 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.203-278T>C | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33592492 | ||||||
chr2:33592509
|
G | C | 1 | a0001c0001t0001g0045 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.203-295C>G | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33592509 | ||||||
chr2:33592558
|
C | T | 3 | a0001c0001t0002g0026a0001c0001t0002g0125a0001c0001t0002g0130 | 5 | HG01167.hp1 HG01169.hp1 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.203-344G>A | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33592558 | ||||||
chr2:33592814
|
T | C | 98 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(95): Show | 261 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(258): Show |
intron_variant | MODIFIER | c.203-600A>G | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33592814 | ||||||
chr2:33592835
|
C | T | 1 | a0001c0001t0001g0142 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.203-621G>A | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33592835 | ||||||
chr2:33592843
|
C | T | 4 | a0001c0001t0001g0010a0001c0001t0001g0036a0001c0001t0001g0090others(1): Show | 11 | HG01167.hp2 HG01993.hp1 NA18957.hp1 others(8): Show |
intron_variant | MODIFIER | c.203-629G>A | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33592843 | ||||||
chr2:33593060
|
G | C | 3 | a0001c0002t0004g0011a0001c0002t0004g0029a0001c0002t0004g0063 | 9 | HG02109.hp2 HG02559.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.203-846C>G | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33593060 | ||||||
chr2:33593131
|
C | T | 51 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(48): Show | 148 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(145): Show |
intron_variant | MODIFIER | c.203-917G>A | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33593131 | ||||||
chr2:33593254
|
A | G | 1 | a0001c0001t0001g0046 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.203-1040T>C | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33593254 | ||||||
chr2:33593694
|
C | T | 1 | a0001c0001t0008g0081 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.203-1480G>A | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33593694 | ||||||
chr2:33594000
|
C | A | 8 | a0001c0001t0002g0042a0001c0001t0002g0043a0001c0001t0002g0137others(5): Show | 13 | HG00735.hp2 HG01074.hp1 HG01074.hp2 others(10): Show |
intron_variant | MODIFIER | c.202+1489G>T | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594000 | ||||||
chr2:33594326
|
C | T | 42 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0018others(39): Show | 103 | HG00323.hp1 HG00423.hp1 HG00738.hp2 others(100): Show |
intron_variant | MODIFIER | c.202+1163G>A | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594326 | ||||||
chr2:33594385
|
G | A | 42 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0018others(39): Show | 103 | HG00323.hp1 HG00423.hp1 HG00738.hp2 others(100): Show |
intron_variant | MODIFIER | c.202+1104C>T | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594385 | ||||||
chr2:33594412
|
G | A | 9 | a0001c0001t0001g0064a0001c0001t0003g0013a0001c0001t0003g0015others(6): Show | 19 | HG01109.hp1 HG01515.hp2 HG01517.hp2 others(16): Show |
intron_variant | MODIFIER | c.202+1077C>T | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594412 | ||||||
chr2:33594535
|
T | TA | 6 | a0001c0001t0002g0008a0001c0001t0002g0048a0001c0001t0002g0130others(3): Show | 13 | HG01175.hp2 HG02056.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.202+953dupT | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594535 | ||||||
chr2:33594535
|
TA | T | 9 | a0001c0001t0001g0006a0001c0001t0001g0030a0001c0001t0001g0064others(6): Show | 20 | HG00323.hp1 HG01081.hp1 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.202+953delT | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594535 | ||||||
chr2:33594555
|
AAAAAATT others(2): Show |
A | 9 | a0001c0001t0001g0046a0001c0001t0001g0084a0001c0001t0001g0089others(6): Show | 9 | HG01257.hp2 HG01358.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.202+925_202+933del others(9): Show |
FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594555 | ||||||
chr2:33594556
|
AAAAATTA others(1): Show |
A | 35 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(32): Show | 132 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.202+925_202+932del others(8): Show |
FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594556 | ||||||
chr2:33594557
|
AAAATTAT | A | 6 | a0001c0001t0001g0079a0001c0001t0001g0106a0001c0001t0001g0107others(3): Show | 9 | HG01243.hp1 HG02280.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.202+925_202+931del others(7): Show |
FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594557 | ||||||
chr2:33594558
|
AAATT | A | 10 | a0001c0001t0001g0014a0001c0001t0001g0044a0001c0001t0001g0143others(7): Show | 18 | HG01361.hp2 HG01517.hp2 HG02056.hp1 others(15): Show |
intron_variant | MODIFIER | c.202+927_202+930del others(4): Show |
FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594558 | ||||||
chr2:33594558
|
AAATTAT | A | 3 | a0001c0001t0005g0120a0001c0002t0004g0011a0001c0002t0004g0029 | 9 | HG02109.hp2 HG02559.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.202+925_202+930del others(6): Show |
FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594558 | ||||||
chr2:33594559
|
AATT | A | 7 | a0001c0001t0001g0075a0001c0001t0001g0144a0001c0001t0003g0013others(4): Show | 14 | HG01109.hp1 HG01515.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.202+927_202+929del others(3): Show |
FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594559 | ||||||
chr2:33594561
|
T | A | 6 | a0001c0001t0001g0019a0001c0001t0001g0032a0001c0001t0001g0060others(3): Show | 10 | HG01516.hp1 HG01517.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.202+928A>T | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594561 | ||||||
chr2:33594561
|
TTATA | T | 6 | a0001c0001t0001g0020a0001c0001t0001g0033a0001c0001t0001g0062others(3): Show | 10 | HG00738.hp2 HG01255.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.202+924_202+927del others(4): Show |
FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594561 | ||||||
chr2:33594562
|
TATA | T | 4 | a0001c0001t0001g0019a0001c0001t0001g0032a0001c0001t0001g0065others(1): Show | 8 | HG01516.hp1 HG01517.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.202+924_202+926del others(3): Show |
FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594562 | ||||||
chr2:33594563
|
A | T | 21 | a0001c0001t0001g0014a0001c0001t0001g0028a0001c0001t0001g0044others(18): Show | 38 | HG01070.hp2 HG01109.hp1 HG01361.hp2 others(35): Show |
intron_variant | MODIFIER | c.202+926T>A | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594563 | ||||||
chr2:33594564
|
T | A | 1 | a0001c0001t0001g0070 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.202+925A>T | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594564 | ||||||
chr2:33594565
|
A | T | 56 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(53): Show | 162 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.202+924T>A | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594565 | ||||||
chr2:33594572
|
T | C | 2 | a0001c0001t0001g0045a0001c0001t0001g0142 | 3 | HG02896.hp2 HG02897.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.202+917A>G | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594572 | ||||||
chr2:33594572
|
TATATAC | T | 14 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0018others(11): Show | 46 | HG00323.hp1 HG00423.hp1 HG00741.hp2 others(43): Show |
intron_variant | MODIFIER | c.202+911_202+916del others(6): Show |
FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594572 | ||||||
chr2:33594572
|
TATATACA others(3): Show |
T | 1 | a0001c0003t0001g0031 | 2 | HG02257.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.202+907_202+916del others(10): Show |
FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594572 | ||||||
chr2:33594572
|
TATATACA others(9): Show |
T | 1 | a0001c0001t0001g0092 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.202+901_202+916del others(16): Show |
FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594572 | ||||||
chr2:33594574
|
T | C | 4 | a0001c0001t0001g0045a0001c0001t0001g0064a0001c0001t0001g0080others(1): Show | 5 | HG02896.hp2 HG02897.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.202+915A>G | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594574 | ||||||
chr2:33594574
|
TATAC | T | 2 | a0001c0001t0001g0024a0001c0001t0001g0094 | 4 | NA18948.hp2 NA18999.hp1 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.202+911_202+914del others(4): Show |
FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594574 | ||||||
chr2:33594576
|
T | C | 30 | a0001c0001t0001g0014a0001c0001t0001g0028a0001c0001t0001g0034others(27): Show | 54 | HG00621.hp2 HG00738.hp2 HG01070.hp2 others(51): Show |
intron_variant | MODIFIER | c.202+913A>G | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594576 | ||||||
chr2:33594576
|
T | TAC | 9 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0043others(6): Show | 16 | HG00597.hp1 HG00735.hp2 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.202+911_202+912dup others(2): Show |
FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594576 | ||||||
chr2:33594578
|
C | T | 3 | a0001c0001t0001g0032a0001c0001t0001g0070a0001c0002t0004g0071 | 4 | HG02615.hp2 HG02886.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.202+911G>A | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594578 | ||||||
chr2:33594600
|
CATACATA others(15): Show |
C | 1 | a0001c0001t0001g0064 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.202+867_202+888del others(22): Show |
FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594600 | ||||||
chr2:33594606
|
T | A | 1 | a0001c0001t0003g0016 | 4 | HG02559.hp2 HG02970.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.202+883A>T | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594606 | ||||||
chr2:33594608
|
C | CACACATA others(21): Show |
2 | a0001c0001t0002g0124a0001c0006t0002g0123 | 2 | HG00544.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.202+853_202+880dup others(28): Show |
FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594608 | ||||||
chr2:33594608
|
CACACATA others(21): Show |
C | 14 | a0001c0001t0001g0014a0001c0001t0001g0028a0001c0001t0001g0034others(11): Show | 21 | HG00408.hp1 HG00597.hp2 HG01070.hp2 others(18): Show |
intron_variant | MODIFIER | c.202+853_202+880del others(28): Show |
FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594608 | ||||||
chr2:33594614
|
T | C | 42 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0018others(39): Show | 104 | HG00323.hp1 HG00423.hp1 HG00738.hp2 others(101): Show |
intron_variant | MODIFIER | c.202+875A>G | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594614 | ||||||
chr2:33594614
|
TATATATA others(19): Show |
T | 5 | a0001c0001t0001g0010a0001c0001t0001g0090a0001c0001t0001g0091others(2): Show | 12 | HG01167.hp2 HG01993.hp1 NA18957.hp1 others(9): Show |
intron_variant | MODIFIER | c.202+849_202+874del others(26): Show |
FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594614 | ||||||
chr2:33594622
|
T | C | 1 | a0001c0001t0001g0109 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.202+867A>G | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594622 | ||||||
chr2:33594632
|
T | C | 1 | a0001c0001t0001g0064 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.202+857A>G | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594632 | ||||||
chr2:33594636
|
T | C | 1 | a0001c0001t0001g0064 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.202+853A>G | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594636 | ||||||
chr2:33594636
|
TACACATA others(37): Show |
T | 1 | a0001c0001t0001g0065 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.202+809_202+852del others(44): Show |
FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594636 | ||||||
chr2:33594642
|
T | C | 1 | a0001c0001t0001g0064 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.202+847A>G | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594642 | ||||||
chr2:33594644
|
TATATATA others(5): Show |
T | 1 | a0001c0001t0001g0018 | 4 | HG01891.hp1 HG02572.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.202+833_202+844del others(12): Show |
FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594644 | ||||||
chr2:33594648
|
TATAC | T | 9 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0032others(6): Show | 16 | HG00738.hp2 HG01255.hp1 HG01516.hp1 others(13): Show |
intron_variant | MODIFIER | c.202+837_202+840del others(4): Show |
FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594648 | ||||||
chr2:33594648
|
TATACACA others(25): Show |
T | 3 | a0001c0001t0001g0033a0001c0001t0001g0060a0001c0001t0001g0076 | 4 | HG01891.hp2 HG02145.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.202+809_202+840del others(32): Show |
FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594648 | ||||||
chr2:33594650
|
T | C | 3 | a0001c0001t0001g0046a0001c0001t0001g0084a0003c0010t0001g0085 | 3 | HG02055.hp1 HG02717.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.202+839A>G | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594650 | ||||||
chr2:33594652
|
CACACATA others(47): Show |
C | 2 | a0001c0001t0001g0084a0003c0010t0001g0085 | 2 | HG02055.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.202+783_202+836del others(54): Show |
FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594652 | ||||||
chr2:33594656
|
C | T | 27 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0024others(24): Show | 77 | HG00323.hp1 HG00423.hp1 HG00741.hp2 others(74): Show |
intron_variant | MODIFIER | c.202+833G>A | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594656 | ||||||
chr2:33594662
|
TATACACA others(27): Show |
T | 1 | a0001c0003t0001g0031 | 2 | HG02257.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.202+793_202+826del others(34): Show |
FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594662 | ||||||
chr2:33594666
|
CACATATA others(33): Show |
C | 6 | a0001c0001t0001g0062a0001c0001t0004g0017a0001c0001t0004g0061others(3): Show | 15 | HG02109.hp2 HG02280.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.202+783_202+822del others(40): Show |
FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594666 | ||||||
chr2:33594668
|
CATATATA others(23): Show |
C | 4 | a0001c0001t0001g0044a0001c0001t0001g0121a0001c0001t0001g0143others(1): Show | 5 | HG02698.hp2 HG03195.hp2 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.202+791_202+820del others(30): Show |
FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594668 | ||||||
chr2:33594668
|
CATATATA others(25): Show |
C | 2 | a0001c0001t0003g0057a0001c0001t0003g0058 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.202+789_202+820del others(32): Show |
FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594668 | ||||||
chr2:33594668
|
CATATATA others(27): Show |
C | 14 | a0001c0001t0001g0020a0001c0001t0001g0032a0001c0001t0001g0070others(11): Show | 28 | HG00738.hp2 HG01109.hp1 HG01255.hp1 others(25): Show |
intron_variant | MODIFIER | c.202+787_202+820del others(34): Show |
FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594668 | ||||||
chr2:33594668
|
CATATATA others(29): Show |
C | 13 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0019others(10): Show | 46 | HG00323.hp1 HG00423.hp1 HG00741.hp2 others(43): Show |
intron_variant | MODIFIER | c.202+785_202+820del others(36): Show |
FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594668 | ||||||
chr2:33594676
|
TATACACA others(25): Show |
T | 1 | a0001c0001t0001g0045 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.202+781_202+812del others(32): Show |
FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594676 | ||||||
chr2:33594678
|
T | C | 36 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(33): Show | 125 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(122): Show |
intron_variant | MODIFIER | c.202+811A>G | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594678 | ||||||
chr2:33594678
|
TACACACA others(23): Show |
T | 1 | a0001c0001t0001g0142 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.202+781_202+810del others(30): Show |
FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594678 | ||||||
chr2:33594680
|
CACACATA others(19): Show |
C | 38 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(35): Show | 127 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(124): Show |
intron_variant | MODIFIER | c.202+783_202+808del others(26): Show |
FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594680 | ||||||
chr2:33594684
|
C | T | 1 | a0001c0001t0001g0064 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.202+805G>A | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594684 | ||||||
chr2:33594684
|
CATATATA others(15): Show |
C | 2 | a0001c0001t0001g0018a0001c0001t0001g0038 | 6 | HG01891.hp1 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.202+783_202+804del others(22): Show |
FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594684 | ||||||
chr2:33594696
|
CATAT | C | 3 | a0001c0001t0001g0033a0001c0001t0001g0060a0001c0001t0001g0076 | 4 | HG01891.hp2 HG02145.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.202+789_202+792del others(4): Show |
FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594696 | ||||||
chr2:33594702
|
T | C | 6 | a0001c0001t0001g0033a0001c0001t0001g0060a0001c0001t0001g0076others(3): Show | 8 | HG01515.hp2 HG01517.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.202+787A>G | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594702 | ||||||
chr2:33594704
|
T | C | 21 | a0001c0001t0001g0020a0001c0001t0001g0032a0001c0001t0001g0033others(18): Show | 37 | HG00408.hp1 HG00738.hp2 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.202+785A>G | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594704 | ||||||
chr2:33594704
|
T | TAC | 4 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0006g0039others(1): Show | 5 | HG01167.hp2 HG01993.hp1 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.202+784_202+785ins others(2): Show |
FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594704 | ||||||
chr2:33594706
|
T | C | 46 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0010others(43): Show | 108 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.202+783A>G | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594706 | ||||||
chr2:33594976
|
T | C | 2 | a0001c0001t0001g0034a0001c0001t0001g0080 | 3 | HG03195.hp1 HG03579.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.202+513A>G | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594976 | ||||||
chr2:33594986
|
T | C | 1 | a0001c0001t0008g0081 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.202+503A>G | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33594986 | ||||||
chr2:33595057
|
C | T | 1 | a0001c0001t0001g0060 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.202+432G>A | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33595057 | ||||||
chr2:33595074
|
T | C | 2 | a0001c0001t0006g0039a0001c0001t0006g0117 | 3 | NA18968.hp2 NA19078.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.202+415A>G | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33595074 | ||||||
chr2:33595085
|
T | A | 1 | a0001c0001t0002g0134 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.202+404A>T | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33595085 | ||||||
chr2:33595319
|
C | T | 1 | a0001c0001t0001g0088 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.202+170G>A | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33595319 | ||||||
chr2:33595347
|
C | T | 1 | a0001c0001t0002g0025 | 3 | NA19076.hp2 NA19078.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.202+142G>A | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 2/7 | chr2 | 33595347 | ||||||
chr2:33595731
|
A | G | 6 | a0001c0001t0003g0013a0001c0001t0003g0015a0001c0001t0003g0016others(3): Show | 16 | HG01109.hp1 HG02055.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.54-94T>C | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 1/7 | chr2 | 33595731 | ||||||
chr2:33595836
|
G | A | 1 | a0001c0001t0002g0135 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.54-199C>T | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 1/7 | chr2 | 33595836 | ||||||
chr2:33595889
|
CTAAAT | C | 8 | a0001c0001t0003g0013a0001c0001t0003g0015a0001c0001t0003g0016others(5): Show | 18 | HG01109.hp1 HG01515.hp2 HG01517.hp2 others(15): Show |
intron_variant | MODIFIER | c.54-257_54-253delAT others(3): Show |
FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 1/7 | chr2 | 33595889 | ||||||
chr2:33595973
|
A | G | 1 | a0001c0001t0001g0142 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.54-336T>C | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 1/7 | chr2 | 33595973 | ||||||
chr2:33596106
|
C | T | 3 | a0001c0001t0001g0030a0001c0001t0001g0053a0001c0001t0001g0059 | 4 | HG01981.hp2 HG03654.hp2 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.54-469G>A | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 1/7 | chr2 | 33596106 | ||||||
chr2:33596254
|
C | T | 3 | a0001c0001t0001g0121a0001c0001t0005g0120a0001c0001t0005g0122 | 3 | HG03195.hp2 HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.54-617G>A | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 1/7 | chr2 | 33596254 | ||||||
chr2:33596269
|
T | G | 1 | a0001c0001t0001g0119 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.54-632A>C | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 1/7 | chr2 | 33596269 | ||||||
chr2:33596331
|
G | C | 117 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(114): Show | 289 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(286): Show |
intron_variant | MODIFIER | c.54-694C>G | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 1/7 | chr2 | 33596331 | ||||||
chr2:33596372
|
C | A | 1 | a0001c0001t0001g0091 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.54-735G>T | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 1/7 | chr2 | 33596372 | ||||||
chr2:33596398
|
A | G | 1 | a0001c0002t0004g0029 | 2 | HG02559.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.54-761T>C | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 1/7 | chr2 | 33596398 | ||||||
chr2:33596405
|
T | A | 1 | a0001c0001t0002g0141 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.54-768A>T | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 1/7 | chr2 | 33596405 | ||||||
chr2:33596444
|
C | T | 3 | a0001c0001t0001g0005a0001c0001t0001g0035a0005c0008t0001g0087 | 15 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(12): Show |
intron_variant | MODIFIER | c.54-807G>A | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 1/7 | chr2 | 33596444 | ||||||
chr2:33596450
|
T | G | 44 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0018others(41): Show | 108 | HG00323.hp1 HG00423.hp1 HG00738.hp2 others(105): Show |
intron_variant | MODIFIER | c.54-813A>C | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 1/7 | chr2 | 33596450 | ||||||
chr2:33596491
|
T | C | 9 | a0001c0001t0001g0007a0001c0001t0001g0038a0001c0001t0001g0082others(6): Show | 19 | HG00438.hp2 HG00597.hp2 HG02027.hp1 others(16): Show |
intron_variant | MODIFIER | c.54-854A>G | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 1/7 | chr2 | 33596491 | ||||||
chr2:33596617
|
C | T | 42 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0018others(39): Show | 103 | HG00323.hp1 HG00423.hp1 HG00738.hp2 others(100): Show |
intron_variant | MODIFIER | c.54-980G>A | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 1/7 | chr2 | 33596617 | ||||||
chr2:33596666
|
T | C | 108 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(105): Show | 275 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(272): Show |
intron_variant | MODIFIER | c.54-1029A>G | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 1/7 | chr2 | 33596666 | ||||||
chr2:33596707
|
C | G | 10 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(7): Show | 45 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.54-1070G>C | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 1/7 | chr2 | 33596707 | ||||||
chr2:33596844
|
A | T | 8 | a0001c0001t0003g0013a0001c0001t0003g0015a0001c0001t0003g0016others(5): Show | 18 | HG01109.hp1 HG01515.hp2 HG01517.hp2 others(15): Show |
intron_variant | MODIFIER | c.54-1207T>A | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 1/7 | chr2 | 33596844 | ||||||
chr2:33596891
|
C | CA | 102 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(99): Show | 269 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(266): Show |
intron_variant | MODIFIER | c.54-1255dupT | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 1/7 | chr2 | 33596891 | ||||||
chr2:33596963
|
A | T | 44 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0018others(41): Show | 106 | HG00323.hp1 HG00423.hp1 HG00738.hp2 others(103): Show |
intron_variant | MODIFIER | c.54-1326T>A | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 1/7 | chr2 | 33596963 | ||||||
chr2:33597046
|
T | C | 1 | a0001c0001t0001g0144 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.54-1409A>G | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 1/7 | chr2 | 33597046 | ||||||
chr2:33597102
|
T | C | 3 | a0001c0001t0001g0083a0001c0001t0001g0084a0003c0010t0001g0085 | 3 | HG01884.hp1 HG02055.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.54-1465A>G | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 1/7 | chr2 | 33597102 | ||||||
chr2:33597132
|
A | G | 1 | a0001c0001t0001g0045 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.54-1495T>C | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 1/7 | chr2 | 33597132 | ||||||
chr2:33597139
|
C | G | 3 | a0001c0001t0001g0121a0001c0001t0005g0120a0001c0001t0005g0122 | 3 | HG03195.hp2 HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.54-1502G>C | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 1/7 | chr2 | 33597139 | ||||||
chr2:33597211
|
T | G | 1 | a0001c0001t0002g0145 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.54-1574A>C | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 1/7 | chr2 | 33597211 | ||||||
chr2:33597253
|
G | A | 43 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(40): Show | 140 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.54-1616C>T | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 1/7 | chr2 | 33597253 | ||||||
chr2:33597459
|
T | G | 2 | a0001c0001t0006g0039a0001c0001t0006g0117 | 3 | NA18968.hp2 NA19078.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.53+1710A>C | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 1/7 | chr2 | 33597459 | ||||||
chr2:33597632
|
G | A | 3 | a0001c0001t0001g0014a0001c0001t0001g0028a0001c0001t0001g0146 | 9 | HG01070.hp2 HG01361.hp2 HG02056.hp1 others(6): Show |
intron_variant | MODIFIER | c.53+1537C>T | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 1/7 | chr2 | 33597632 | ||||||
chr2:33597892
|
C | A | 1 | a0001c0001t0002g0147 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.53+1277G>T | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 1/7 | chr2 | 33597892 | ||||||
chr2:33597896
|
A | G | 1 | a0001c0001t0001g0050 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.53+1273T>C | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 1/7 | chr2 | 33597896 | ||||||
chr2:33598120
|
T | G | 2 | a0001c0001t0001g0118a0001c0001t0001g0119 | 2 | HG01243.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.53+1049A>C | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 1/7 | chr2 | 33598120 | ||||||
chr2:33598224
|
T | C | 2 | a0001c0001t0002g0023a0001c0001t0011g0148 | 5 | HG02293.hp1 NA18952.hp2 NA18977.hp1 others(2): Show |
intron_variant | MODIFIER | c.53+945A>G | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 1/7 | chr2 | 33598224 | ||||||
chr2:33598227
|
A | G | 1 | a0001c0001t0001g0046 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.53+942T>C | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 1/7 | chr2 | 33598227 | ||||||
chr2:33598472
|
A | C | 100 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(97): Show | 263 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(260): Show |
intron_variant | MODIFIER | c.53+697T>G | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 1/7 | chr2 | 33598472 | ||||||
chr2:33598571
|
C | G | 2 | a0001c0001t0002g0009a0001c0001t0002g0049 | 8 | HG02132.hp1 NA18950.hp2 NA18990.hp2 others(5): Show |
intron_variant | MODIFIER | c.53+598G>C | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 1/7 | chr2 | 33598571 | ||||||
chr2:33598777
|
G | C | 1 | a0001c0001t0001g0045 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.53+392C>G | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 1/7 | chr2 | 33598777 | ||||||
chr2:33598803
|
C | T | 1 | a0001c0001t0002g0048 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.53+366G>A | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 1/7 | chr2 | 33598803 | ||||||
chr2:33599028
|
G | T | 1 | a0001c0001t0002g0047 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.53+141C>A | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 1/7 | chr2 | 33599028 | ||||||
chr2:33599052
|
A | C | 1 | a0001c0001t0001g0046 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.53+117T>G | FAM98A | ENSG00000119812.20 | transcript | ENST00000238823.13 | protein_coding | 1/7 | chr2 | 33599052 |