geneid | 203259 |
---|---|
ensemblid | ENSG00000164970.15 |
hgncid | 19920 |
symbol | FAM219A |
name | family with sequence similarity 219 member A |
refseq_nuc | NM_001184940.2 |
refseq_prot | NP_001171869.1 |
ensembl_nuc | ENST00000651358.1 |
ensembl_prot | ENSP00000499069.1 |
mane_status | MANE Select |
chr | chr9 |
start | 34398184 |
end | 34458570 |
strand | - |
ver | v1.2 |
region | chr9:34398184-34458570 |
region5000 | chr9:34393184-34463570 |
regionname0 | FAM219A_chr9_34398184_34458570 |
regionname5000 | FAM219A_chr9_34393184_34463570 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 185 | 396 | 84 | 74 | 186 | 12 | 38 | 140 | FAM219A_chr9_34393184_34463570 | FAM219A | copy fasta | chr9 | 34393184 | 34463570 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 558 | 391 | 84 | 72 | 184 | 12 | 37 | FAM219A_chr9_34393184_34463570 | FAM219A | copy fasta | chr9 | 34393184 | 34463570 |
c0002 | 0/0 | 558 | 3 | 0 | 2 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | copy fasta | chr9 | 34393184 | 34463570 |
c0003 | 0/0 | 558 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | copy fasta | chr9 | 34393184 | 34463570 |
c0004 | 0/0 | 558 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | copy fasta | chr9 | 34393184 | 34463570 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/0 | 3088 | 120 | 30 | 15 | 59 | 2 | 13 | FAM219A_chr9_34393184_34463570 | FAM219A | copy fasta | chr9 | 34393184 | 34463570 |
t0002 | 0/1 | 3088 | 107 | 21 | 25 | 39 | 5 | 16 | FAM219A_chr9_34393184_34463570 | FAM219A | copy fasta | chr9 | 34393184 | 34463570 |
t0003 | 0/0 | 3084 | 46 | 1 | 6 | 36 | 0 | 3 | FAM219A_chr9_34393184_34463570 | FAM219A | copy fasta | chr9 | 34393184 | 34463570 |
t0004 | 0/0 | 3088 | 36 | 1 | 11 | 18 | 2 | 4 | FAM219A_chr9_34393184_34463570 | FAM219A | copy fasta | chr9 | 34393184 | 34463570 |
t0005 | 0/0 | 3088 | 29 | 3 | 3 | 23 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | copy fasta | chr9 | 34393184 | 34463570 |
t0006 | 0/0 | 3088 | 14 | 13 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | copy fasta | chr9 | 34393184 | 34463570 |
t0007 | 0/0 | 3088 | 13 | 0 | 9 | 0 | 2 | 2 | FAM219A_chr9_34393184_34463570 | FAM219A | copy fasta | chr9 | 34393184 | 34463570 |
t0008 | 0/0 | 3087 | 4 | 0 | 0 | 4 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | copy fasta | chr9 | 34393184 | 34463570 |
t0009 | 0/0 | 3088 | 4 | 4 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | copy fasta | chr9 | 34393184 | 34463570 |
t0010 | 0/0 | 3088 | 3 | 3 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | copy fasta | chr9 | 34393184 | 34463570 |
t0011 | 0/0 | 3088 | 2 | 2 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | copy fasta | chr9 | 34393184 | 34463570 |
t0012 | 0/0 | 3088 | 2 | 2 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | copy fasta | chr9 | 34393184 | 34463570 |
t0013 | 0/0 | 3088 | 2 | 2 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | copy fasta | chr9 | 34393184 | 34463570 |
t0014 | 0/0 | 3088 | 2 | 0 | 0 | 2 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | copy fasta | chr9 | 34393184 | 34463570 |
t0015 | 0/0 | 3088 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | copy fasta | chr9 | 34393184 | 34463570 |
t0016 | 0/0 | 3088 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | copy fasta | chr9 | 34393184 | 34463570 |
t0017 | 0/0 | 3088 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | copy fasta | chr9 | 34393184 | 34463570 |
t0018 | 0/0 | 3088 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | copy fasta | chr9 | 34393184 | 34463570 |
t0019 | 0/0 | 3088 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | copy fasta | chr9 | 34393184 | 34463570 |
t0020 | 0/0 | 3088 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | copy fasta | chr9 | 34393184 | 34463570 |
t0021 | 0/0 | 3088 | 1 | 0 | 0 | 0 | 1 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | copy fasta | chr9 | 34393184 | 34463570 |
t0022 | 0/0 | 3088 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | copy fasta | chr9 | 34393184 | 34463570 |
t0023 | 0/0 | 3088 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | copy fasta | chr9 | 34393184 | 34463570 |
t0024 | 0/0 | 3088 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | copy fasta | chr9 | 34393184 | 34463570 |
t0025 | 0/0 | 3088 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | copy fasta | chr9 | 34393184 | 34463570 |
t0026 | 0/0 | 3088 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | copy fasta | chr9 | 34393184 | 34463570 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0005 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0190 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0219 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0321 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0355 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0362 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0364 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0365 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0366 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0370 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0371 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0373 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0374 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0375 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0376 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0377 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0378 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0379 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0380 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0381 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
g0382 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 558 | 391 | 84 | 72 | 184 | 12 | 37 | FAM219A_chr9_34393184_34463570 | FAM219A | copy fasta | chr9 | 34393184 | 34463570 |
a0001c0002 | 0/0 | 558 | 3 | 0 | 2 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | copy fasta | chr9 | 34393184 | 34463570 |
a0001c0003 | 0/0 | 558 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | copy fasta | chr9 | 34393184 | 34463570 |
a0001c0004 | 0/0 | 558 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | copy fasta | chr9 | 34393184 | 34463570 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 3645 | 116 | 30 | 13 | 58 | 2 | 12 | FAM219A_chr9_34393184_34463570 | FAM219A | copy fasta | chr9 | 34393184 | 34463570 |
a0001c0001t0002 | 0/1 | 3645 | 107 | 21 | 25 | 39 | 5 | 16 | FAM219A_chr9_34393184_34463570 | FAM219A | copy fasta | chr9 | 34393184 | 34463570 |
a0001c0001t0003 | 0/0 | 3641 | 45 | 1 | 6 | 35 | 0 | 3 | FAM219A_chr9_34393184_34463570 | FAM219A | copy fasta | chr9 | 34393184 | 34463570 |
a0001c0001t0004 | 0/0 | 3645 | 36 | 1 | 11 | 18 | 2 | 4 | FAM219A_chr9_34393184_34463570 | FAM219A | copy fasta | chr9 | 34393184 | 34463570 |
a0001c0001t0005 | 0/0 | 3645 | 29 | 3 | 3 | 23 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | copy fasta | chr9 | 34393184 | 34463570 |
a0001c0001t0006 | 0/0 | 3645 | 14 | 13 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | copy fasta | chr9 | 34393184 | 34463570 |
a0001c0001t0007 | 0/0 | 3645 | 13 | 0 | 9 | 0 | 2 | 2 | FAM219A_chr9_34393184_34463570 | FAM219A | copy fasta | chr9 | 34393184 | 34463570 |
a0001c0001t0008 | 0/0 | 3644 | 4 | 0 | 0 | 4 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | copy fasta | chr9 | 34393184 | 34463570 |
a0001c0001t0009 | 0/0 | 3645 | 4 | 4 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | copy fasta | chr9 | 34393184 | 34463570 |
a0001c0001t0010 | 0/0 | 3645 | 3 | 3 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | copy fasta | chr9 | 34393184 | 34463570 |
a0001c0001t0011 | 0/0 | 3645 | 2 | 2 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | copy fasta | chr9 | 34393184 | 34463570 |
a0001c0001t0012 | 0/0 | 3645 | 2 | 2 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | copy fasta | chr9 | 34393184 | 34463570 |
a0001c0001t0013 | 0/0 | 3645 | 2 | 2 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | copy fasta | chr9 | 34393184 | 34463570 |
a0001c0001t0014 | 0/0 | 3645 | 2 | 0 | 0 | 2 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | copy fasta | chr9 | 34393184 | 34463570 |
a0001c0001t0015 | 0/0 | 3645 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | copy fasta | chr9 | 34393184 | 34463570 |
a0001c0001t0016 | 0/0 | 3645 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | copy fasta | chr9 | 34393184 | 34463570 |
a0001c0001t0017 | 0/0 | 3645 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | copy fasta | chr9 | 34393184 | 34463570 |
a0001c0001t0018 | 0/0 | 3645 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | copy fasta | chr9 | 34393184 | 34463570 |
a0001c0001t0019 | 0/0 | 3645 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | copy fasta | chr9 | 34393184 | 34463570 |
a0001c0001t0020 | 0/0 | 3645 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | copy fasta | chr9 | 34393184 | 34463570 |
a0001c0001t0021 | 0/0 | 3645 | 1 | 0 | 0 | 0 | 1 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | copy fasta | chr9 | 34393184 | 34463570 |
a0001c0001t0022 | 0/0 | 3645 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | copy fasta | chr9 | 34393184 | 34463570 |
a0001c0001t0023 | 0/0 | 3645 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | copy fasta | chr9 | 34393184 | 34463570 |
a0001c0001t0024 | 0/0 | 3645 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | copy fasta | chr9 | 34393184 | 34463570 |
a0001c0001t0025 | 0/0 | 3645 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | copy fasta | chr9 | 34393184 | 34463570 |
a0001c0001t0026 | 0/0 | 3645 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | copy fasta | chr9 | 34393184 | 34463570 |
a0001c0002t0001 | 0/0 | 3645 | 3 | 0 | 2 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | copy fasta | chr9 | 34393184 | 34463570 |
a0001c0003t0001 | 0/0 | 3645 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | copy fasta | chr9 | 34393184 | 34463570 |
a0001c0004t0003 | 0/0 | 3641 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | copy fasta | chr9 | 34393184 | 34463570 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0001g0190 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0001g0355 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0001g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0001g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0001g0374 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0001g0375 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0001g0376 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0001g0377 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0001g0380 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0001g0381 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0002g0005 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0002g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0002g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0002g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0002g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0002g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0002g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0002g0219 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0002g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0002g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0002g0321 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0002g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0002g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0002g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0002g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0002g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0002g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0002g0379 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0003g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0003g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0003g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0003g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0003g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0003g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0003g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0003g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0003g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0003g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0003g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0003g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0003g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0003g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0003g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0003g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0003g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0003g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0003g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0003g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0003g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0003g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0003g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0003g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0003g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0003g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0003g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0003g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0003g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0003g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0003g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0003g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0003g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0003g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0003g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0003g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0003g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0003g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0003g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0003g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0003g0373 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0004g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0004g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0004g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0004g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0004g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0004g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0004g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0004g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0004g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0004g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0004g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0004g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0004g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0004g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0004g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0004g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0004g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0004g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0004g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0004g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0004g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0004g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0004g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0004g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0004g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0004g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0004g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0004g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0004g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0004g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0004g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0004g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0004g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0004g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0004g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0005g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0005g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0005g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0005g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0005g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0005g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0005g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0005g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0005g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0005g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0005g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0005g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0005g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0005g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0005g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0005g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0005g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0005g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0005g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0005g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0005g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0005g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0005g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0005g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0005g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0005g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0005g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0005g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0005g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0006g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0006g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0006g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0006g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0006g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0006g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0006g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0006g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0006g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0006g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0006g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0006g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0006g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0006g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0007g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0007g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0007g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0007g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0007g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0007g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0007g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0007g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0007g0362 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0007g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0007g0364 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0007g0365 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0007g0382 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0008g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0008g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0008g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0008g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0009g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0009g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0009g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0009g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0010g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0010g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0010g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0011g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0011g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0012g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0012g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0013g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0013g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0014g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0014g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0015g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0016g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0017g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0018g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0019g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0020g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0021g0366 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0022g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0023g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0024g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0025g0378 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0001t0026g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0002t0001g0370 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0002t0001g0371 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0003t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
a0001c0004t0003g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0007 | g0362 | EUR | GBR | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0146 | EUR | GBR | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0251 | EUR | FIN | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG00280 | hp2 | a0001 | c0001 | t0004 | g0048 | EUR | FIN | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0321 | EUR | FIN | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG00323 | hp2 | a0001 | c0001 | t0002 | g0130 | EUR | FIN | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG00423 | hp1 | a0001 | c0001 | t0004 | g0212 | EAS | CHS | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | CHS | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0258 | EAS | CHS | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | CHS | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG00544 | hp2 | a0001 | c0001 | t0002 | g0343 | EAS | CHS | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG00558 | hp1 | a0001 | c0001 | t0005 | g0025 | EAS | CHS | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG00558 | hp2 | a0001 | c0001 | t0003 | g0339 | EAS | CHS | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG00597 | hp1 | a0001 | c0001 | t0014 | g0272 | EAS | CHS | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0176 | EAS | CHS | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | CHS | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0124 | EAS | CHS | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG00621 | hp1 | a0001 | c0001 | t0020 | g0281 | EAS | CHS | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG00621 | hp2 | a0001 | c0001 | t0003 | g0120 | EAS | CHS | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0248 | AMR | PUR | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0128 | AMR | PUR | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0179 | AMR | PUR | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG00673 | hp1 | a0001 | c0001 | t0003 | g0352 | EAS | CHS | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG00673 | hp2 | a0001 | c0001 | t0002 | g0173 | EAS | CHS | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG00735 | hp2 | a0001 | c0001 | t0003 | g0336 | AMR | PUR | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG00741 | hp1 | a0001 | c0001 | t0007 | g0364 | AMR | PUR | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG00741 | hp2 | a0001 | c0001 | t0007 | g0169 | AMR | PUR | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG01070 | hp1 | a0001 | c0001 | t0007 | g0196 | AMR | PUR | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG01070 | hp2 | a0001 | c0001 | t0007 | g0360 | AMR | PUR | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG01074 | hp1 | a0001 | c0001 | t0004 | g0061 | AMR | PUR | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0279 | AMR | PUR | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG01081 | hp1 | a0001 | c0001 | t0004 | g0056 | AMR | PUR | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG01081 | hp2 | a0001 | c0001 | t0002 | g0199 | AMR | PUR | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG01099 | hp1 | a0001 | c0001 | t0004 | g0054 | AMR | PUR | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG01099 | hp2 | a0001 | c0002 | t0001 | g0370 | AMR | PUR | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG01106 | hp1 | a0001 | c0001 | t0002 | g0150 | AMR | PUR | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0183 | AMR | PUR | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0136 | AMR | PUR | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0216 | AMR | PUR | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG01167 | hp1 | a0001 | c0001 | t0002 | g0116 | AMR | PUR | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG01167 | hp2 | a0001 | c0001 | t0007 | g0359 | AMR | PUR | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG01168 | hp1 | a0001 | c0001 | t0002 | g0197 | AMR | PUR | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0246 | AMR | PUR | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0247 | AMR | PUR | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0121 | AMR | PUR | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG01175 | hp1 | a0001 | c0001 | t0004 | g0065 | AMR | PUR | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG01243 | hp2 | a0001 | c0001 | t0004 | g0096 | AMR | PUR | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG01255 | hp1 | a0001 | c0001 | t0026 | g0144 | AMR | CLM | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG01255 | hp2 | a0001 | c0001 | t0024 | g0095 | AMR | CLM | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG01257 | hp1 | a0001 | c0001 | t0004 | g0064 | AMR | CLM | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0172 | AMR | CLM | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG01258 | hp1 | a0001 | c0001 | t0004 | g0055 | AMR | CLM | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0122 | AMR | CLM | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0374 | AMR | CLM | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0125 | AMR | CLM | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG01346 | hp1 | a0001 | c0001 | t0002 | g0119 | AMR | CLM | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0201 | AMR | CLM | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0376 | AMR | CLM | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG01358 | hp2 | a0001 | c0001 | t0002 | g0135 | AMR | CLM | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG01361 | hp1 | a0001 | c0001 | t0002 | g0221 | AMR | CLM | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG01361 | hp2 | a0001 | c0002 | t0001 | g0371 | AMR | CLM | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG01433 | hp1 | a0001 | c0001 | t0003 | g0373 | AMR | CLM | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG01433 | hp2 | a0001 | c0001 | t0016 | g0063 | AMR | CLM | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG01496 | hp1 | a0001 | c0001 | t0003 | g0098 | AMR | CLM | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG01496 | hp2 | a0001 | c0001 | t0006 | g0051 | AMR | CLM | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG01516 | hp1 | a0001 | c0001 | t0002 | g0105 | EUR | IBS | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG01516 | hp2 | a0001 | c0001 | t0021 | g0366 | EUR | IBS | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG01891 | hp1 | a0001 | c0001 | t0010 | g0082 | AFR | ACB | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG01891 | hp2 | a0001 | c0001 | t0011 | g0041 | AFR | ACB | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG01928 | hp1 | a0001 | c0001 | t0005 | g0032 | AMR | PEL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0381 | AMR | PEL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG01934 | hp1 | a0001 | c0001 | t0005 | g0021 | AMR | PEL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG01934 | hp2 | a0001 | c0001 | t0004 | g0049 | AMR | PEL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG01943 | hp1 | a0001 | c0001 | t0007 | g0361 | AMR | PEL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG01943 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | PEL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG01952 | hp1 | a0001 | c0001 | t0003 | g0345 | AMR | PEL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG01952 | hp2 | a0001 | c0001 | t0004 | g0060 | AMR | PEL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG01975 | hp1 | a0001 | c0001 | t0003 | g0338 | AMR | PEL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0377 | AMR | PEL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG01978 | hp1 | a0001 | c0001 | t0004 | g0053 | AMR | PEL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG01978 | hp2 | a0001 | c0001 | t0007 | g0203 | AMR | PEL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0113 | AMR | PEL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG01981 | hp2 | a0001 | c0001 | t0025 | g0378 | AMR | PEL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PEL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0307 | AMR | PEL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0380 | AMR | PEL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG02004 | hp2 | a0001 | c0001 | t0003 | g0337 | AMR | PEL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG02015 | hp1 | a0001 | c0001 | t0002 | g0222 | EAS | KHV | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | KHV | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG02027 | hp1 | a0001 | c0001 | t0005 | g0017 | EAS | KHV | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG02027 | hp2 | a0001 | c0001 | t0003 | g0319 | EAS | KHV | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | KHV | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0320 | EAS | KHV | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0253 | AFR | ACB | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | ACB | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | KHV | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG02056 | hp2 | a0001 | c0001 | t0004 | g0156 | EAS | KHV | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG02071 | hp1 | a0001 | c0001 | t0002 | g0261 | EAS | KHV | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG02074 | hp1 | a0001 | c0001 | t0005 | g0037 | EAS | KHV | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | KHV | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | KHV | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0160 | EAS | KHV | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG02083 | hp1 | a0001 | c0001 | t0004 | g0225 | EAS | KHV | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | KHV | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG02129 | hp1 | a0001 | c0001 | t0002 | g0171 | EAS | KHV | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0344 | EAS | KHV | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | KHV | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG02132 | hp2 | a0001 | c0001 | t0003 | g0332 | EAS | KHV | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | KHV | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | KHV | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG02145 | hp1 | a0001 | c0001 | t0002 | g0213 | AFR | ACB | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG02145 | hp2 | a0001 | c0001 | t0002 | g0200 | AFR | ACB | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG02155 | hp1 | a0001 | c0001 | t0019 | g0267 | EAS | CDX | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG02155 | hp2 | a0001 | c0001 | t0002 | g0147 | EAS | CDX | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG02165 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | CDX | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0180 | EAS | CDX | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG02257 | hp1 | a0001 | c0001 | t0006 | g0072 | AFR | ACB | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0237 | AFR | ACB | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0269 | AFR | ACB | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0372 | AFR | ACB | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG02273 | hp1 | a0001 | c0001 | t0005 | g0020 | AMR | PEL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | PEL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG02280 | hp1 | a0001 | c0001 | t0006 | g0069 | AFR | ACB | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | ACB | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0245 | AMR | PEL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG02293 | hp2 | a0001 | c0001 | t0002 | g0149 | AMR | PEL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0010 | AMR | PEL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG02300 | hp2 | a0001 | c0001 | t0007 | g0151 | AMR | PEL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | ACB | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG02451 | hp2 | a0001 | c0001 | t0017 | g0094 | AFR | ACB | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG02523 | hp1 | a0001 | c0001 | t0005 | g0036 | EAS | KHV | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG02523 | hp2 | a0001 | c0001 | t0003 | g0333 | EAS | KHV | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG02572 | hp1 | a0001 | c0001 | t0006 | g0080 | AFR | GWD | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | GWD | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG02602 | hp1 | a0001 | c0001 | t0003 | g0341 | SAS | PJL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0175 | SAS | PJL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG02615 | hp1 | a0001 | c0001 | t0002 | g0215 | AFR | GWD | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | GWD | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG02622 | hp1 | a0001 | c0001 | t0011 | g0042 | AFR | GWD | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG02622 | hp2 | a0001 | c0001 | t0006 | g0111 | AFR | GWD | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG02630 | hp1 | a0001 | c0001 | t0010 | g0093 | AFR | GWD | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0242 | AFR | GWD | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG02647 | hp1 | a0001 | c0001 | t0018 | g0099 | AFR | GWD | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG02647 | hp2 | a0001 | c0001 | t0002 | g0227 | AFR | GWD | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0260 | SAS | PJL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG02683 | hp2 | a0001 | c0001 | t0002 | g0127 | SAS | PJL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0118 | SAS | PJL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG02698 | hp2 | a0001 | c0002 | t0001 | g0193 | SAS | PJL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | GWD | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG02717 | hp2 | a0001 | c0001 | t0002 | g0206 | AFR | GWD | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0235 | SAS | PJL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG02735 | hp2 | a0001 | c0001 | t0007 | g0382 | SAS | PJL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0188 | SAS | PJL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0355 | SAS | PJL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | GWD | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0189 | AFR | GWD | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | GWD | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG02818 | hp2 | a0001 | c0001 | t0009 | g0142 | AFR | GWD | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0330 | AFR | GWD | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG02895 | hp2 | a0001 | c0001 | t0006 | g0071 | AFR | GWD | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG02896 | hp1 | a0001 | c0001 | t0006 | g0143 | AFR | GWD | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | GWD | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG02897 | hp1 | a0001 | c0001 | t0006 | g0073 | AFR | GWD | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG02897 | hp2 | a0001 | c0001 | t0006 | g0138 | AFR | GWD | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | ESN | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG02922 | hp2 | a0001 | c0001 | t0002 | g0194 | AFR | ESN | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | ESN | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG02965 | hp2 | a0001 | c0001 | t0002 | g0070 | AFR | ESN | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG02970 | hp1 | a0001 | c0001 | t0002 | g0115 | AFR | ESN | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0255 | AFR | ESN | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0114 | SAS | PJL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG03017 | hp2 | a0001 | c0001 | t0004 | g0059 | SAS | PJL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG03041 | hp1 | a0001 | c0001 | t0002 | g0214 | AFR | GWD | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0270 | AFR | GWD | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | MSL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | MSL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG03139 | hp1 | a0001 | c0001 | t0002 | g0228 | AFR | ESN | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0296 | AFR | ESN | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG03195 | hp1 | a0001 | c0001 | t0012 | g0044 | AFR | ESN | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG03195 | hp2 | a0001 | c0001 | t0002 | g0087 | AFR | ESN | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0264 | AFR | MSL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG03225 | hp2 | a0001 | c0001 | t0006 | g0047 | AFR | MSL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0278 | AFR | MSL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG03453 | hp2 | a0001 | c0001 | t0002 | g0205 | AFR | MSL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG03486 | hp1 | a0001 | c0001 | t0002 | g0078 | AFR | MSL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | MSL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0236 | SAS | PJL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG03490 | hp2 | a0001 | c0001 | t0002 | g0202 | SAS | PJL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0379 | SAS | PJL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0291 | SAS | PJL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG03516 | hp1 | a0001 | c0001 | t0013 | g0083 | AFR | ESN | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG03516 | hp2 | a0001 | c0001 | t0012 | g0043 | AFR | ESN | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG03540 | hp1 | a0001 | c0001 | t0010 | g0086 | AFR | GWD | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG03540 | hp2 | a0001 | c0001 | t0002 | g0207 | AFR | GWD | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG03579 | hp1 | a0001 | c0001 | t0002 | g0192 | AFR | MSL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG03579 | hp2 | a0001 | c0001 | t0009 | g0139 | AFR | MSL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0271 | SAS | PJL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG03654 | hp2 | a0001 | c0001 | t0007 | g0365 | SAS | PJL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0170 | SAS | PJL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG03669 | hp2 | a0001 | c0001 | t0002 | g0005 | SAS | PJL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0131 | SAS | STU | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0292 | SAS | STU | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG03704 | hp1 | a0001 | c0001 | t0003 | g0290 | SAS | PJL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0148 | SAS | PJL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG03834 | hp1 | a0001 | c0001 | t0004 | g0062 | SAS | BEB | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0187 | SAS | BEB | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG03927 | hp1 | a0001 | c0001 | t0004 | g0249 | SAS | BEB | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG03927 | hp2 | a0001 | c0001 | t0002 | g0223 | SAS | BEB | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0234 | SAS | BEB | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG03942 | hp2 | a0001 | c0001 | t0002 | g0145 | SAS | BEB | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0375 | SAS | STU | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0233 | SAS | STU | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0168 | SAS | BEB | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG04184 | hp2 | a0001 | c0001 | t0003 | g0347 | SAS | BEB | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0286 | SAS | STU | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0204 | SAS | STU | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG04228 | hp1 | a0001 | c0001 | t0004 | g0066 | SAS | STU | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0134 | SAS | STU | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA18747 | hp1 | a0001 | c0001 | t0008 | g0161 | EAS | CHB | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | CHB | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA18906 | hp1 | a0001 | c0001 | t0005 | g0035 | AFR | YRI | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA18906 | hp2 | a0001 | c0001 | t0006 | g0369 | AFR | YRI | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA18939 | hp1 | a0001 | c0001 | t0005 | g0022 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA18939 | hp2 | a0001 | c0001 | t0003 | g0316 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA18940 | hp1 | a0001 | c0001 | t0004 | g0157 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA18940 | hp2 | a0001 | c0001 | t0005 | g0014 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA18941 | hp1 | a0001 | c0001 | t0005 | g0016 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA18944 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA18945 | hp2 | a0001 | c0001 | t0005 | g0040 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA18947 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA18948 | hp1 | a0001 | c0001 | t0005 | g0023 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA18948 | hp2 | a0001 | c0001 | t0003 | g0334 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA18949 | hp1 | a0001 | c0001 | t0002 | g0282 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA18950 | hp1 | a0001 | c0001 | t0004 | g0211 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA18950 | hp2 | a0001 | c0001 | t0003 | g0349 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA18952 | hp1 | a0001 | c0001 | t0003 | g0335 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA18953 | hp1 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA18956 | hp1 | a0001 | c0001 | t0003 | g0353 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA18956 | hp2 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA18957 | hp2 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA18959 | hp1 | a0001 | c0001 | t0005 | g0027 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA18960 | hp2 | a0001 | c0001 | t0003 | g0318 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA18962 | hp1 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA18962 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA18964 | hp2 | a0001 | c0001 | t0003 | g0356 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA18965 | hp2 | a0001 | c0001 | t0005 | g0013 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA18967 | hp2 | a0001 | c0001 | t0003 | g0315 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA18971 | hp1 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA18971 | hp2 | a0001 | c0001 | t0004 | g0153 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA18973 | hp2 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA18974 | hp1 | a0001 | c0001 | t0004 | g0209 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA18974 | hp2 | a0001 | c0001 | t0002 | g0257 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA18975 | hp1 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA18977 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA18979 | hp1 | a0001 | c0001 | t0003 | g0323 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA18979 | hp2 | a0001 | c0001 | t0015 | g0011 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA18980 | hp2 | a0001 | c0001 | t0005 | g0029 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA18981 | hp1 | a0001 | c0001 | t0003 | g0324 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA18981 | hp2 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA18982 | hp1 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0162 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA18983 | hp1 | a0001 | c0001 | t0003 | g0357 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA18983 | hp2 | a0001 | c0001 | t0005 | g0031 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0368 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA18984 | hp2 | a0001 | c0001 | t0002 | g0297 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA18988 | hp2 | a0001 | c0001 | t0003 | g0317 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA18989 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA18989 | hp2 | a0001 | c0001 | t0003 | g0325 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA18990 | hp1 | a0001 | c0001 | t0023 | g0159 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA18991 | hp1 | a0001 | c0001 | t0005 | g0018 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA18991 | hp2 | a0001 | c0001 | t0002 | g0259 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA18992 | hp2 | a0001 | c0001 | t0005 | g0026 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA18993 | hp1 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA18994 | hp1 | a0001 | c0001 | t0003 | g0322 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA18994 | hp2 | a0001 | c0001 | t0004 | g0067 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA18998 | hp1 | a0001 | c0001 | t0003 | g0328 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA18999 | hp1 | a0001 | c0001 | t0005 | g0038 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA19000 | hp1 | a0001 | c0001 | t0004 | g0107 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA19001 | hp1 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA19001 | hp2 | a0001 | c0001 | t0003 | g0350 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA19002 | hp1 | a0001 | c0001 | t0004 | g0137 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0367 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA19003 | hp2 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA19005 | hp1 | a0001 | c0001 | t0003 | g0326 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA19005 | hp2 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA19007 | hp2 | a0001 | c0001 | t0003 | g0327 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA19010 | hp1 | a0001 | c0001 | t0004 | g0208 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA19030 | hp1 | a0001 | c0001 | t0002 | g0186 | AFR | LWK | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | LWK | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA19043 | hp1 | a0001 | c0001 | t0005 | g0012 | AFR | LWK | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | LWK | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA19054 | hp1 | a0001 | c0001 | t0003 | g0348 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA19055 | hp2 | a0001 | c0001 | t0005 | g0015 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA19057 | hp1 | a0001 | c0001 | t0004 | g0152 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA19060 | hp1 | a0001 | c0001 | t0003 | g0342 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA19060 | hp2 | a0001 | c0001 | t0008 | g0164 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA19062 | hp1 | a0001 | c0001 | t0005 | g0030 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA19063 | hp2 | a0001 | c0001 | t0005 | g0019 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA19065 | hp1 | a0001 | c0001 | t0022 | g0305 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA19065 | hp2 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA19067 | hp1 | a0001 | c0001 | t0003 | g0314 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA19067 | hp2 | a0001 | c0001 | t0004 | g0108 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA19068 | hp1 | a0001 | c0001 | t0004 | g0226 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA19068 | hp2 | a0001 | c0001 | t0003 | g0354 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA19070 | hp1 | a0001 | c0001 | t0002 | g0329 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA19070 | hp2 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA19077 | hp1 | a0001 | c0001 | t0003 | g0340 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA19077 | hp2 | a0001 | c0001 | t0008 | g0165 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA19078 | hp2 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA19079 | hp1 | a0001 | c0001 | t0003 | g0346 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA19079 | hp2 | a0001 | c0001 | t0004 | g0210 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA19080 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA19080 | hp2 | a0001 | c0001 | t0014 | g0268 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA19081 | hp1 | a0001 | c0001 | t0008 | g0163 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA19081 | hp2 | a0001 | c0004 | t0003 | g0358 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA19084 | hp1 | a0001 | c0001 | t0005 | g0024 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA19084 | hp2 | a0001 | c0003 | t0001 | g0293 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA19085 | hp1 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA19087 | hp1 | a0001 | c0001 | t0004 | g0158 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA19087 | hp2 | a0001 | c0001 | t0005 | g0033 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA19088 | hp2 | a0001 | c0001 | t0005 | g0028 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA19240 | hp1 | a0001 | c0001 | t0002 | g0351 | AFR | YRI | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA19240 | hp2 | a0001 | c0001 | t0013 | g0081 | AFR | YRI | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0331 | AFR | ASW | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA20129 | hp2 | a0001 | c0001 | t0006 | g0068 | AFR | ASW | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0198 | EUR | TSI | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA20752 | hp2 | a0001 | c0001 | t0004 | g0058 | EUR | TSI | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA20805 | hp1 | a0001 | c0001 | t0007 | g0224 | EUR | TSI | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0117 | EUR | TSI | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG01123 | hp1 | a0001 | c0001 | t0004 | g0057 | AMR | CLM | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG01123 | hp2 | a0001 | c0001 | t0007 | g0363 | AMR | CLM | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG02109 | hp1 | a0001 | c0001 | t0002 | g0195 | AFR | ACB | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG02109 | hp2 | a0001 | c0001 | t0006 | g0052 | AFR | ACB | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG02559 | hp1 | a0001 | c0001 | t0009 | g0140 | AFR | ACB | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG02559 | hp2 | a0001 | c0001 | t0005 | g0039 | AFR | ACB | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG03471 | hp1 | a0001 | c0001 | t0006 | g0084 | AFR | MSL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0241 | AFR | MSL | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG06807 | hp1 | a0001 | c0001 | t0003 | g0100 | AFR | USA | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | USA | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA18955 | hp2 | a0001 | c0001 | t0005 | g0034 | EAS | JPT | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0310 | AFR | USA | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0240 | AFR | USA | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA21309 | hp1 | a0001 | c0001 | t0004 | g0089 | AFR | LWK | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
NA21309 | hp2 | a0001 | c0001 | t0009 | g0141 | AFR | LWK | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0219 | REF | REF | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0190 | REF | REF | FAM219A_chr9_34393184_34463570 | FAM219A | chr9 | 34393184 | 34463570 |
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 |
---|
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:34400982
|
G | A | 1 | a0001c0002 | 3 | HG01099.hp2 HG01361.hp2 HG02698.hp2 |
synonymous_variant | LOW | c.540C>T | p.Thr180Thr | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 6/6 | 847/3645 | 540/558 | 180/185 | chr9 | 34400982 | ||
chr9:34401030
|
G | T | 1 | a0001c0003 | 1 | NA19084.hp2 | synonymous_variant | LOW | c.492C>A | p.Pro164Pro | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 6/6 | 799/3645 | 492/558 | 164/185 | chr9 | 34401030 | ||
chr9:34402706
|
T | G | 1 | a0001c0004 | 1 | NA19081.hp2 | splice_region_variant&synonymous_variant | LOW | c.262A>C | p.Arg88Arg | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 3/6 | 569/3645 | 262/558 | 88/185 | chr9 | 34402706 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:34398268
|
TA | T | 1 | a0001c0001t0008 | 4 | NA18747.hp1 NA19060.hp2 NA19077.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2695delT | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 6/6 | 2695 | chr9 | 34398268 | |||||
chr9:34398587
|
G | C | 2 | a0001c0001t0010a0001c0001t0018 | 4 | HG01891.hp1 HG02630.hp1 HG02647.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2377C>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 6/6 | 2377 | chr9 | 34398587 | |||||
chr9:34399004
|
C | A | 11 | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(8): Show | 211 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(208): Show |
3_prime_UTR_variant | MODIFIER | c.*1960G>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 6/6 | 1960 | chr9 | 34399004 | |||||
chr9:34399172
|
G | A | 2 | a0001c0001t0004a0001c0001t0006 | 50 | HG00280.hp2 HG00423.hp1 HG01074.hp1 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*1792C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 6/6 | 1792 | chr9 | 34399172 | |||||
chr9:34399340
|
A | G | 2 | a0001c0001t0007a0001c0001t0021 | 14 | HG00099.hp1 HG00741.hp1 HG00741.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1624T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 6/6 | 1624 | chr9 | 34399340 | |||||
chr9:34399504
|
C | G | 1 | a0001c0001t0020 | 1 | HG00621.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1460G>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 6/6 | 1460 | chr9 | 34399504 | |||||
chr9:34399505
|
CCAAA | C | 2 | a0001c0001t0003a0001c0004t0003 | 46 | HG00558.hp2 HG00621.hp2 HG00673.hp1 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*1455_*1458delTTTG | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 6/6 | 1455 | chr9 | 34399505 | |||||
chr9:34399663
|
A | C | 1 | a0001c0001t0024 | 1 | HG01255.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1301T>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 6/6 | 1301 | chr9 | 34399663 | |||||
chr9:34399683
|
A | G | 1 | a0001c0001t0019 | 1 | HG02155.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1281T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 6/6 | 1281 | chr9 | 34399683 | |||||
chr9:34399892
|
G | A | 1 | a0001c0001t0021 | 1 | HG01516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1072C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 6/6 | 1072 | chr9 | 34399892 | |||||
chr9:34400188
|
C | A | 1 | a0001c0001t0024 | 1 | HG01255.hp2 | 3_prime_UTR_variant | MODIFIER | c.*776G>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 6/6 | 776 | chr9 | 34400188 | |||||
chr9:34400204
|
G | A | 1 | a0001c0001t0022 | 1 | NA19065.hp1 | 3_prime_UTR_variant | MODIFIER | c.*760C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 6/6 | 760 | chr9 | 34400204 | |||||
chr9:34400251
|
G | A | 1 | a0001c0001t0023 | 1 | NA18990.hp1 | 3_prime_UTR_variant | MODIFIER | c.*713C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 6/6 | 713 | chr9 | 34400251 | |||||
chr9:34400304
|
A | G | 1 | a0001c0001t0018 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*660T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 6/6 | 660 | chr9 | 34400304 | |||||
chr9:34400340
|
G | A | 1 | a0001c0001t0014 | 2 | HG00597.hp1 NA19080.hp2 |
3_prime_UTR_variant | MODIFIER | c.*624C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 6/6 | 624 | chr9 | 34400340 | |||||
chr9:34400475
|
T | C | 1 | a0001c0001t0024 | 1 | HG01255.hp2 | 3_prime_UTR_variant | MODIFIER | c.*489A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 6/6 | 489 | chr9 | 34400475 | |||||
chr9:34400503
|
G | A | 1 | a0001c0001t0025 | 1 | HG01981.hp2 | 3_prime_UTR_variant | MODIFIER | c.*461C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 6/6 | 461 | chr9 | 34400503 | |||||
chr9:34400583
|
C | T | 7 | a0001c0001t0002a0001c0001t0005a0001c0001t0008others(4): Show | 144 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(141): Show |
3_prime_UTR_variant | MODIFIER | c.*381G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 6/6 | 381 | chr9 | 34400583 | |||||
chr9:34400598
|
A | G | 1 | a0001c0001t0013 | 2 | HG03516.hp1 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*366T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 6/6 | 366 | chr9 | 34400598 | |||||
chr9:34400607
|
G | A | 1 | a0001c0001t0004 | 36 | HG00280.hp2 HG00423.hp1 HG01074.hp1 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*357C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 6/6 | 357 | chr9 | 34400607 | |||||
chr9:34400687
|
A | G | 1 | a0001c0001t0016 | 1 | HG01433.hp2 | 3_prime_UTR_variant | MODIFIER | c.*277T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 6/6 | 277 | chr9 | 34400687 | |||||
chr9:34400952
|
T | C | 1 | a0001c0001t0026 | 1 | HG01255.hp1 | 3_prime_UTR_variant | MODIFIER | c.*12A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 6/6 | 12 | chr9 | 34400952 | |||||
chr9:34458322
|
C | T | 1 | a0001c0001t0012 | 2 | HG03195.hp1 HG03516.hp2 |
5_prime_UTR_variant | MODIFIER | c.-59G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/6 | 59 | chr9 | 34458322 | |||||
chr9:34458380
|
C | G | 2 | a0001c0001t0005a0001c0001t0011 | 31 | HG00558.hp1 HG01891.hp2 HG01928.hp1 others(28): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-117G>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/6 | chr9 | 34458380 | ||||||
chr9:34458536
|
G | T | 1 | a0001c0001t0015 | 1 | NA18979.hp2 | 5_prime_UTR_variant | MODIFIER | c.-273C>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/6 | 273 | chr9 | 34458536 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:34401184
|
C | T | 1 | a0001c0001t0004g0058 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.400-62G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 5/5 | chr9 | 34401184 | ||||||
chr9:34401372
|
C | A | 1 | a0001c0001t0004g0061 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.400-250G>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 5/5 | chr9 | 34401372 | ||||||
chr9:34401461
|
G | A | 1 | a0001c0001t0018g0099 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.399+205C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 5/5 | chr9 | 34401461 | ||||||
chr9:34401494
|
AGGCCAGT others(15): Show |
A | 1 | a0001c0004t0003g0358 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.399+150_399+171del others(22): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 5/5 | chr9 | 34401494 | ||||||
chr9:34401766
|
T | C | 45 | a0001c0001t0001g0355a0001c0001t0002g0233a0001c0001t0003g0003others(42): Show | 48 | HG00558.hp2 HG00621.hp2 HG00673.hp1 others(45): Show |
intron_variant | MODIFIER | c.345-46A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 4/5 | chr9 | 34401766 | ||||||
chr9:34401970
|
A | G | 1 | a0001c0001t0006g0080 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.345-250T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 4/5 | chr9 | 34401970 | ||||||
chr9:34401972
|
CT | C | 145 | a0001c0001t0001g0250a0001c0001t0001g0306a0001c0001t0001g0320others(142): Show | 149 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.345-253delA | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 4/5 | chr9 | 34401972 | ||||||
chr9:34402096
|
T | C | 49 | a0001c0001t0004g0004a0001c0001t0004g0048a0001c0001t0004g0049others(46): Show | 50 | HG00280.hp2 HG00423.hp1 HG01074.hp1 others(47): Show |
intron_variant | MODIFIER | c.344+291A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 4/5 | chr9 | 34402096 | ||||||
chr9:34402120
|
C | T | 1 | a0001c0001t0006g0111 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.344+267G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 4/5 | chr9 | 34402120 | ||||||
chr9:34402175
|
A | G | 380 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(377): Show | 394 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(391): Show |
intron_variant | MODIFIER | c.344+212T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 4/5 | chr9 | 34402175 | ||||||
chr9:34402486
|
G | A | 2 | a0001c0001t0001g0288a0001c0001t0001g0289 | 2 | HG00423.hp2 HG02015.hp2 |
intron_variant | MODIFIER | c.264-19C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 3/5 | chr9 | 34402486 | ||||||
chr9:34402665
|
C | T | 14 | a0001c0001t0007g0151a0001c0001t0007g0169a0001c0001t0007g0196others(11): Show | 14 | HG00099.hp1 HG00741.hp1 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.263+40G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 3/5 | chr9 | 34402665 | ||||||
chr9:34402703
|
A | T | 1 | a0001c0004t0003g0358 | 1 | NA19081.hp2 | splice_donor_variant&intron_variant | HIGH | c.263+2T>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 3/5 | chr9 | 34402703 | ||||||
chr9:34402886
|
G | T | 1 | a0001c0004t0003g0358 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.161-79C>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 2/5 | chr9 | 34402886 | ||||||
chr9:34402898
|
G | A | 2 | a0001c0001t0001g0372a0001c0001t0001g0375 | 2 | HG02258.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.161-91C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 2/5 | chr9 | 34402898 | ||||||
chr9:34402989
|
G | A | 1 | a0001c0001t0001g0229 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.161-182C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 2/5 | chr9 | 34402989 | ||||||
chr9:34403028
|
T | C | 1 | a0001c0004t0003g0358 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.161-221A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 2/5 | chr9 | 34403028 | ||||||
chr9:34403029
|
G | T | 1 | a0001c0004t0003g0358 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.161-222C>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 2/5 | chr9 | 34403029 | ||||||
chr9:34403030
|
T | G | 1 | a0001c0004t0003g0358 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.161-223A>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 2/5 | chr9 | 34403030 | ||||||
chr9:34403033
|
T | C | 1 | a0001c0001t0002g0006 | 2 | HG01943.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.161-226A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 2/5 | chr9 | 34403033 | ||||||
chr9:34403097
|
G | A | 3 | a0001c0001t0002g0258a0001c0001t0002g0259a0001c0001t0002g0282 | 3 | HG00438.hp1 NA18949.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.161-290C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 2/5 | chr9 | 34403097 | ||||||
chr9:34403284
|
T | C | 1 | a0001c0004t0003g0358 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.161-477A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 2/5 | chr9 | 34403284 | ||||||
chr9:34403289
|
T | C | 1 | a0001c0001t0006g0084 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.161-482A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 2/5 | chr9 | 34403289 | ||||||
chr9:34403313
|
A | G | 4 | a0001c0001t0001g0074a0001c0001t0001g0270a0001c0001t0012g0043others(1): Show | 4 | HG02055.hp2 HG03041.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.161-506T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 2/5 | chr9 | 34403313 | ||||||
chr9:34403355
|
C | T | 1 | a0001c0001t0001g0242 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.161-548G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 2/5 | chr9 | 34403355 | ||||||
chr9:34403356
|
G | A | 1 | a0001c0001t0005g0015 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.161-549C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 2/5 | chr9 | 34403356 | ||||||
chr9:34403375
|
A | G | 4 | a0001c0001t0009g0139a0001c0001t0009g0140a0001c0001t0009g0141others(1): Show | 4 | HG02559.hp1 HG02818.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.161-568T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 2/5 | chr9 | 34403375 | ||||||
chr9:34403380
|
C | G | 1 | a0001c0001t0003g0098 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.161-573G>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 2/5 | chr9 | 34403380 | ||||||
chr9:34403421
|
A | T | 1 | a0001c0004t0003g0358 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.161-614T>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 2/5 | chr9 | 34403421 | ||||||
chr9:34403426
|
C | T | 47 | a0001c0001t0004g0004a0001c0001t0004g0048a0001c0001t0004g0049others(44): Show | 48 | HG00280.hp2 HG00423.hp1 HG01074.hp1 others(45): Show |
intron_variant | MODIFIER | c.161-619G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 2/5 | chr9 | 34403426 | ||||||
chr9:34403524
|
C | T | 2 | a0001c0001t0011g0041a0001c0001t0011g0042 | 2 | HG01891.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.161-717G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 2/5 | chr9 | 34403524 | ||||||
chr9:34403603
|
C | G | 1 | a0001c0001t0003g0120 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.161-796G>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 2/5 | chr9 | 34403603 | ||||||
chr9:34403666
|
T | A | 1 | a0001c0004t0003g0358 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.161-859A>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 2/5 | chr9 | 34403666 | ||||||
chr9:34403813
|
C | T | 1 | a0001c0001t0001g0117 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.161-1006G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 2/5 | chr9 | 34403813 | ||||||
chr9:34403868
|
T | A | 1 | a0001c0004t0003g0358 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.161-1061A>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 2/5 | chr9 | 34403868 | ||||||
chr9:34403906
|
T | C | 3 | a0001c0001t0002g0258a0001c0001t0002g0259a0001c0001t0002g0282 | 3 | HG00438.hp1 NA18949.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.161-1099A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 2/5 | chr9 | 34403906 | ||||||
chr9:34403984
|
G | C | 1 | a0001c0001t0001g0185 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.161-1177C>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 2/5 | chr9 | 34403984 | ||||||
chr9:34404417
|
A | G | 1 | a0001c0001t0003g0332 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.160+1448T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 2/5 | chr9 | 34404417 | ||||||
chr9:34404490
|
T | A | 1 | a0001c0004t0003g0358 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.160+1375A>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 2/5 | chr9 | 34404490 | ||||||
chr9:34404578
|
C | G | 2 | a0001c0001t0003g0340a0001c0001t0003g0346 | 2 | NA19077.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.160+1287G>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 2/5 | chr9 | 34404578 | ||||||
chr9:34404701
|
C | CT | 6 | a0001c0001t0001g0050a0001c0001t0001g0075a0001c0001t0001g0076others(3): Show | 6 | HG01175.hp2 HG02818.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.160+1163dupA | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 2/5 | chr9 | 34404701 | ||||||
chr9:34404709
|
AAAC | A | 115 | a0001c0001t0001g0355a0001c0001t0002g0233a0001c0001t0003g0003others(112): Show | 119 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.160+1153_160+1155d others(5): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 2/5 | chr9 | 34404709 | ||||||
chr9:34404736
|
C | A | 1 | a0001c0004t0003g0358 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.160+1129G>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 2/5 | chr9 | 34404736 | ||||||
chr9:34404737
|
A | C | 1 | a0001c0004t0003g0358 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.160+1128T>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 2/5 | chr9 | 34404737 | ||||||
chr9:34404739
|
C | A | 1 | a0001c0004t0003g0358 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.160+1126G>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 2/5 | chr9 | 34404739 | ||||||
chr9:34404742
|
A | C | 1 | a0001c0004t0003g0358 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.160+1123T>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 2/5 | chr9 | 34404742 | ||||||
chr9:34405013
|
G | A | 1 | a0001c0001t0002g0145 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.160+852C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 2/5 | chr9 | 34405013 | ||||||
chr9:34405620
|
G | C | 288 | a0001c0001t0001g0050a0001c0001t0001g0074a0001c0001t0001g0075others(285): Show | 295 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(292): Show |
intron_variant | MODIFIER | c.160+245C>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 2/5 | chr9 | 34405620 | ||||||
chr9:34405683
|
G | C | 20 | a0001c0001t0002g0005a0001c0001t0002g0105a0001c0001t0002g0114others(17): Show | 21 | HG00609.hp2 HG01106.hp2 HG01167.hp1 others(18): Show |
intron_variant | MODIFIER | c.160+182C>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 2/5 | chr9 | 34405683 | ||||||
chr9:34406161
|
C | G | 1 | a0001c0001t0001g0376 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.61-197G>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34406161 | ||||||
chr9:34406386
|
G | A | 161 | a0001c0001t0001g0050a0001c0001t0001g0075a0001c0001t0001g0076others(158): Show | 164 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.61-422C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34406386 | ||||||
chr9:34406507
|
A | C | 2 | a0001c0001t0011g0041a0001c0001t0011g0042 | 2 | HG01891.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.61-543T>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34406507 | ||||||
chr9:34406803
|
C | CT | 87 | a0001c0001t0001g0008a0001c0001t0001g0050a0001c0001t0001g0074others(84): Show | 91 | HG00099.hp1 HG00544.hp1 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.61-840dupA | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34406803 | ||||||
chr9:34406803
|
CT | C | 195 | a0001c0001t0001g0109a0001c0001t0001g0112a0001c0001t0001g0182others(192): Show | 199 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.61-840delA | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34406803 | ||||||
chr9:34406895
|
C | T | 2 | a0001c0001t0002g0233a0001c0001t0003g0290 | 2 | HG03704.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.61-931G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34406895 | ||||||
chr9:34407033
|
C | T | 19 | a0001c0001t0002g0005a0001c0001t0002g0105a0001c0001t0002g0114others(16): Show | 20 | HG00609.hp2 HG01106.hp2 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.61-1069G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34407033 | ||||||
chr9:34407039
|
G | C | 1 | a0001c0001t0001g0278 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.61-1075C>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34407039 | ||||||
chr9:34407043
|
C | T | 14 | a0001c0001t0007g0151a0001c0001t0007g0169a0001c0001t0007g0196others(11): Show | 14 | HG00099.hp1 HG00741.hp1 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.61-1079G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34407043 | ||||||
chr9:34407206
|
T | C | 135 | a0001c0001t0001g0050a0001c0001t0001g0074a0001c0001t0001g0075others(132): Show | 139 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(136): Show |
intron_variant | MODIFIER | c.61-1242A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34407206 | ||||||
chr9:34407241
|
A | T | 2 | a0001c0001t0001g0312a0001c0001t0001g0313 | 2 | NA19054.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.61-1277T>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34407241 | ||||||
chr9:34407312
|
T | C | 45 | a0001c0001t0001g0355a0001c0001t0002g0233a0001c0001t0003g0003others(42): Show | 48 | HG00558.hp2 HG00621.hp2 HG00673.hp1 others(45): Show |
intron_variant | MODIFIER | c.61-1348A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34407312 | ||||||
chr9:34407333
|
G | A | 135 | a0001c0001t0001g0050a0001c0001t0001g0074a0001c0001t0001g0075others(132): Show | 139 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(136): Show |
intron_variant | MODIFIER | c.61-1369C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34407333 | ||||||
chr9:34407358
|
G | T | 2 | a0001c0001t0009g0140a0001c0001t0009g0142 | 2 | HG02559.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.61-1394C>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34407358 | ||||||
chr9:34407400
|
T | C | 1 | a0001c0001t0002g0189 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.61-1436A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34407400 | ||||||
chr9:34407425
|
C | T | 86 | a0001c0001t0001g0050a0001c0001t0001g0074a0001c0001t0001g0075others(83): Show | 89 | HG00099.hp1 HG00558.hp2 HG00621.hp2 others(86): Show |
intron_variant | MODIFIER | c.61-1461G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34407425 | ||||||
chr9:34407471
|
CAACTT | C | 11 | a0001c0001t0002g0145a0001c0001t0002g0168a0001c0001t0002g0171others(8): Show | 11 | HG01361.hp1 HG01433.hp2 HG02071.hp1 others(8): Show |
intron_variant | MODIFIER | c.61-1512_61-1508del others(5): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34407471 | ||||||
chr9:34407533
|
G | C | 11 | a0001c0001t0002g0145a0001c0001t0002g0168a0001c0001t0002g0171others(8): Show | 11 | HG01361.hp1 HG01433.hp2 HG02071.hp1 others(8): Show |
intron_variant | MODIFIER | c.61-1569C>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34407533 | ||||||
chr9:34407548
|
G | A | 1 | a0001c0001t0003g0354 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.61-1584C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34407548 | ||||||
chr9:34407574
|
G | C | 135 | a0001c0001t0001g0050a0001c0001t0001g0074a0001c0001t0001g0075others(132): Show | 139 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(136): Show |
intron_variant | MODIFIER | c.61-1610C>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34407574 | ||||||
chr9:34407992
|
C | T | 8 | a0001c0001t0001g0050a0001c0001t0001g0075a0001c0001t0001g0076others(5): Show | 8 | HG01175.hp2 HG01891.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.61-2028G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34407992 | ||||||
chr9:34408052
|
C | T | 1 | a0001c0001t0002g0146 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.61-2088G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34408052 | ||||||
chr9:34408083
|
T | C | 2 | a0001c0001t0001g0074a0001c0001t0024g0095 | 2 | HG01255.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.61-2119A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34408083 | ||||||
chr9:34408206
|
T | G | 287 | a0001c0001t0001g0050a0001c0001t0001g0074a0001c0001t0001g0075others(284): Show | 294 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(291): Show |
intron_variant | MODIFIER | c.61-2242A>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34408206 | ||||||
chr9:34408387
|
T | C | 1 | a0001c0001t0018g0099 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.61-2423A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34408387 | ||||||
chr9:34408396
|
A | G | 135 | a0001c0001t0001g0050a0001c0001t0001g0074a0001c0001t0001g0075others(132): Show | 139 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(136): Show |
intron_variant | MODIFIER | c.61-2432T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34408396 | ||||||
chr9:34408857
|
T | G | 86 | a0001c0001t0001g0050a0001c0001t0001g0074a0001c0001t0001g0075others(83): Show | 89 | HG00099.hp1 HG00558.hp2 HG00621.hp2 others(86): Show |
intron_variant | MODIFIER | c.61-2893A>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34408857 | ||||||
chr9:34408943
|
A | G | 4 | a0001c0001t0009g0139a0001c0001t0009g0140a0001c0001t0009g0141others(1): Show | 4 | HG02559.hp1 HG02818.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.61-2979T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34408943 | ||||||
chr9:34409174
|
C | T | 2 | a0001c0001t0001g0074a0001c0001t0024g0095 | 2 | HG01255.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.61-3210G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34409174 | ||||||
chr9:34409382
|
C | T | 14 | a0001c0001t0007g0151a0001c0001t0007g0169a0001c0001t0007g0196others(11): Show | 14 | HG00099.hp1 HG00741.hp1 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.61-3418G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34409382 | ||||||
chr9:34409420
|
G | A | 57 | a0001c0001t0001g0050a0001c0001t0001g0075a0001c0001t0001g0076others(54): Show | 60 | HG00558.hp2 HG00621.hp2 HG00673.hp1 others(57): Show |
intron_variant | MODIFIER | c.61-3456C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34409420 | ||||||
chr9:34409861
|
AG | A | 27 | a0001c0001t0002g0155a0001c0001t0005g0013a0001c0001t0005g0014others(24): Show | 27 | HG00558.hp1 HG01928.hp1 HG01934.hp1 others(24): Show |
intron_variant | MODIFIER | c.61-3898delC | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34409861 | ||||||
chr9:34409979
|
C | T | 49 | a0001c0001t0004g0004a0001c0001t0004g0048a0001c0001t0004g0049others(46): Show | 50 | HG00280.hp2 HG00423.hp1 HG01074.hp1 others(47): Show |
intron_variant | MODIFIER | c.61-4015G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34409979 | ||||||
chr9:34410040
|
G | C | 49 | a0001c0001t0004g0004a0001c0001t0004g0048a0001c0001t0004g0049others(46): Show | 50 | HG00280.hp2 HG00423.hp1 HG01074.hp1 others(47): Show |
intron_variant | MODIFIER | c.61-4076C>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34410040 | ||||||
chr9:34410167
|
C | T | 14 | a0001c0001t0007g0151a0001c0001t0007g0169a0001c0001t0007g0196others(11): Show | 14 | HG00099.hp1 HG00741.hp1 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.61-4203G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34410167 | ||||||
chr9:34410264
|
C | T | 380 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(377): Show | 394 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(391): Show |
intron_variant | MODIFIER | c.61-4300G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34410264 | ||||||
chr9:34410302
|
G | T | 5 | a0001c0001t0001g0097a0001c0001t0001g0101a0001c0001t0001g0102others(2): Show | 5 | HG01243.hp1 HG02451.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.61-4338C>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34410302 | ||||||
chr9:34410336
|
G | C | 13 | a0001c0001t0001g0088a0001c0001t0001g0090a0001c0001t0001g0091others(10): Show | 13 | HG01891.hp1 HG02451.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.61-4372C>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34410336 | ||||||
chr9:34410583
|
T | C | 49 | a0001c0001t0004g0004a0001c0001t0004g0048a0001c0001t0004g0049others(46): Show | 50 | HG00280.hp2 HG00423.hp1 HG01074.hp1 others(47): Show |
intron_variant | MODIFIER | c.61-4619A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34410583 | ||||||
chr9:34410853
|
A | G | 1 | a0001c0001t0007g0359 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.61-4889T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34410853 | ||||||
chr9:34410980
|
T | C | 14 | a0001c0001t0007g0151a0001c0001t0007g0169a0001c0001t0007g0196others(11): Show | 14 | HG00099.hp1 HG00741.hp1 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.61-5016A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34410980 | ||||||
chr9:34411007
|
G | A | 1 | a0001c0001t0007g0364 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.61-5043C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34411007 | ||||||
chr9:34411028
|
T | C | 378 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(375): Show | 392 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(389): Show |
intron_variant | MODIFIER | c.61-5064A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34411028 | ||||||
chr9:34411114
|
A | G | 20 | a0001c0001t0001g0074a0001c0001t0007g0151a0001c0001t0007g0169others(17): Show | 20 | HG00099.hp1 HG00741.hp1 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.61-5150T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34411114 | ||||||
chr9:34411231
|
A | T | 1 | a0001c0001t0026g0144 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.61-5267T>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34411231 | ||||||
chr9:34411358
|
C | A | 1 | a0001c0001t0011g0042 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.61-5394G>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34411358 | ||||||
chr9:34411359
|
G | A | 1 | a0001c0001t0005g0039 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.61-5395C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34411359 | ||||||
chr9:34411417
|
C | T | 16 | a0001c0001t0001g0074a0001c0001t0007g0151a0001c0001t0007g0169others(13): Show | 16 | HG00099.hp1 HG00741.hp1 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.61-5453G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34411417 | ||||||
chr9:34411494
|
A | G | 16 | a0001c0001t0001g0074a0001c0001t0007g0151a0001c0001t0007g0169others(13): Show | 16 | HG00099.hp1 HG00741.hp1 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.61-5530T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34411494 | ||||||
chr9:34411569
|
C | T | 16 | a0001c0001t0001g0074a0001c0001t0007g0151a0001c0001t0007g0169others(13): Show | 16 | HG00099.hp1 HG00741.hp1 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.61-5605G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34411569 | ||||||
chr9:34411609
|
G | A | 1 | a0001c0001t0001g0301 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.61-5645C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34411609 | ||||||
chr9:34411656
|
G | A | 2 | a0001c0001t0009g0140a0001c0001t0009g0142 | 2 | HG02559.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.61-5692C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34411656 | ||||||
chr9:34411664
|
G | A | 1 | a0001c0001t0002g0200 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.61-5700C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34411664 | ||||||
chr9:34411676
|
CA | C | 151 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0092others(148): Show | 154 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.61-5713delT | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34411676 | ||||||
chr9:34411688
|
AAAAAAG | A | 54 | a0001c0001t0001g0050a0001c0001t0001g0075a0001c0001t0001g0076others(51): Show | 57 | HG00558.hp2 HG00673.hp1 HG00735.hp2 others(54): Show |
intron_variant | MODIFIER | c.61-5730_61-5725del others(6): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34411688 | ||||||
chr9:34411689
|
AAAAAG | A | 46 | a0001c0001t0003g0120a0001c0001t0003g0333a0001c0001t0003g0334others(43): Show | 47 | HG00280.hp2 HG00423.hp1 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.61-5730_61-5726del others(5): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34411689 | ||||||
chr9:34411690
|
AAAAG | A | 18 | a0001c0001t0004g0137a0001c0001t0006g0068a0001c0001t0006g0069others(15): Show | 18 | HG00099.hp1 HG00741.hp1 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.61-5730_61-5727del others(4): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34411690 | ||||||
chr9:34411803
|
G | A | 14 | a0001c0001t0007g0151a0001c0001t0007g0169a0001c0001t0007g0196others(11): Show | 14 | HG00099.hp1 HG00741.hp1 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.61-5839C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34411803 | ||||||
chr9:34411848
|
C | A | 8 | a0001c0001t0001g0050a0001c0001t0001g0075a0001c0001t0001g0076others(5): Show | 8 | HG01175.hp2 HG01891.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.61-5884G>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34411848 | ||||||
chr9:34411900
|
T | C | 6 | a0001c0001t0001g0050a0001c0001t0001g0075a0001c0001t0001g0076others(3): Show | 6 | HG01175.hp2 HG02818.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.61-5936A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34411900 | ||||||
chr9:34412005
|
A | C | 1 | a0001c0001t0001g0112 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.61-6041T>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34412005 | ||||||
chr9:34412399
|
A | G | 14 | a0001c0001t0007g0151a0001c0001t0007g0169a0001c0001t0007g0196others(11): Show | 14 | HG00099.hp1 HG00741.hp1 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.61-6435T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34412399 | ||||||
chr9:34412597
|
G | A | 122 | a0001c0001t0001g0050a0001c0001t0001g0074a0001c0001t0001g0075others(119): Show | 126 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.61-6633C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34412597 | ||||||
chr9:34412602
|
G | GA | 116 | a0001c0001t0001g0050a0001c0001t0001g0075a0001c0001t0001g0076others(113): Show | 120 | HG00280.hp2 HG00423.hp1 HG00558.hp2 others(117): Show |
intron_variant | MODIFIER | c.61-6639dupT | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34412602 | ||||||
chr9:34412602
|
G | GAA | 149 | a0001c0001t0001g0109a0001c0001t0001g0112a0001c0001t0001g0182others(146): Show | 152 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.61-6640_61-6639dup others(2): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34412602 | ||||||
chr9:34412602
|
G | GAAA | 8 | a0001c0001t0002g0124a0001c0001t0002g0145a0001c0001t0002g0227others(5): Show | 8 | HG00609.hp2 HG02273.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.61-6641_61-6639dup others(3): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34412602 | ||||||
chr9:34412608
|
A | G | 2 | a0001c0001t0001g0287a0001c0003t0001g0293 | 2 | NA18993.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.61-6644T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34412608 | ||||||
chr9:34412733
|
T | G | 1 | a0001c0001t0002g0329 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.61-6769A>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34412733 | ||||||
chr9:34412870
|
T | C | 1 | a0001c0001t0007g0362 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.61-6906A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34412870 | ||||||
chr9:34412914
|
G | C | 1 | a0001c0001t0011g0041 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.61-6950C>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34412914 | ||||||
chr9:34412918
|
G | A | 9 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0092others(6): Show | 9 | HG01891.hp1 HG02451.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.61-6954C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34412918 | ||||||
chr9:34413142
|
A | G | 1 | a0001c0001t0017g0094 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.61-7178T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34413142 | ||||||
chr9:34413409
|
G | A | 2 | a0001c0001t0001g0074a0001c0001t0024g0095 | 2 | HG01255.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.61-7445C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34413409 | ||||||
chr9:34413422
|
G | A | 16 | a0001c0001t0001g0074a0001c0001t0007g0151a0001c0001t0007g0169others(13): Show | 16 | HG00099.hp1 HG00741.hp1 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.61-7458C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34413422 | ||||||
chr9:34413483
|
C | T | 286 | a0001c0001t0001g0050a0001c0001t0001g0074a0001c0001t0001g0075others(283): Show | 293 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(290): Show |
intron_variant | MODIFIER | c.61-7519G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34413483 | ||||||
chr9:34413511
|
C | T | 1 | a0001c0001t0001g0312 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.61-7547G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34413511 | ||||||
chr9:34413519
|
G | C | 1 | a0001c0001t0002g0106 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.61-7555C>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34413519 | ||||||
chr9:34413675
|
T | C | 1 | a0001c0001t0002g0106 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.61-7711A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34413675 | ||||||
chr9:34413745
|
TTTATTTT others(7): Show |
T | 1 | a0001c0001t0002g0106 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.61-7795_61-7782del others(14): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34413745 | ||||||
chr9:34413758
|
G | C | 1 | a0001c0001t0002g0297 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.61-7794C>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34413758 | ||||||
chr9:34413769
|
G | A | 1 | a0001c0001t0003g0319 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.61-7805C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34413769 | ||||||
chr9:34413804
|
C | G | 1 | a0001c0001t0002g0261 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.61-7840G>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34413804 | ||||||
chr9:34413838
|
G | C | 2 | a0001c0001t0004g0209a0001c0001t0004g0211 | 2 | NA18950.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.61-7874C>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34413838 | ||||||
chr9:34413849
|
A | G | 1 | a0001c0001t0002g0106 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.61-7885T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34413849 | ||||||
chr9:34413919
|
C | A | 49 | a0001c0001t0004g0004a0001c0001t0004g0048a0001c0001t0004g0049others(46): Show | 50 | HG00280.hp2 HG00423.hp1 HG01074.hp1 others(47): Show |
intron_variant | MODIFIER | c.61-7955G>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34413919 | ||||||
chr9:34413929
|
A | G | 40 | a0001c0001t0004g0004a0001c0001t0004g0048a0001c0001t0004g0049others(37): Show | 41 | HG00280.hp2 HG00423.hp1 HG01074.hp1 others(38): Show |
intron_variant | MODIFIER | c.61-7965T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34413929 | ||||||
chr9:34413937
|
C | T | 3 | a0001c0001t0001g0241a0001c0001t0001g0253a0001c0001t0001g0279 | 3 | HG01074.hp2 HG02055.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.61-7973G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34413937 | ||||||
chr9:34414086
|
C | G | 286 | a0001c0001t0001g0050a0001c0001t0001g0074a0001c0001t0001g0075others(283): Show | 293 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(290): Show |
intron_variant | MODIFIER | c.61-8122G>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34414086 | ||||||
chr9:34414291
|
C | T | 2 | a0001c0001t0013g0081a0001c0001t0013g0083 | 2 | HG03516.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.61-8327G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34414291 | ||||||
chr9:34414341
|
C | T | 151 | a0001c0001t0001g0109a0001c0001t0001g0112a0001c0001t0001g0182others(148): Show | 154 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.61-8377G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34414341 | ||||||
chr9:34414420
|
A | G | 16 | a0001c0001t0001g0074a0001c0001t0007g0151a0001c0001t0007g0169others(13): Show | 16 | HG00099.hp1 HG00741.hp1 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.61-8456T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34414420 | ||||||
chr9:34414499
|
G | A | 14 | a0001c0001t0001g0008a0001c0001t0001g0299a0001c0001t0001g0300others(11): Show | 15 | HG00438.hp2 HG00544.hp1 HG01993.hp2 others(12): Show |
intron_variant | MODIFIER | c.61-8535C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34414499 | ||||||
chr9:34414543
|
C | T | 1 | a0001c0001t0002g0170 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.61-8579G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34414543 | ||||||
chr9:34414654
|
G | A | 2 | a0001c0001t0001g0288a0001c0001t0001g0289 | 2 | HG00423.hp2 HG02015.hp2 |
intron_variant | MODIFIER | c.61-8690C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34414654 | ||||||
chr9:34414861
|
A | G | 2 | a0001c0001t0002g0179a0001c0001t0002g0213 | 2 | HG00642.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.61-8897T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34414861 | ||||||
chr9:34415121
|
AT | A | 234 | a0001c0001t0001g0074a0001c0001t0001g0088a0001c0001t0001g0090others(231): Show | 241 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(238): Show |
intron_variant | MODIFIER | c.61-9158delA | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34415121 | ||||||
chr9:34415121
|
ATT | A | 21 | a0001c0001t0001g0050a0001c0001t0001g0075a0001c0001t0001g0076others(18): Show | 21 | HG00099.hp1 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.61-9159_61-9158del others(2): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34415121 | ||||||
chr9:34415224
|
G | A | 16 | a0001c0001t0001g0312a0001c0001t0001g0313a0001c0001t0007g0151others(13): Show | 16 | HG00099.hp1 HG00741.hp1 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.61-9260C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34415224 | ||||||
chr9:34415650
|
C | T | 151 | a0001c0001t0001g0109a0001c0001t0001g0112a0001c0001t0001g0182others(148): Show | 154 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.61-9686G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34415650 | ||||||
chr9:34415714
|
T | C | 1 | a0001c0001t0001g0255 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.61-9750A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34415714 | ||||||
chr9:34415745
|
T | G | 1 | a0001c0001t0002g0106 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.61-9781A>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34415745 | ||||||
chr9:34415787
|
G | GTAAAGTT others(33): Show |
1 | a0001c0001t0005g0013 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.61-9824_61-9823ins others(40): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34415787 | ||||||
chr9:34415883
|
G | A | 2 | a0001c0001t0002g0343a0001c0001t0002g0344 | 2 | HG00544.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.61-9919C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34415883 | ||||||
chr9:34416173
|
G | GAAGAAGA others(3): Show |
1 | a0001c0001t0002g0239 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.61-10210_61-10209i others(12): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416173 | ||||||
chr9:34416182
|
G | A | 2 | a0001c0001t0001g0088a0001c0001t0002g0239 | 2 | HG02572.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.61-10218C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416182 | ||||||
chr9:34416182
|
GAA | G | 3 | a0001c0001t0002g0129a0001c0001t0002g0343a0001c0001t0014g0272 | 3 | HG00544.hp2 HG00597.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.61-10220_61-10219d others(4): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416182 | ||||||
chr9:34416183
|
A | AAAAG | 34 | a0001c0001t0001g0091a0001c0001t0001g0117a0001c0001t0001g0229others(31): Show | 34 | HG00323.hp1 HG00438.hp1 HG00621.hp2 others(31): Show |
intron_variant | MODIFIER | c.61-10223_61-10220d others(6): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416183 | ||||||
chr9:34416183
|
A | AAAAGAAA others(1): Show |
18 | a0001c0001t0001g0002a0001c0001t0001g0097a0001c0001t0001g0187others(15): Show | 20 | HG01074.hp2 HG01361.hp2 HG02647.hp2 others(17): Show |
intron_variant | MODIFIER | c.61-10227_61-10220d others(10): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416183 | ||||||
chr9:34416183
|
A | AAAAGAAA others(5): Show |
11 | a0001c0001t0001g0101a0001c0001t0001g0188a0001c0001t0001g0262others(8): Show | 11 | HG00673.hp2 HG02027.hp1 HG02155.hp2 others(8): Show |
intron_variant | MODIFIER | c.61-10231_61-10220d others(14): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416183 | ||||||
chr9:34416183
|
A | AAAAGAAA others(9): Show |
1 | a0001c0001t0001g0381 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.61-10235_61-10220d others(18): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416183 | ||||||
chr9:34416183
|
A | AAAAGAAA others(13): Show |
1 | a0001c0002t0001g0370 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.61-10239_61-10220d others(22): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416183 | ||||||
chr9:34416183
|
A | AGAAAGAA others(6): Show |
1 | a0001c0001t0001g0088 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.61-10220_61-10219i others(15): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416183 | ||||||
chr9:34416183
|
AAAAG | A | 18 | a0001c0001t0001g0104a0001c0001t0001g0191a0001c0001t0001g0236others(15): Show | 19 | HG01070.hp1 HG01070.hp2 HG01978.hp2 others(16): Show |
intron_variant | MODIFIER | c.61-10223_61-10220d others(6): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416183 | ||||||
chr9:34416183
|
AAAAGAAA others(1): Show |
A | 12 | a0001c0001t0001g0103a0001c0001t0001g0235a0001c0001t0001g0245others(9): Show | 12 | HG00099.hp1 HG00621.hp1 HG00639.hp1 others(9): Show |
intron_variant | MODIFIER | c.61-10227_61-10220d others(10): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416183 | ||||||
chr9:34416183
|
AAAAGAAA others(5): Show |
A | 13 | a0001c0001t0001g0246a0001c0001t0001g0247a0001c0001t0001g0280others(10): Show | 13 | HG00438.hp2 HG01168.hp2 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.61-10231_61-10220d others(14): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416183 | ||||||
chr9:34416183
|
AAAAGAAA others(9): Show |
A | 7 | a0001c0001t0001g0008a0001c0001t0001g0285a0001c0001t0001g0306others(4): Show | 8 | HG00544.hp1 HG01106.hp2 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.61-10235_61-10220d others(18): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416183 | ||||||
chr9:34416183
|
AAAAGAAA others(13): Show |
A | 5 | a0001c0001t0001g0001a0001c0001t0001g0074a0001c0001t0001g0302others(2): Show | 8 | HG01255.hp2 HG02055.hp2 NA18940.hp1 others(5): Show |
intron_variant | MODIFIER | c.61-10239_61-10220d others(22): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416183 | ||||||
chr9:34416183
|
AAAAGAAA others(17): Show |
A | 1 | a0001c0001t0004g0048 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.61-10243_61-10220d others(26): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416183 | ||||||
chr9:34416191
|
G | T | 1 | a0001c0001t0001g0236 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.61-10227C>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416191 | ||||||
chr9:34416192
|
A | AAAGAAAG others(12): Show |
1 | a0001c0001t0001g0283 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.61-10247_61-10229d others(21): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416192 | ||||||
chr9:34416195
|
G | T | 1 | a0001c0001t0001g0235 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.61-10231C>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416195 | ||||||
chr9:34416195
|
GAAAGAAA others(6): Show |
G | 1 | a0001c0001t0001g0301 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.61-10244_61-10232d others(15): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416195 | ||||||
chr9:34416205
|
A | T | 12 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0130others(9): Show | 14 | HG00323.hp2 HG00639.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.61-10241T>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416205 | ||||||
chr9:34416212
|
A | AAAGAAAG others(14): Show |
1 | a0001c0001t0002g0106 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.61-10249_61-10248i others(23): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416212 | ||||||
chr9:34416228
|
A | G | 5 | a0001c0001t0006g0068a0001c0001t0006g0069a0001c0001t0006g0071others(2): Show | 5 | HG02280.hp1 HG02572.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.61-10264T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416228 | ||||||
chr9:34416229
|
A | G | 5 | a0001c0001t0006g0068a0001c0001t0006g0069a0001c0001t0006g0071others(2): Show | 5 | HG02280.hp1 HG02572.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.61-10265T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416229 | ||||||
chr9:34416230
|
A | G | 5 | a0001c0001t0006g0068a0001c0001t0006g0069a0001c0001t0006g0071others(2): Show | 5 | HG02280.hp1 HG02572.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.61-10266T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416230 | ||||||
chr9:34416232
|
A | G | 1 | a0001c0001t0006g0072 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.61-10268T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416232 | ||||||
chr9:34416232
|
AAAGAAAG others(21): Show |
A | 5 | a0001c0001t0006g0068a0001c0001t0006g0069a0001c0001t0006g0071others(2): Show | 5 | HG02280.hp1 HG02572.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.61-10296_61-10269d others(30): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416232 | ||||||
chr9:34416233
|
A | G | 1 | a0001c0001t0006g0072 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.61-10269T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416233 | ||||||
chr9:34416234
|
A | G | 1 | a0001c0001t0006g0072 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.61-10270T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416234 | ||||||
chr9:34416236
|
A | G | 13 | a0001c0001t0003g0315a0001c0001t0003g0323a0001c0001t0003g0356others(10): Show | 13 | HG01081.hp1 HG01243.hp2 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.61-10272T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416236 | ||||||
chr9:34416236
|
AAAGAAAG others(17): Show |
A | 1 | a0001c0001t0006g0072 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.61-10296_61-10273d others(26): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416236 | ||||||
chr9:34416237
|
A | G | 13 | a0001c0001t0003g0315a0001c0001t0003g0323a0001c0001t0003g0356others(10): Show | 13 | HG01081.hp1 HG01243.hp2 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.61-10273T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416237 | ||||||
chr9:34416238
|
A | G | 13 | a0001c0001t0003g0315a0001c0001t0003g0323a0001c0001t0003g0356others(10): Show | 13 | HG01081.hp1 HG01243.hp2 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.61-10274T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416238 | ||||||
chr9:34416240
|
A | G | 13 | a0001c0001t0002g0114a0001c0001t0003g0314a0001c0001t0003g0317others(10): Show | 14 | HG01074.hp1 HG01099.hp1 HG01175.hp1 others(11): Show |
intron_variant | MODIFIER | c.61-10276T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416240 | ||||||
chr9:34416240
|
AAAGAAAG others(13): Show |
A | 10 | a0001c0001t0004g0055a0001c0001t0004g0056a0001c0001t0004g0059others(7): Show | 10 | HG01081.hp1 HG01243.hp2 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.61-10296_61-10277d others(22): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416240 | ||||||
chr9:34416241
|
A | G | 16 | a0001c0001t0002g0114a0001c0001t0003g0314a0001c0001t0003g0315others(13): Show | 17 | HG01074.hp1 HG01099.hp1 HG01175.hp1 others(14): Show |
intron_variant | MODIFIER | c.61-10277T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416241 | ||||||
chr9:34416242
|
A | G | 16 | a0001c0001t0002g0114a0001c0001t0003g0314a0001c0001t0003g0315others(13): Show | 17 | HG01074.hp1 HG01099.hp1 HG01175.hp1 others(14): Show |
intron_variant | MODIFIER | c.61-10278T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416242 | ||||||
chr9:34416244
|
A | G | 35 | a0001c0001t0002g0118a0001c0001t0002g0122a0001c0001t0002g0125others(32): Show | 37 | HG00558.hp1 HG01123.hp1 HG01168.hp1 others(34): Show |
intron_variant | MODIFIER | c.61-10280T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416244 | ||||||
chr9:34416244
|
AAAGAAAG others(9): Show |
A | 7 | a0001c0001t0002g0114a0001c0001t0004g0004a0001c0001t0004g0049others(4): Show | 8 | HG01074.hp1 HG01099.hp1 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.61-10296_61-10281d others(18): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416244 | ||||||
chr9:34416245
|
A | G | 45 | a0001c0001t0002g0118a0001c0001t0002g0122a0001c0001t0002g0125others(42): Show | 47 | HG00558.hp1 HG01123.hp1 HG01168.hp1 others(44): Show |
intron_variant | MODIFIER | c.61-10281T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416245 | ||||||
chr9:34416246
|
A | AGG | 5 | a0001c0001t0003g0009a0001c0001t0003g0346a0001c0001t0003g0347others(2): Show | 6 | HG00673.hp1 HG02165.hp1 HG04184.hp2 others(3): Show |
intron_variant | MODIFIER | c.61-10283_61-10282i others(4): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416246 | ||||||
chr9:34416246
|
A | G | 45 | a0001c0001t0002g0118a0001c0001t0002g0122a0001c0001t0002g0125others(42): Show | 47 | HG00558.hp1 HG01123.hp1 HG01168.hp1 others(44): Show |
intron_variant | MODIFIER | c.61-10282T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416246 | ||||||
chr9:34416248
|
A | G | 42 | a0001c0001t0001g0075a0001c0001t0001g0079a0001c0001t0001g0182others(39): Show | 44 | HG00423.hp1 HG00609.hp2 HG00642.hp2 others(41): Show |
intron_variant | MODIFIER | c.61-10284T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416248 | ||||||
chr9:34416248
|
AAAGAAAG others(5): Show |
A | 13 | a0001c0001t0002g0118a0001c0001t0002g0122a0001c0001t0002g0125others(10): Show | 13 | HG01123.hp1 HG01258.hp2 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.61-10296_61-10285d others(14): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416248 | ||||||
chr9:34416249
|
A | G | 76 | a0001c0001t0001g0075a0001c0001t0001g0079a0001c0001t0001g0182others(73): Show | 80 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(77): Show |
intron_variant | MODIFIER | c.61-10285T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416249 | ||||||
chr9:34416250
|
A | AGGGG | 11 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0270others(8): Show | 11 | HG01109.hp1 HG01433.hp1 HG02293.hp2 others(8): Show |
intron_variant | MODIFIER | c.61-10287_61-10286i others(6): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416250 | ||||||
chr9:34416250
|
A | AGGGGGAG others(5): Show |
1 | a0001c0001t0003g0100 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.61-10287_61-10286i others(14): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416250 | ||||||
chr9:34416250
|
A | G | 71 | a0001c0001t0001g0075a0001c0001t0001g0079a0001c0001t0001g0182others(68): Show | 74 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(71): Show |
intron_variant | MODIFIER | c.61-10286T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416250 | ||||||
chr9:34416252
|
A | AAAGAAAG others(3): Show |
1 | a0001c0001t0001g0252 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.61-10289_61-10288i others(12): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416252 | ||||||
chr9:34416252
|
A | G | 35 | a0001c0001t0001g0050a0001c0001t0001g0076a0001c0001t0001g0077others(32): Show | 38 | HG00323.hp2 HG00558.hp2 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.61-10288T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416252 | ||||||
chr9:34416252
|
AAAGAAAG others(1): Show |
A | 27 | a0001c0001t0002g0116a0001c0001t0002g0123a0001c0001t0002g0124others(24): Show | 27 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(24): Show |
intron_variant | MODIFIER | c.61-10296_61-10289d others(10): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416252 | ||||||
chr9:34416253
|
A | G | 90 | a0001c0001t0001g0050a0001c0001t0001g0075a0001c0001t0001g0076others(87): Show | 96 | HG00323.hp2 HG00558.hp2 HG00639.hp2 others(93): Show |
intron_variant | MODIFIER | c.61-10289T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416253 | ||||||
chr9:34416254
|
A | AGGGG | 10 | a0001c0001t0001g0109a0001c0001t0001g0218a0001c0001t0001g0231others(7): Show | 10 | HG01109.hp2 HG02622.hp1 HG02970.hp1 others(7): Show |
intron_variant | MODIFIER | c.61-10291_61-10290i others(6): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416254 | ||||||
chr9:34416254
|
A | G | 84 | a0001c0001t0001g0050a0001c0001t0001g0075a0001c0001t0001g0076others(81): Show | 89 | HG00323.hp2 HG00558.hp2 HG00639.hp2 others(86): Show |
intron_variant | MODIFIER | c.61-10290T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416254 | ||||||
chr9:34416256
|
A | AAAGAAAG others(8): Show |
1 | a0001c0002t0001g0193 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.61-10293_61-10292i others(17): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416256 | ||||||
chr9:34416256
|
A | G | 24 | a0001c0001t0001g0256a0001c0001t0002g0119a0001c0001t0002g0131others(21): Show | 25 | HG00673.hp1 HG01346.hp1 HG01975.hp1 others(22): Show |
intron_variant | MODIFIER | c.61-10292T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416256 | ||||||
chr9:34416256
|
AAAGG | A | 36 | a0001c0001t0001g0075a0001c0001t0001g0079a0001c0001t0001g0182others(33): Show | 40 | HG01081.hp2 HG01106.hp1 HG01169.hp2 others(37): Show |
intron_variant | MODIFIER | c.61-10296_61-10293d others(6): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416256 | ||||||
chr9:34416257
|
A | AAGAAAGA others(3): Show |
1 | a0001c0001t0002g0167 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.61-10294_61-10293i others(12): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416257 | ||||||
chr9:34416257
|
A | G | 75 | a0001c0001t0001g0050a0001c0001t0001g0076a0001c0001t0001g0077others(72): Show | 77 | HG00323.hp2 HG00558.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.61-10293T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416257 | ||||||
chr9:34416257
|
AAGGG | A | 3 | a0001c0001t0003g0317a0001c0001t0003g0327a0001c0001t0003g0357 | 3 | NA18983.hp1 NA18988.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.61-10297_61-10294d others(6): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416257 | ||||||
chr9:34416258
|
A | AGAAAGAA others(13): Show |
1 | a0001c0001t0011g0041 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.61-10295_61-10294i others(22): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416258 | ||||||
chr9:34416258
|
A | G | 74 | a0001c0001t0001g0050a0001c0001t0001g0076a0001c0001t0001g0077others(71): Show | 75 | HG00323.hp2 HG00558.hp2 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.61-10294T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416258 | ||||||
chr9:34416260
|
G | A | 79 | a0001c0001t0001g0050a0001c0001t0001g0076a0001c0001t0001g0077others(76): Show | 80 | HG00323.hp2 HG00558.hp2 HG00639.hp2 others(77): Show |
intron_variant | MODIFIER | c.61-10296C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416260 | ||||||
chr9:34416261
|
G | A | 12 | a0001c0001t0001g0320a0001c0001t0003g0100a0001c0001t0003g0318others(9): Show | 12 | HG01123.hp2 HG02027.hp2 HG02040.hp2 others(9): Show |
intron_variant | MODIFIER | c.61-10297C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416261 | ||||||
chr9:34416261
|
G | GAA | 6 | a0001c0001t0003g0009a0001c0001t0003g0346a0001c0001t0003g0347others(3): Show | 7 | HG00673.hp1 HG02165.hp1 HG04184.hp2 others(4): Show |
intron_variant | MODIFIER | c.61-10298_61-10297i others(4): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416261 | ||||||
chr9:34416262
|
G | A | 4 | a0001c0001t0001g0320a0001c0001t0007g0151a0001c0001t0007g0224others(1): Show | 4 | HG01123.hp2 HG02040.hp2 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.61-10298C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416262 | ||||||
chr9:34416264
|
A | G | 2 | a0001c0001t0001g0320a0001c0001t0007g0363 | 2 | HG01123.hp2 HG02040.hp2 |
intron_variant | MODIFIER | c.61-10300T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416264 | ||||||
chr9:34416265
|
G | A | 48 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0270others(45): Show | 51 | HG00642.hp2 HG00673.hp1 HG01109.hp1 others(48): Show |
intron_variant | MODIFIER | c.61-10301C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416265 | ||||||
chr9:34416265
|
G | GGGAAGGA others(1): Show |
6 | a0001c0001t0001g0355a0001c0001t0003g0335a0001c0001t0003g0339others(3): Show | 6 | HG00558.hp2 HG02630.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.61-10302_61-10301i others(10): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416265 | ||||||
chr9:34416266
|
G | A | 2 | a0001c0001t0007g0151a0001c0001t0007g0224 | 2 | HG02300.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.61-10302C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416266 | ||||||
chr9:34416268
|
A | G | 1 | a0001c0001t0007g0151 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.61-10304T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416268 | ||||||
chr9:34416269
|
G | A | 104 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0109others(101): Show | 109 | HG00323.hp2 HG00558.hp1 HG00558.hp2 others(106): Show |
intron_variant | MODIFIER | c.61-10305C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416269 | ||||||
chr9:34416269
|
G | GGGAAGGA others(1): Show |
6 | a0001c0001t0002g0131a0001c0001t0002g0175a0001c0001t0002g0207others(3): Show | 6 | HG02129.hp2 HG02602.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.61-10306_61-10305i others(10): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416269 | ||||||
chr9:34416269
|
G | GGGAAGGA others(5): Show |
7 | a0001c0001t0002g0180a0001c0001t0002g0204a0001c0001t0002g0206others(4): Show | 7 | HG01975.hp1 HG02132.hp2 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.61-10306_61-10305i others(14): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416269 | ||||||
chr9:34416269
|
G | GGGAAGGA others(9): Show |
1 | a0001c0001t0002g0170 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.61-10306_61-10305i others(18): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416269 | ||||||
chr9:34416270
|
G | A | 1 | a0001c0001t0007g0224 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.61-10306C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416270 | ||||||
chr9:34416272
|
A | G | 1 | a0001c0001t0007g0224 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.61-10308T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416272 | ||||||
chr9:34416273
|
G | A | 182 | a0001c0001t0001g0050a0001c0001t0001g0075a0001c0001t0001g0076others(179): Show | 189 | HG00323.hp2 HG00423.hp1 HG00558.hp1 others(186): Show |
intron_variant | MODIFIER | c.61-10309C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416273 | ||||||
chr9:34416273
|
G | GGGAA | 11 | a0001c0001t0001g0254a0001c0001t0002g0127a0001c0001t0002g0181others(8): Show | 11 | HG01496.hp2 HG02109.hp2 HG02683.hp2 others(8): Show |
intron_variant | MODIFIER | c.61-10313_61-10310d others(6): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416273 | ||||||
chr9:34416273
|
G | GGGAAGGA others(1): Show |
22 | a0001c0001t0001g0112a0001c0001t0001g0188a0001c0001t0001g0220others(19): Show | 22 | HG00323.hp1 HG00438.hp1 HG02559.hp2 others(19): Show |
intron_variant | MODIFIER | c.61-10317_61-10310d others(10): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416273 | ||||||
chr9:34416273
|
G | GGGAAGGA others(5): Show |
25 | a0001c0001t0001g0088a0001c0001t0001g0091a0001c0001t0001g0238others(22): Show | 25 | HG00099.hp2 HG00544.hp2 HG00597.hp2 others(22): Show |
intron_variant | MODIFIER | c.61-10321_61-10310d others(14): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416273 | ||||||
chr9:34416273
|
G | GGGAAGGA others(9): Show |
10 | a0001c0001t0002g0205a0001c0001t0002g0222a0001c0001t0002g0368others(7): Show | 10 | HG00735.hp2 HG01433.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.61-10325_61-10310d others(18): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416273 | ||||||
chr9:34416273
|
G | GGGAAGGA others(13): Show |
7 | a0001c0001t0002g0162a0001c0001t0002g0166a0001c0001t0002g0217others(4): Show | 7 | HG01496.hp1 NA18955.hp1 NA18982.hp2 others(4): Show |
intron_variant | MODIFIER | c.61-10329_61-10310d others(22): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416273 | ||||||
chr9:34416273
|
G | GGGAGGGA others(9): Show |
1 | a0001c0001t0002g0128 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.61-10310_61-10309i others(18): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416273 | ||||||
chr9:34416273
|
GGGAA | G | 15 | a0001c0001t0001g0008a0001c0001t0001g0299a0001c0001t0001g0300others(12): Show | 16 | HG00438.hp2 HG00544.hp1 HG01993.hp2 others(13): Show |
intron_variant | MODIFIER | c.61-10313_61-10310d others(6): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416273 | ||||||
chr9:34416273
|
GGGAAGGA others(1): Show |
G | 3 | a0001c0001t0009g0139a0001c0001t0009g0141a0001c0001t0017g0094 | 3 | HG02451.hp2 HG03579.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.61-10317_61-10310d others(10): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416273 | ||||||
chr9:34416273
|
GGGAAGGA others(9): Show |
G | 2 | a0001c0001t0001g0074a0001c0001t0024g0095 | 2 | HG01255.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.61-10325_61-10310d others(18): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416273 | ||||||
chr9:34416277
|
A | G | 4 | a0001c0001t0001g0320a0001c0001t0007g0151a0001c0001t0007g0224others(1): Show | 4 | HG01123.hp2 HG02040.hp2 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.61-10313T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416277 | ||||||
chr9:34416281
|
A | G | 2 | a0001c0001t0007g0151a0001c0001t0007g0224 | 2 | HG02300.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.61-10317T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416281 | ||||||
chr9:34416285
|
A | G | 1 | a0001c0001t0007g0224 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.61-10321T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416285 | ||||||
chr9:34416298
|
GGAAGGAA others(5): Show |
G | 11 | a0001c0001t0007g0169a0001c0001t0007g0196a0001c0001t0007g0203others(8): Show | 11 | HG00099.hp1 HG00741.hp1 HG00741.hp2 others(8): Show |
intron_variant | MODIFIER | c.61-10346_61-10335d others(14): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416298 | ||||||
chr9:34416310
|
C | G | 2 | a0001c0001t0002g0115a0001c0001t0007g0224 | 2 | HG02970.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.61-10346G>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416310 | ||||||
chr9:34416311
|
G | A | 8 | a0001c0001t0001g0050a0001c0001t0001g0075a0001c0001t0001g0076others(5): Show | 8 | HG01175.hp2 HG01891.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.61-10347C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416311 | ||||||
chr9:34416314
|
G | C | 13 | a0001c0001t0007g0169a0001c0001t0007g0196a0001c0001t0007g0203others(10): Show | 13 | HG00099.hp1 HG00741.hp1 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.61-10350C>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416314 | ||||||
chr9:34416322
|
G | A | 1 | a0001c0001t0003g0327 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.61-10358C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416322 | ||||||
chr9:34416543
|
C | T | 8 | a0001c0001t0001g0050a0001c0001t0001g0075a0001c0001t0001g0076others(5): Show | 8 | HG01175.hp2 HG01891.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.61-10579G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416543 | ||||||
chr9:34416737
|
C | CA | 63 | a0001c0001t0001g0074a0001c0001t0001g0220a0001c0001t0004g0004others(60): Show | 64 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.61-10774dupT | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416737 | ||||||
chr9:34416756
|
T | TA | 286 | a0001c0001t0001g0050a0001c0001t0001g0074a0001c0001t0001g0075others(283): Show | 293 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(290): Show |
intron_variant | MODIFIER | c.61-10793_61-10792i others(3): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416756 | ||||||
chr9:34416808
|
A | AT | 17 | a0001c0001t0001g0097a0001c0001t0001g0101a0001c0001t0001g0102others(14): Show | 17 | HG01099.hp2 HG01243.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.61-10845dupA | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416808 | ||||||
chr9:34416808
|
A | ATG | 126 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0092others(123): Show | 129 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.61-10845_61-10844i others(4): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416808 | ||||||
chr9:34416808
|
A | ATGT | 56 | a0001c0001t0001g0088a0001c0001t0001g0109a0001c0001t0001g0185others(53): Show | 59 | HG00558.hp2 HG00597.hp2 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.61-10845_61-10844i others(5): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416808 | ||||||
chr9:34416808
|
A | ATGTT | 19 | a0001c0001t0001g0050a0001c0001t0001g0076a0001c0001t0001g0077others(16): Show | 19 | HG01175.hp2 HG01433.hp1 HG01496.hp1 others(16): Show |
intron_variant | MODIFIER | c.61-10845_61-10844i others(6): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416808 | ||||||
chr9:34416808
|
A | ATGTTT | 41 | a0001c0001t0001g0075a0001c0001t0004g0004a0001c0001t0004g0048others(38): Show | 42 | HG00280.hp2 HG00423.hp1 HG01081.hp1 others(39): Show |
intron_variant | MODIFIER | c.61-10845_61-10844i others(7): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416808 | ||||||
chr9:34416808
|
A | ATGTTTT | 10 | a0001c0001t0004g0049a0001c0001t0004g0053a0001c0001t0004g0058others(7): Show | 10 | HG01074.hp1 HG01175.hp1 HG01934.hp2 others(7): Show |
intron_variant | MODIFIER | c.61-10845_61-10844i others(8): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416808 | ||||||
chr9:34416808
|
AT | A | 13 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0236others(10): Show | 13 | HG00280.hp1 HG02155.hp1 HG02735.hp1 others(10): Show |
intron_variant | MODIFIER | c.61-10845delA | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416808 | ||||||
chr9:34416809
|
T | TG | 12 | a0001c0001t0002g0126a0001c0001t0002g0133a0001c0001t0002g0162others(9): Show | 12 | HG01891.hp1 HG02630.hp1 HG03540.hp1 others(9): Show |
intron_variant | MODIFIER | c.61-10846_61-10845i others(3): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416809 | ||||||
chr9:34416809
|
T | TGTTC | 14 | a0001c0001t0001g0074a0001c0001t0007g0151a0001c0001t0007g0169others(11): Show | 14 | HG00099.hp1 HG00741.hp2 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.61-10846_61-10845i others(6): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416809 | ||||||
chr9:34416810
|
T | C | 1 | a0001c0001t0007g0360 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.61-10846A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416810 | ||||||
chr9:34416813
|
T | G | 1 | a0001c0001t0002g0180 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.61-10849A>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416813 | ||||||
chr9:34416831
|
A | T | 1 | a0001c0001t0004g0137 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.61-10867T>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416831 | ||||||
chr9:34416865
|
G | A | 2 | a0001c0001t0001g0255a0001c0001t0001g0256 | 2 | HG02280.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.61-10901C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416865 | ||||||
chr9:34416916
|
C | T | 1 | a0001c0001t0006g0111 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.61-10952G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416916 | ||||||
chr9:34416961
|
G | A | 2 | a0001c0001t0001g0074a0001c0001t0024g0095 | 2 | HG01255.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.61-10997C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34416961 | ||||||
chr9:34417000
|
CTCCTTCT | C | 3 | a0001c0001t0001g0074a0001c0001t0005g0016a0001c0001t0024g0095 | 3 | HG01255.hp2 HG02055.hp2 NA18941.hp1 |
intron_variant | MODIFIER | c.61-11043_61-11037d others(9): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34417000 | ||||||
chr9:34417070
|
CCTT | C | 16 | a0001c0001t0001g0074a0001c0001t0007g0151a0001c0001t0007g0169others(13): Show | 16 | HG00099.hp1 HG00741.hp1 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.61-11109_61-11107d others(5): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34417070 | ||||||
chr9:34417197
|
C | T | 1 | a0001c0001t0002g0154 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.61-11233G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34417197 | ||||||
chr9:34417367
|
T | C | 2 | a0001c0001t0002g0233a0001c0001t0003g0290 | 2 | HG03704.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.61-11403A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34417367 | ||||||
chr9:34417445
|
A | C | 1 | a0001c0001t0002g0106 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.61-11481T>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34417445 | ||||||
chr9:34417597
|
C | T | 49 | a0001c0001t0004g0004a0001c0001t0004g0048a0001c0001t0004g0049others(46): Show | 50 | HG00280.hp2 HG00423.hp1 HG01074.hp1 others(47): Show |
intron_variant | MODIFIER | c.61-11633G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34417597 | ||||||
chr9:34417752
|
C | T | 6 | a0001c0001t0007g0151a0001c0001t0007g0169a0001c0001t0007g0196others(3): Show | 6 | HG00741.hp2 HG01070.hp1 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.61-11788G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34417752 | ||||||
chr9:34417875
|
T | G | 16 | a0001c0001t0001g0074a0001c0001t0007g0151a0001c0001t0007g0169others(13): Show | 16 | HG00099.hp1 HG00741.hp1 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.61-11911A>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34417875 | ||||||
chr9:34417918
|
A | G | 286 | a0001c0001t0001g0050a0001c0001t0001g0074a0001c0001t0001g0075others(283): Show | 293 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(290): Show |
intron_variant | MODIFIER | c.61-11954T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34417918 | ||||||
chr9:34418200
|
T | TA | 10 | a0001c0001t0001g0275a0001c0001t0002g0046a0001c0001t0002g0106others(7): Show | 10 | HG01346.hp2 HG01358.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.61-12237dupT | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34418200 | ||||||
chr9:34418268
|
G | T | 1 | a0001c0001t0002g0192 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.61-12304C>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34418268 | ||||||
chr9:34418460
|
G | C | 1 | a0001c0001t0001g0182 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.61-12496C>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34418460 | ||||||
chr9:34418554
|
C | G | 1 | a0001c0001t0003g0334 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.61-12590G>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34418554 | ||||||
chr9:34418690
|
C | A | 1 | a0001c0001t0003g0314 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.61-12726G>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34418690 | ||||||
chr9:34418712
|
A | C | 1 | a0001c0001t0003g0350 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.61-12748T>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34418712 | ||||||
chr9:34418776
|
A | G | 1 | a0001c0001t0001g0286 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.61-12812T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34418776 | ||||||
chr9:34418957
|
C | T | 46 | a0001c0001t0004g0004a0001c0001t0004g0048a0001c0001t0004g0049others(43): Show | 47 | HG00280.hp2 HG00423.hp1 HG01074.hp1 others(44): Show |
intron_variant | MODIFIER | c.61-12993G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34418957 | ||||||
chr9:34419073
|
T | TCAAA | 15 | a0001c0001t0001g0185a0001c0001t0001g0309a0001c0001t0001g0311others(12): Show | 15 | HG00642.hp1 HG01109.hp1 HG01981.hp1 others(12): Show |
intron_variant | MODIFIER | c.61-13113_61-13110d others(6): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34419073 | ||||||
chr9:34419073
|
TCAAA | T | 14 | a0001c0001t0001g0050a0001c0001t0001g0074a0001c0001t0001g0075others(11): Show | 14 | HG00741.hp2 HG01175.hp2 HG01255.hp2 others(11): Show |
intron_variant | MODIFIER | c.61-13113_61-13110d others(6): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34419073 | ||||||
chr9:34419166
|
T | A | 59 | a0001c0001t0001g0088a0001c0001t0001g0355a0001c0001t0001g0380others(56): Show | 62 | HG00099.hp1 HG00558.hp2 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.61-13202A>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34419166 | ||||||
chr9:34419167
|
A | T | 22 | a0001c0001t0001g0050a0001c0001t0001g0075a0001c0001t0001g0076others(19): Show | 24 | HG00323.hp2 HG00639.hp2 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.61-13203T>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34419167 | ||||||
chr9:34419191
|
G | A | 2 | a0001c0001t0001g0074a0001c0001t0024g0095 | 2 | HG01255.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.61-13227C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34419191 | ||||||
chr9:34419297
|
T | C | 7 | a0001c0001t0002g0162a0001c0001t0002g0166a0001c0001t0002g0217others(4): Show | 7 | NA18747.hp1 NA18955.hp1 NA18982.hp2 others(4): Show |
intron_variant | MODIFIER | c.61-13333A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34419297 | ||||||
chr9:34419354
|
G | A | 1 | a0001c0001t0001g0251 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.61-13390C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34419354 | ||||||
chr9:34419583
|
T | C | 16 | a0001c0001t0001g0074a0001c0001t0007g0151a0001c0001t0007g0169others(13): Show | 16 | HG00099.hp1 HG00741.hp1 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.61-13619A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34419583 | ||||||
chr9:34419626
|
C | G | 4 | a0001c0001t0001g0273a0001c0001t0001g0274a0001c0001t0001g0277others(1): Show | 4 | NA18960.hp1 NA18975.hp2 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.61-13662G>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34419626 | ||||||
chr9:34419754
|
G | C | 16 | a0001c0001t0001g0074a0001c0001t0007g0151a0001c0001t0007g0169others(13): Show | 16 | HG00099.hp1 HG00741.hp1 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.61-13790C>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34419754 | ||||||
chr9:34419935
|
C | A | 1 | a0001c0001t0017g0094 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.61-13971G>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34419935 | ||||||
chr9:34420023
|
A | G | 1 | a0001c0001t0002g0146 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.61-14059T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34420023 | ||||||
chr9:34420046
|
C | A | 1 | a0001c0001t0002g0175 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.61-14082G>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34420046 | ||||||
chr9:34420289
|
T | C | 20 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0113others(17): Show | 22 | HG00323.hp2 HG00639.hp2 HG00642.hp1 others(19): Show |
intron_variant | MODIFIER | c.61-14325A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34420289 | ||||||
chr9:34420323
|
G | A | 8 | a0001c0001t0001g0050a0001c0001t0001g0075a0001c0001t0001g0076others(5): Show | 8 | HG01175.hp2 HG01891.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.61-14359C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34420323 | ||||||
chr9:34420415
|
G | A | 45 | a0001c0001t0001g0355a0001c0001t0002g0233a0001c0001t0003g0003others(42): Show | 48 | HG00558.hp2 HG00621.hp2 HG00673.hp1 others(45): Show |
intron_variant | MODIFIER | c.61-14451C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34420415 | ||||||
chr9:34420480
|
G | A | 1 | a0001c0001t0001g0218 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.61-14516C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34420480 | ||||||
chr9:34420690
|
A | G | 2 | a0001c0001t0001g0246a0001c0001t0001g0247 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.61-14726T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34420690 | ||||||
chr9:34420796
|
G | A | 14 | a0001c0001t0007g0151a0001c0001t0007g0169a0001c0001t0007g0196others(11): Show | 14 | HG00099.hp1 HG00741.hp1 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.61-14832C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34420796 | ||||||
chr9:34420808
|
C | G | 1 | a0001c0001t0004g0157 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.61-14844G>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34420808 | ||||||
chr9:34420821
|
A | G | 1 | a0001c0001t0001g0231 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.61-14857T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34420821 | ||||||
chr9:34420973
|
C | CGT | 4 | a0001c0001t0001g0091a0001c0001t0001g0241a0001c0001t0002g0010others(1): Show | 5 | HG02273.hp2 HG02300.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.61-15011_61-15010d others(4): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34420973 | ||||||
chr9:34420974
|
G | A | 1 | a0001c0001t0002g0124 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.61-15010C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34420974 | ||||||
chr9:34420986
|
G | A | 8 | a0001c0001t0001g0050a0001c0001t0001g0075a0001c0001t0001g0076others(5): Show | 8 | HG01175.hp2 HG01891.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.61-15022C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34420986 | ||||||
chr9:34420992
|
A | C | 14 | a0001c0001t0007g0151a0001c0001t0007g0169a0001c0001t0007g0196others(11): Show | 14 | HG00099.hp1 HG00741.hp1 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.61-15028T>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34420992 | ||||||
chr9:34420992
|
A | G | 23 | a0001c0001t0001g0050a0001c0001t0001g0075a0001c0001t0001g0076others(20): Show | 23 | HG01074.hp2 HG01175.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.61-15028T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34420992 | ||||||
chr9:34420994
|
G | A | 12 | a0001c0001t0001g0088a0001c0001t0001g0090a0001c0001t0001g0092others(9): Show | 12 | HG01891.hp1 HG02451.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.61-15030C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34420994 | ||||||
chr9:34421001
|
T | TGAGAGAG others(7): Show |
1 | a0001c0001t0011g0041 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.61-15038_61-15037i others(16): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34421001 | ||||||
chr9:34421003
|
T | A | 3 | a0001c0001t0001g0091a0001c0001t0011g0041a0001c0001t0011g0042 | 3 | HG01891.hp2 HG02622.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.61-15039A>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34421003 | ||||||
chr9:34421003
|
T | TGAGAGAG others(1): Show |
6 | a0001c0001t0001g0050a0001c0001t0001g0075a0001c0001t0001g0076others(3): Show | 6 | HG01175.hp2 HG02896.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.61-15040_61-15039i others(10): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34421003 | ||||||
chr9:34421003
|
T | TGAGAGAG others(3): Show |
4 | a0001c0001t0001g0077a0001c0001t0001g0085a0001c0001t0010g0082others(1): Show | 4 | HG01891.hp1 HG02818.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.61-15040_61-15039i others(12): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34421003 | ||||||
chr9:34421003
|
T | TGAGAGAG others(7): Show |
1 | a0001c0001t0001g0090 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.61-15040_61-15039i others(16): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34421003 | ||||||
chr9:34421005
|
T | A | 14 | a0001c0001t0001g0050a0001c0001t0001g0075a0001c0001t0001g0076others(11): Show | 14 | HG01175.hp2 HG01891.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.61-15041A>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34421005 | ||||||
chr9:34421005
|
T | TGAGAGAG others(9): Show |
1 | a0001c0001t0002g0115 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.61-15042_61-15041i others(18): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34421005 | ||||||
chr9:34421005
|
T | TGAGAGAG others(11): Show |
1 | a0001c0001t0002g0127 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.61-15042_61-15041i others(20): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34421005 | ||||||
chr9:34421007
|
T | A | 18 | a0001c0001t0001g0050a0001c0001t0001g0075a0001c0001t0001g0076others(15): Show | 18 | HG01175.hp2 HG01891.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.61-15043A>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34421007 | ||||||
chr9:34421007
|
T | TGAGA | 20 | a0001c0001t0002g0351a0001c0001t0003g0003a0001c0001t0003g0009others(17): Show | 23 | HG00558.hp2 HG00621.hp2 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.61-15044_61-15043i others(6): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34421007 | ||||||
chr9:34421007
|
T | TGAGAGA | 14 | a0001c0001t0001g0270a0001c0001t0003g0314a0001c0001t0003g0315others(11): Show | 14 | HG02559.hp1 HG03041.hp2 HG04184.hp2 others(11): Show |
intron_variant | MODIFIER | c.61-15044_61-15043i others(8): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34421007 | ||||||
chr9:34421007
|
T | TGAGAGAG others(1): Show |
7 | a0001c0001t0003g0316a0001c0001t0003g0326a0001c0001t0003g0327others(4): Show | 7 | HG03516.hp2 NA18939.hp2 NA18950.hp2 others(4): Show |
intron_variant | MODIFIER | c.61-15044_61-15043i others(10): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34421007 | ||||||
chr9:34421007
|
T | TGAGAGAG others(3): Show |
13 | a0001c0001t0002g0070a0001c0001t0002g0114a0001c0001t0002g0128others(10): Show | 13 | HG00642.hp1 HG02559.hp2 HG02965.hp2 others(10): Show |
intron_variant | MODIFIER | c.61-15044_61-15043i others(12): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34421007 | ||||||
chr9:34421007
|
T | TGAGAGAG others(5): Show |
24 | a0001c0001t0002g0105a0001c0001t0002g0116a0001c0001t0002g0121others(21): Show | 24 | HG00323.hp2 HG00558.hp1 HG00609.hp2 others(21): Show |
intron_variant | MODIFIER | c.61-15044_61-15043i others(14): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34421007 | ||||||
chr9:34421007
|
T | TGAGAGAG others(7): Show |
12 | a0001c0001t0002g0118a0001c0001t0002g0119a0001c0001t0002g0125others(9): Show | 12 | HG01081.hp2 HG01106.hp2 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.61-15044_61-15043i others(16): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34421007 | ||||||
chr9:34421007
|
T | TGAGAGAG others(9): Show |
15 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0133others(12): Show | 17 | HG01255.hp1 HG01346.hp2 HG01928.hp1 others(14): Show |
intron_variant | MODIFIER | c.61-15044_61-15043i others(18): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34421007 | ||||||
chr9:34421007
|
T | TGAGAGAG others(11): Show |
7 | a0001c0001t0002g0007a0001c0001t0002g0136a0001c0001t0002g0150others(4): Show | 8 | HG00639.hp2 HG00735.hp1 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.61-15044_61-15043i others(20): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34421007 | ||||||
chr9:34421007
|
T | TGAGAGAG others(13): Show |
5 | a0001c0001t0002g0087a0001c0001t0002g0113a0001c0001t0002g0202others(2): Show | 5 | HG01981.hp1 HG03195.hp2 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.61-15044_61-15043i others(22): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34421007 | ||||||
chr9:34421007
|
T | TGAGAGAG others(15): Show |
2 | a0001c0001t0002g0078a0001c0001t0002g0228 | 2 | HG03139.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.61-15044_61-15043i others(24): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34421007 | ||||||
chr9:34421007
|
T | TGAGAGAG others(19): Show |
1 | a0001c0001t0002g0216 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.61-15044_61-15043i others(28): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34421007 | ||||||
chr9:34421007
|
TGTGAGAG others(3): Show |
T | 1 | a0001c0001t0003g0332 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.61-15053_61-15044d others(12): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34421007 | ||||||
chr9:34421009
|
T | A | 147 | a0001c0001t0001g0050a0001c0001t0001g0075a0001c0001t0001g0076others(144): Show | 153 | HG00323.hp2 HG00558.hp1 HG00558.hp2 others(150): Show |
intron_variant | MODIFIER | c.61-15045A>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34421009 | ||||||
chr9:34421009
|
T | TGA | 6 | a0001c0001t0001g0110a0001c0001t0001g0288a0001c0001t0001g0294others(3): Show | 6 | HG00597.hp1 HG01928.hp2 HG02015.hp2 others(3): Show |
intron_variant | MODIFIER | c.61-15047_61-15046d others(4): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34421009 | ||||||
chr9:34421009
|
T | TGAGA | 5 | a0001c0001t0001g0117a0001c0001t0001g0289a0001c0001t0002g0148others(2): Show | 5 | HG00423.hp2 HG01433.hp1 HG02293.hp2 others(2): Show |
intron_variant | MODIFIER | c.61-15049_61-15046d others(6): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34421009 | ||||||
chr9:34421009
|
T | TGAGAGAG others(1): Show |
42 | a0001c0001t0001g0109a0001c0001t0001g0218a0001c0001t0001g0229others(39): Show | 42 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(39): Show |
intron_variant | MODIFIER | c.61-15053_61-15046d others(10): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34421009 | ||||||
chr9:34421009
|
T | TGAGAGAG others(3): Show |
23 | a0001c0001t0001g0112a0001c0001t0001g0182a0001c0001t0001g0185others(20): Show | 23 | HG00099.hp1 HG00597.hp2 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.61-15055_61-15046d others(12): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34421009 | ||||||
chr9:34421009
|
T | TGAGAGAG others(5): Show |
2 | a0001c0001t0002g0257a0001c0001t0007g0364 | 2 | HG00741.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.61-15057_61-15046d others(14): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34421009 | ||||||
chr9:34421009
|
T | TGAGAGAG others(7): Show |
3 | a0001c0001t0005g0018a0001c0001t0005g0040a0001c0001t0021g0366 | 3 | HG01516.hp2 NA18945.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.61-15059_61-15046d others(16): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34421009 | ||||||
chr9:34421009
|
T | TGAGAGAG others(9): Show |
4 | a0001c0001t0002g0186a0001c0001t0005g0015a0001c0001t0005g0016others(1): Show | 4 | HG01943.hp1 NA18941.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.61-15061_61-15046d others(18): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34421009 | ||||||
chr9:34421009
|
T | TGTGAGAG others(3): Show |
7 | a0001c0001t0002g0106a0001c0001t0004g0048a0001c0001t0006g0084others(4): Show | 7 | HG00280.hp2 HG00741.hp2 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.61-15046_61-15045i others(12): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34421009 | ||||||
chr9:34421009
|
T | TGTGAGAG others(5): Show |
1 | a0001c0001t0007g0151 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.61-15046_61-15045i others(14): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34421009 | ||||||
chr9:34421009
|
T | TGTGAGAG others(7): Show |
1 | a0001c0001t0007g0196 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.61-15046_61-15045i others(16): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34421009 | ||||||
chr9:34421009
|
T | TGTGAGAG others(9): Show |
1 | a0001c0001t0001g0074 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.61-15046_61-15045i others(18): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34421009 | ||||||
chr9:34421009
|
T | TGTGAGAG others(11): Show |
1 | a0001c0001t0024g0095 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.61-15046_61-15045i others(20): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34421009 | ||||||
chr9:34421009
|
TGAGAGAG others(3): Show |
T | 1 | a0001c0001t0002g0170 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.61-15055_61-15046d others(12): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34421009 | ||||||
chr9:34421011
|
A | T | 7 | a0001c0001t0001g0097a0001c0001t0001g0101a0001c0001t0001g0102others(4): Show | 7 | HG01243.hp1 HG02040.hp1 HG02074.hp2 others(4): Show |
intron_variant | MODIFIER | c.61-15047T>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34421011 | ||||||
chr9:34421044
|
G | C | 2 | a0001c0001t0004g0048a0001c0001t0006g0084 | 2 | HG00280.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.61-15080C>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34421044 | ||||||
chr9:34421044
|
G | GAGAGAGA others(3): Show |
21 | a0001c0001t0004g0004a0001c0001t0004g0053a0001c0001t0004g0054others(18): Show | 22 | HG00423.hp1 HG01081.hp1 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.61-15081_61-15080i others(12): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34421044 | ||||||
chr9:34421044
|
G | GAGAGAGA others(5): Show |
6 | a0001c0001t0004g0049a0001c0001t0004g0060a0001c0001t0004g0067others(3): Show | 6 | HG01934.hp2 HG01952.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.61-15081_61-15080i others(14): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34421044 | ||||||
chr9:34421044
|
G | GAGAGAGA others(7): Show |
6 | a0001c0001t0004g0065a0001c0001t0004g0066a0001c0001t0004g0249others(3): Show | 6 | HG01175.hp1 HG02257.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.61-15081_61-15080i others(16): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34421044 | ||||||
chr9:34421044
|
G | GAGAGAGA others(9): Show |
5 | a0001c0001t0004g0061a0001c0001t0004g0157a0001c0001t0006g0069others(2): Show | 5 | HG01074.hp1 HG02280.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.61-15081_61-15080i others(18): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34421044 | ||||||
chr9:34421044
|
G | GAGAGAGA others(13): Show |
4 | a0001c0001t0006g0051a0001c0001t0006g0052a0001c0001t0006g0138others(1): Show | 4 | HG01496.hp2 HG02109.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.61-15081_61-15080i others(22): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34421044 | ||||||
chr9:34421044
|
G | GAGAGAGA others(15): Show |
1 | a0001c0001t0004g0062 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.61-15081_61-15080i others(24): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34421044 | ||||||
chr9:34421205
|
G | A | 39 | a0001c0001t0004g0004a0001c0001t0004g0048a0001c0001t0004g0049others(36): Show | 40 | HG00280.hp2 HG00423.hp1 HG01074.hp1 others(37): Show |
intron_variant | MODIFIER | c.61-15241C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34421205 | ||||||
chr9:34421217
|
C | T | 64 | a0001c0001t0001g0109a0001c0001t0001g0112a0001c0001t0001g0182others(61): Show | 64 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.61-15253G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34421217 | ||||||
chr9:34421281
|
G | A | 4 | a0001c0001t0009g0139a0001c0001t0009g0140a0001c0001t0009g0141others(1): Show | 4 | HG02559.hp1 HG02818.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.61-15317C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34421281 | ||||||
chr9:34421315
|
G | A | 1 | a0001c0001t0001g0269 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.61-15351C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34421315 | ||||||
chr9:34421473
|
C | T | 1 | a0001c0001t0005g0036 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.61-15509G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34421473 | ||||||
chr9:34421523
|
G | T | 4 | a0001c0001t0009g0139a0001c0001t0009g0140a0001c0001t0009g0141others(1): Show | 4 | HG02559.hp1 HG02818.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.61-15559C>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34421523 | ||||||
chr9:34421553
|
G | A | 1 | a0001c0001t0003g0328 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.61-15589C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34421553 | ||||||
chr9:34421593
|
G | C | 281 | a0001c0001t0001g0050a0001c0001t0001g0074a0001c0001t0001g0075others(278): Show | 288 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(285): Show |
intron_variant | MODIFIER | c.61-15629C>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34421593 | ||||||
chr9:34421668
|
C | T | 22 | a0001c0001t0002g0129a0001c0001t0005g0013a0001c0001t0005g0014others(19): Show | 22 | HG00558.hp1 HG02027.hp1 HG02523.hp1 others(19): Show |
intron_variant | MODIFIER | c.61-15704G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34421668 | ||||||
chr9:34421881
|
C | A | 52 | a0001c0001t0004g0004a0001c0001t0004g0048a0001c0001t0004g0049others(49): Show | 53 | HG00280.hp2 HG00423.hp1 HG01074.hp1 others(50): Show |
intron_variant | MODIFIER | c.61-15917G>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34421881 | ||||||
chr9:34421881
|
C | G | 1 | a0001c0001t0002g0222 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.61-15917G>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34421881 | ||||||
chr9:34422066
|
T | C | 16 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0130others(13): Show | 18 | HG00323.hp2 HG00639.hp2 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.61-16102A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34422066 | ||||||
chr9:34422080
|
A | G | 4 | a0001c0001t0009g0139a0001c0001t0009g0140a0001c0001t0009g0141others(1): Show | 4 | HG02559.hp1 HG02818.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.61-16116T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34422080 | ||||||
chr9:34422113
|
G | A | 1 | a0001c0001t0001g0278 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.61-16149C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34422113 | ||||||
chr9:34422187
|
G | A | 129 | a0001c0001t0001g0355a0001c0001t0002g0005a0001c0001t0002g0006others(126): Show | 135 | HG00323.hp2 HG00558.hp1 HG00558.hp2 others(132): Show |
intron_variant | MODIFIER | c.61-16223C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34422187 | ||||||
chr9:34422215
|
T | G | 17 | a0001c0001t0001g0074a0001c0001t0007g0151a0001c0001t0007g0169others(14): Show | 17 | HG00099.hp1 HG00741.hp1 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.61-16251A>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34422215 | ||||||
chr9:34422248
|
A | T | 2 | a0001c0001t0011g0041a0001c0001t0011g0042 | 2 | HG01891.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.61-16284T>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34422248 | ||||||
chr9:34422281
|
T | C | 1 | a0001c0001t0002g0128 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.61-16317A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34422281 | ||||||
chr9:34422341
|
G | A | 1 | a0001c0001t0003g0100 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.61-16377C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34422341 | ||||||
chr9:34422457
|
T | A | 1 | a0001c0001t0012g0043 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.61-16493A>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34422457 | ||||||
chr9:34422480
|
C | T | 1 | a0001c0001t0001g0245 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.61-16516G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34422480 | ||||||
chr9:34422492
|
T | C | 3 | a0001c0001t0001g0276a0001c0001t0001g0294a0001c0001t0001g0320 | 3 | HG02040.hp2 HG02083.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.61-16528A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34422492 | ||||||
chr9:34422493
|
G | T | 2 | a0001c0001t0011g0041a0001c0001t0011g0042 | 2 | HG01891.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.61-16529C>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34422493 | ||||||
chr9:34422779
|
G | A | 6 | a0001c0001t0001g0050a0001c0001t0001g0075a0001c0001t0001g0076others(3): Show | 6 | HG01175.hp2 HG02818.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.61-16815C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34422779 | ||||||
chr9:34422832
|
G | T | 1 | a0001c0001t0008g0161 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.61-16868C>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34422832 | ||||||
chr9:34423133
|
G | A | 3 | a0001c0001t0001g0270a0001c0001t0012g0043a0001c0001t0012g0044 | 3 | HG03041.hp2 HG03195.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.61-17169C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34423133 | ||||||
chr9:34423207
|
G | C | 195 | a0001c0001t0001g0109a0001c0001t0001g0112a0001c0001t0001g0182others(192): Show | 201 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.61-17243C>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34423207 | ||||||
chr9:34423420
|
G | A | 24 | a0001c0001t0002g0129a0001c0001t0005g0013a0001c0001t0005g0014others(21): Show | 24 | HG00558.hp1 HG02027.hp1 HG02074.hp1 others(21): Show |
intron_variant | MODIFIER | c.61-17456C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34423420 | ||||||
chr9:34423500
|
C | T | 54 | a0001c0001t0001g0050a0001c0001t0001g0075a0001c0001t0001g0076others(51): Show | 55 | HG00280.hp2 HG00423.hp1 HG01074.hp1 others(52): Show |
intron_variant | MODIFIER | c.61-17536G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34423500 | ||||||
chr9:34423743
|
A | G | 1 | a0001c0001t0003g0316 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.61-17779T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34423743 | ||||||
chr9:34423761
|
G | A | 11 | a0001c0001t0007g0151a0001c0001t0007g0169a0001c0001t0007g0224others(8): Show | 11 | HG00099.hp1 HG00741.hp1 HG00741.hp2 others(8): Show |
intron_variant | MODIFIER | c.61-17797C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34423761 | ||||||
chr9:34423778
|
G | A | 1 | a0001c0001t0001g0308 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.61-17814C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34423778 | ||||||
chr9:34423808
|
C | T | 193 | a0001c0001t0001g0109a0001c0001t0001g0112a0001c0001t0001g0182others(190): Show | 199 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(196): Show |
intron_variant | MODIFIER | c.61-17844G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34423808 | ||||||
chr9:34424095
|
C | G | 6 | a0001c0001t0001g0074a0001c0001t0009g0139a0001c0001t0009g0140others(3): Show | 6 | HG01255.hp2 HG02055.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.61-18131G>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34424095 | ||||||
chr9:34424400
|
A | G | 4 | a0001c0001t0009g0139a0001c0001t0009g0140a0001c0001t0009g0141others(1): Show | 4 | HG02559.hp1 HG02818.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.61-18436T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34424400 | ||||||
chr9:34424443
|
T | TGGGCAAG others(11): Show |
63 | a0001c0001t0001g0109a0001c0001t0001g0112a0001c0001t0001g0182others(60): Show | 63 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.61-18497_61-18480d others(20): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34424443 | ||||||
chr9:34424458
|
C | T | 1 | a0001c0001t0011g0041 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.61-18494G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34424458 | ||||||
chr9:34424651
|
C | CGG | 45 | a0001c0001t0001g0355a0001c0001t0002g0233a0001c0001t0003g0003others(42): Show | 48 | HG00558.hp2 HG00621.hp2 HG00673.hp1 others(45): Show |
intron_variant | MODIFIER | c.61-18689_61-18688d others(4): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34424651 | ||||||
chr9:34424861
|
T | G | 1 | a0001c0001t0001g0306 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.61-18897A>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34424861 | ||||||
chr9:34424949
|
T | C | 15 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0130others(12): Show | 17 | HG00323.hp2 HG00639.hp2 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.61-18985A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34424949 | ||||||
chr9:34424951
|
T | C | 1 | a0001c0001t0002g0181 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.61-18987A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34424951 | ||||||
chr9:34424993
|
A | G | 1 | a0001c0001t0002g0167 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.61-19029T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34424993 | ||||||
chr9:34425005
|
C | T | 14 | a0001c0001t0007g0151a0001c0001t0007g0169a0001c0001t0007g0224others(11): Show | 14 | HG00099.hp1 HG00741.hp2 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.61-19041G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34425005 | ||||||
chr9:34425051
|
C | G | 1 | a0001c0001t0004g0249 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.61-19087G>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34425051 | ||||||
chr9:34425137
|
C | T | 4 | a0001c0001t0009g0139a0001c0001t0009g0140a0001c0001t0009g0141others(1): Show | 4 | HG02559.hp1 HG02818.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.61-19173G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34425137 | ||||||
chr9:34425218
|
T | C | 17 | a0001c0001t0001g0074a0001c0001t0007g0151a0001c0001t0007g0169others(14): Show | 17 | HG00099.hp1 HG00741.hp1 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.61-19254A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34425218 | ||||||
chr9:34425230
|
A | T | 55 | a0001c0001t0001g0050a0001c0001t0001g0075a0001c0001t0001g0076others(52): Show | 56 | HG00280.hp2 HG00423.hp1 HG01074.hp1 others(53): Show |
intron_variant | MODIFIER | c.61-19266T>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34425230 | ||||||
chr9:34425244
|
C | G | 1 | a0001c0001t0003g0316 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.61-19280G>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34425244 | ||||||
chr9:34425246
|
A | C | 1 | a0001c0001t0003g0316 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.61-19282T>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34425246 | ||||||
chr9:34425248
|
G | A | 1 | a0001c0001t0003g0316 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.61-19284C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34425248 | ||||||
chr9:34425317
|
C | T | 17 | a0001c0001t0001g0074a0001c0001t0007g0151a0001c0001t0007g0169others(14): Show | 17 | HG00099.hp1 HG00741.hp1 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.61-19353G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34425317 | ||||||
chr9:34425497
|
T | C | 65 | a0001c0001t0001g0109a0001c0001t0001g0112a0001c0001t0001g0182others(62): Show | 65 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.61-19533A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34425497 | ||||||
chr9:34425577
|
G | A | 1 | a0001c0001t0002g0131 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.61-19613C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34425577 | ||||||
chr9:34425584
|
C | T | 3 | a0001c0001t0002g0145a0001c0001t0002g0219a0001c0001t0002g0221 | 3 | HG01361.hp1 HG03942.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.61-19620G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34425584 | ||||||
chr9:34425619
|
G | A | 192 | a0001c0001t0001g0109a0001c0001t0001g0112a0001c0001t0001g0182others(189): Show | 198 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(195): Show |
intron_variant | MODIFIER | c.61-19655C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34425619 | ||||||
chr9:34425718
|
C | T | 1 | a0001c0001t0007g0365 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.61-19754G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34425718 | ||||||
chr9:34425800
|
A | T | 6 | a0001c0001t0009g0139a0001c0001t0009g0140a0001c0001t0009g0141others(3): Show | 6 | HG02559.hp1 HG02818.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.61-19836T>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34425800 | ||||||
chr9:34425930
|
A | C | 1 | a0001c0001t0006g0047 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.61-19966T>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34425930 | ||||||
chr9:34426126
|
G | C | 267 | a0001c0001t0001g0050a0001c0001t0001g0074a0001c0001t0001g0075others(264): Show | 274 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(271): Show |
intron_variant | MODIFIER | c.61-20162C>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34426126 | ||||||
chr9:34426189
|
T | A | 7 | a0001c0001t0006g0138a0001c0001t0006g0143a0001c0001t0009g0139others(4): Show | 7 | HG02559.hp1 HG02622.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.61-20225A>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34426189 | ||||||
chr9:34426340
|
TG | T | 7 | a0001c0001t0001g0097a0001c0001t0001g0101a0001c0001t0001g0102others(4): Show | 7 | HG01243.hp1 HG02451.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.61-20377delC | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34426340 | ||||||
chr9:34426590
|
G | A | 1 | a0001c0001t0020g0281 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.61-20626C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34426590 | ||||||
chr9:34426660
|
G | C | 76 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(73): Show | 83 | HG00099.hp1 HG00323.hp2 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.61-20696C>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34426660 | ||||||
chr9:34426685
|
CCAG | C | 3 | a0001c0001t0003g0356a0001c0001t0003g0357a0001c0004t0003g0358 | 3 | NA18964.hp2 NA18983.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.61-20724_61-20722d others(5): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34426685 | ||||||
chr9:34426773
|
G | A | 19 | a0001c0001t0004g0004a0001c0001t0004g0048a0001c0001t0004g0049others(16): Show | 20 | HG00280.hp2 HG01074.hp1 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.61-20809C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34426773 | ||||||
chr9:34426774
|
G | A | 1 | a0001c0001t0001g0307 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.61-20810C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34426774 | ||||||
chr9:34426863
|
G | A | 5 | a0001c0001t0001g0097a0001c0001t0001g0101a0001c0001t0001g0102others(2): Show | 5 | HG01243.hp1 HG02451.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.61-20899C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34426863 | ||||||
chr9:34426920
|
G | C | 1 | a0001c0001t0006g0369 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.61-20956C>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34426920 | ||||||
chr9:34426923
|
C | T | 1 | a0001c0001t0010g0086 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.61-20959G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34426923 | ||||||
chr9:34426935
|
T | C | 1 | a0001c0001t0024g0095 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.61-20971A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34426935 | ||||||
chr9:34426984
|
G | A | 31 | a0001c0001t0005g0012a0001c0001t0005g0013a0001c0001t0005g0014others(28): Show | 31 | HG00558.hp1 HG01891.hp2 HG01928.hp1 others(28): Show |
intron_variant | MODIFIER | c.61-21020C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34426984 | ||||||
chr9:34427023
|
C | T | 1 | a0001c0001t0024g0095 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.61-21059G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34427023 | ||||||
chr9:34427048
|
C | G | 31 | a0001c0001t0005g0012a0001c0001t0005g0013a0001c0001t0005g0014others(28): Show | 31 | HG00558.hp1 HG01891.hp2 HG01928.hp1 others(28): Show |
intron_variant | MODIFIER | c.61-21084G>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34427048 | ||||||
chr9:34427194
|
C | T | 2 | a0001c0001t0012g0043a0001c0001t0012g0044 | 2 | HG03195.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.61-21230G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34427194 | ||||||
chr9:34427199
|
C | T | 7 | a0001c0001t0007g0360a0001c0001t0007g0361a0001c0001t0007g0362others(4): Show | 7 | HG00099.hp1 HG00741.hp1 HG01070.hp2 others(4): Show |
intron_variant | MODIFIER | c.61-21235G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34427199 | ||||||
chr9:34427200
|
C | T | 1 | a0001c0001t0002g0192 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.61-21236G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34427200 | ||||||
chr9:34427333
|
G | C | 1 | a0001c0001t0001g0252 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.61-21369C>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34427333 | ||||||
chr9:34427349
|
C | T | 7 | a0001c0001t0007g0360a0001c0001t0007g0361a0001c0001t0007g0362others(4): Show | 7 | HG00099.hp1 HG00741.hp1 HG01070.hp2 others(4): Show |
intron_variant | MODIFIER | c.61-21385G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34427349 | ||||||
chr9:34427378
|
C | T | 49 | a0001c0001t0001g0097a0001c0001t0001g0101a0001c0001t0001g0102others(46): Show | 49 | HG00099.hp1 HG00558.hp1 HG00741.hp1 others(46): Show |
intron_variant | MODIFIER | c.61-21414G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34427378 | ||||||
chr9:34427495
|
T | C | 31 | a0001c0001t0005g0012a0001c0001t0005g0013a0001c0001t0005g0014others(28): Show | 31 | HG00558.hp1 HG01891.hp2 HG01928.hp1 others(28): Show |
intron_variant | MODIFIER | c.61-21531A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34427495 | ||||||
chr9:34427540
|
T | G | 1 | a0001c0001t0002g0207 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.61-21576A>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34427540 | ||||||
chr9:34428530
|
T | C | 1 | a0001c0001t0002g0146 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.61-22566A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34428530 | ||||||
chr9:34428539
|
G | C | 5 | a0001c0001t0001g0109a0001c0001t0001g0112a0001c0001t0001g0182others(2): Show | 5 | NA18949.hp2 NA18953.hp2 NA18985.hp2 others(2): Show |
intron_variant | MODIFIER | c.61-22575C>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34428539 | ||||||
chr9:34428602
|
T | C | 1 | a0001c0001t0001g0251 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.61-22638A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34428602 | ||||||
chr9:34428990
|
G | C | 10 | a0001c0001t0001g0097a0001c0001t0001g0101a0001c0001t0001g0102others(7): Show | 10 | HG01243.hp1 HG01496.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.61-23026C>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34428990 | ||||||
chr9:34429019
|
A | G | 31 | a0001c0001t0005g0012a0001c0001t0005g0013a0001c0001t0005g0014others(28): Show | 31 | HG00558.hp1 HG01891.hp2 HG01928.hp1 others(28): Show |
intron_variant | MODIFIER | c.61-23055T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34429019 | ||||||
chr9:34429027
|
T | G | 1 | a0001c0001t0006g0111 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.61-23063A>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34429027 | ||||||
chr9:34429077
|
C | T | 8 | a0001c0001t0007g0359a0001c0001t0007g0360a0001c0001t0007g0361others(5): Show | 8 | HG00099.hp1 HG00741.hp1 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.61-23113G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34429077 | ||||||
chr9:34429250
|
G | A | 10 | a0001c0001t0001g0097a0001c0001t0001g0101a0001c0001t0001g0102others(7): Show | 10 | HG01243.hp1 HG01496.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.61-23286C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34429250 | ||||||
chr9:34429352
|
T | C | 2 | a0001c0001t0001g0312a0001c0001t0001g0313 | 2 | NA19054.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.61-23388A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34429352 | ||||||
chr9:34429480
|
G | A | 8 | a0001c0001t0007g0359a0001c0001t0007g0360a0001c0001t0007g0361others(5): Show | 8 | HG00099.hp1 HG00741.hp1 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.61-23516C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34429480 | ||||||
chr9:34429728
|
T | A | 98 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(95): Show | 105 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.61-23764A>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34429728 | ||||||
chr9:34429734
|
T | C | 8 | a0001c0001t0007g0359a0001c0001t0007g0360a0001c0001t0007g0361others(5): Show | 8 | HG00099.hp1 HG00741.hp1 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.61-23770A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34429734 | ||||||
chr9:34430101
|
C | T | 1 | a0001c0001t0002g0213 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.61-24137G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34430101 | ||||||
chr9:34430107
|
T | G | 1 | a0001c0001t0002g0221 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.61-24143A>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34430107 | ||||||
chr9:34430204
|
C | T | 31 | a0001c0001t0005g0012a0001c0001t0005g0013a0001c0001t0005g0014others(28): Show | 31 | HG00558.hp1 HG01891.hp2 HG01928.hp1 others(28): Show |
intron_variant | MODIFIER | c.61-24240G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34430204 | ||||||
chr9:34430247
|
G | C | 1 | a0001c0001t0002g0183 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.61-24283C>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34430247 | ||||||
chr9:34430299
|
T | C | 26 | a0001c0001t0001g0117a0001c0001t0002g0005a0001c0001t0002g0105others(23): Show | 27 | HG00323.hp2 HG00609.hp2 HG00621.hp2 others(24): Show |
intron_variant | MODIFIER | c.61-24335A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34430299 | ||||||
chr9:34430632
|
G | A | 9 | a0001c0001t0007g0359a0001c0001t0007g0360a0001c0001t0007g0361others(6): Show | 9 | HG00099.hp1 HG00741.hp1 HG01070.hp2 others(6): Show |
intron_variant | MODIFIER | c.61-24668C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34430632 | ||||||
chr9:34430636
|
C | CA | 50 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0076others(47): Show | 50 | HG00280.hp2 HG01074.hp1 HG01081.hp1 others(47): Show |
intron_variant | MODIFIER | c.61-24673dupT | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34430636 | ||||||
chr9:34430636
|
C | CAA | 88 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(85): Show | 95 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.61-24674_61-24673d others(4): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34430636 | ||||||
chr9:34430636
|
C | CAAA | 25 | a0001c0001t0001g0237a0001c0001t0001g0271a0001c0001t0001g0291others(22): Show | 26 | HG00099.hp1 HG00597.hp1 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.61-24675_61-24673d others(5): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34430636 | ||||||
chr9:34430636
|
C | CAAAAAAA others(3): Show |
5 | a0001c0001t0005g0013a0001c0001t0005g0016a0001c0001t0005g0017others(2): Show | 5 | HG02027.hp1 NA18941.hp1 NA18945.hp2 others(2): Show |
intron_variant | MODIFIER | c.61-24682_61-24673d others(12): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34430636 | ||||||
chr9:34430636
|
C | CAAAAAAA others(4): Show |
12 | a0001c0001t0005g0012a0001c0001t0005g0020a0001c0001t0005g0021others(9): Show | 12 | HG00558.hp1 HG01934.hp1 HG02273.hp1 others(9): Show |
intron_variant | MODIFIER | c.61-24683_61-24673d others(13): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34430636 | ||||||
chr9:34430636
|
C | CAAAAAAA others(5): Show |
11 | a0001c0001t0005g0014a0001c0001t0005g0015a0001c0001t0005g0018others(8): Show | 11 | HG01891.hp2 HG02074.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.61-24684_61-24673d others(14): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34430636 | ||||||
chr9:34430636
|
C | CAAAAAAA others(6): Show |
3 | a0001c0001t0005g0032a0001c0001t0005g0033a0001c0001t0005g0034 | 3 | HG01928.hp1 NA18955.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.61-24685_61-24673d others(15): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34430636 | ||||||
chr9:34430636
|
CA | C | 8 | a0001c0001t0001g0367a0001c0001t0002g0166a0001c0001t0002g0167others(5): Show | 8 | HG01496.hp1 HG02622.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.61-24673delT | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34430636 | ||||||
chr9:34430846
|
T | TAACAACA others(2): Show |
31 | a0001c0001t0005g0012a0001c0001t0005g0013a0001c0001t0005g0014others(28): Show | 31 | HG00558.hp1 HG01891.hp2 HG01928.hp1 others(28): Show |
intron_variant | MODIFIER | c.61-24891_61-24883d others(11): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34430846 | ||||||
chr9:34430846
|
T | TAACAACA others(5): Show |
50 | a0001c0001t0001g0050a0001c0001t0001g0074a0001c0001t0001g0075others(47): Show | 51 | HG00280.hp2 HG01074.hp1 HG01081.hp1 others(48): Show |
intron_variant | MODIFIER | c.61-24894_61-24883d others(14): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34430846 | ||||||
chr9:34430846
|
T | TAACAACA others(8): Show |
2 | a0001c0001t0001g0079a0001c0001t0017g0094 | 2 | HG02451.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.61-24897_61-24883d others(17): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34430846 | ||||||
chr9:34430846
|
T | TAACAACA others(11): Show |
7 | a0001c0001t0007g0359a0001c0001t0007g0360a0001c0001t0007g0362others(4): Show | 7 | HG00099.hp1 HG00741.hp1 HG01070.hp2 others(4): Show |
intron_variant | MODIFIER | c.61-24900_61-24883d others(20): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34430846 | ||||||
chr9:34430846
|
T | TAACAACA others(14): Show |
3 | a0001c0001t0003g0098a0001c0001t0012g0043a0001c0001t0018g0099 | 3 | HG01496.hp1 HG02647.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.61-24883_61-24882i others(23): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34430846 | ||||||
chr9:34430846
|
T | TAACAACA others(17): Show |
2 | a0001c0001t0003g0100a0001c0001t0012g0044 | 2 | HG03195.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.61-24883_61-24882i others(26): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34430846 | ||||||
chr9:34430846
|
T | TAACAACA others(20): Show |
4 | a0001c0001t0001g0097a0001c0001t0001g0101a0001c0001t0001g0102others(1): Show | 4 | HG01243.hp1 HG02451.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.61-24883_61-24882i others(29): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34430846 | ||||||
chr9:34430846
|
T | TAACAACA others(23): Show |
1 | a0001c0001t0001g0104 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.61-24883_61-24882i others(32): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34430846 | ||||||
chr9:34430867
|
T | C | 9 | a0001c0001t0007g0359a0001c0001t0007g0360a0001c0001t0007g0361others(6): Show | 9 | HG00099.hp1 HG00741.hp1 HG01070.hp2 others(6): Show |
intron_variant | MODIFIER | c.61-24903A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34430867 | ||||||
chr9:34431081
|
C | T | 51 | a0001c0001t0001g0050a0001c0001t0001g0074a0001c0001t0001g0075others(48): Show | 52 | HG00280.hp2 HG01074.hp1 HG01081.hp1 others(49): Show |
intron_variant | MODIFIER | c.61-25117G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34431081 | ||||||
chr9:34431401
|
C | T | 1 | a0001c0001t0021g0366 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.61-25437G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34431401 | ||||||
chr9:34431485
|
T | G | 10 | a0001c0001t0001g0097a0001c0001t0001g0101a0001c0001t0001g0102others(7): Show | 10 | HG01243.hp1 HG01496.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.61-25521A>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34431485 | ||||||
chr9:34431976
|
A | G | 205 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(202): Show | 213 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.61-26012T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34431976 | ||||||
chr9:34432272
|
G | T | 31 | a0001c0001t0005g0012a0001c0001t0005g0013a0001c0001t0005g0014others(28): Show | 31 | HG00558.hp1 HG01891.hp2 HG01928.hp1 others(28): Show |
intron_variant | MODIFIER | c.60+25932C>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34432272 | ||||||
chr9:34432489
|
C | T | 6 | a0001c0001t0006g0138a0001c0001t0006g0143a0001c0001t0009g0139others(3): Show | 6 | HG02559.hp1 HG02818.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.60+25715G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34432489 | ||||||
chr9:34432500
|
T | C | 4 | a0001c0001t0001g0097a0001c0001t0001g0101a0001c0001t0001g0102others(1): Show | 4 | HG01243.hp1 HG02451.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.60+25704A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34432500 | ||||||
chr9:34432541
|
C | T | 40 | a0001c0001t0001g0320a0001c0001t0002g0321a0001c0001t0002g0329others(37): Show | 43 | HG00323.hp1 HG00544.hp2 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.60+25663G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34432541 | ||||||
chr9:34432554
|
C | T | 31 | a0001c0001t0005g0012a0001c0001t0005g0013a0001c0001t0005g0014others(28): Show | 31 | HG00558.hp1 HG01891.hp2 HG01928.hp1 others(28): Show |
intron_variant | MODIFIER | c.60+25650G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34432554 | ||||||
chr9:34432555
|
G | A | 1 | a0001c0001t0001g0088 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.60+25649C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34432555 | ||||||
chr9:34432639
|
C | T | 10 | a0001c0001t0001g0097a0001c0001t0001g0101a0001c0001t0001g0102others(7): Show | 10 | HG01243.hp1 HG01496.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.60+25565G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34432639 | ||||||
chr9:34432738
|
C | T | 9 | a0001c0001t0001g0050a0001c0001t0001g0074a0001c0001t0001g0075others(6): Show | 9 | HG01175.hp2 HG02055.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.60+25466G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34432738 | ||||||
chr9:34432751
|
T | G | 1 | a0001c0001t0024g0095 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.60+25453A>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34432751 | ||||||
chr9:34432819
|
C | G | 10 | a0001c0001t0001g0097a0001c0001t0001g0101a0001c0001t0001g0102others(7): Show | 10 | HG01243.hp1 HG01496.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.60+25385G>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34432819 | ||||||
chr9:34432903
|
G | T | 1 | a0001c0001t0005g0038 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.60+25301C>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34432903 | ||||||
chr9:34432966
|
G | C | 1 | a0001c0001t0001g0285 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.60+25238C>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34432966 | ||||||
chr9:34432980
|
G | A | 1 | a0001c0001t0006g0111 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.60+25224C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34432980 | ||||||
chr9:34433259
|
T | C | 8 | a0001c0001t0007g0359a0001c0001t0007g0360a0001c0001t0007g0361others(5): Show | 8 | HG00099.hp1 HG00741.hp1 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.60+24945A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34433259 | ||||||
chr9:34433315
|
A | G | 98 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(95): Show | 105 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.60+24889T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34433315 | ||||||
chr9:34433329
|
C | T | 1 | a0001c0001t0001g0088 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.60+24875G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34433329 | ||||||
chr9:34433348
|
G | A | 3 | a0001c0001t0003g0356a0001c0001t0003g0357a0001c0004t0003g0358 | 3 | NA18964.hp2 NA18983.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.60+24856C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34433348 | ||||||
chr9:34433380
|
A | G | 1 | a0001c0001t0005g0016 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.60+24824T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34433380 | ||||||
chr9:34433818
|
G | A | 1 | a0001c0001t0011g0042 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.60+24386C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34433818 | ||||||
chr9:34433877
|
G | C | 31 | a0001c0001t0005g0012a0001c0001t0005g0013a0001c0001t0005g0014others(28): Show | 31 | HG00558.hp1 HG01891.hp2 HG01928.hp1 others(28): Show |
intron_variant | MODIFIER | c.60+24327C>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34433877 | ||||||
chr9:34433931
|
G | A | 4 | a0001c0001t0001g0273a0001c0001t0001g0274a0001c0001t0001g0277others(1): Show | 4 | NA18960.hp1 NA18975.hp2 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.60+24273C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34433931 | ||||||
chr9:34434030
|
G | A | 1 | a0001c0001t0001g0283 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.60+24174C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34434030 | ||||||
chr9:34434045
|
A | T | 1 | a0001c0001t0001g0302 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.60+24159T>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34434045 | ||||||
chr9:34434046
|
C | A | 1 | a0001c0001t0001g0302 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.60+24158G>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34434046 | ||||||
chr9:34434047
|
A | C | 1 | a0001c0001t0001g0302 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.60+24157T>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34434047 | ||||||
chr9:34434181
|
A | G | 1 | a0001c0001t0002g0184 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.60+24023T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34434181 | ||||||
chr9:34434201
|
C | CA | 25 | a0001c0001t0001g0092a0001c0001t0001g0101a0001c0001t0001g0102others(22): Show | 25 | HG01243.hp1 HG01358.hp2 HG01361.hp1 others(22): Show |
intron_variant | MODIFIER | c.60+24002dupT | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34434201 | ||||||
chr9:34434201
|
C | CAA | 6 | a0001c0001t0001g0088a0001c0001t0001g0097a0001c0001t0001g0104others(3): Show | 6 | HG01496.hp1 HG02572.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.60+24001_60+24002d others(4): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34434201 | ||||||
chr9:34434201
|
CA | C | 105 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(102): Show | 112 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.60+24002delT | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34434201 | ||||||
chr9:34434201
|
CAA | C | 39 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0002g0282others(36): Show | 40 | HG00280.hp1 HG00558.hp1 HG01081.hp1 others(37): Show |
intron_variant | MODIFIER | c.60+24001_60+24002d others(4): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34434201 | ||||||
chr9:34434201
|
CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0004g0048 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.60+23990_60+24002d others(15): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34434201 | ||||||
chr9:34434355
|
T | C | 98 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(95): Show | 105 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.60+23849A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34434355 | ||||||
chr9:34434434
|
A | G | 1 | a0001c0001t0017g0094 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.60+23770T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34434434 | ||||||
chr9:34434526
|
ATCCAGAA others(26): Show |
A | 1 | a0001c0001t0017g0094 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.60+23645_60+23677d others(35): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34434526 | ||||||
chr9:34434570
|
C | T | 31 | a0001c0001t0005g0012a0001c0001t0005g0013a0001c0001t0005g0014others(28): Show | 31 | HG00558.hp1 HG01891.hp2 HG01928.hp1 others(28): Show |
intron_variant | MODIFIER | c.60+23634G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34434570 | ||||||
chr9:34434680
|
T | C | 1 | a0001c0001t0001g0278 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.60+23524A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34434680 | ||||||
chr9:34434812
|
TTTTC | T | 51 | a0001c0001t0001g0050a0001c0001t0001g0074a0001c0001t0001g0075others(48): Show | 52 | HG00280.hp2 HG01074.hp1 HG01081.hp1 others(49): Show |
intron_variant | MODIFIER | c.60+23388_60+23391d others(6): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34434812 | ||||||
chr9:34434827
|
TC | T | 31 | a0001c0001t0005g0012a0001c0001t0005g0013a0001c0001t0005g0014others(28): Show | 31 | HG00558.hp1 HG01891.hp2 HG01928.hp1 others(28): Show |
intron_variant | MODIFIER | c.60+23376delG | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34434827 | ||||||
chr9:34434832
|
T | C | 3 | a0001c0001t0003g0098a0001c0001t0003g0100a0001c0001t0018g0099 | 3 | HG01496.hp1 HG02647.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.60+23372A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34434832 | ||||||
chr9:34434979
|
C | G | 1 | a0001c0001t0001g0088 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.60+23225G>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34434979 | ||||||
chr9:34435011
|
G | T | 2 | a0001c0001t0003g0317a0001c0001t0003g0318 | 2 | NA18960.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.60+23193C>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34435011 | ||||||
chr9:34435059
|
G | A | 1 | a0001c0001t0024g0095 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.60+23145C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34435059 | ||||||
chr9:34435175
|
G | C | 1 | a0001c0001t0004g0226 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.60+23029C>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34435175 | ||||||
chr9:34435377
|
A | G | 1 | a0001c0001t0001g0372 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.60+22827T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34435377 | ||||||
chr9:34435377
|
A | T | 31 | a0001c0001t0005g0012a0001c0001t0005g0013a0001c0001t0005g0014others(28): Show | 31 | HG00558.hp1 HG01891.hp2 HG01928.hp1 others(28): Show |
intron_variant | MODIFIER | c.60+22827T>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34435377 | ||||||
chr9:34435414
|
T | C | 3 | a0001c0001t0003g0098a0001c0001t0003g0100a0001c0001t0018g0099 | 3 | HG01496.hp1 HG02647.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.60+22790A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34435414 | ||||||
chr9:34435425
|
A | C | 31 | a0001c0001t0005g0012a0001c0001t0005g0013a0001c0001t0005g0014others(28): Show | 31 | HG00558.hp1 HG01891.hp2 HG01928.hp1 others(28): Show |
intron_variant | MODIFIER | c.60+22779T>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34435425 | ||||||
chr9:34435430
|
GA | G | 31 | a0001c0001t0005g0012a0001c0001t0005g0013a0001c0001t0005g0014others(28): Show | 31 | HG00558.hp1 HG01891.hp2 HG01928.hp1 others(28): Show |
intron_variant | MODIFIER | c.60+22773delT | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34435430 | ||||||
chr9:34435514
|
C | G | 31 | a0001c0001t0005g0012a0001c0001t0005g0013a0001c0001t0005g0014others(28): Show | 31 | HG00558.hp1 HG01891.hp2 HG01928.hp1 others(28): Show |
intron_variant | MODIFIER | c.60+22690G>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34435514 | ||||||
chr9:34435634
|
T | C | 381 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(378): Show | 395 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(392): Show |
intron_variant | MODIFIER | c.60+22570A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34435634 | ||||||
chr9:34435723
|
C | T | 1 | a0001c0001t0017g0094 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.60+22481G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34435723 | ||||||
chr9:34435813
|
C | CT | 98 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(95): Show | 105 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.60+22390dupA | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34435813 | ||||||
chr9:34435824
|
G | T | 1 | a0001c0001t0017g0094 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.60+22380C>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34435824 | ||||||
chr9:34435875
|
G | A | 2 | a0001c0001t0002g0148a0001c0001t0002g0149 | 2 | HG02293.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.60+22329C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34435875 | ||||||
chr9:34435962
|
C | T | 1 | a0001c0001t0016g0063 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.60+22242G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34435962 | ||||||
chr9:34435966
|
T | C | 1 | a0001c0001t0001g0232 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.60+22238A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34435966 | ||||||
chr9:34436004
|
C | T | 1 | a0001c0004t0003g0358 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.60+22200G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34436004 | ||||||
chr9:34436026
|
A | G | 7 | a0001c0001t0002g0162a0001c0001t0002g0166a0001c0001t0002g0217others(4): Show | 7 | NA18747.hp1 NA18955.hp1 NA18982.hp2 others(4): Show |
intron_variant | MODIFIER | c.60+22178T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34436026 | ||||||
chr9:34436095
|
G | A | 6 | a0001c0001t0006g0138a0001c0001t0006g0143a0001c0001t0009g0139others(3): Show | 6 | HG02559.hp1 HG02818.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.60+22109C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34436095 | ||||||
chr9:34436248
|
T | C | 1 | a0001c0001t0001g0110 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.60+21956A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34436248 | ||||||
chr9:34436422
|
T | A | 99 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(96): Show | 106 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.60+21782A>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34436422 | ||||||
chr9:34436494
|
C | T | 1 | a0001c0001t0001g0218 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.60+21710G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34436494 | ||||||
chr9:34436617
|
T | G | 1 | a0001c0001t0001g0355 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.60+21587A>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34436617 | ||||||
chr9:34436773
|
C | CTA | 98 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(95): Show | 105 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.60+21430_60+21431i others(4): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34436773 | ||||||
chr9:34436775
|
C | T | 98 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(95): Show | 105 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.60+21429G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34436775 | ||||||
chr9:34436849
|
T | C | 1 | a0001c0001t0017g0094 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.60+21355A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34436849 | ||||||
chr9:34437026
|
C | G | 2 | a0001c0001t0003g0317a0001c0001t0003g0318 | 2 | NA18960.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.60+21178G>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34437026 | ||||||
chr9:34437179
|
A | ACT | 3 | a0001c0001t0006g0051a0001c0001t0006g0052a0001c0001t0006g0369 | 3 | HG01496.hp2 HG02109.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.60+21023_60+21024d others(4): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34437179 | ||||||
chr9:34437194
|
A | G | 31 | a0001c0001t0005g0012a0001c0001t0005g0013a0001c0001t0005g0014others(28): Show | 31 | HG00558.hp1 HG01891.hp2 HG01928.hp1 others(28): Show |
intron_variant | MODIFIER | c.60+21010T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34437194 | ||||||
chr9:34437471
|
G | A | 98 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(95): Show | 105 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.60+20733C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34437471 | ||||||
chr9:34437798
|
C | A | 1 | a0001c0001t0001g0187 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.60+20406G>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34437798 | ||||||
chr9:34437895
|
G | A | 1 | a0001c0001t0003g0354 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.60+20309C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34437895 | ||||||
chr9:34437911
|
A | G | 1 | a0001c0001t0026g0144 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.60+20293T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34437911 | ||||||
chr9:34437967
|
G | T | 1 | a0001c0001t0004g0066 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.60+20237C>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34437967 | ||||||
chr9:34437973
|
C | G | 31 | a0001c0001t0005g0012a0001c0001t0005g0013a0001c0001t0005g0014others(28): Show | 31 | HG00558.hp1 HG01891.hp2 HG01928.hp1 others(28): Show |
intron_variant | MODIFIER | c.60+20231G>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34437973 | ||||||
chr9:34437986
|
G | A | 31 | a0001c0001t0005g0012a0001c0001t0005g0013a0001c0001t0005g0014others(28): Show | 31 | HG00558.hp1 HG01891.hp2 HG01928.hp1 others(28): Show |
intron_variant | MODIFIER | c.60+20218C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34437986 | ||||||
chr9:34438004
|
G | A | 3 | a0001c0001t0003g0098a0001c0001t0003g0100a0001c0001t0018g0099 | 3 | HG01496.hp1 HG02647.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.60+20200C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34438004 | ||||||
chr9:34438015
|
C | G | 3 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0092 | 3 | HG02615.hp2 HG02809.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.60+20189G>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34438015 | ||||||
chr9:34438021
|
A | G | 50 | a0001c0001t0001g0050a0001c0001t0001g0074a0001c0001t0001g0075others(47): Show | 51 | HG00280.hp2 HG01074.hp1 HG01081.hp1 others(48): Show |
intron_variant | MODIFIER | c.60+20183T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34438021 | ||||||
chr9:34438113
|
C | G | 1 | a0001c0001t0002g0189 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.60+20091G>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34438113 | ||||||
chr9:34438122
|
G | A | 1 | a0001c0001t0001g0188 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.60+20082C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34438122 | ||||||
chr9:34438144
|
G | A | 1 | a0001c0001t0001g0104 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.60+20060C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34438144 | ||||||
chr9:34438246
|
G | A | 199 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(196): Show | 207 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.60+19958C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34438246 | ||||||
chr9:34438266
|
A | G | 1 | a0001c0001t0007g0224 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.60+19938T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34438266 | ||||||
chr9:34438275
|
A | AC | 6 | a0001c0001t0001g0355a0001c0001t0002g0116a0001c0001t0002g0133others(3): Show | 6 | HG01167.hp1 HG02080.hp2 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.60+19928dupG | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34438275 | ||||||
chr9:34438292
|
G | A | 1 | a0001c0001t0002g0240 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.60+19912C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34438292 | ||||||
chr9:34438309
|
A | G | 2 | a0001c0002t0001g0370a0001c0002t0001g0371 | 2 | HG01099.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.60+19895T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34438309 | ||||||
chr9:34438315
|
G | A | 1 | a0001c0001t0024g0095 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.60+19889C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34438315 | ||||||
chr9:34438343
|
G | A | 1 | a0001c0001t0001g0279 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.60+19861C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34438343 | ||||||
chr9:34438374
|
G | A | 1 | a0001c0001t0002g0150 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.60+19830C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34438374 | ||||||
chr9:34438378
|
C | T | 4 | a0001c0001t0001g0237a0001c0001t0001g0246a0001c0001t0001g0247others(1): Show | 4 | HG00639.hp1 HG01168.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.60+19826G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34438378 | ||||||
chr9:34438446
|
G | C | 1 | a0001c0001t0006g0080 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.60+19758C>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34438446 | ||||||
chr9:34438456
|
T | C | 1 | a0001c0001t0017g0094 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.60+19748A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34438456 | ||||||
chr9:34438471
|
C | G | 74 | a0001c0001t0001g0109a0001c0001t0001g0112a0001c0001t0001g0182others(71): Show | 74 | HG00423.hp1 HG00597.hp2 HG00642.hp2 others(71): Show |
intron_variant | MODIFIER | c.60+19733G>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34438471 | ||||||
chr9:34438521
|
G | GT | 31 | a0001c0001t0005g0012a0001c0001t0005g0013a0001c0001t0005g0014others(28): Show | 31 | HG00558.hp1 HG01891.hp2 HG01928.hp1 others(28): Show |
intron_variant | MODIFIER | c.60+19682dupA | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34438521 | ||||||
chr9:34438681
|
G | A | 33 | a0001c0001t0002g0204a0001c0001t0005g0012a0001c0001t0005g0013others(30): Show | 33 | HG00558.hp1 HG01891.hp1 HG01891.hp2 others(30): Show |
intron_variant | MODIFIER | c.60+19523C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34438681 | ||||||
chr9:34438799
|
G | C | 1 | a0001c0001t0005g0038 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.60+19405C>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34438799 | ||||||
chr9:34438873
|
A | T | 2 | a0001c0002t0001g0370a0001c0002t0001g0371 | 2 | HG01099.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.60+19331T>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34438873 | ||||||
chr9:34438885
|
T | C | 1 | a0001c0001t0001g0280 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.60+19319A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34438885 | ||||||
chr9:34439017
|
G | A | 4 | a0001c0001t0005g0015a0001c0001t0005g0017a0001c0001t0005g0018others(1): Show | 4 | HG02027.hp1 NA18945.hp2 NA18991.hp1 others(1): Show |
intron_variant | MODIFIER | c.60+19187C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34439017 | ||||||
chr9:34439068
|
C | T | 1 | a0001c0001t0001g0008 | 2 | HG00544.hp1 HG02071.hp2 |
intron_variant | MODIFIER | c.60+19136G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34439068 | ||||||
chr9:34439175
|
C | T | 1 | a0001c0001t0023g0159 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.60+19029G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34439175 | ||||||
chr9:34439257
|
G | A | 1 | a0001c0001t0001g0242 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.60+18947C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34439257 | ||||||
chr9:34439308
|
G | A | 1 | a0001c0001t0001g0296 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.60+18896C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34439308 | ||||||
chr9:34439342
|
A | C | 1 | a0001c0001t0002g0133 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.60+18862T>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34439342 | ||||||
chr9:34439593
|
A | G | 1 | a0001c0001t0002g0115 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.60+18611T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34439593 | ||||||
chr9:34439662
|
G | A | 6 | a0001c0001t0002g0205a0001c0001t0002g0206a0001c0001t0002g0207others(3): Show | 6 | HG01109.hp2 HG02615.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.60+18542C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34439662 | ||||||
chr9:34439750
|
G | A | 1 | a0001c0001t0012g0043 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.60+18454C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34439750 | ||||||
chr9:34439785
|
G | A | 2 | a0001c0001t0001g0231a0001c0001t0001g0232 | 2 | NA18942.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.60+18419C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34439785 | ||||||
chr9:34439978
|
C | T | 1 | a0001c0001t0002g0115 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.60+18226G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34439978 | ||||||
chr9:34439994
|
G | A | 1 | a0001c0001t0020g0281 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.60+18210C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34439994 | ||||||
chr9:34440037
|
A | T | 1 | a0001c0001t0001g0245 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.60+18167T>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34440037 | ||||||
chr9:34440078
|
A | G | 18 | a0001c0001t0002g0154a0001c0001t0002g0155a0001c0001t0003g0314others(15): Show | 18 | HG00423.hp1 HG02056.hp2 HG02083.hp1 others(15): Show |
intron_variant | MODIFIER | c.60+18126T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34440078 | ||||||
chr9:34440174
|
A | C | 1 | a0001c0001t0001g0091 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.60+18030T>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34440174 | ||||||
chr9:34440239
|
C | T | 1 | a0001c0001t0002g0106 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.60+17965G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34440239 | ||||||
chr9:34440315
|
G | A | 1 | a0001c0001t0015g0011 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.60+17889C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34440315 | ||||||
chr9:34440477
|
T | C | 1 | a0001c0001t0006g0084 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.60+17727A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34440477 | ||||||
chr9:34440503
|
C | T | 3 | a0001c0001t0003g0098a0001c0001t0003g0100a0001c0001t0018g0099 | 3 | HG01496.hp1 HG02647.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.60+17701G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34440503 | ||||||
chr9:34440564
|
T | C | 4 | a0001c0001t0004g0208a0001c0001t0004g0209a0001c0001t0004g0210others(1): Show | 4 | NA18950.hp1 NA18974.hp1 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.60+17640A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34440564 | ||||||
chr9:34440625
|
C | T | 9 | a0001c0001t0001g0050a0001c0001t0001g0074a0001c0001t0001g0075others(6): Show | 9 | HG01175.hp2 HG02055.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.60+17579G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34440625 | ||||||
chr9:34440800
|
G | A | 98 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(95): Show | 105 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.60+17404C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34440800 | ||||||
chr9:34440844
|
C | A | 26 | a0001c0001t0001g0117a0001c0001t0002g0005a0001c0001t0002g0105others(23): Show | 27 | HG00323.hp2 HG00609.hp2 HG00621.hp2 others(24): Show |
intron_variant | MODIFIER | c.60+17360G>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34440844 | ||||||
chr9:34440850
|
C | CA | 16 | a0001c0001t0001g0112a0001c0001t0001g0283a0001c0001t0001g0284others(13): Show | 16 | HG00423.hp1 HG01106.hp1 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.60+17353dupT | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34440850 | ||||||
chr9:34440850
|
CA | C | 16 | a0001c0001t0001g0229a0001c0001t0001g0243a0001c0001t0001g0244others(13): Show | 16 | HG01070.hp2 HG01496.hp1 HG02027.hp1 others(13): Show |
intron_variant | MODIFIER | c.60+17353delT | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34440850 | ||||||
chr9:34440867
|
A | T | 27 | a0001c0001t0005g0013a0001c0001t0005g0014a0001c0001t0005g0015others(24): Show | 27 | HG00558.hp1 HG01928.hp1 HG01934.hp1 others(24): Show |
intron_variant | MODIFIER | c.60+17337T>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34440867 | ||||||
chr9:34440868
|
A | T | 33 | a0001c0001t0001g0367a0001c0001t0002g0368a0001c0001t0005g0012others(30): Show | 33 | HG00558.hp1 HG01891.hp2 HG01928.hp1 others(30): Show |
intron_variant | MODIFIER | c.60+17336T>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34440868 | ||||||
chr9:34440869
|
T | A | 1 | a0001c0001t0017g0094 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.60+17335A>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34440869 | ||||||
chr9:34441025
|
C | T | 2 | a0001c0001t0003g0317a0001c0001t0003g0318 | 2 | NA18960.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.60+17179G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34441025 | ||||||
chr9:34441098
|
C | T | 2 | a0001c0001t0003g0317a0001c0001t0003g0318 | 2 | NA18960.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.60+17106G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34441098 | ||||||
chr9:34441226
|
G | T | 1 | a0001c0001t0007g0151 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.60+16978C>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34441226 | ||||||
chr9:34441268
|
C | T | 9 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0092others(6): Show | 9 | HG01891.hp1 HG02615.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.60+16936G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34441268 | ||||||
chr9:34441288
|
A | G | 8 | a0001c0001t0007g0359a0001c0001t0007g0360a0001c0001t0007g0361others(5): Show | 8 | HG00099.hp1 HG00741.hp1 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.60+16916T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34441288 | ||||||
chr9:34441532
|
A | G | 1 | a0001c0001t0002g0150 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.60+16672T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34441532 | ||||||
chr9:34441582
|
C | T | 2 | a0001c0001t0002g0148a0001c0001t0002g0149 | 2 | HG02293.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.60+16622G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34441582 | ||||||
chr9:34441653
|
T | G | 1 | a0001c0001t0001g0310 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.60+16551A>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34441653 | ||||||
chr9:34442131
|
G | A | 1 | a0001c0001t0002g0213 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.60+16073C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34442131 | ||||||
chr9:34442346
|
A | C | 1 | a0001c0001t0001g0242 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.60+15858T>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34442346 | ||||||
chr9:34442422
|
C | T | 1 | a0001c0001t0001g0218 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.60+15782G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34442422 | ||||||
chr9:34442633
|
C | T | 7 | a0001c0001t0001g0097a0001c0001t0001g0101a0001c0001t0001g0102others(4): Show | 7 | HG01243.hp1 HG02451.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.60+15571G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34442633 | ||||||
chr9:34442684
|
CA | C | 198 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(195): Show | 206 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.60+15519delT | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34442684 | ||||||
chr9:34442697
|
C | A | 3 | a0001c0001t0002g0214a0001c0001t0002g0215a0001c0001t0002g0216 | 3 | HG01109.hp2 HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.60+15507G>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34442697 | ||||||
chr9:34442699
|
A | C | 1 | a0001c0001t0003g0100 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.60+15505T>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34442699 | ||||||
chr9:34442830
|
T | A | 9 | a0001c0001t0001g0286a0001c0001t0001g0287a0001c0001t0001g0288others(6): Show | 9 | HG00423.hp2 HG02015.hp2 HG03491.hp2 others(6): Show |
intron_variant | MODIFIER | c.60+15374A>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34442830 | ||||||
chr9:34442957
|
T | G | 1 | a0001c0001t0003g0348 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.60+15247A>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34442957 | ||||||
chr9:34443193
|
T | C | 6 | a0001c0001t0006g0138a0001c0001t0006g0143a0001c0001t0009g0139others(3): Show | 6 | HG02559.hp1 HG02818.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.60+15011A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34443193 | ||||||
chr9:34443491
|
T | G | 98 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(95): Show | 105 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.60+14713A>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34443491 | ||||||
chr9:34443528
|
A | T | 1 | a0001c0001t0007g0365 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.60+14676T>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34443528 | ||||||
chr9:34443793
|
A | G | 1 | a0001c0001t0001g0241 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.60+14411T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34443793 | ||||||
chr9:34444171
|
T | C | 1 | a0001c0001t0001g0088 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.60+14033A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34444171 | ||||||
chr9:34444223
|
T | C | 1 | a0001c0001t0001g0294 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.60+13981A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34444223 | ||||||
chr9:34444579
|
C | T | 1 | a0001c0001t0017g0094 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.60+13625G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34444579 | ||||||
chr9:34444587
|
A | G | 1 | a0001c0001t0017g0094 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.60+13617T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34444587 | ||||||
chr9:34444606
|
T | C | 3 | a0001c0001t0005g0012a0001c0001t0005g0039a0001c0001t0011g0041 | 3 | HG01891.hp2 HG02559.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.60+13598A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34444606 | ||||||
chr9:34444717
|
G | A | 52 | a0001c0001t0001g0050a0001c0001t0001g0074a0001c0001t0001g0075others(49): Show | 53 | HG00280.hp2 HG01074.hp1 HG01081.hp1 others(50): Show |
intron_variant | MODIFIER | c.60+13487C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34444717 | ||||||
chr9:34444784
|
C | A | 31 | a0001c0001t0005g0012a0001c0001t0005g0013a0001c0001t0005g0014others(28): Show | 31 | HG00558.hp1 HG01891.hp2 HG01928.hp1 others(28): Show |
intron_variant | MODIFIER | c.60+13420G>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34444784 | ||||||
chr9:34444951
|
G | C | 1 | a0001c0001t0001g0088 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.60+13253C>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34444951 | ||||||
chr9:34445176
|
T | C | 199 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(196): Show | 207 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.60+13028A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34445176 | ||||||
chr9:34445187
|
C | T | 1 | a0001c0001t0001g0088 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.60+13017G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34445187 | ||||||
chr9:34445262
|
T | C | 31 | a0001c0001t0005g0012a0001c0001t0005g0013a0001c0001t0005g0014others(28): Show | 31 | HG00558.hp1 HG01891.hp2 HG01928.hp1 others(28): Show |
intron_variant | MODIFIER | c.60+12942A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34445262 | ||||||
chr9:34445283
|
A | G | 1 | a0001c0001t0004g0049 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.60+12921T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34445283 | ||||||
chr9:34445564
|
T | C | 3 | a0001c0001t0002g0240a0001c0001t0013g0081a0001c0001t0013g0083 | 3 | HG03516.hp1 NA19240.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.60+12640A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34445564 | ||||||
chr9:34445624
|
G | A | 1 | a0001c0001t0007g0365 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.60+12580C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34445624 | ||||||
chr9:34445719
|
C | A | 1 | a0001c0001t0002g0217 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.60+12485G>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34445719 | ||||||
chr9:34445734
|
C | T | 8 | a0001c0001t0007g0359a0001c0001t0007g0360a0001c0001t0007g0361others(5): Show | 8 | HG00099.hp1 HG00741.hp1 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.60+12470G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34445734 | ||||||
chr9:34445875
|
A | T | 1 | a0001c0001t0002g0240 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.60+12329T>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34445875 | ||||||
chr9:34446164
|
C | T | 2 | a0001c0001t0002g0113a0001c0001t0002g0136 | 2 | HG01109.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.60+12040G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34446164 | ||||||
chr9:34446172
|
C | CA | 9 | a0001c0001t0001g0109a0001c0001t0001g0218a0001c0001t0001g0220others(6): Show | 9 | HG01358.hp2 HG01361.hp1 HG03942.hp2 others(6): Show |
intron_variant | MODIFIER | c.60+12031dupT | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34446172 | ||||||
chr9:34446172
|
C | CAA | 6 | a0001c0001t0006g0138a0001c0001t0006g0143a0001c0001t0009g0139others(3): Show | 6 | HG02559.hp1 HG02818.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.60+12030_60+12031d others(4): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34446172 | ||||||
chr9:34446172
|
CA | C | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(179): Show | 190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.60+12031delT | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34446172 | ||||||
chr9:34446201
|
G | T | 8 | a0001c0001t0007g0359a0001c0001t0007g0360a0001c0001t0007g0361others(5): Show | 8 | HG00099.hp1 HG00741.hp1 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.60+12003C>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34446201 | ||||||
chr9:34446209
|
A | G | 4 | a0001c0001t0001g0320a0001c0001t0002g0321a0001c0001t0003g0319others(1): Show | 4 | HG00323.hp1 HG02027.hp2 HG02040.hp2 others(1): Show |
intron_variant | MODIFIER | c.60+11995T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34446209 | ||||||
chr9:34446273
|
A | T | 2 | a0001c0001t0001g0238a0001c0001t0002g0239 | 2 | NA18957.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.60+11931T>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34446273 | ||||||
chr9:34446324
|
G | A | 1 | a0001c0001t0011g0041 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.60+11880C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34446324 | ||||||
chr9:34446355
|
T | C | 31 | a0001c0001t0005g0012a0001c0001t0005g0013a0001c0001t0005g0014others(28): Show | 31 | HG00558.hp1 HG01891.hp2 HG01928.hp1 others(28): Show |
intron_variant | MODIFIER | c.60+11849A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34446355 | ||||||
chr9:34446646
|
C | G | 8 | a0001c0001t0007g0359a0001c0001t0007g0360a0001c0001t0007g0361others(5): Show | 8 | HG00099.hp1 HG00741.hp1 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.60+11558G>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34446646 | ||||||
chr9:34446721
|
C | G | 26 | a0001c0001t0001g0117a0001c0001t0002g0005a0001c0001t0002g0105others(23): Show | 27 | HG00323.hp2 HG00609.hp2 HG00621.hp2 others(24): Show |
intron_variant | MODIFIER | c.60+11483G>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34446721 | ||||||
chr9:34446979
|
T | C | 31 | a0001c0001t0005g0012a0001c0001t0005g0013a0001c0001t0005g0014others(28): Show | 31 | HG00558.hp1 HG01891.hp2 HG01928.hp1 others(28): Show |
intron_variant | MODIFIER | c.60+11225A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34446979 | ||||||
chr9:34447342
|
C | T | 26 | a0001c0001t0001g0117a0001c0001t0002g0005a0001c0001t0002g0105others(23): Show | 27 | HG00323.hp2 HG00609.hp2 HG00621.hp2 others(24): Show |
intron_variant | MODIFIER | c.60+10862G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34447342 | ||||||
chr9:34447361
|
T | C | 98 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(95): Show | 105 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.60+10843A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34447361 | ||||||
chr9:34447384
|
C | T | 1 | a0001c0001t0024g0095 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.60+10820G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34447384 | ||||||
chr9:34447457
|
T | C | 98 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(95): Show | 105 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.60+10747A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34447457 | ||||||
chr9:34447506
|
G | A | 8 | a0001c0001t0007g0359a0001c0001t0007g0360a0001c0001t0007g0361others(5): Show | 8 | HG00099.hp1 HG00741.hp1 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.60+10698C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34447506 | ||||||
chr9:34447560
|
G | A | 99 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(96): Show | 106 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.60+10644C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34447560 | ||||||
chr9:34447569
|
G | T | 1 | a0001c0001t0004g0048 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.60+10635C>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34447569 | ||||||
chr9:34447825
|
A | G | 1 | a0001c0001t0024g0095 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.60+10379T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34447825 | ||||||
chr9:34447876
|
AT | A | 50 | a0001c0001t0001g0088a0001c0001t0001g0097a0001c0001t0001g0101others(47): Show | 50 | HG00099.hp1 HG00558.hp1 HG00741.hp1 others(47): Show |
intron_variant | MODIFIER | c.60+10327delA | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34447876 | ||||||
chr9:34447921
|
G | C | 98 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(95): Show | 105 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.60+10283C>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34447921 | ||||||
chr9:34447991
|
C | T | 1 | a0001c0001t0002g0146 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.60+10213G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34447991 | ||||||
chr9:34448038
|
C | G | 31 | a0001c0001t0005g0012a0001c0001t0005g0013a0001c0001t0005g0014others(28): Show | 31 | HG00558.hp1 HG01891.hp2 HG01928.hp1 others(28): Show |
intron_variant | MODIFIER | c.60+10166G>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34448038 | ||||||
chr9:34448072
|
TG | T | 31 | a0001c0001t0005g0012a0001c0001t0005g0013a0001c0001t0005g0014others(28): Show | 31 | HG00558.hp1 HG01891.hp2 HG01928.hp1 others(28): Show |
intron_variant | MODIFIER | c.60+10131delC | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34448072 | ||||||
chr9:34448248
|
C | A | 1 | a0001c0001t0002g0222 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.60+9956G>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34448248 | ||||||
chr9:34448306
|
C | T | 3 | a0001c0001t0001g0008a0001c0001t0001g0298a0001c0001t0001g0299 | 4 | HG00438.hp2 HG00544.hp1 HG02071.hp2 others(1): Show |
intron_variant | MODIFIER | c.60+9898G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34448306 | ||||||
chr9:34448443
|
C | T | 8 | a0001c0001t0007g0359a0001c0001t0007g0360a0001c0001t0007g0361others(5): Show | 8 | HG00099.hp1 HG00741.hp1 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.60+9761G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34448443 | ||||||
chr9:34448612
|
C | A | 1 | a0001c0001t0001g0088 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.60+9592G>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34448612 | ||||||
chr9:34448764
|
A | C | 1 | a0001c0001t0002g0145 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.60+9440T>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34448764 | ||||||
chr9:34448779
|
G | T | 1 | a0001c0001t0001g0001 | 4 | NA18964.hp1 NA18985.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.60+9425C>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34448779 | ||||||
chr9:34448861
|
G | A | 18 | a0001c0001t0002g0343a0001c0001t0002g0344a0001c0001t0003g0009others(15): Show | 19 | HG00544.hp2 HG00558.hp2 HG00673.hp1 others(16): Show |
intron_variant | MODIFIER | c.60+9343C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34448861 | ||||||
chr9:34448973
|
C | T | 1 | a0001c0001t0003g0317 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.60+9231G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34448973 | ||||||
chr9:34448993
|
G | GA | 10 | a0001c0001t0003g0098a0001c0001t0007g0359a0001c0001t0007g0360others(7): Show | 10 | HG00099.hp1 HG00741.hp1 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.60+9210_60+9211ins others(1): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34448993 | ||||||
chr9:34448993
|
G | GAA | 8 | a0001c0001t0001g0090a0001c0001t0001g0097a0001c0001t0001g0101others(5): Show | 8 | HG01243.hp1 HG02451.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.60+9210_60+9211ins others(2): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34448993 | ||||||
chr9:34448993
|
G | GAAA | 10 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0104others(7): Show | 10 | HG01255.hp2 HG01891.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.60+9210_60+9211ins others(3): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34448993 | ||||||
chr9:34448994
|
G | A | 158 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(155): Show | 165 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(162): Show |
intron_variant | MODIFIER | c.60+9210C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34448994 | ||||||
chr9:34448994
|
G | GA | 11 | a0001c0001t0002g0136a0001c0001t0002g0223a0001c0001t0002g0351others(8): Show | 11 | HG00673.hp1 HG01109.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.60+9209dupT | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34448994 | ||||||
chr9:34448994
|
G | GAAA | 33 | a0001c0001t0001g0050a0001c0001t0001g0074a0001c0001t0001g0075others(30): Show | 34 | HG00280.hp2 HG01074.hp1 HG01081.hp1 others(31): Show |
intron_variant | MODIFIER | c.60+9207_60+9209dup others(3): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34448994 | ||||||
chr9:34448994
|
G | GAAAA | 7 | a0001c0001t0002g0070a0001c0001t0004g0067a0001c0001t0006g0068others(4): Show | 7 | HG02257.hp1 HG02280.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.60+9206_60+9209dup others(4): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34448994 | ||||||
chr9:34449005
|
A | C | 31 | a0001c0001t0005g0012a0001c0001t0005g0013a0001c0001t0005g0014others(28): Show | 31 | HG00558.hp1 HG01891.hp2 HG01928.hp1 others(28): Show |
intron_variant | MODIFIER | c.60+9199T>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34449005 | ||||||
chr9:34449006
|
A | AAG | 96 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(93): Show | 103 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.60+9197_60+9198ins others(2): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34449006 | ||||||
chr9:34449009
|
C | A | 199 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(196): Show | 207 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.60+9195G>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34449009 | ||||||
chr9:34449330
|
G | A | 205 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(202): Show | 213 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.60+8874C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34449330 | ||||||
chr9:34449470
|
T | C | 1 | a0001c0001t0006g0084 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.60+8734A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34449470 | ||||||
chr9:34449505
|
C | G | 2 | a0001c0001t0003g0317a0001c0001t0003g0318 | 2 | NA18960.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.60+8699G>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34449505 | ||||||
chr9:34449530
|
C | T | 3 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0092 | 3 | HG02615.hp2 HG02809.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.60+8674G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34449530 | ||||||
chr9:34449842
|
G | A | 1 | a0001c0001t0007g0224 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.60+8362C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34449842 | ||||||
chr9:34450049
|
C | T | 1 | a0001c0001t0026g0144 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.60+8155G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34450049 | ||||||
chr9:34450091
|
C | G | 31 | a0001c0001t0005g0012a0001c0001t0005g0013a0001c0001t0005g0014others(28): Show | 31 | HG00558.hp1 HG01891.hp2 HG01928.hp1 others(28): Show |
intron_variant | MODIFIER | c.60+8113G>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34450091 | ||||||
chr9:34450091
|
C | T | 6 | a0001c0001t0006g0138a0001c0001t0006g0143a0001c0001t0009g0139others(3): Show | 6 | HG02559.hp1 HG02818.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.60+8113G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34450091 | ||||||
chr9:34450221
|
G | A | 8 | a0001c0001t0007g0359a0001c0001t0007g0360a0001c0001t0007g0361others(5): Show | 8 | HG00099.hp1 HG00741.hp1 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.60+7983C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34450221 | ||||||
chr9:34450245
|
G | T | 1 | a0001c0001t0001g0237 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.60+7959C>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34450245 | ||||||
chr9:34450293
|
A | T | 98 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(95): Show | 105 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.60+7911T>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34450293 | ||||||
chr9:34450308
|
C | CA | 72 | a0001c0001t0001g0050a0001c0001t0001g0074a0001c0001t0001g0075others(69): Show | 73 | HG00280.hp2 HG00558.hp1 HG01074.hp1 others(70): Show |
intron_variant | MODIFIER | c.60+7895dupT | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34450308 | ||||||
chr9:34450308
|
C | CAA | 10 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0092others(7): Show | 10 | HG01891.hp1 HG02615.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.60+7894_60+7895dup others(2): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34450308 | ||||||
chr9:34450308
|
CA | C | 98 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(95): Show | 105 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.60+7895delT | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34450308 | ||||||
chr9:34450505
|
C | T | 1 | a0001c0001t0004g0137 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.60+7699G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34450505 | ||||||
chr9:34450534
|
T | C | 1 | a0001c0001t0002g0297 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.60+7670A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34450534 | ||||||
chr9:34450570
|
C | T | 3 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0236 | 3 | HG02735.hp1 HG03490.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.60+7634G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34450570 | ||||||
chr9:34450597
|
T | G | 1 | a0001c0001t0006g0084 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.60+7607A>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34450597 | ||||||
chr9:34450646
|
C | T | 1 | a0001c0001t0017g0094 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.60+7558G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34450646 | ||||||
chr9:34450707
|
C | T | 1 | a0001c0001t0003g0319 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.60+7497G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34450707 | ||||||
chr9:34450757
|
G | A | 1 | a0001c0001t0002g0228 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.60+7447C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34450757 | ||||||
chr9:34450772
|
C | G | 10 | a0001c0001t0001g0097a0001c0001t0001g0101a0001c0001t0001g0102others(7): Show | 10 | HG01243.hp1 HG01496.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.60+7432G>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34450772 | ||||||
chr9:34450799
|
T | C | 1 | a0001c0001t0001g0109 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.60+7405A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34450799 | ||||||
chr9:34450942
|
A | G | 8 | a0001c0001t0007g0359a0001c0001t0007g0360a0001c0001t0007g0361others(5): Show | 8 | HG00099.hp1 HG00741.hp1 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.60+7262T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34450942 | ||||||
chr9:34450943
|
T | C | 31 | a0001c0001t0005g0012a0001c0001t0005g0013a0001c0001t0005g0014others(28): Show | 31 | HG00558.hp1 HG01891.hp2 HG01928.hp1 others(28): Show |
intron_variant | MODIFIER | c.60+7261A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34450943 | ||||||
chr9:34450963
|
C | T | 2 | a0001c0001t0005g0013a0001c0001t0005g0014 | 2 | NA18940.hp2 NA18965.hp2 |
intron_variant | MODIFIER | c.60+7241G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34450963 | ||||||
chr9:34451009
|
G | A | 50 | a0001c0001t0001g0050a0001c0001t0001g0074a0001c0001t0001g0075others(47): Show | 51 | HG00280.hp2 HG01074.hp1 HG01081.hp1 others(48): Show |
intron_variant | MODIFIER | c.60+7195C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34451009 | ||||||
chr9:34451118
|
A | G | 1 | a0001c0001t0005g0012 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.60+7086T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34451118 | ||||||
chr9:34451225
|
A | G | 1 | a0001c0001t0003g0354 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.60+6979T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34451225 | ||||||
chr9:34451347
|
A | C | 31 | a0001c0001t0005g0012a0001c0001t0005g0013a0001c0001t0005g0014others(28): Show | 31 | HG00558.hp1 HG01891.hp2 HG01928.hp1 others(28): Show |
intron_variant | MODIFIER | c.60+6857T>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34451347 | ||||||
chr9:34451385
|
C | G | 8 | a0001c0001t0007g0359a0001c0001t0007g0360a0001c0001t0007g0361others(5): Show | 8 | HG00099.hp1 HG00741.hp1 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.60+6819G>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34451385 | ||||||
chr9:34451414
|
G | A | 1 | a0001c0001t0017g0094 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.60+6790C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34451414 | ||||||
chr9:34451574
|
G | A | 4 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0001t0001g0231others(1): Show | 4 | NA18747.hp2 NA18942.hp2 NA18952.hp2 others(1): Show |
intron_variant | MODIFIER | c.60+6630C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34451574 | ||||||
chr9:34451810
|
C | A | 31 | a0001c0001t0005g0012a0001c0001t0005g0013a0001c0001t0005g0014others(28): Show | 31 | HG00558.hp1 HG01891.hp2 HG01928.hp1 others(28): Show |
intron_variant | MODIFIER | c.60+6394G>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34451810 | ||||||
chr9:34451952
|
G | C | 50 | a0001c0001t0001g0050a0001c0001t0001g0074a0001c0001t0001g0075others(47): Show | 51 | HG00280.hp2 HG01074.hp1 HG01081.hp1 others(48): Show |
intron_variant | MODIFIER | c.60+6252C>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34451952 | ||||||
chr9:34452034
|
C | A | 1 | a0001c0001t0001g0085 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.60+6170G>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34452034 | ||||||
chr9:34452098
|
TAAC | T | 98 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(95): Show | 105 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.60+6103_60+6105del others(3): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34452098 | ||||||
chr9:34452270
|
G | C | 199 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(196): Show | 207 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.60+5934C>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34452270 | ||||||
chr9:34452290
|
A | G | 1 | a0001c0001t0006g0047 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.60+5914T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34452290 | ||||||
chr9:34452533
|
C | T | 2 | a0001c0001t0012g0043a0001c0001t0012g0044 | 2 | HG03195.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.60+5671G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34452533 | ||||||
chr9:34452650
|
C | G | 2 | a0001c0001t0003g0317a0001c0001t0003g0318 | 2 | NA18960.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.60+5554G>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34452650 | ||||||
chr9:34452707
|
T | C | 1 | a0001c0001t0021g0366 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.60+5497A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34452707 | ||||||
chr9:34452928
|
C | T | 1 | a0001c0001t0003g0316 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.60+5276G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34452928 | ||||||
chr9:34452977
|
A | C | 26 | a0001c0001t0001g0117a0001c0001t0002g0005a0001c0001t0002g0105others(23): Show | 27 | HG00323.hp2 HG00609.hp2 HG00621.hp2 others(24): Show |
intron_variant | MODIFIER | c.60+5227T>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34452977 | ||||||
chr9:34453006
|
G | A | 1 | a0001c0001t0003g0354 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.60+5198C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34453006 | ||||||
chr9:34453009
|
T | C | 98 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(95): Show | 105 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.60+5195A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34453009 | ||||||
chr9:34453105
|
A | G | 1 | a0001c0001t0002g0233 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.60+5099T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34453105 | ||||||
chr9:34453269
|
T | C | 1 | a0001c0001t0001g0355 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.60+4935A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34453269 | ||||||
chr9:34453279
|
G | A | 8 | a0001c0001t0007g0359a0001c0001t0007g0360a0001c0001t0007g0361others(5): Show | 8 | HG00099.hp1 HG00741.hp1 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.60+4925C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34453279 | ||||||
chr9:34453295
|
G | A | 1 | a0001c0001t0011g0042 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.60+4909C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34453295 | ||||||
chr9:34453592
|
G | A | 98 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(95): Show | 105 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.60+4612C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34453592 | ||||||
chr9:34454166
|
G | A | 1 | a0001c0001t0017g0094 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.60+4038C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34454166 | ||||||
chr9:34454219
|
T | C | 2 | a0001c0001t0002g0087a0001c0001t0010g0086 | 2 | HG03195.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.60+3985A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34454219 | ||||||
chr9:34454584
|
A | G | 1 | a0001c0001t0001g0112 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.60+3620T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34454584 | ||||||
chr9:34454585
|
A | G | 1 | a0001c0001t0001g0097 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.60+3619T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34454585 | ||||||
chr9:34454799
|
A | T | 1 | a0001c0001t0006g0068 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.60+3405T>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34454799 | ||||||
chr9:34454968
|
C | T | 1 | a0001c0001t0006g0111 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.60+3236G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34454968 | ||||||
chr9:34455005
|
C | T | 8 | a0001c0001t0007g0359a0001c0001t0007g0360a0001c0001t0007g0361others(5): Show | 8 | HG00099.hp1 HG00741.hp1 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.60+3199G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34455005 | ||||||
chr9:34455036
|
G | A | 1 | a0001c0001t0017g0094 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.60+3168C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34455036 | ||||||
chr9:34455069
|
T | G | 1 | a0001c0001t0024g0095 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.60+3135A>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34455069 | ||||||
chr9:34455252
|
C | G | 10 | a0001c0001t0001g0097a0001c0001t0001g0101a0001c0001t0001g0102others(7): Show | 10 | HG01243.hp1 HG01496.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.60+2952G>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34455252 | ||||||
chr9:34455297
|
CGAG | C | 3 | a0001c0001t0003g0356a0001c0001t0003g0357a0001c0004t0003g0358 | 3 | NA18964.hp2 NA18983.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.60+2904_60+2906del others(3): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34455297 | ||||||
chr9:34455448
|
T | G | 31 | a0001c0001t0005g0012a0001c0001t0005g0013a0001c0001t0005g0014others(28): Show | 31 | HG00558.hp1 HG01891.hp2 HG01928.hp1 others(28): Show |
intron_variant | MODIFIER | c.60+2756A>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34455448 | ||||||
chr9:34455465
|
A | AT | 68 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0076others(65): Show | 68 | HG00558.hp1 HG01243.hp1 HG01496.hp1 others(65): Show |
intron_variant | MODIFIER | c.60+2738dupA | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34455465 | ||||||
chr9:34455465
|
A | ATT | 25 | a0001c0001t0001g0050a0001c0001t0004g0004a0001c0001t0004g0048others(22): Show | 26 | HG00280.hp2 HG01074.hp1 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.60+2737_60+2738dup others(2): Show |
FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34455465 | ||||||
chr9:34455814
|
G | A | 15 | a0001c0001t0001g0008a0001c0001t0001g0298a0001c0001t0001g0299others(12): Show | 16 | HG00438.hp2 HG00544.hp1 HG01993.hp2 others(13): Show |
intron_variant | MODIFIER | c.60+2390C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34455814 | ||||||
chr9:34456054
|
G | A | 2 | a0001c0001t0001g0312a0001c0001t0001g0313 | 2 | NA19054.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.60+2150C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34456054 | ||||||
chr9:34456107
|
C | T | 1 | a0001c0001t0006g0047 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.60+2097G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34456107 | ||||||
chr9:34456184
|
C | A | 1 | a0001c0001t0004g0096 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.60+2020G>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34456184 | ||||||
chr9:34456272
|
T | G | 47 | a0001c0001t0001g0320a0001c0001t0001g0330a0001c0001t0001g0355others(44): Show | 50 | HG00323.hp1 HG00544.hp2 HG00558.hp2 others(47): Show |
intron_variant | MODIFIER | c.60+1932A>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34456272 | ||||||
chr9:34456580
|
G | A | 8 | a0001c0001t0007g0359a0001c0001t0007g0360a0001c0001t0007g0361others(5): Show | 8 | HG00099.hp1 HG00741.hp1 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.60+1624C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34456580 | ||||||
chr9:34456600
|
A | C | 52 | a0001c0001t0001g0050a0001c0001t0001g0074a0001c0001t0001g0075others(49): Show | 53 | HG00280.hp2 HG01074.hp1 HG01081.hp1 others(50): Show |
intron_variant | MODIFIER | c.60+1604T>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34456600 | ||||||
chr9:34456720
|
A | G | 2 | a0001c0001t0002g0045a0001c0001t0002g0046 | 2 | NA18947.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.60+1484T>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34456720 | ||||||
chr9:34456726
|
G | A | 2 | a0001c0001t0001g0367a0001c0001t0002g0368 | 2 | NA18984.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.60+1478C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34456726 | ||||||
chr9:34456886
|
C | T | 31 | a0001c0001t0005g0012a0001c0001t0005g0013a0001c0001t0005g0014others(28): Show | 31 | HG00558.hp1 HG01891.hp2 HG01928.hp1 others(28): Show |
intron_variant | MODIFIER | c.60+1318G>A | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34456886 | ||||||
chr9:34457198
|
G | A | 1 | a0001c0001t0006g0369 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.60+1006C>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34457198 | ||||||
chr9:34457262
|
C | G | 2 | a0001c0001t0002g0045a0001c0001t0002g0046 | 2 | NA18947.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.60+942G>C | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34457262 | ||||||
chr9:34457854
|
C | A | 13 | a0001c0001t0001g0372a0001c0001t0001g0374a0001c0001t0001g0375others(10): Show | 14 | HG01099.hp2 HG01261.hp1 HG01358.hp1 others(11): Show |
intron_variant | MODIFIER | c.60+350G>T | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34457854 | ||||||
chr9:34458075
|
T | C | 1 | a0001c0001t0007g0382 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.60+129A>G | FAM219A | ENSG00000164970.15 | transcript | ENST00000651358.1 | protein_coding | 1/5 | chr9 | 34458075 |