geneid | 81558 |
---|---|
ensemblid | ENSG00000121104.8 |
hgncid | 24179 |
symbol | FAM117A |
name | family with sequence similarity 117 member A |
refseq_nuc | NM_030802.4 |
refseq_prot | NP_110429.1 |
ensembl_nuc | ENST00000240364.7 |
ensembl_prot | ENSP00000240364.2 |
mane_status | MANE Select |
chr | chr17 |
start | 49710332 |
end | 49764131 |
strand | - |
ver | v1.2 |
region | chr17:49710332-49764131 |
region5000 | chr17:49705332-49769131 |
regionname0 | FAM117A_chr17_49710332_49764131 |
regionname5000 | FAM117A_chr17_49705332_49769131 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 453 | 330 | 93 | 71 | 120 | 10 | 34 | 85 | FAM117A_chr17_49705332_49769131 | FAM117A | copy fasta | chr17 | 49705332 | 49769131 |
a0002 | 0/0 | 453 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | copy fasta | chr17 | 49705332 | 49769131 |
a0003 | 0/0 | 453 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | copy fasta | chr17 | 49705332 | 49769131 |
a0004 | 0/0 | 453 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | copy fasta | chr17 | 49705332 | 49769131 |
a0005 | 0/0 | 453 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | copy fasta | chr17 | 49705332 | 49769131 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1362 | 293 | 84 | 61 | 110 | 7 | 29 | FAM117A_chr17_49705332_49769131 | FAM117A | copy fasta | chr17 | 49705332 | 49769131 |
c0002 | 0/0 | 1362 | 28 | 5 | 10 | 9 | 2 | 2 | FAM117A_chr17_49705332_49769131 | FAM117A | copy fasta | chr17 | 49705332 | 49769131 |
c0003 | 0/0 | 1362 | 5 | 4 | 0 | 0 | 0 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | copy fasta | chr17 | 49705332 | 49769131 |
c0004 | 0/0 | 1362 | 3 | 3 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | copy fasta | chr17 | 49705332 | 49769131 |
c0005 | 0/0 | 1362 | 2 | 0 | 0 | 0 | 1 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | copy fasta | chr17 | 49705332 | 49769131 |
c0006 | 0/0 | 1362 | 2 | 0 | 0 | 1 | 0 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | copy fasta | chr17 | 49705332 | 49769131 |
c0007 | 0/0 | 1362 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | copy fasta | chr17 | 49705332 | 49769131 |
c0008 | 0/0 | 1362 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | copy fasta | chr17 | 49705332 | 49769131 |
c0009 | 0/0 | 1362 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | copy fasta | chr17 | 49705332 | 49769131 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 968 | 297 | 84 | 60 | 111 | 8 | 32 | FAM117A_chr17_49705332_49769131 | FAM117A | copy fasta | chr17 | 49705332 | 49769131 |
t0002 | 0/0 | 968 | 28 | 5 | 10 | 9 | 2 | 2 | FAM117A_chr17_49705332_49769131 | FAM117A | copy fasta | chr17 | 49705332 | 49769131 |
t0003 | 0/0 | 968 | 3 | 3 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | copy fasta | chr17 | 49705332 | 49769131 |
t0004 | 0/0 | 968 | 3 | 1 | 2 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | copy fasta | chr17 | 49705332 | 49769131 |
t0005 | 0/0 | 968 | 2 | 2 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | copy fasta | chr17 | 49705332 | 49769131 |
t0006 | 0/0 | 968 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | copy fasta | chr17 | 49705332 | 49769131 |
t0007 | 0/0 | 968 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | copy fasta | chr17 | 49705332 | 49769131 |
t0008 | 0/0 | 968 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | copy fasta | chr17 | 49705332 | 49769131 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0003 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0010 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0011 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0016 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0018 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0065 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1362 | 293 | 84 | 61 | 110 | 7 | 29 | FAM117A_chr17_49705332_49769131 | FAM117A | copy fasta | chr17 | 49705332 | 49769131 |
a0001c0002 | 0/0 | 1362 | 28 | 5 | 10 | 9 | 2 | 2 | FAM117A_chr17_49705332_49769131 | FAM117A | copy fasta | chr17 | 49705332 | 49769131 |
a0001c0003 | 0/0 | 1362 | 5 | 4 | 0 | 0 | 0 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | copy fasta | chr17 | 49705332 | 49769131 |
a0001c0005 | 0/0 | 1362 | 2 | 0 | 0 | 0 | 1 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | copy fasta | chr17 | 49705332 | 49769131 |
a0001c0006 | 0/0 | 1362 | 2 | 0 | 0 | 1 | 0 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | copy fasta | chr17 | 49705332 | 49769131 |
a0002c0004 | 0/0 | 1362 | 3 | 3 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | copy fasta | chr17 | 49705332 | 49769131 |
a0003c0007 | 0/0 | 1362 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | copy fasta | chr17 | 49705332 | 49769131 |
a0004c0009 | 0/0 | 1362 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | copy fasta | chr17 | 49705332 | 49769131 |
a0005c0008 | 0/0 | 1362 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | copy fasta | chr17 | 49705332 | 49769131 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 2329 | 285 | 80 | 59 | 108 | 7 | 29 | FAM117A_chr17_49705332_49769131 | FAM117A | copy fasta | chr17 | 49705332 | 49769131 |
a0001c0001t0004 | 0/0 | 2329 | 3 | 1 | 2 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | copy fasta | chr17 | 49705332 | 49769131 |
a0001c0001t0005 | 0/0 | 2329 | 2 | 2 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | copy fasta | chr17 | 49705332 | 49769131 |
a0001c0001t0006 | 0/0 | 2329 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | copy fasta | chr17 | 49705332 | 49769131 |
a0001c0001t0007 | 0/0 | 2329 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | copy fasta | chr17 | 49705332 | 49769131 |
a0001c0001t0008 | 0/0 | 2329 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | copy fasta | chr17 | 49705332 | 49769131 |
a0001c0002t0002 | 0/0 | 2329 | 28 | 5 | 10 | 9 | 2 | 2 | FAM117A_chr17_49705332_49769131 | FAM117A | copy fasta | chr17 | 49705332 | 49769131 |
a0001c0003t0001 | 0/0 | 2329 | 2 | 1 | 0 | 0 | 0 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | copy fasta | chr17 | 49705332 | 49769131 |
a0001c0003t0003 | 0/0 | 2329 | 3 | 3 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | copy fasta | chr17 | 49705332 | 49769131 |
a0001c0005t0001 | 0/0 | 2329 | 2 | 0 | 0 | 0 | 1 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | copy fasta | chr17 | 49705332 | 49769131 |
a0001c0006t0001 | 0/0 | 2329 | 2 | 0 | 0 | 1 | 0 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | copy fasta | chr17 | 49705332 | 49769131 |
a0002c0004t0001 | 0/0 | 2329 | 3 | 3 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | copy fasta | chr17 | 49705332 | 49769131 |
a0003c0007t0001 | 0/0 | 2329 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | copy fasta | chr17 | 49705332 | 49769131 |
a0004c0009t0001 | 0/0 | 2329 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | copy fasta | chr17 | 49705332 | 49769131 |
a0005c0008t0001 | 0/0 | 2329 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | copy fasta | chr17 | 49705332 | 49769131 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0003 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0010 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0011 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0065 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0004g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0004g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0004g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0005g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0005g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0006g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0007g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0001t0008g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0002t0002g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0002t0002g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0002t0002g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0002t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0002t0002g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0002t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0002t0002g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0002t0002g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0002t0002g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0002t0002g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0002t0002g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0002t0002g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0002t0002g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0002t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0002t0002g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0002t0002g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0002t0002g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0002t0002g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0002t0002g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0002t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0002t0002g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0003t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0003t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0003t0003g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0003t0003g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0003t0003g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0005t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0005t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0006t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0001c0006t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0002c0004t0001g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0002c0004t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0003c0007t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0004c0009t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
a0005c0008t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0002 | t0002 | g0282 | EUR | GBR | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0205 | EUR | GBR | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0016 | EUR | GBR | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0171 | EUR | GBR | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0241 | EUR | FIN | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0023 | EUR | FIN | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0289 | EUR | FIN | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0086 | EUR | FIN | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | CHS | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | CHS | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | CHS | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | CHS | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | CHS | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | CHS | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | CHS | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG00609 | hp1 | a0001 | c0001 | t0008 | g0315 | EAS | CHS | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | CHS | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | CHS | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | CHS | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | PUR | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0224 | AMR | PUR | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | PUR | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG00673 | hp1 | a0001 | c0002 | t0002 | g0049 | EAS | CHS | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | CHS | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0211 | AMR | PUR | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0254 | AMR | PUR | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0276 | AMR | PUR | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0274 | AMR | PUR | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG01069 | hp1 | a0001 | c0001 | t0004 | g0312 | AMR | PUR | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0275 | AMR | PUR | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG01071 | hp2 | a0001 | c0001 | t0004 | g0313 | AMR | PUR | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0250 | AMR | PUR | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0302 | AMR | PUR | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0267 | AMR | PUR | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0221 | AMR | PUR | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0210 | AMR | PUR | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0308 | AMR | PUR | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0251 | AMR | CLM | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | CLM | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | CLM | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG01256 | hp2 | a0001 | c0002 | t0002 | g0255 | AMR | CLM | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | CLM | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | CLM | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG01258 | hp1 | a0001 | c0002 | t0002 | g0021 | AMR | CLM | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | CLM | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0298 | AMR | CLM | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | CLM | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG01346 | hp2 | a0001 | c0002 | t0002 | g0263 | AMR | CLM | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG01358 | hp2 | a0001 | c0002 | t0002 | g0021 | AMR | CLM | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | CLM | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | CLM | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG01496 | hp1 | a0001 | c0002 | t0002 | g0305 | AMR | CLM | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | ACB | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | ACB | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | ACB | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | ACB | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | PEL | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0223 | AMR | PEL | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0247 | AMR | PEL | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | PEL | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0218 | AMR | PEL | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PEL | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG01952 | hp1 | a0003 | c0007 | t0001 | g0179 | AMR | PEL | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | PEL | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | PEL | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | PEL | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0262 | AMR | PEL | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG02027 | hp1 | a0004 | c0009 | t0001 | g0194 | EAS | KHV | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG02027 | hp2 | a0001 | c0002 | t0002 | g0294 | EAS | KHV | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | ACB | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | ACB | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | KHV | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | KHV | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | KHV | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | KHV | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | KHV | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | KHV | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | KHV | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | KHV | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | KHV | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | KHV | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | KHV | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | ACB | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | PEL | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | CDX | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | CDX | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | ACB | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | ACB | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG02258 | hp1 | a0001 | c0002 | t0002 | g0279 | AFR | ACB | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG02258 | hp2 | a0001 | c0001 | t0004 | g0314 | AFR | ACB | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG02273 | hp1 | a0001 | c0002 | t0002 | g0264 | AMR | PEL | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG02273 | hp2 | a0001 | c0002 | t0002 | g0260 | AMR | PEL | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0249 | AFR | ACB | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG02293 | hp1 | a0001 | c0002 | t0002 | g0269 | AMR | PEL | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG02293 | hp2 | a0001 | c0002 | t0002 | g0259 | AMR | PEL | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0293 | AMR | PEL | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG02300 | hp2 | a0001 | c0002 | t0002 | g0266 | AMR | PEL | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | ACB | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | ACB | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | KHV | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | KHV | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | GWD | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | GWD | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0166 | SAS | PJL | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | GWD | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | GWD | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | GWD | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG02630 | hp1 | a0001 | c0002 | t0002 | g0017 | AFR | GWD | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | GWD | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG02647 | hp1 | a0002 | c0004 | t0001 | g0125 | AFR | GWD | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | GWD | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0209 | SAS | PJL | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0200 | SAS | PJL | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG02698 | hp1 | a0001 | c0005 | t0001 | g0127 | SAS | PJL | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0252 | SAS | PJL | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG02717 | hp1 | a0001 | c0003 | t0003 | g0129 | AFR | GWD | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | GWD | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | GWD | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0283 | SAS | PJL | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0077 | SAS | PJL | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0303 | SAS | PJL | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0306 | SAS | PJL | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0299 | AFR | GWD | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG02809 | hp2 | a0001 | c0001 | t0005 | g0296 | AFR | GWD | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | GWD | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | GWD | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | GWD | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG02896 | hp1 | a0001 | c0001 | t0006 | g0261 | AFR | GWD | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | GWD | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG02922 | hp2 | a0001 | c0003 | t0003 | g0227 | AFR | ESN | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG02965 | hp1 | a0001 | c0002 | t0002 | g0017 | AFR | ESN | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | ESN | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | ESN | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG02970 | hp2 | a0001 | c0001 | t0005 | g0063 | AFR | ESN | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG02976 | hp1 | a0002 | c0004 | t0001 | g0004 | AFR | ESN | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | ESN | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0147 | SAS | PJL | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0229 | SAS | PJL | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | GWD | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | MSL | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | MSL | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ESN | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | ESN | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ESN | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | MSL | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0217 | AFR | MSL | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG03225 | hp1 | a0001 | c0003 | t0001 | g0067 | AFR | MSL | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0246 | SAS | PJL | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0165 | SAS | PJL | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | MSL | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | MSL | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | MSL | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0309 | AFR | MSL | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | ESN | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | ESN | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | GWD | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0290 | AFR | GWD | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | MSL | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0230 | SAS | PJL | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG03710 | hp2 | a0001 | c0003 | t0001 | g0134 | SAS | PJL | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG03831 | hp1 | a0001 | c0006 | t0001 | g0311 | SAS | BEB | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0253 | SAS | BEB | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0056 | SAS | BEB | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG03834 | hp2 | a0001 | c0002 | t0002 | g0142 | SAS | BEB | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0297 | SAS | BEB | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0206 | SAS | BEB | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | BEB | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG03942 | hp2 | a0001 | c0002 | t0002 | g0226 | SAS | BEB | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | STU | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0245 | SAS | STU | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0088 | SAS | STU | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0093 | SAS | STU | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
NA18522 | hp1 | a0002 | c0004 | t0001 | g0004 | AFR | YRI | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | YRI | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | CHB | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | CHB | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHB | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | CHB | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
NA18906 | hp1 | a0001 | c0003 | t0003 | g0228 | AFR | YRI | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | YRI | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
NA18952 | hp1 | a0001 | c0002 | t0002 | g0265 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
NA18953 | hp2 | a0005 | c0008 | t0001 | g0156 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
NA18959 | hp1 | a0001 | c0002 | t0002 | g0100 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
NA18962 | hp2 | a0001 | c0002 | t0002 | g0097 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
NA18994 | hp1 | a0001 | c0006 | t0001 | g0310 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
NA19005 | hp2 | a0001 | c0002 | t0002 | g0096 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | LWK | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | LWK | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | LWK | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | LWK | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
NA19058 | hp2 | a0001 | c0001 | t0007 | g0216 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
NA19063 | hp2 | a0001 | c0002 | t0002 | g0015 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
NA19074 | hp1 | a0001 | c0002 | t0002 | g0015 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
NA19075 | hp2 | a0001 | c0002 | t0002 | g0135 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | YRI | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | YRI | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | ASW | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | ASW | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
NA20752 | hp1 | a0001 | c0005 | t0001 | g0128 | EUR | TSI | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
NA20752 | hp2 | a0001 | c0002 | t0002 | g0258 | EUR | TSI | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | GIH | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0052 | SAS | GIH | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0240 | AMR | CLM | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | CLM | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | ACB | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | ACB | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | ACB | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | ACB | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | ACB | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | MSL | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0280 | AFR | MSL | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | USA | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | USA | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
NA20300 | hp1 | a0001 | c0002 | t0002 | g0278 | AFR | USA | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | USA | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | LWK | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
NA21309 | hp2 | a0001 | c0002 | t0002 | g0175 | AFR | LWK | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0065 | REF | REF | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0010 | REF | REF | FAM117A_chr17_49705332_49769131 | FAM117A | chr17 | 49705332 | 49769131 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:49710332
|
T | G | 1 | a0001 | 2 | HG02809.hp2 HG02970.hp2 |
splice_region_variant | LOW | c.*923A>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 8/8 | chr17 | 49710332 | ||||||
chr17:49719854
|
C | T | 1 | a0004 | 1 | HG02027.hp1 | missense_variant | MODERATE | c.614G>A | p.Arg205Gln | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 5/8 | 658/2329 | 614/1362 | 205/453 | chr17 | 49719854 | ||
chr17:49720330
|
A | G | 1 | a0005 | 1 | NA18953.hp2 | missense_variant | MODERATE | c.569T>C | p.Leu190Pro | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 4/8 | 613/2329 | 569/1362 | 190/453 | chr17 | 49720330 | ||
chr17:49720396
|
C | T | 1 | a0002 | 3 | HG02647.hp1 HG02976.hp1 NA18522.hp1 |
missense_variant | MODERATE | c.503G>A | p.Ser168Asn | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 4/8 | 547/2329 | 503/1362 | 168/453 | chr17 | 49720396 | ||
chr17:49722560
|
C | G | 1 | a0003 | 1 | HG01952.hp1 | missense_variant | MODERATE | c.401G>C | p.Arg134Pro | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 3/8 | 445/2329 | 401/1362 | 134/453 | chr17 | 49722560 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:49711348
|
T | C | 1 | a0001c0003 | 5 | HG02717.hp1 HG02922.hp2 HG03225.hp1 others(2): Show |
synonymous_variant | LOW | c.1269A>G | p.Glu423Glu | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 8/8 | 1313/2329 | 1269/1362 | 423/453 | chr17 | 49711348 | ||
chr17:49711393
|
G | A | 1 | a0001c0002 | 28 | HG00099.hp1 HG00673.hp1 HG01256.hp2 others(25): Show |
synonymous_variant | LOW | c.1224C>T | p.Pro408Pro | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 8/8 | 1268/2329 | 1224/1362 | 408/453 | chr17 | 49711393 | ||
chr17:49717547
|
G | A | 1 | a0001c0005 | 2 | HG02698.hp1 NA20752.hp1 |
synonymous_variant | LOW | c.876C>T | p.Ala292Ala | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 6/8 | 920/2329 | 876/1362 | 292/453 | chr17 | 49717547 | ||
chr17:49763941
|
G | A | 1 | a0001c0006 | 2 | HG03831.hp1 NA18994.hp1 |
synonymous_variant | LOW | c.147C>T | p.Pro49Pro | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/8 | 191/2329 | 147/1362 | 49/453 | chr17 | 49763941 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:49710574
|
G | A | 1 | a0001c0003t0003 | 3 | HG02717.hp1 HG02922.hp2 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*681C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 8/8 | 681 | chr17 | 49710574 | |||||
chr17:49710691
|
C | T | 1 | a0001c0001t0006 | 1 | HG02896.hp1 | 3_prime_UTR_variant | MODIFIER | c.*564G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 8/8 | 564 | chr17 | 49710691 | |||||
chr17:49710743
|
C | G | 1 | a0001c0002t0002 | 28 | HG00099.hp1 HG00673.hp1 HG01256.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*512G>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 8/8 | 512 | chr17 | 49710743 | |||||
chr17:49711228
|
T | C | 1 | a0001c0001t0007 | 1 | NA19058.hp2 | 3_prime_UTR_variant | MODIFIER | c.*27A>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 8/8 | 27 | chr17 | 49711228 | |||||
chr17:49764097
|
G | A | 1 | a0001c0001t0004 | 3 | HG01069.hp1 HG01071.hp2 HG02258.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-10C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/8 | chr17 | 49764097 | ||||||
chr17:49764099
|
C | A | 1 | a0001c0001t0008 | 1 | HG00609.hp1 | 5_prime_UTR_variant | MODIFIER | c.-12G>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/8 | 12 | chr17 | 49764099 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:49711589
|
C | T | 2 | a0001c0001t0001g0050a0001c0001t0001g0051 | 2 | HG01884.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1062-34G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 7/7 | chr17 | 49711589 | ||||||
chr17:49711664
|
C | T | 1 | a0001c0003t0001g0134 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1062-109G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 7/7 | chr17 | 49711664 | ||||||
chr17:49711704
|
CT | C | 3 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0035 | 4 | HG01106.hp2 HG02486.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1062-150delA | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 7/7 | chr17 | 49711704 | ||||||
chr17:49711720
|
T | A | 72 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0022others(69): Show | 74 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.1062-165A>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 7/7 | chr17 | 49711720 | ||||||
chr17:49711899
|
C | T | 1 | a0001c0001t0001g0020 | 2 | HG03130.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1062-344G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 7/7 | chr17 | 49711899 | ||||||
chr17:49711942
|
C | T | 3 | a0001c0001t0004g0312a0001c0001t0004g0313a0001c0001t0004g0314 | 3 | HG01069.hp1 HG01071.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.1062-387G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 7/7 | chr17 | 49711942 | ||||||
chr17:49711943
|
G | A | 4 | a0001c0001t0001g0102a0001c0001t0001g0106a0001c0001t0001g0122others(1): Show | 4 | HG02630.hp2 HG02717.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1062-388C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 7/7 | chr17 | 49711943 | ||||||
chr17:49711996
|
A | G | 3 | a0001c0001t0001g0168a0001c0001t0001g0230a0001c0001t0001g0240 | 3 | HG01123.hp1 HG01361.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1062-441T>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 7/7 | chr17 | 49711996 | ||||||
chr17:49712023
|
G | A | 14 | a0001c0001t0001g0003a0001c0001t0001g0038a0001c0001t0001g0039others(11): Show | 16 | HG00558.hp1 HG00621.hp2 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.1062-468C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 7/7 | chr17 | 49712023 | ||||||
chr17:49712184
|
GT | G | 14 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0029others(11): Show | 15 | HG01106.hp2 HG02145.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.1062-630delA | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 7/7 | chr17 | 49712184 | ||||||
chr17:49712364
|
T | C | 4 | a0001c0001t0001g0039a0001c0001t0001g0041a0001c0001t0001g0043others(1): Show | 4 | HG01070.hp1 HG01943.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.1062-809A>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 7/7 | chr17 | 49712364 | ||||||
chr17:49712406
|
A | G | 2 | a0001c0005t0001g0127a0001c0005t0001g0128 | 2 | HG02698.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1062-851T>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 7/7 | chr17 | 49712406 | ||||||
chr17:49712503
|
G | C | 261 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(258): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.1062-948C>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 7/7 | chr17 | 49712503 | ||||||
chr17:49712514
|
T | A | 72 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0022others(69): Show | 74 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.1062-959A>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 7/7 | chr17 | 49712514 | ||||||
chr17:49713022
|
C | T | 1 | a0001c0001t0001g0291 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1062-1467G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 7/7 | chr17 | 49713022 | ||||||
chr17:49713048
|
T | C | 1 | a0001c0001t0001g0103 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1062-1493A>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 7/7 | chr17 | 49713048 | ||||||
chr17:49713062
|
T | A | 1 | a0001c0001t0001g0200 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1062-1507A>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 7/7 | chr17 | 49713062 | ||||||
chr17:49713178
|
G | A | 7 | a0001c0001t0001g0012a0001c0001t0001g0047a0001c0001t0001g0062others(4): Show | 8 | HG02109.hp2 HG02622.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1062-1623C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 7/7 | chr17 | 49713178 | ||||||
chr17:49713346
|
T | C | 1 | a0001c0001t0001g0107 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1062-1791A>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 7/7 | chr17 | 49713346 | ||||||
chr17:49713505
|
T | C | 1 | a0001c0002t0002g0226 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1062-1950A>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 7/7 | chr17 | 49713505 | ||||||
chr17:49713524
|
T | C | 1 | a0001c0001t0001g0115 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1062-1969A>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 7/7 | chr17 | 49713524 | ||||||
chr17:49713823
|
C | T | 1 | a0001c0001t0001g0032 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1062-2268G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 7/7 | chr17 | 49713823 | ||||||
chr17:49713921
|
G | A | 8 | a0001c0001t0001g0019a0001c0001t0001g0119a0001c0001t0001g0203others(5): Show | 9 | HG00639.hp1 HG00738.hp1 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1061+2244C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 7/7 | chr17 | 49713921 | ||||||
chr17:49713941
|
G | A | 1 | a0001c0001t0001g0056 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1061+2224C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 7/7 | chr17 | 49713941 | ||||||
chr17:49714015
|
C | T | 1 | a0001c0003t0001g0134 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1061+2150G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 7/7 | chr17 | 49714015 | ||||||
chr17:49714334
|
C | CT | 6 | a0001c0001t0001g0094a0001c0001t0001g0109a0001c0001t0001g0163others(3): Show | 6 | HG00438.hp1 HG01256.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1061+1830dupA | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 7/7 | chr17 | 49714334 | ||||||
chr17:49714334
|
CT | C | 6 | a0001c0001t0001g0029a0001c0001t0001g0111a0001c0001t0001g0169others(3): Show | 6 | HG00639.hp2 HG01070.hp2 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.1061+1830delA | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 7/7 | chr17 | 49714334 | ||||||
chr17:49714416
|
C | A | 32 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0038others(29): Show | 35 | HG00140.hp1 HG00558.hp1 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.1061+1749G>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 7/7 | chr17 | 49714416 | ||||||
chr17:49714701
|
C | T | 4 | a0001c0001t0001g0059a0001c0001t0001g0099a0001c0001t0001g0308others(1): Show | 4 | HG01243.hp1 HG02055.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1061+1464G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 7/7 | chr17 | 49714701 | ||||||
chr17:49714708
|
G | A | 1 | a0001c0003t0001g0134 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1061+1457C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 7/7 | chr17 | 49714708 | ||||||
chr17:49714749
|
C | T | 1 | a0001c0001t0001g0253 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1061+1416G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 7/7 | chr17 | 49714749 | ||||||
chr17:49715338
|
C | A | 1 | a0001c0001t0001g0052 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1061+827G>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 7/7 | chr17 | 49715338 | ||||||
chr17:49715680
|
G | A | 61 | a0001c0001t0001g0009a0001c0001t0001g0018a0001c0001t0001g0019others(58): Show | 65 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(62): Show |
intron_variant | MODIFIER | c.1061+485C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 7/7 | chr17 | 49715680 | ||||||
chr17:49715800
|
C | G | 1 | a0001c0001t0001g0002 | 2 | HG03195.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1061+365G>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 7/7 | chr17 | 49715800 | ||||||
chr17:49715806
|
A | G | 1 | a0001c0001t0001g0149 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1061+359T>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 7/7 | chr17 | 49715806 | ||||||
chr17:49715806
|
A | T | 1 | a0001c0001t0001g0002 | 2 | HG03195.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1061+359T>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 7/7 | chr17 | 49715806 | ||||||
chr17:49715813
|
G | A | 18 | a0001c0001t0001g0005a0001c0001t0001g0073a0001c0001t0001g0075others(15): Show | 19 | HG00544.hp1 HG01934.hp2 HG02080.hp1 others(16): Show |
intron_variant | MODIFIER | c.1061+352C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 7/7 | chr17 | 49715813 | ||||||
chr17:49716590
|
C | T | 1 | a0001c0002t0002g0142 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.911-275G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 6/7 | chr17 | 49716590 | ||||||
chr17:49716651
|
G | A | 7 | a0001c0002t0002g0015a0001c0002t0002g0135a0001c0002t0002g0263others(4): Show | 8 | HG01346.hp2 HG01496.hp1 HG02027.hp2 others(5): Show |
intron_variant | MODIFIER | c.911-336C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 6/7 | chr17 | 49716651 | ||||||
chr17:49716652
|
A | G | 2 | a0001c0001t0001g0184a0001c0001t0001g0186 | 2 | HG00438.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.911-337T>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 6/7 | chr17 | 49716652 | ||||||
chr17:49716679
|
C | T | 1 | a0001c0001t0001g0074 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.911-364G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 6/7 | chr17 | 49716679 | ||||||
chr17:49716698
|
C | T | 4 | a0001c0002t0002g0259a0001c0002t0002g0260a0001c0002t0002g0265others(1): Show | 4 | HG02273.hp2 HG02293.hp2 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.911-383G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 6/7 | chr17 | 49716698 | ||||||
chr17:49717041
|
G | A | 3 | a0001c0001t0004g0312a0001c0001t0004g0313a0001c0001t0004g0314 | 3 | HG01069.hp1 HG01071.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.910+472C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 6/7 | chr17 | 49717041 | ||||||
chr17:49717073
|
A | G | 12 | a0001c0001t0001g0006a0001c0001t0001g0023a0001c0001t0001g0024others(9): Show | 13 | HG00280.hp2 HG00323.hp2 HG01255.hp2 others(10): Show |
intron_variant | MODIFIER | c.910+440T>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 6/7 | chr17 | 49717073 | ||||||
chr17:49717220
|
C | G | 1 | a0001c0002t0002g0265 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.910+293G>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 6/7 | chr17 | 49717220 | ||||||
chr17:49717469
|
T | C | 33 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0038others(30): Show | 36 | HG00140.hp1 HG00558.hp1 HG00621.hp2 others(33): Show |
intron_variant | MODIFIER | c.910+44A>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 6/7 | chr17 | 49717469 | ||||||
chr17:49717783
|
A | G | 1 | a0001c0003t0001g0134 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.709-69T>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 5/7 | chr17 | 49717783 | ||||||
chr17:49717824
|
C | A | 1 | a0001c0001t0001g0306 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.709-110G>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 5/7 | chr17 | 49717824 | ||||||
chr17:49717863
|
C | T | 1 | a0001c0001t0001g0061 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.709-149G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 5/7 | chr17 | 49717863 | ||||||
chr17:49717948
|
A | G | 19 | a0001c0001t0001g0005a0001c0001t0001g0073a0001c0001t0001g0075others(16): Show | 20 | HG00544.hp1 HG01934.hp2 HG02080.hp1 others(17): Show |
intron_variant | MODIFIER | c.709-234T>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 5/7 | chr17 | 49717948 | ||||||
chr17:49718673
|
A | G | 1 | a0001c0001t0001g0217 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.709-959T>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 5/7 | chr17 | 49718673 | ||||||
chr17:49718742
|
G | A | 1 | a0001c0003t0001g0134 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.708+1018C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 5/7 | chr17 | 49718742 | ||||||
chr17:49718742
|
G | T | 1 | a0001c0001t0001g0197 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.708+1018C>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 5/7 | chr17 | 49718742 | ||||||
chr17:49718868
|
T | C | 1 | a0002c0004t0001g0125 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.708+892A>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 5/7 | chr17 | 49718868 | ||||||
chr17:49718954
|
C | T | 1 | a0001c0001t0001g0057 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.708+806G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 5/7 | chr17 | 49718954 | ||||||
chr17:49718973
|
C | CA | 6 | a0001c0001t0001g0085a0001c0001t0001g0151a0001c0001t0001g0236others(3): Show | 6 | HG02135.hp1 HG02698.hp1 NA18939.hp1 others(3): Show |
intron_variant | MODIFIER | c.708+786dupT | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 5/7 | chr17 | 49718973 | ||||||
chr17:49718973
|
CA | C | 15 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0029others(12): Show | 16 | HG01106.hp2 HG02145.hp2 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.708+786delT | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 5/7 | chr17 | 49718973 | ||||||
chr17:49718974
|
A | C | 4 | a0001c0001t0001g0115a0001c0001t0001g0193a0001c0001t0001g0197others(1): Show | 4 | HG00642.hp1 HG01891.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.708+786T>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 5/7 | chr17 | 49718974 | ||||||
chr17:49718992
|
G | A | 1 | a0001c0001t0001g0208 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.708+768C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 5/7 | chr17 | 49718992 | ||||||
chr17:49719185
|
C | T | 1 | a0001c0001t0001g0289 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.708+575G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 5/7 | chr17 | 49719185 | ||||||
chr17:49719186
|
G | A | 1 | a0001c0001t0001g0307 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.708+574C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 5/7 | chr17 | 49719186 | ||||||
chr17:49719252
|
A | T | 1 | a0001c0001t0001g0077 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.708+508T>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 5/7 | chr17 | 49719252 | ||||||
chr17:49719432
|
G | A | 1 | a0001c0006t0001g0310 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.708+328C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 5/7 | chr17 | 49719432 | ||||||
chr17:49720153
|
C | T | 91 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0014others(88): Show | 94 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.573+173G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 4/7 | chr17 | 49720153 | ||||||
chr17:49720229
|
G | T | 1 | a0001c0001t0001g0170 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.573+97C>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 4/7 | chr17 | 49720229 | ||||||
chr17:49720284
|
T | G | 1 | a0001c0003t0001g0134 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.573+42A>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 4/7 | chr17 | 49720284 | ||||||
chr17:49720317
|
A | G | 11 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0029others(8): Show | 12 | HG01106.hp2 HG02145.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.573+9T>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 4/7 | chr17 | 49720317 | ||||||
chr17:49720496
|
C | G | 10 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0029others(7): Show | 11 | HG01106.hp2 HG02145.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.463-60G>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 3/7 | chr17 | 49720496 | ||||||
chr17:49720750
|
C | T | 10 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0092others(7): Show | 10 | HG01123.hp1 HG01346.hp1 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.463-314G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 3/7 | chr17 | 49720750 | ||||||
chr17:49720783
|
G | A | 1 | a0001c0001t0001g0230 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.463-347C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 3/7 | chr17 | 49720783 | ||||||
chr17:49721005
|
G | A | 1 | a0001c0001t0001g0249 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.463-569C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 3/7 | chr17 | 49721005 | ||||||
chr17:49721160
|
T | G | 1 | a0001c0001t0001g0039 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.463-724A>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 3/7 | chr17 | 49721160 | ||||||
chr17:49721363
|
A | G | 261 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(258): Show | 278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.463-927T>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 3/7 | chr17 | 49721363 | ||||||
chr17:49721373
|
A | G | 2 | a0001c0001t0001g0099a0001c0001t0001g0123 | 2 | HG02647.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.463-937T>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 3/7 | chr17 | 49721373 | ||||||
chr17:49721600
|
G | A | 1 | a0001c0001t0001g0248 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.462+899C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 3/7 | chr17 | 49721600 | ||||||
chr17:49721811
|
T | G | 1 | a0001c0001t0001g0276 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.462+688A>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 3/7 | chr17 | 49721811 | ||||||
chr17:49721854
|
C | G | 1 | a0001c0001t0001g0217 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.462+645G>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 3/7 | chr17 | 49721854 | ||||||
chr17:49721876
|
G | A | 2 | a0001c0005t0001g0127a0001c0005t0001g0128 | 2 | HG02698.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.462+623C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 3/7 | chr17 | 49721876 | ||||||
chr17:49721926
|
T | TA | 12 | a0001c0001t0001g0035a0001c0001t0001g0081a0001c0001t0001g0082others(9): Show | 12 | HG01123.hp1 HG01346.hp1 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.462+572dupT | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 3/7 | chr17 | 49721926 | ||||||
chr17:49721926
|
TA | T | 6 | a0001c0001t0001g0131a0001c0001t0001g0169a0001c0001t0001g0185others(3): Show | 6 | HG01167.hp1 HG02896.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.462+572delT | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 3/7 | chr17 | 49721926 | ||||||
chr17:49721942
|
T | A | 5 | a0001c0001t0001g0146a0001c0001t0001g0152a0001c0001t0001g0174others(2): Show | 5 | NA18961.hp2 NA18983.hp2 NA18995.hp2 others(2): Show |
intron_variant | MODIFIER | c.462+557A>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 3/7 | chr17 | 49721942 | ||||||
chr17:49722043
|
G | A | 6 | a0001c0001t0001g0066a0001c0001t0001g0068a0001c0001t0001g0069others(3): Show | 6 | HG01243.hp2 HG01884.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.462+456C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 3/7 | chr17 | 49722043 | ||||||
chr17:49722044
|
A | G | 6 | a0001c0001t0001g0066a0001c0001t0001g0068a0001c0001t0001g0069others(3): Show | 6 | HG01243.hp2 HG01884.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.462+455T>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 3/7 | chr17 | 49722044 | ||||||
chr17:49722053
|
C | T | 25 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0038others(22): Show | 28 | HG00140.hp1 HG00558.hp1 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.462+446G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 3/7 | chr17 | 49722053 | ||||||
chr17:49722305
|
G | T | 3 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0209 | 3 | HG01074.hp1 HG02257.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.462+194C>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 3/7 | chr17 | 49722305 | ||||||
chr17:49722694
|
C | T | 1 | a0001c0002t0002g0049 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.367-100G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49722694 | ||||||
chr17:49722728
|
G | A | 2 | a0001c0002t0002g0021a0001c0002t0002g0255 | 3 | HG01256.hp2 HG01258.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.367-134C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49722728 | ||||||
chr17:49722871
|
T | C | 1 | a0001c0001t0001g0098 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.367-277A>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49722871 | ||||||
chr17:49723036
|
A | C | 1 | a0001c0001t0001g0031 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.367-442T>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49723036 | ||||||
chr17:49723182
|
C | T | 1 | a0001c0001t0001g0089 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.367-588G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49723182 | ||||||
chr17:49723526
|
C | T | 2 | a0001c0001t0001g0275a0001c0001t0001g0306 | 2 | HG01069.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.367-932G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49723526 | ||||||
chr17:49724050
|
T | C | 10 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0029others(7): Show | 11 | HG01106.hp2 HG02145.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.367-1456A>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49724050 | ||||||
chr17:49724202
|
A | T | 1 | a0001c0001t0001g0086 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.367-1608T>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49724202 | ||||||
chr17:49724264
|
C | T | 1 | a0004c0009t0001g0194 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.367-1670G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49724264 | ||||||
chr17:49724289
|
A | G | 253 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(250): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.367-1695T>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49724289 | ||||||
chr17:49724384
|
C | G | 1 | a0001c0001t0001g0309 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.367-1790G>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49724384 | ||||||
chr17:49724387
|
T | A | 1 | a0001c0001t0001g0086 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.367-1793A>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49724387 | ||||||
chr17:49724822
|
GA | G | 6 | a0001c0001t0001g0039a0001c0001t0001g0256a0001c0001t0001g0270others(3): Show | 6 | HG00408.hp1 HG01069.hp1 HG01070.hp1 others(3): Show |
intron_variant | MODIFIER | c.367-2229delT | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49724822 | ||||||
chr17:49725066
|
G | A | 2 | a0001c0001t0001g0047a0001c0001t0001g0062 | 2 | HG02723.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.367-2472C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49725066 | ||||||
chr17:49725395
|
G | A | 1 | a0001c0001t0001g0149 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.367-2801C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49725395 | ||||||
chr17:49725489
|
G | C | 13 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0029others(10): Show | 14 | HG01106.hp2 HG02145.hp2 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.367-2895C>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49725489 | ||||||
chr17:49725848
|
C | T | 1 | a0001c0003t0001g0134 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.367-3254G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49725848 | ||||||
chr17:49726032
|
C | T | 1 | a0001c0001t0001g0057 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.367-3438G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49726032 | ||||||
chr17:49726207
|
C | T | 1 | a0001c0001t0001g0289 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.367-3613G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49726207 | ||||||
chr17:49726400
|
C | T | 1 | a0001c0001t0001g0122 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.367-3806G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49726400 | ||||||
chr17:49726432
|
G | A | 1 | a0001c0001t0001g0133 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.367-3838C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49726432 | ||||||
chr17:49726561
|
C | T | 1 | a0001c0002t0002g0096 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.367-3967G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49726561 | ||||||
chr17:49726618
|
A | G | 1 | a0001c0001t0001g0108 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.367-4024T>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49726618 | ||||||
chr17:49726732
|
C | T | 1 | a0001c0002t0002g0049 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.367-4138G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49726732 | ||||||
chr17:49726813
|
A | G | 4 | a0001c0002t0002g0263a0001c0002t0002g0264a0001c0002t0002g0269others(1): Show | 4 | HG01346.hp2 HG01496.hp1 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.367-4219T>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49726813 | ||||||
chr17:49726911
|
C | T | 1 | a0001c0003t0001g0134 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.367-4317G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49726911 | ||||||
chr17:49726923
|
G | A | 1 | a0001c0003t0001g0134 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.367-4329C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49726923 | ||||||
chr17:49726945
|
C | T | 22 | a0001c0002t0002g0015a0001c0002t0002g0021a0001c0002t0002g0049others(19): Show | 24 | HG00099.hp1 HG00673.hp1 HG01256.hp2 others(21): Show |
intron_variant | MODIFIER | c.367-4351G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49726945 | ||||||
chr17:49727394
|
C | G | 1 | a0001c0002t0002g0135 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.367-4800G>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49727394 | ||||||
chr17:49727565
|
A | T | 1 | a0001c0001t0001g0050 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.367-4971T>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49727565 | ||||||
chr17:49727583
|
A | G | 1 | a0001c0001t0001g0037 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.366+4968T>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49727583 | ||||||
chr17:49727703
|
T | C | 1 | a0001c0001t0001g0274 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.366+4848A>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49727703 | ||||||
chr17:49727884
|
C | T | 1 | a0001c0003t0001g0134 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.366+4667G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49727884 | ||||||
chr17:49727913
|
C | T | 1 | a0001c0001t0001g0022 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.366+4638G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49727913 | ||||||
chr17:49727949
|
A | G | 2 | a0001c0005t0001g0127a0001c0005t0001g0128 | 2 | HG02698.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.366+4602T>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49727949 | ||||||
chr17:49728018
|
C | T | 7 | a0001c0002t0002g0015a0001c0002t0002g0135a0001c0002t0002g0263others(4): Show | 8 | HG01346.hp2 HG01496.hp1 HG02027.hp2 others(5): Show |
intron_variant | MODIFIER | c.366+4533G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49728018 | ||||||
chr17:49728112
|
C | A | 1 | a0001c0001t0001g0027 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.366+4439G>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49728112 | ||||||
chr17:49728305
|
T | C | 1 | a0001c0001t0001g0130 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.366+4246A>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49728305 | ||||||
chr17:49728389
|
G | A | 1 | a0001c0001t0001g0054 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.366+4162C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49728389 | ||||||
chr17:49728409
|
C | CT | 6 | a0001c0001t0001g0038a0001c0001t0001g0050a0001c0001t0001g0051others(3): Show | 6 | HG01884.hp2 HG02132.hp2 HG02148.hp1 others(3): Show |
intron_variant | MODIFIER | c.366+4141dupA | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49728409 | ||||||
chr17:49728688
|
A | G | 14 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0029others(11): Show | 15 | HG01106.hp2 HG02145.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.366+3863T>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49728688 | ||||||
chr17:49729077
|
A | ATTCAAGA others(32): Show |
1 | a0001c0002t0002g0135 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.366+3435_366+3473d others(41): Show |
FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49729077 | ||||||
chr17:49729083
|
G | T | 1 | a0001c0001t0001g0098 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.366+3468C>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49729083 | ||||||
chr17:49729292
|
T | A | 11 | a0001c0001t0001g0016a0001c0001t0001g0064a0001c0001t0001g0126others(8): Show | 12 | HG00140.hp1 HG00741.hp1 HG00741.hp2 others(9): Show |
intron_variant | MODIFIER | c.366+3259A>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49729292 | ||||||
chr17:49729450
|
G | A | 1 | a0001c0001t0001g0095 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.366+3101C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49729450 | ||||||
chr17:49729503
|
CT | C | 92 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(89): Show | 97 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.366+3047delA | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49729503 | ||||||
chr17:49729503
|
CTT | C | 208 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(205): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.366+3046_366+3047d others(4): Show |
FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49729503 | ||||||
chr17:49729503
|
CTTT | C | 7 | a0001c0001t0001g0047a0001c0001t0001g0163a0001c0001t0007g0216others(4): Show | 7 | HG01256.hp1 HG02717.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.366+3045_366+3047d others(5): Show |
FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49729503 | ||||||
chr17:49729538
|
C | T | 2 | a0001c0001t0001g0050a0001c0001t0001g0051 | 2 | HG01884.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.366+3013G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49729538 | ||||||
chr17:49729728
|
C | T | 186 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(183): Show | 197 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.366+2823G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49729728 | ||||||
chr17:49729755
|
C | T | 1 | a0001c0001t0001g0074 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.366+2796G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49729755 | ||||||
chr17:49729853
|
T | C | 18 | a0001c0001t0001g0005a0001c0001t0001g0073a0001c0001t0001g0075others(15): Show | 19 | HG00544.hp1 HG01934.hp2 HG02080.hp1 others(16): Show |
intron_variant | MODIFIER | c.366+2698A>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49729853 | ||||||
chr17:49730334
|
C | T | 1 | a0001c0001t0001g0285 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.366+2217G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49730334 | ||||||
chr17:49730524
|
A | G | 1 | a0001c0001t0001g0101 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.366+2027T>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49730524 | ||||||
chr17:49730625
|
C | A | 1 | a0001c0001t0001g0309 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.366+1926G>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49730625 | ||||||
chr17:49730760
|
C | G | 1 | a0001c0002t0002g0175 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.366+1791G>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49730760 | ||||||
chr17:49730845
|
C | A | 2 | a0001c0005t0001g0127a0001c0005t0001g0128 | 2 | HG02698.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.366+1706G>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49730845 | ||||||
chr17:49730891
|
T | C | 2 | a0001c0001t0001g0022a0001c0001t0001g0110 | 2 | HG03490.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.366+1660A>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49730891 | ||||||
chr17:49731403
|
G | A | 4 | a0001c0001t0001g0274a0001c0001t0001g0275a0001c0001t0001g0276others(1): Show | 4 | HG00741.hp1 HG00741.hp2 HG01069.hp2 others(1): Show |
intron_variant | MODIFIER | c.366+1148C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49731403 | ||||||
chr17:49731463
|
G | GTGCTCAG others(5): Show |
14 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0029others(11): Show | 15 | HG01106.hp2 HG02145.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.366+1087_366+1088i others(14): Show |
FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49731463 | ||||||
chr17:49731520
|
G | A | 1 | a0001c0003t0001g0134 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.366+1031C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49731520 | ||||||
chr17:49731522
|
G | C | 1 | a0001c0001t0001g0154 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.366+1029C>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49731522 | ||||||
chr17:49731616
|
G | C | 1 | a0001c0001t0001g0160 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.366+935C>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49731616 | ||||||
chr17:49731618
|
C | T | 18 | a0001c0001t0001g0005a0001c0001t0001g0073a0001c0001t0001g0075others(15): Show | 19 | HG00544.hp1 HG01934.hp2 HG02080.hp1 others(16): Show |
intron_variant | MODIFIER | c.366+933G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49731618 | ||||||
chr17:49731748
|
G | A | 10 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0029others(7): Show | 11 | HG01106.hp2 HG02145.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.366+803C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49731748 | ||||||
chr17:49731787
|
A | AT | 10 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0029others(7): Show | 11 | HG01106.hp2 HG02145.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.366+763dupA | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49731787 | ||||||
chr17:49731888
|
C | T | 3 | a0001c0002t0002g0096a0001c0002t0002g0097a0001c0002t0002g0100 | 3 | NA18959.hp1 NA18962.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.366+663G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49731888 | ||||||
chr17:49731975
|
G | A | 1 | a0001c0001t0001g0126 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.366+576C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49731975 | ||||||
chr17:49732170
|
A | G | 1 | a0001c0001t0001g0309 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.366+381T>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 2/7 | chr17 | 49732170 | ||||||
chr17:49732991
|
C | T | 18 | a0001c0001t0001g0005a0001c0001t0001g0073a0001c0001t0001g0075others(15): Show | 19 | HG00544.hp1 HG01934.hp2 HG02080.hp1 others(16): Show |
intron_variant | MODIFIER | c.197-271G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49732991 | ||||||
chr17:49733294
|
G | C | 51 | a0001c0001t0001g0009a0001c0001t0001g0018a0001c0001t0001g0019others(48): Show | 55 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(52): Show |
intron_variant | MODIFIER | c.197-574C>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49733294 | ||||||
chr17:49733631
|
C | T | 18 | a0001c0001t0001g0005a0001c0001t0001g0073a0001c0001t0001g0075others(15): Show | 19 | HG00544.hp1 HG01934.hp2 HG02080.hp1 others(16): Show |
intron_variant | MODIFIER | c.197-911G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49733631 | ||||||
chr17:49733908
|
C | T | 1 | a0001c0001t0001g0299 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.197-1188G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49733908 | ||||||
chr17:49733959
|
G | A | 3 | a0001c0001t0004g0312a0001c0001t0004g0313a0001c0001t0004g0314 | 3 | HG01069.hp1 HG01071.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.197-1239C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49733959 | ||||||
chr17:49733967
|
C | T | 18 | a0001c0001t0001g0005a0001c0001t0001g0073a0001c0001t0001g0075others(15): Show | 19 | HG00544.hp1 HG01934.hp2 HG02080.hp1 others(16): Show |
intron_variant | MODIFIER | c.197-1247G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49733967 | ||||||
chr17:49734100
|
G | A | 1 | a0001c0001t0001g0023 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.197-1380C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49734100 | ||||||
chr17:49734142
|
C | CA | 6 | a0001c0001t0001g0093a0001c0001t0001g0098a0001c0002t0002g0135others(3): Show | 6 | HG02717.hp1 HG02922.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.197-1423dupT | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49734142 | ||||||
chr17:49734381
|
G | A | 1 | a0001c0003t0001g0134 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.197-1661C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49734381 | ||||||
chr17:49734431
|
C | CA | 7 | a0001c0001t0001g0109a0001c0001t0001g0131a0001c0001t0001g0132others(4): Show | 7 | HG04115.hp1 NA18941.hp2 NA18980.hp1 others(4): Show |
intron_variant | MODIFIER | c.197-1712dupT | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49734431 | ||||||
chr17:49734435
|
A | C | 1 | a0001c0001t0001g0171 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.197-1715T>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49734435 | ||||||
chr17:49734475
|
C | G | 1 | a0001c0003t0001g0067 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.197-1755G>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49734475 | ||||||
chr17:49734478
|
G | C | 1 | a0001c0003t0001g0134 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.197-1758C>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49734478 | ||||||
chr17:49734613
|
A | T | 1 | a0001c0003t0001g0134 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.197-1893T>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49734613 | ||||||
chr17:49734667
|
A | T | 3 | a0001c0001t0001g0124a0001c0001t0001g0222a0001c0001t0001g0301 | 3 | NA18939.hp2 NA18963.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.197-1947T>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49734667 | ||||||
chr17:49734690
|
C | T | 1 | a0001c0001t0001g0293 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.197-1970G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49734690 | ||||||
chr17:49735385
|
G | A | 3 | a0001c0001t0001g0198a0001c0002t0002g0021a0001c0002t0002g0255 | 4 | HG01256.hp2 HG01257.hp1 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.197-2665C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49735385 | ||||||
chr17:49735396
|
A | C | 1 | a0001c0001t0001g0165 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.197-2676T>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49735396 | ||||||
chr17:49735495
|
G | A | 1 | a0001c0001t0001g0037 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.197-2775C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49735495 | ||||||
chr17:49735716
|
T | C | 1 | a0001c0001t0001g0229 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.197-2996A>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49735716 | ||||||
chr17:49735904
|
T | C | 1 | a0001c0001t0001g0007 | 2 | HG00438.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.197-3184A>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49735904 | ||||||
chr17:49735974
|
G | A | 1 | a0001c0001t0001g0233 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.197-3254C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49735974 | ||||||
chr17:49736074
|
CTGTGTGT others(5): Show |
C | 5 | a0001c0001t0001g0001a0001c0001t0001g0030a0001c0001t0001g0031others(2): Show | 6 | HG01106.hp2 HG02486.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.197-3366_197-3355d others(14): Show |
FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49736074 | ||||||
chr17:49736203
|
A | G | 1 | a0001c0001t0001g0079 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.197-3483T>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49736203 | ||||||
chr17:49736260
|
CT | C | 10 | a0001c0001t0001g0016a0001c0001t0001g0078a0001c0001t0001g0169others(7): Show | 11 | HG00140.hp1 HG00741.hp1 HG00741.hp2 others(8): Show |
intron_variant | MODIFIER | c.197-3541delA | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49736260 | ||||||
chr17:49736470
|
C | T | 2 | a0001c0001t0001g0308a0001c0001t0001g0309 | 2 | HG01243.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.197-3750G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49736470 | ||||||
chr17:49736766
|
C | T | 1 | a0001c0001t0001g0308 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.197-4046G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49736766 | ||||||
chr17:49736857
|
C | G | 1 | a0001c0001t0001g0284 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.197-4137G>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49736857 | ||||||
chr17:49737116
|
C | G | 1 | a0001c0001t0001g0143 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.197-4396G>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49737116 | ||||||
chr17:49737217
|
C | T | 4 | a0001c0001t0001g0159a0001c0001t0001g0198a0001c0001t0001g0199others(1): Show | 4 | HG00323.hp1 HG00733.hp1 HG00735.hp2 others(1): Show |
intron_variant | MODIFIER | c.197-4497G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49737217 | ||||||
chr17:49737375
|
C | T | 1 | a0001c0001t0001g0054 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.197-4655G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49737375 | ||||||
chr17:49737458
|
A | T | 1 | a0001c0001t0001g0029 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.197-4738T>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49737458 | ||||||
chr17:49737476
|
A | G | 2 | a0001c0001t0001g0280a0001c0001t0001g0290 | 2 | HG03471.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.197-4756T>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49737476 | ||||||
chr17:49737592
|
C | T | 2 | a0001c0001t0001g0002a0001c0001t0001g0060 | 3 | HG03195.hp2 HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.197-4872G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49737592 | ||||||
chr17:49737884
|
C | G | 20 | a0001c0001t0001g0005a0001c0001t0001g0073a0001c0001t0001g0075others(17): Show | 21 | HG00544.hp1 HG01934.hp2 HG02027.hp1 others(18): Show |
intron_variant | MODIFIER | c.197-5164G>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49737884 | ||||||
chr17:49737927
|
G | T | 3 | a0001c0001t0004g0312a0001c0001t0004g0313a0001c0001t0004g0314 | 3 | HG01069.hp1 HG01071.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.197-5207C>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49737927 | ||||||
chr17:49737960
|
T | C | 1 | a0001c0002t0002g0279 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.197-5240A>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49737960 | ||||||
chr17:49738195
|
C | T | 1 | a0001c0003t0001g0134 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.197-5475G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49738195 | ||||||
chr17:49738200
|
A | C | 1 | a0001c0001t0001g0149 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.197-5480T>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49738200 | ||||||
chr17:49738392
|
C | A | 1 | a0001c0003t0001g0134 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.197-5672G>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49738392 | ||||||
chr17:49738718
|
C | G | 10 | a0001c0001t0001g0012a0001c0001t0001g0047a0001c0001t0001g0057others(7): Show | 11 | HG02109.hp2 HG02145.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.197-5998G>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49738718 | ||||||
chr17:49738742
|
C | A | 3 | a0001c0001t0001g0076a0001c0001t0001g0137a0001c0001t0001g0257 | 3 | NA18747.hp2 NA18969.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.197-6022G>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49738742 | ||||||
chr17:49738757
|
G | A | 1 | a0001c0001t0001g0155 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.197-6037C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49738757 | ||||||
chr17:49738865
|
G | A | 1 | a0001c0002t0002g0097 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.197-6145C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49738865 | ||||||
chr17:49739229
|
G | A | 1 | a0001c0006t0001g0311 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.197-6509C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49739229 | ||||||
chr17:49739297
|
A | G | 1 | a0001c0003t0001g0134 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.197-6577T>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49739297 | ||||||
chr17:49739405
|
C | A | 46 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0038others(43): Show | 49 | HG00544.hp1 HG00558.hp1 HG00621.hp2 others(46): Show |
intron_variant | MODIFIER | c.197-6685G>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49739405 | ||||||
chr17:49739442
|
G | A | 1 | a0001c0001t0001g0025 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.197-6722C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49739442 | ||||||
chr17:49739467
|
A | G | 1 | a0001c0001t0001g0170 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.197-6747T>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49739467 | ||||||
chr17:49739641
|
C | T | 1 | a0001c0001t0001g0234 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.197-6921G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49739641 | ||||||
chr17:49739647
|
C | T | 2 | a0001c0001t0001g0083a0001c0001t0001g0297 | 2 | HG02602.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.197-6927G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49739647 | ||||||
chr17:49740010
|
C | G | 1 | a0001c0001t0001g0076 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.197-7290G>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49740010 | ||||||
chr17:49740011
|
A | T | 25 | a0001c0002t0002g0015a0001c0002t0002g0017a0001c0002t0002g0021others(22): Show | 28 | HG00099.hp1 HG00673.hp1 HG01256.hp2 others(25): Show |
intron_variant | MODIFIER | c.197-7291T>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49740011 | ||||||
chr17:49740173
|
C | T | 5 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0236others(2): Show | 5 | NA18959.hp2 NA18963.hp2 NA18971.hp2 others(2): Show |
intron_variant | MODIFIER | c.197-7453G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49740173 | ||||||
chr17:49740235
|
C | T | 2 | a0001c0001t0001g0042a0001c0001t0007g0216 | 2 | HG00621.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.197-7515G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49740235 | ||||||
chr17:49740249
|
A | AT | 8 | a0001c0001t0001g0072a0001c0001t0001g0122a0001c0001t0001g0141others(5): Show | 8 | HG01123.hp2 HG01361.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.197-7530dupA | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49740249 | ||||||
chr17:49740325
|
T | C | 28 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0028others(25): Show | 30 | HG00544.hp1 HG01106.hp2 HG01934.hp2 others(27): Show |
intron_variant | MODIFIER | c.197-7605A>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49740325 | ||||||
chr17:49740350
|
C | T | 5 | a0001c0001t0001g0048a0001c0001t0001g0091a0001c0001t0001g0140others(2): Show | 5 | HG02451.hp1 HG02559.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.197-7630G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49740350 | ||||||
chr17:49740351
|
G | A | 5 | a0001c0001t0001g0059a0001c0001t0001g0099a0001c0001t0001g0123others(2): Show | 5 | HG01243.hp1 HG02055.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.197-7631C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49740351 | ||||||
chr17:49740440
|
G | A | 2 | a0001c0001t0001g0006a0001c0001t0001g0080 | 3 | HG02922.hp1 HG03471.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.197-7720C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49740440 | ||||||
chr17:49740466
|
G | A | 1 | a0001c0001t0001g0052 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.197-7746C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49740466 | ||||||
chr17:49740470
|
T | C | 1 | a0001c0001t0001g0246 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.197-7750A>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49740470 | ||||||
chr17:49740623
|
G | A | 2 | a0001c0001t0001g0113a0001c0001t0001g0114 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.197-7903C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49740623 | ||||||
chr17:49740628
|
T | C | 4 | a0001c0001t0001g0274a0001c0001t0001g0275a0001c0001t0001g0276others(1): Show | 4 | HG00741.hp1 HG00741.hp2 HG01069.hp2 others(1): Show |
intron_variant | MODIFIER | c.197-7908A>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49740628 | ||||||
chr17:49740686
|
A | C | 14 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0029others(11): Show | 15 | HG01106.hp2 HG02145.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.197-7966T>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49740686 | ||||||
chr17:49740876
|
C | T | 1 | a0001c0001t0001g0137 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.197-8156G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49740876 | ||||||
chr17:49741459
|
C | T | 10 | a0001c0001t0001g0016a0001c0001t0001g0168a0001c0001t0001g0169others(7): Show | 11 | HG00140.hp1 HG00741.hp1 HG00741.hp2 others(8): Show |
intron_variant | MODIFIER | c.197-8739G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49741459 | ||||||
chr17:49741517
|
C | T | 4 | a0001c0001t0001g0159a0001c0001t0001g0198a0001c0001t0001g0199others(1): Show | 4 | HG00323.hp1 HG00733.hp1 HG00735.hp2 others(1): Show |
intron_variant | MODIFIER | c.197-8797G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49741517 | ||||||
chr17:49741570
|
C | G | 10 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0029others(7): Show | 11 | HG01106.hp2 HG02145.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.197-8850G>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49741570 | ||||||
chr17:49741590
|
C | T | 2 | a0001c0001t0001g0308a0001c0001t0001g0309 | 2 | HG01243.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.197-8870G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49741590 | ||||||
chr17:49741689
|
G | A | 314 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(311): Show | 334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.197-8969C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49741689 | ||||||
chr17:49741812
|
G | A | 1 | a0001c0001t0001g0123 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.197-9092C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49741812 | ||||||
chr17:49741849
|
A | G | 1 | a0001c0001t0001g0038 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.197-9129T>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49741849 | ||||||
chr17:49742282
|
A | G | 1 | a0001c0001t0001g0208 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.197-9562T>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49742282 | ||||||
chr17:49742319
|
C | T | 2 | a0001c0001t0001g0044a0001c0001t0001g0045 | 2 | HG00558.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.197-9599G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49742319 | ||||||
chr17:49742343
|
A | G | 2 | a0001c0001t0001g0050a0001c0001t0001g0051 | 2 | HG01884.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.197-9623T>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49742343 | ||||||
chr17:49742439
|
T | C | 1 | a0001c0001t0001g0048 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.197-9719A>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49742439 | ||||||
chr17:49742771
|
C | G | 1 | a0001c0001t0001g0126 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.197-10051G>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49742771 | ||||||
chr17:49742966
|
T | C | 1 | a0001c0001t0001g0053 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.197-10246A>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49742966 | ||||||
chr17:49743500
|
C | T | 1 | a0001c0001t0001g0221 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.197-10780G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49743500 | ||||||
chr17:49743860
|
G | A | 1 | a0001c0001t0001g0145 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.197-11140C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49743860 | ||||||
chr17:49743952
|
C | T | 3 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0209 | 3 | HG01074.hp1 HG02257.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.197-11232G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49743952 | ||||||
chr17:49744218
|
T | C | 1 | a0001c0003t0001g0134 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.197-11498A>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49744218 | ||||||
chr17:49744360
|
A | G | 2 | a0001c0001t0001g0002a0001c0001t0001g0060 | 3 | HG03195.hp2 HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.197-11640T>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49744360 | ||||||
chr17:49744478
|
C | T | 1 | a0001c0003t0001g0134 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.197-11758G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49744478 | ||||||
chr17:49744548
|
G | A | 1 | a0003c0007t0001g0179 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.197-11828C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49744548 | ||||||
chr17:49744696
|
G | A | 3 | a0001c0003t0003g0129a0001c0003t0003g0227a0001c0003t0003g0228 | 3 | HG02717.hp1 HG02922.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.197-11976C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49744696 | ||||||
chr17:49744761
|
C | T | 1 | a0001c0001t0001g0059 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.197-12041G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49744761 | ||||||
chr17:49745013
|
C | CA | 22 | a0001c0001t0001g0012a0001c0001t0001g0042a0001c0001t0001g0066others(19): Show | 23 | HG00621.hp2 HG01243.hp2 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.197-12294dupT | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49745013 | ||||||
chr17:49745013
|
C | CAA | 31 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0029others(28): Show | 35 | HG00099.hp1 HG00673.hp1 HG01106.hp2 others(32): Show |
intron_variant | MODIFIER | c.197-12295_197-1229 others(6): Show |
FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49745013 | ||||||
chr17:49745013
|
CA | C | 47 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(44): Show | 50 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(47): Show |
intron_variant | MODIFIER | c.197-12294delT | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49745013 | ||||||
chr17:49745029
|
A | C | 1 | a0001c0001t0001g0249 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.197-12309T>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49745029 | ||||||
chr17:49745032
|
A | C | 6 | a0001c0001t0001g0056a0001c0001t0001g0117a0001c0001t0001g0205others(3): Show | 6 | HG00099.hp2 HG01192.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.197-12312T>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49745032 | ||||||
chr17:49745034
|
C | A | 3 | a0001c0001t0001g0059a0001c0001t0001g0308a0001c0001t0001g0309 | 3 | HG01243.hp1 HG02055.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.197-12314G>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49745034 | ||||||
chr17:49745306
|
T | C | 1 | a0001c0001t0001g0196 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.197-12586A>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49745306 | ||||||
chr17:49745505
|
T | C | 1 | a0001c0001t0001g0080 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.197-12785A>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49745505 | ||||||
chr17:49745572
|
G | C | 1 | a0001c0001t0001g0057 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.197-12852C>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49745572 | ||||||
chr17:49745697
|
G | A | 1 | a0001c0001t0001g0126 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.197-12977C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49745697 | ||||||
chr17:49746337
|
C | T | 1 | a0001c0001t0001g0090 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.197-13617G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49746337 | ||||||
chr17:49746692
|
C | T | 8 | a0001c0001t0001g0111a0001c0001t0001g0115a0001c0001t0001g0116others(5): Show | 8 | HG00642.hp1 HG00735.hp1 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.197-13972G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49746692 | ||||||
chr17:49746753
|
G | A | 1 | a0001c0001t0001g0053 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.197-14033C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49746753 | ||||||
chr17:49746769
|
G | A | 1 | a0001c0003t0003g0227 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.197-14049C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49746769 | ||||||
chr17:49747139
|
GA | G | 11 | a0001c0001t0001g0012a0001c0001t0001g0047a0001c0001t0001g0057others(8): Show | 12 | HG02109.hp2 HG02145.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.197-14420delT | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49747139 | ||||||
chr17:49747243
|
A | G | 107 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0013others(104): Show | 111 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.197-14523T>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49747243 | ||||||
chr17:49747352
|
G | A | 3 | a0001c0001t0001g0139a0001c0001t0001g0153a0001c0001t0001g0154 | 3 | HG02135.hp2 NA18612.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.197-14632C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49747352 | ||||||
chr17:49747442
|
G | T | 13 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0029others(10): Show | 14 | HG01106.hp2 HG02145.hp2 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.197-14722C>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49747442 | ||||||
chr17:49747575
|
C | T | 93 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0014others(90): Show | 96 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.197-14855G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49747575 | ||||||
chr17:49747892
|
G | T | 6 | a0001c0001t0001g0066a0001c0001t0001g0068a0001c0001t0001g0069others(3): Show | 6 | HG01243.hp2 HG01884.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.197-15172C>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49747892 | ||||||
chr17:49747918
|
G | A | 1 | a0001c0001t0001g0283 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.197-15198C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49747918 | ||||||
chr17:49747949
|
G | A | 7 | a0001c0001t0001g0243a0001c0001t0001g0281a0001c0001t0001g0284others(4): Show | 7 | HG00408.hp2 HG02056.hp1 NA18942.hp2 others(4): Show |
intron_variant | MODIFIER | c.197-15229C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49747949 | ||||||
chr17:49748139
|
A | G | 1 | a0001c0003t0001g0134 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.197-15419T>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49748139 | ||||||
chr17:49748248
|
A | G | 1 | a0001c0001t0001g0220 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.197-15528T>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49748248 | ||||||
chr17:49748304
|
A | C | 2 | a0001c0005t0001g0127a0001c0005t0001g0128 | 2 | HG02698.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.197-15584T>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49748304 | ||||||
chr17:49748402
|
C | A | 1 | a0001c0001t0001g0225 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.196+15490G>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49748402 | ||||||
chr17:49748420
|
C | T | 1 | a0001c0001t0001g0016 | 2 | HG00140.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.196+15472G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49748420 | ||||||
chr17:49748456
|
A | G | 1 | a0001c0003t0001g0134 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.196+15436T>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49748456 | ||||||
chr17:49748457
|
A | C | 1 | a0001c0003t0001g0134 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.196+15435T>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49748457 | ||||||
chr17:49748650
|
T | C | 2 | a0001c0001t0001g0155a0004c0009t0001g0194 | 2 | HG02027.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.196+15242A>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49748650 | ||||||
chr17:49748915
|
G | A | 2 | a0002c0004t0001g0004a0002c0004t0001g0125 | 3 | HG02647.hp1 HG02976.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.196+14977C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49748915 | ||||||
chr17:49748934
|
G | T | 1 | a0001c0001t0006g0261 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.196+14958C>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49748934 | ||||||
chr17:49749005
|
T | C | 41 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0044others(38): Show | 43 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.196+14887A>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49749005 | ||||||
chr17:49749105
|
C | T | 2 | a0001c0001t0001g0099a0001c0001t0001g0123 | 2 | HG02647.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.196+14787G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49749105 | ||||||
chr17:49749171
|
C | T | 1 | a0001c0001t0001g0248 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.196+14721G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49749171 | ||||||
chr17:49749300
|
A | G | 1 | a0001c0001t0001g0233 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.196+14592T>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49749300 | ||||||
chr17:49749312
|
T | A | 1 | a0001c0001t0001g0107 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.196+14580A>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49749312 | ||||||
chr17:49749380
|
T | G | 1 | a0001c0001t0001g0020 | 2 | HG03130.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.196+14512A>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49749380 | ||||||
chr17:49749387
|
C | T | 2 | a0001c0001t0001g0230a0001c0001t0001g0240 | 2 | HG01123.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.196+14505G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49749387 | ||||||
chr17:49749403
|
C | T | 1 | a0001c0001t0001g0025 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.196+14489G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49749403 | ||||||
chr17:49749404
|
A | G | 1 | a0001c0001t0001g0025 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.196+14488T>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49749404 | ||||||
chr17:49749450
|
G | A | 6 | a0001c0002t0002g0015a0001c0002t0002g0263a0001c0002t0002g0264others(3): Show | 7 | HG01346.hp2 HG01496.hp1 HG02027.hp2 others(4): Show |
intron_variant | MODIFIER | c.196+14442C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49749450 | ||||||
chr17:49749457
|
GTCCCAGC others(1056): Show |
G | 10 | a0001c0001t0001g0016a0001c0001t0001g0168a0001c0001t0001g0169others(7): Show | 11 | HG00140.hp1 HG00741.hp1 HG00741.hp2 others(8): Show |
intron_variant | MODIFIER | c.196+13372_196+1443 others(4): Show |
FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49749457 | ||||||
chr17:49749575
|
C | CA | 32 | a0001c0001t0001g0006a0001c0001t0001g0023a0001c0001t0001g0028others(29): Show | 33 | HG00280.hp2 HG01255.hp2 HG01346.hp1 others(30): Show |
intron_variant | MODIFIER | c.196+14316dupT | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49749575 | ||||||
chr17:49749575
|
CA | C | 57 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(54): Show | 63 | HG00438.hp2 HG00544.hp1 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.196+14316delT | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49749575 | ||||||
chr17:49750163
|
G | A | 1 | a0001c0001t0001g0046 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.196+13729C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49750163 | ||||||
chr17:49750255
|
G | C | 1 | a0001c0001t0001g0062 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.196+13637C>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49750255 | ||||||
chr17:49750265
|
T | C | 1 | a0001c0003t0001g0134 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.196+13627A>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49750265 | ||||||
chr17:49750293
|
C | T | 1 | a0001c0003t0001g0134 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.196+13599G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49750293 | ||||||
chr17:49750445
|
C | T | 1 | a0001c0001t0001g0247 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.196+13447G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49750445 | ||||||
chr17:49750599
|
A | AC | 8 | a0001c0001t0001g0095a0001c0002t0002g0096a0001c0002t0002g0097others(5): Show | 8 | HG02717.hp1 HG02922.hp2 HG03710.hp2 others(5): Show |
intron_variant | MODIFIER | c.196+13292dupG | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49750599 | ||||||
chr17:49750600
|
C | A | 1 | a0001c0001t0001g0147 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.196+13292G>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49750600 | ||||||
chr17:49750605
|
C | A | 5 | a0001c0001t0001g0059a0001c0001t0001g0099a0001c0001t0001g0123others(2): Show | 5 | HG01243.hp1 HG02055.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.196+13287G>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49750605 | ||||||
chr17:49750727
|
G | T | 1 | a0001c0001t0001g0158 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.196+13165C>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49750727 | ||||||
chr17:49750931
|
T | G | 1 | a0001c0001t0001g0046 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.196+12961A>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49750931 | ||||||
chr17:49751213
|
G | T | 1 | a0001c0001t0001g0205 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.196+12679C>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49751213 | ||||||
chr17:49751237
|
G | A | 1 | a0001c0001t0005g0296 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.196+12655C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49751237 | ||||||
chr17:49751275
|
T | C | 1 | a0001c0001t0001g0304 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.196+12617A>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49751275 | ||||||
chr17:49751279
|
C | CA | 20 | a0001c0001t0001g0005a0001c0001t0001g0073a0001c0001t0001g0076others(17): Show | 21 | HG00408.hp1 HG00438.hp1 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.196+12612dupT | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49751279 | ||||||
chr17:49751279
|
C | CAAAAAAA others(3): Show |
1 | a0001c0003t0001g0134 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.196+12603_196+1261 others(14): Show |
FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49751279 | ||||||
chr17:49751299
|
A | AG | 4 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0308others(1): Show | 4 | HG00558.hp1 HG01243.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.196+12592dupC | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49751299 | ||||||
chr17:49751299
|
A | G | 23 | a0001c0001t0001g0003a0001c0001t0001g0038a0001c0001t0001g0039others(20): Show | 25 | HG00621.hp2 HG01069.hp1 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.196+12593T>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49751299 | ||||||
chr17:49751473
|
G | A | 26 | a0001c0001t0001g0095a0001c0002t0002g0015a0001c0002t0002g0017others(23): Show | 29 | HG00099.hp1 HG00673.hp1 HG01256.hp2 others(26): Show |
intron_variant | MODIFIER | c.196+12419C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49751473 | ||||||
chr17:49751528
|
C | T | 1 | a0001c0001t0005g0063 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.196+12364G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49751528 | ||||||
chr17:49751943
|
C | CA | 51 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(48): Show | 54 | HG00099.hp1 HG00673.hp1 HG01106.hp2 others(51): Show |
intron_variant | MODIFIER | c.196+11948dupT | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49751943 | ||||||
chr17:49751943
|
CA | C | 43 | a0001c0001t0001g0009a0001c0001t0001g0018a0001c0001t0001g0019others(40): Show | 47 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(44): Show |
intron_variant | MODIFIER | c.196+11948delT | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49751943 | ||||||
chr17:49752185
|
A | C | 1 | a0001c0003t0001g0134 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.196+11707T>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49752185 | ||||||
chr17:49752189
|
G | A | 9 | a0001c0001t0001g0016a0001c0001t0001g0168a0001c0001t0001g0169others(6): Show | 10 | HG00140.hp1 HG00741.hp1 HG01069.hp2 others(7): Show |
intron_variant | MODIFIER | c.196+11703C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49752189 | ||||||
chr17:49752302
|
C | T | 1 | a0001c0001t0001g0188 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.196+11590G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49752302 | ||||||
chr17:49752488
|
A | T | 1 | a0001c0001t0001g0200 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.196+11404T>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49752488 | ||||||
chr17:49752808
|
T | C | 1 | a0001c0001t0001g0267 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.196+11084A>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49752808 | ||||||
chr17:49753003
|
A | G | 1 | a0001c0003t0001g0134 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.196+10889T>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49753003 | ||||||
chr17:49753407
|
C | T | 6 | a0001c0001t0001g0066a0001c0001t0001g0068a0001c0001t0001g0069others(3): Show | 6 | HG01243.hp2 HG01884.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.196+10485G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49753407 | ||||||
chr17:49753419
|
T | C | 1 | a0001c0001t0001g0254 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.196+10473A>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49753419 | ||||||
chr17:49753543
|
C | T | 4 | a0001c0001t0001g0095a0001c0002t0002g0096a0001c0002t0002g0097others(1): Show | 4 | NA18959.hp1 NA18962.hp2 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.196+10349G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49753543 | ||||||
chr17:49753558
|
G | C | 1 | a0001c0001t0001g0093 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.196+10334C>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49753558 | ||||||
chr17:49753595
|
C | T | 10 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0029others(7): Show | 11 | HG01106.hp2 HG02145.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.196+10297G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49753595 | ||||||
chr17:49753618
|
C | G | 2 | a0001c0001t0001g0050a0001c0001t0001g0051 | 2 | HG01884.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.196+10274G>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49753618 | ||||||
chr17:49753852
|
G | A | 10 | a0001c0001t0001g0012a0001c0001t0001g0047a0001c0001t0001g0057others(7): Show | 11 | HG02109.hp2 HG02145.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.196+10040C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49753852 | ||||||
chr17:49753942
|
C | G | 1 | a0001c0002t0002g0175 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.196+9950G>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49753942 | ||||||
chr17:49754461
|
C | T | 2 | a0001c0001t0001g0058a0001c0001t0001g0214 | 2 | HG02145.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.196+9431G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49754461 | ||||||
chr17:49754487
|
G | C | 68 | a0001c0001t0001g0009a0001c0001t0001g0016a0001c0001t0001g0018others(65): Show | 73 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(70): Show |
intron_variant | MODIFIER | c.196+9405C>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49754487 | ||||||
chr17:49754550
|
C | T | 2 | a0001c0001t0001g0193a0001c0001t0001g0197 | 2 | HG00642.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.196+9342G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49754550 | ||||||
chr17:49754600
|
G | A | 3 | a0001c0003t0003g0129a0001c0003t0003g0227a0001c0003t0003g0228 | 3 | HG02717.hp1 HG02922.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.196+9292C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49754600 | ||||||
chr17:49754750
|
C | T | 2 | a0001c0001t0001g0176a0001c0001t0001g0177 | 2 | NA19058.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.196+9142G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49754750 | ||||||
chr17:49754981
|
T | C | 3 | a0001c0001t0004g0312a0001c0001t0004g0313a0001c0001t0004g0314 | 3 | HG01069.hp1 HG01071.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.196+8911A>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49754981 | ||||||
chr17:49754986
|
C | T | 2 | a0001c0001t0001g0050a0001c0001t0001g0051 | 2 | HG01884.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.196+8906G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49754986 | ||||||
chr17:49755038
|
C | CA | 31 | a0001c0001t0001g0036a0001c0001t0001g0045a0001c0001t0001g0058others(28): Show | 31 | HG00140.hp2 HG00558.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.196+8853dupT | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49755038 | ||||||
chr17:49755038
|
CA | C | 34 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(31): Show | 37 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.196+8853delT | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49755038 | ||||||
chr17:49755276
|
T | C | 1 | a0001c0003t0001g0134 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.196+8616A>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49755276 | ||||||
chr17:49755715
|
C | T | 1 | a0001c0003t0001g0134 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.196+8177G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49755715 | ||||||
chr17:49755724
|
C | T | 1 | a0004c0009t0001g0194 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.196+8168G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49755724 | ||||||
chr17:49755740
|
G | A | 1 | a0001c0001t0001g0082 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.196+8152C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49755740 | ||||||
chr17:49755789
|
C | G | 1 | a0001c0001t0001g0193 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.196+8103G>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49755789 | ||||||
chr17:49756299
|
G | A | 1 | a0001c0002t0002g0100 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.196+7593C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49756299 | ||||||
chr17:49756624
|
A | G | 1 | a0001c0001t0001g0147 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.196+7268T>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49756624 | ||||||
chr17:49756916
|
CA | C | 170 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(167): Show | 180 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.196+6975delT | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49756916 | ||||||
chr17:49756916
|
CAA | C | 6 | a0001c0001t0001g0028a0001c0001t0001g0101a0001c0001t0001g0102others(3): Show | 6 | HG00673.hp1 HG01943.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.196+6974_196+6975d others(4): Show |
FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49756916 | ||||||
chr17:49756945
|
A | G | 1 | a0001c0003t0001g0134 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.196+6947T>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49756945 | ||||||
chr17:49756967
|
C | T | 1 | a0001c0002t0002g0260 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.196+6925G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49756967 | ||||||
chr17:49757025
|
G | A | 1 | a0001c0001t0001g0231 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.196+6867C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49757025 | ||||||
chr17:49757056
|
C | A | 1 | a0001c0001t0001g0280 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.196+6836G>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49757056 | ||||||
chr17:49757086
|
G | A | 2 | a0001c0001t0001g0012a0001c0001t0001g0217 | 3 | HG02886.hp1 HG03209.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.196+6806C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49757086 | ||||||
chr17:49757211
|
C | G | 3 | a0001c0001t0001g0192a0001c0001t0001g0212a0001c0001t0001g0213 | 3 | HG02109.hp2 HG02622.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.196+6681G>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49757211 | ||||||
chr17:49757414
|
A | G | 14 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0029others(11): Show | 15 | HG01106.hp2 HG02145.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.196+6478T>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49757414 | ||||||
chr17:49757697
|
C | T | 1 | a0001c0001t0001g0057 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.196+6195G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49757697 | ||||||
chr17:49757813
|
G | A | 1 | a0001c0001t0001g0006 | 2 | HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.196+6079C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49757813 | ||||||
chr17:49757817
|
G | A | 3 | a0001c0001t0001g0009a0001c0001t0001g0211a0001c0001t0001g0241 | 4 | HG00280.hp1 HG00733.hp2 HG01099.hp1 others(1): Show |
intron_variant | MODIFIER | c.196+6075C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49757817 | ||||||
chr17:49757971
|
A | G | 1 | a0001c0003t0001g0134 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.196+5921T>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49757971 | ||||||
chr17:49758008
|
C | T | 2 | a0001c0001t0001g0146a0001c0001t0001g0231 | 2 | NA19060.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.196+5884G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49758008 | ||||||
chr17:49758159
|
G | A | 3 | a0001c0001t0001g0082a0001c0001t0001g0094a0001c0001t0001g0172 | 3 | HG01346.hp1 HG02486.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.196+5733C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49758159 | ||||||
chr17:49758186
|
G | T | 2 | a0001c0001t0001g0083a0001c0001t0001g0297 | 2 | HG02602.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.196+5706C>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49758186 | ||||||
chr17:49758231
|
C | G | 1 | a0001c0003t0001g0134 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.196+5661G>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49758231 | ||||||
chr17:49758511
|
C | T | 3 | a0001c0003t0003g0129a0001c0003t0003g0227a0001c0003t0003g0228 | 3 | HG02717.hp1 HG02922.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.196+5381G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49758511 | ||||||
chr17:49758621
|
C | CA | 59 | a0001c0001t0001g0013a0001c0001t0001g0022a0001c0001t0001g0052others(56): Show | 60 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.196+5270dupT | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49758621 | ||||||
chr17:49758632
|
A | AT | 4 | a0001c0001t0001g0083a0001c0001t0001g0173a0001c0001t0001g0174others(1): Show | 4 | HG02602.hp2 HG03927.hp1 NA18961.hp1 others(1): Show |
intron_variant | MODIFIER | c.196+5259_196+5260i others(3): Show |
FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49758632 | ||||||
chr17:49758632
|
A | T | 133 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(130): Show | 142 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.196+5260T>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49758632 | ||||||
chr17:49758633
|
A | T | 6 | a0001c0001t0001g0048a0001c0001t0001g0192a0001c0001t0004g0312others(3): Show | 6 | HG01069.hp1 HG01071.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.196+5259T>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49758633 | ||||||
chr17:49758634
|
A | AT | 4 | a0001c0001t0001g0006a0001c0001t0001g0024a0001c0001t0001g0086others(1): Show | 5 | HG00323.hp2 HG01255.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.196+5257_196+5258i others(3): Show |
FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49758634 | ||||||
chr17:49758634
|
A | T | 1 | a0001c0001t0001g0023 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.196+5258T>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49758634 | ||||||
chr17:49758634
|
AAAT | A | 10 | a0001c0001t0001g0046a0001c0001t0001g0068a0001c0001t0001g0069others(7): Show | 10 | HG01884.hp1 HG02559.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.196+5255_196+5257d others(5): Show |
FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49758634 | ||||||
chr17:49758634
|
AAATAAAA others(9): Show |
A | 1 | a0001c0003t0001g0134 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.196+5242_196+5257d others(18): Show |
FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49758634 | ||||||
chr17:49758637
|
T | A | 26 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0048others(23): Show | 28 | HG00558.hp2 HG00639.hp2 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.196+5255A>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49758637 | ||||||
chr17:49758638
|
A | AAAAT | 23 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0083others(20): Show | 24 | HG00673.hp1 HG01167.hp2 HG01346.hp2 others(21): Show |
intron_variant | MODIFIER | c.196+5250_196+5253d others(6): Show |
FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49758638 | ||||||
chr17:49758638
|
A | AT | 4 | a0001c0001t0001g0014a0001c0001t0001g0085a0001c0001t0001g0130others(1): Show | 5 | HG02129.hp2 NA18945.hp2 NA18967.hp1 others(2): Show |
intron_variant | MODIFIER | c.196+5253_196+5254i others(3): Show |
FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49758638 | ||||||
chr17:49758638
|
A | T | 5 | a0001c0001t0001g0048a0001c0001t0001g0143a0001c0001t0001g0144others(2): Show | 5 | HG02293.hp1 HG02451.hp1 NA18945.hp1 others(2): Show |
intron_variant | MODIFIER | c.196+5254T>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49758638 | ||||||
chr17:49758638
|
AAAAT | A | 92 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(89): Show | 101 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(98): Show |
intron_variant | MODIFIER | c.196+5250_196+5253d others(6): Show |
FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49758638 | ||||||
chr17:49758638
|
AAAATAAA others(5): Show |
A | 8 | a0001c0001t0001g0005a0001c0001t0001g0073a0001c0001t0001g0075others(5): Show | 9 | HG01934.hp2 HG02055.hp2 HG02080.hp1 others(6): Show |
intron_variant | MODIFIER | c.196+5242_196+5253d others(14): Show |
FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49758638 | ||||||
chr17:49758638
|
AAAATAAA others(9): Show |
A | 1 | a0001c0001t0001g0062 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.196+5238_196+5253d others(18): Show |
FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49758638 | ||||||
chr17:49758640
|
A | T | 1 | a0001c0001t0001g0080 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.196+5252T>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49758640 | ||||||
chr17:49758641
|
A | T | 7 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(4): Show | 7 | HG01884.hp1 HG02559.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.196+5251T>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49758641 | ||||||
chr17:49758642
|
T | A | 23 | a0001c0001t0001g0013a0001c0001t0001g0046a0001c0001t0001g0061others(20): Show | 24 | HG00639.hp2 HG01106.hp1 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.196+5250A>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49758642 | ||||||
chr17:49758646
|
T | A | 5 | a0001c0001t0001g0061a0001c0001t0001g0133a0001c0001t0001g0137others(2): Show | 5 | HG00639.hp2 HG01928.hp2 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.196+5246A>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49758646 | ||||||
chr17:49758669
|
A | T | 3 | a0001c0003t0003g0129a0001c0003t0003g0227a0001c0003t0003g0228 | 3 | HG02717.hp1 HG02922.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.196+5223T>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49758669 | ||||||
chr17:49758678
|
T | A | 3 | a0001c0001t0001g0003a0002c0004t0001g0004a0002c0004t0001g0125 | 5 | HG01358.hp1 HG02109.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.196+5214A>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49758678 | ||||||
chr17:49758993
|
A | G | 7 | a0001c0001t0001g0005a0001c0001t0001g0073a0001c0001t0001g0075others(4): Show | 8 | HG01934.hp2 HG02080.hp1 HG02735.hp2 others(5): Show |
intron_variant | MODIFIER | c.196+4899T>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49758993 | ||||||
chr17:49759088
|
C | T | 2 | a0001c0005t0001g0127a0001c0005t0001g0128 | 2 | HG02698.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.196+4804G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49759088 | ||||||
chr17:49759526
|
C | A | 1 | a0001c0001t0001g0071 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.196+4366G>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49759526 | ||||||
chr17:49759544
|
T | C | 1 | a0001c0001t0001g0072 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.196+4348A>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49759544 | ||||||
chr17:49759783
|
C | T | 1 | a0001c0001t0001g0074 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.196+4109G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49759783 | ||||||
chr17:49759865
|
A | G | 1 | a0001c0002t0002g0259 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.196+4027T>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49759865 | ||||||
chr17:49759995
|
G | T | 1 | a0001c0002t0002g0258 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.196+3897C>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49759995 | ||||||
chr17:49760049
|
A | G | 1 | a0001c0001t0001g0138 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.196+3843T>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49760049 | ||||||
chr17:49760058
|
A | T | 1 | a0001c0001t0001g0073 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.196+3834T>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49760058 | ||||||
chr17:49760092
|
A | G | 1 | a0001c0001t0001g0230 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.196+3800T>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49760092 | ||||||
chr17:49760189
|
G | A | 4 | a0001c0001t0001g0064a0001c0001t0001g0126a0001c0001t0005g0063others(1): Show | 4 | HG02615.hp1 HG02809.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.196+3703C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49760189 | ||||||
chr17:49760321
|
A | C | 3 | a0001c0001t0004g0312a0001c0001t0004g0313a0001c0001t0004g0314 | 3 | HG01069.hp1 HG01071.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.196+3571T>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49760321 | ||||||
chr17:49760417
|
A | T | 1 | a0001c0001t0001g0047 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.196+3475T>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49760417 | ||||||
chr17:49760484
|
A | G | 3 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0257 | 3 | NA18747.hp2 NA18969.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.196+3408T>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49760484 | ||||||
chr17:49760666
|
T | C | 1 | a0001c0002t0002g0294 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.196+3226A>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49760666 | ||||||
chr17:49760680
|
C | T | 1 | a0001c0001t0001g0072 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.196+3212G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49760680 | ||||||
chr17:49760717
|
T | C | 1 | a0001c0002t0002g0226 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.196+3175A>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49760717 | ||||||
chr17:49760723
|
A | T | 1 | a0001c0003t0001g0134 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.196+3169T>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49760723 | ||||||
chr17:49761008
|
C | A | 2 | a0001c0005t0001g0127a0001c0005t0001g0128 | 2 | HG02698.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.196+2884G>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49761008 | ||||||
chr17:49761014
|
A | G | 6 | a0001c0001t0001g0066a0001c0001t0001g0068a0001c0001t0001g0069others(3): Show | 6 | HG01243.hp2 HG01884.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.196+2878T>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49761014 | ||||||
chr17:49761037
|
C | A | 10 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0029others(7): Show | 11 | HG01106.hp2 HG02145.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.196+2855G>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49761037 | ||||||
chr17:49761094
|
A | C | 1 | a0001c0002t0002g0135 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.196+2798T>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49761094 | ||||||
chr17:49761154
|
G | C | 3 | a0001c0003t0003g0129a0001c0003t0003g0227a0001c0003t0003g0228 | 3 | HG02717.hp1 HG02922.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.196+2738C>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49761154 | ||||||
chr17:49761556
|
C | T | 1 | a0001c0001t0001g0065 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.196+2336G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49761556 | ||||||
chr17:49761775
|
T | C | 1 | a0001c0001t0001g0130 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.196+2117A>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49761775 | ||||||
chr17:49762039
|
G | A | 10 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0029others(7): Show | 11 | HG01106.hp2 HG02145.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.196+1853C>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49762039 | ||||||
chr17:49762164
|
T | C | 4 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0256others(1): Show | 4 | NA18941.hp2 NA18980.hp1 NA19074.hp2 others(1): Show |
intron_variant | MODIFIER | c.196+1728A>G | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49762164 | ||||||
chr17:49762168
|
C | T | 1 | a0001c0001t0001g0229 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.196+1724G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49762168 | ||||||
chr17:49762263
|
C | T | 1 | a0001c0003t0001g0134 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.196+1629G>A | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49762263 | ||||||
chr17:49762668
|
A | G | 1 | a0001c0001t0001g0133 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.196+1224T>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49762668 | ||||||
chr17:49763123
|
T | TAC | 32 | a0001c0001t0001g0014a0001c0001t0001g0229a0001c0001t0001g0230others(29): Show | 33 | HG00280.hp1 HG00738.hp1 HG01074.hp2 others(30): Show |
intron_variant | MODIFIER | c.196+767_196+768dup others(2): Show |
FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49763123 | ||||||
chr17:49763123
|
T | TACAC | 49 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0019others(46): Show | 56 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(53): Show |
intron_variant | MODIFIER | c.196+765_196+768dup others(4): Show |
FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49763123 | ||||||
chr17:49763123
|
TAC | T | 78 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0022others(75): Show | 80 | HG00323.hp2 HG00544.hp2 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.196+767_196+768del others(2): Show |
FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49763123 | ||||||
chr17:49763123
|
TACAC | T | 23 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0047others(20): Show | 26 | HG00673.hp1 HG01243.hp1 HG01358.hp1 others(23): Show |
intron_variant | MODIFIER | c.196+765_196+768del others(4): Show |
FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49763123 | ||||||
chr17:49763123
|
TACACAC | T | 10 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(7): Show | 10 | HG00558.hp1 HG00621.hp2 HG01070.hp1 others(7): Show |
intron_variant | MODIFIER | c.196+763_196+768del others(6): Show |
FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49763123 | ||||||
chr17:49763123
|
TACACACA others(1): Show |
T | 10 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0029others(7): Show | 11 | HG01106.hp2 HG02145.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.196+761_196+768del others(8): Show |
FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49763123 | ||||||
chr17:49763123
|
TACACACA others(3): Show |
T | 1 | a0001c0001t0001g0027 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.196+759_196+768del others(10): Show |
FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49763123 | ||||||
chr17:49763123
|
TACACACA others(5): Show |
T | 4 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(1): Show | 4 | HG00280.hp2 HG00673.hp2 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.196+757_196+768del others(12): Show |
FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49763123 | ||||||
chr17:49763698
|
C | G | 1 | a0001c0001t0001g0022 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.196+194G>C | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49763698 | ||||||
chr17:49763838
|
G | GC | 12 | a0001c0001t0001g0297a0001c0001t0001g0298a0001c0001t0001g0299others(9): Show | 12 | HG00408.hp1 HG01109.hp1 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.196+53dupG | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49763838 | ||||||
chr17:49763864
|
C | A | 2 | a0001c0001t0001g0308a0001c0001t0001g0309 | 2 | HG01243.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.196+28G>T | FAM117A | ENSG00000121104.8 | transcript | ENST00000240364.7 | protein_coding | 1/7 | chr17 | 49763864 |