geneid | 130074 |
---|---|
ensemblid | ENSG00000152102.18 |
hgncid | 27016 |
symbol | FAM168B |
name | family with sequence similarity 168 member B |
refseq_nuc | NM_001009993.4 |
refseq_prot | NP_001009993.2 |
ensembl_nuc | ENST00000389915.4 |
ensembl_prot | ENSP00000374565.3 |
mane_status | MANE Select |
chr | chr2 |
start | 131047876 |
end | 131093460 |
strand | - |
ver | v1.2 |
region | chr2:131047876-131093460 |
region5000 | chr2:131042876-131098460 |
regionname0 | FAM168B_chr2_131047876_131093460 |
regionname5000 | FAM168B_chr2_131042876_131098460 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 195 | 260 | 94 | 58 | 68 | 10 | 28 | 44 | FAM168B_chr2_131042876_131098460 | FAM168B | copy fasta | chr2 | 131042876 | 131098460 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 588 | 260 | 94 | 58 | 68 | 10 | 28 | FAM168B_chr2_131042876_131098460 | FAM168B | copy fasta | chr2 | 131042876 | 131098460 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/0 | 4848 | 140 | 34 | 38 | 42 | 5 | 20 | FAM168B_chr2_131042876_131098460 | FAM168B | copy fasta | chr2 | 131042876 | 131098460 |
t0002 | 0/0 | 4847 | 32 | 1 | 6 | 19 | 3 | 3 | FAM168B_chr2_131042876_131098460 | FAM168B | copy fasta | chr2 | 131042876 | 131098460 |
t0003 | 0/0 | 4847 | 15 | 12 | 0 | 1 | 0 | 2 | FAM168B_chr2_131042876_131098460 | FAM168B | copy fasta | chr2 | 131042876 | 131098460 |
t0004 | 0/0 | 4848 | 9 | 9 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | copy fasta | chr2 | 131042876 | 131098460 |
t0005 | 0/0 | 4847 | 7 | 6 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | copy fasta | chr2 | 131042876 | 131098460 |
t0006 | 0/0 | 4848 | 6 | 4 | 2 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | copy fasta | chr2 | 131042876 | 131098460 |
t0007 | 0/0 | 4847 | 5 | 4 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | copy fasta | chr2 | 131042876 | 131098460 |
t0008 | 0/0 | 4847 | 5 | 4 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | copy fasta | chr2 | 131042876 | 131098460 |
t0009 | 0/0 | 4847 | 3 | 1 | 2 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | copy fasta | chr2 | 131042876 | 131098460 |
t0010 | 0/0 | 4847 | 3 | 3 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | copy fasta | chr2 | 131042876 | 131098460 |
t0011 | 0/1 | 4847 | 3 | 0 | 1 | 0 | 1 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | copy fasta | chr2 | 131042876 | 131098460 |
t0012 | 0/0 | 4848 | 3 | 3 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | copy fasta | chr2 | 131042876 | 131098460 |
t0013 | 0/0 | 4847 | 3 | 3 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | copy fasta | chr2 | 131042876 | 131098460 |
t0014 | 0/0 | 4847 | 2 | 2 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | copy fasta | chr2 | 131042876 | 131098460 |
t0015 | 0/0 | 4847 | 2 | 0 | 1 | 0 | 1 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | copy fasta | chr2 | 131042876 | 131098460 |
t0016 | 0/0 | 4848 | 2 | 2 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | copy fasta | chr2 | 131042876 | 131098460 |
t0017 | 0/0 | 4848 | 2 | 2 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | copy fasta | chr2 | 131042876 | 131098460 |
t0018 | 0/0 | 4847 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | copy fasta | chr2 | 131042876 | 131098460 |
t0019 | 0/0 | 4847 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168B_chr2_131042876_131098460 | FAM168B | copy fasta | chr2 | 131042876 | 131098460 |
t0020 | 0/0 | 4847 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168B_chr2_131042876_131098460 | FAM168B | copy fasta | chr2 | 131042876 | 131098460 |
t0021 | 0/0 | 4848 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | copy fasta | chr2 | 131042876 | 131098460 |
t0022 | 0/0 | 4848 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | copy fasta | chr2 | 131042876 | 131098460 |
t0023 | 0/0 | 4847 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | copy fasta | chr2 | 131042876 | 131098460 |
t0024 | 0/0 | 4847 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | copy fasta | chr2 | 131042876 | 131098460 |
t0025 | 0/0 | 4847 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | copy fasta | chr2 | 131042876 | 131098460 |
t0026 | 0/0 | 4847 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | copy fasta | chr2 | 131042876 | 131098460 |
t0027 | 0/0 | 4847 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168B_chr2_131042876_131098460 | FAM168B | copy fasta | chr2 | 131042876 | 131098460 |
t0028 | 0/0 | 4848 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | copy fasta | chr2 | 131042876 | 131098460 |
t0029 | 0/0 | 4848 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | copy fasta | chr2 | 131042876 | 131098460 |
t0030 | 0/0 | 4848 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | copy fasta | chr2 | 131042876 | 131098460 |
t0031 | 0/0 | 4848 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | copy fasta | chr2 | 131042876 | 131098460 |
t0032 | 0/0 | 4848 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | copy fasta | chr2 | 131042876 | 131098460 |
t0033 | 0/0 | 4848 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | copy fasta | chr2 | 131042876 | 131098460 |
t0034 | 0/0 | 4848 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | copy fasta | chr2 | 131042876 | 131098460 |
t0035 | 0/0 | 4847 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | copy fasta | chr2 | 131042876 | 131098460 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 10 | 0 | 2 | 6 | 2 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0002 | 0/0 | 7 | 2 | 3 | 2 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0003 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0004 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0006 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0007 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0008 | 0/1 | 3 | 0 | 1 | 0 | 1 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0011 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0015 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0019 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0020 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0022 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0046 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 588 | 260 | 94 | 58 | 68 | 10 | 28 | FAM168B_chr2_131042876_131098460 | FAM168B | copy fasta | chr2 | 131042876 | 131098460 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 5435 | 140 | 34 | 38 | 42 | 5 | 20 | FAM168B_chr2_131042876_131098460 | FAM168B | copy fasta | chr2 | 131042876 | 131098460 |
a0001c0001t0002 | 0/0 | 5434 | 32 | 1 | 6 | 19 | 3 | 3 | FAM168B_chr2_131042876_131098460 | FAM168B | copy fasta | chr2 | 131042876 | 131098460 |
a0001c0001t0003 | 0/0 | 5434 | 15 | 12 | 0 | 1 | 0 | 2 | FAM168B_chr2_131042876_131098460 | FAM168B | copy fasta | chr2 | 131042876 | 131098460 |
a0001c0001t0004 | 0/0 | 5435 | 9 | 9 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | copy fasta | chr2 | 131042876 | 131098460 |
a0001c0001t0005 | 0/0 | 5434 | 7 | 6 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | copy fasta | chr2 | 131042876 | 131098460 |
a0001c0001t0006 | 0/0 | 5435 | 6 | 4 | 2 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | copy fasta | chr2 | 131042876 | 131098460 |
a0001c0001t0007 | 0/0 | 5434 | 5 | 4 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | copy fasta | chr2 | 131042876 | 131098460 |
a0001c0001t0008 | 0/0 | 5434 | 5 | 4 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | copy fasta | chr2 | 131042876 | 131098460 |
a0001c0001t0009 | 0/0 | 5434 | 3 | 1 | 2 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | copy fasta | chr2 | 131042876 | 131098460 |
a0001c0001t0010 | 0/0 | 5434 | 3 | 3 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | copy fasta | chr2 | 131042876 | 131098460 |
a0001c0001t0011 | 0/1 | 5434 | 3 | 0 | 1 | 0 | 1 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | copy fasta | chr2 | 131042876 | 131098460 |
a0001c0001t0012 | 0/0 | 5435 | 3 | 3 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | copy fasta | chr2 | 131042876 | 131098460 |
a0001c0001t0013 | 0/0 | 5434 | 3 | 3 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | copy fasta | chr2 | 131042876 | 131098460 |
a0001c0001t0014 | 0/0 | 5434 | 2 | 2 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | copy fasta | chr2 | 131042876 | 131098460 |
a0001c0001t0015 | 0/0 | 5434 | 2 | 0 | 1 | 0 | 1 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | copy fasta | chr2 | 131042876 | 131098460 |
a0001c0001t0016 | 0/0 | 5435 | 2 | 2 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | copy fasta | chr2 | 131042876 | 131098460 |
a0001c0001t0017 | 0/0 | 5435 | 2 | 2 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | copy fasta | chr2 | 131042876 | 131098460 |
a0001c0001t0018 | 0/0 | 5434 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | copy fasta | chr2 | 131042876 | 131098460 |
a0001c0001t0019 | 0/0 | 5434 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168B_chr2_131042876_131098460 | FAM168B | copy fasta | chr2 | 131042876 | 131098460 |
a0001c0001t0020 | 0/0 | 5434 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168B_chr2_131042876_131098460 | FAM168B | copy fasta | chr2 | 131042876 | 131098460 |
a0001c0001t0021 | 0/0 | 5435 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | copy fasta | chr2 | 131042876 | 131098460 |
a0001c0001t0022 | 0/0 | 5435 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | copy fasta | chr2 | 131042876 | 131098460 |
a0001c0001t0023 | 0/0 | 5434 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | copy fasta | chr2 | 131042876 | 131098460 |
a0001c0001t0024 | 0/0 | 5434 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | copy fasta | chr2 | 131042876 | 131098460 |
a0001c0001t0025 | 0/0 | 5434 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | copy fasta | chr2 | 131042876 | 131098460 |
a0001c0001t0026 | 0/0 | 5434 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | copy fasta | chr2 | 131042876 | 131098460 |
a0001c0001t0027 | 0/0 | 5434 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168B_chr2_131042876_131098460 | FAM168B | copy fasta | chr2 | 131042876 | 131098460 |
a0001c0001t0028 | 0/0 | 5435 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | copy fasta | chr2 | 131042876 | 131098460 |
a0001c0001t0029 | 0/0 | 5435 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | copy fasta | chr2 | 131042876 | 131098460 |
a0001c0001t0030 | 0/0 | 5435 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | copy fasta | chr2 | 131042876 | 131098460 |
a0001c0001t0031 | 0/0 | 5435 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | copy fasta | chr2 | 131042876 | 131098460 |
a0001c0001t0032 | 0/0 | 5435 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | copy fasta | chr2 | 131042876 | 131098460 |
a0001c0001t0033 | 0/0 | 5435 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | copy fasta | chr2 | 131042876 | 131098460 |
a0001c0001t0034 | 0/0 | 5435 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | copy fasta | chr2 | 131042876 | 131098460 |
a0001c0001t0035 | 0/0 | 5434 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | copy fasta | chr2 | 131042876 | 131098460 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 10 | 0 | 2 | 6 | 2 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0002 | 0/0 | 7 | 2 | 3 | 2 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0006 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0007 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0046 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0002g0003 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0002g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0002g0019 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0002g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0002g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0003g0004 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0003g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0003g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0003g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0003g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0003g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0003g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0003g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0003g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0004g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0004g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0004g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0004g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0004g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0004g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0004g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0005g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0005g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0005g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0005g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0005g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0005g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0006g0022 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0006g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0006g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0006g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0006g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0007g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0007g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0007g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0007g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0008g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0008g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0008g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0008g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0008g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0009g0020 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0009g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0010g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0011g0008 | 0/1 | 3 | 0 | 1 | 0 | 1 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0012g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0012g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0013g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0013g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0013g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0014g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0014g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0015g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0015g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0016g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0016g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0017g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0018g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0019g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0020g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0021g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0022g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0023g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0024g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0025g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0026g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0027g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0028g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0029g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0030g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0031g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0032g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0033g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0034g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
a0001c0001t0035g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0011 | g0008 | EUR | GBR | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG00280 | hp1 | a0001 | c0001 | t0002 | g0019 | EUR | FIN | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0077 | EUR | FIN | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | CHS | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | CHS | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG00544 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | CHS | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | CHS | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | CHS | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG00639 | hp1 | a0001 | c0001 | t0032 | g0082 | AMR | PUR | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG00642 | hp1 | a0001 | c0001 | t0011 | g0008 | AMR | PUR | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | CHS | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | CHS | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG00733 | hp1 | a0001 | c0001 | t0002 | g0189 | AMR | PUR | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0153 | AMR | PUR | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG00741 | hp2 | a0001 | c0001 | t0015 | g0172 | AMR | PUR | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG01099 | hp1 | a0001 | c0001 | t0030 | g0092 | AMR | PUR | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG01106 | hp2 | a0001 | c0001 | t0034 | g0067 | AMR | PUR | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG01109 | hp2 | a0001 | c0001 | t0031 | g0045 | AMR | PUR | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG01175 | hp2 | a0001 | c0001 | t0009 | g0195 | AMR | PUR | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0177 | AMR | PUR | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG01243 | hp1 | a0001 | c0001 | t0005 | g0171 | AMR | PUR | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG01243 | hp2 | a0001 | c0001 | t0007 | g0151 | AMR | PUR | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | CLM | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG01257 | hp1 | a0001 | c0001 | t0006 | g0201 | AMR | CLM | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | CLM | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG01258 | hp2 | a0001 | c0001 | t0006 | g0022 | AMR | CLM | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | CLM | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG01261 | hp2 | a0001 | c0001 | t0009 | g0020 | AMR | CLM | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0135 | AMR | CLM | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG01515 | hp2 | a0001 | c0001 | t0002 | g0137 | EUR | IBS | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG01517 | hp1 | a0001 | c0001 | t0002 | g0136 | EUR | IBS | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0025 | EUR | IBS | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG01884 | hp1 | a0001 | c0001 | t0008 | g0026 | AFR | ACB | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | ACB | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG01891 | hp1 | a0001 | c0001 | t0005 | g0162 | AFR | ACB | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | ACB | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0182 | AMR | PEL | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PEL | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG01943 | hp1 | a0001 | c0001 | t0023 | g0169 | AMR | PEL | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG01943 | hp2 | a0001 | c0001 | t0008 | g0127 | AMR | PEL | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | PEL | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG01975 | hp2 | a0001 | c0001 | t0002 | g0152 | AMR | PEL | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PEL | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PEL | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG02015 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | KHV | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | KHV | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG02055 | hp1 | a0001 | c0001 | t0013 | g0024 | AFR | ACB | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | ACB | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0191 | EAS | KHV | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | KHV | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | KHV | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | KHV | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | ACB | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | ACB | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PEL | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PEL | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | CDX | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG02155 | hp2 | a0001 | c0001 | t0002 | g0185 | EAS | CDX | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0180 | EAS | CDX | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG02257 | hp1 | a0001 | c0001 | t0003 | g0016 | AFR | ACB | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG02257 | hp2 | a0001 | c0001 | t0014 | g0197 | AFR | ACB | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG02258 | hp1 | a0001 | c0001 | t0008 | g0053 | AFR | ACB | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | PEL | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG02280 | hp1 | a0001 | c0001 | t0004 | g0209 | AFR | ACB | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | ACB | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG02451 | hp1 | a0001 | c0001 | t0013 | g0174 | AFR | ACB | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG02451 | hp2 | a0001 | c0001 | t0004 | g0208 | AFR | ACB | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG02572 | hp1 | a0001 | c0001 | t0004 | g0212 | AFR | GWD | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG02572 | hp2 | a0001 | c0001 | t0003 | g0004 | AFR | GWD | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG02615 | hp1 | a0001 | c0001 | t0010 | g0009 | AFR | GWD | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG02615 | hp2 | a0001 | c0001 | t0028 | g0204 | AFR | GWD | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG02622 | hp1 | a0001 | c0001 | t0006 | g0022 | AFR | GWD | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG02622 | hp2 | a0001 | c0001 | t0012 | g0196 | AFR | GWD | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | GWD | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG02630 | hp2 | a0001 | c0001 | t0005 | g0018 | AFR | GWD | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG02647 | hp1 | a0001 | c0001 | t0009 | g0020 | AFR | GWD | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG02647 | hp2 | a0001 | c0001 | t0006 | g0205 | AFR | GWD | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG02698 | hp1 | a0001 | c0001 | t0003 | g0156 | SAS | PJL | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | GWD | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | GWD | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG02723 | hp2 | a0001 | c0001 | t0003 | g0167 | AFR | GWD | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG02738 | hp1 | a0001 | c0001 | t0020 | g0193 | SAS | PJL | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG02809 | hp1 | a0001 | c0001 | t0003 | g0004 | AFR | GWD | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG02809 | hp2 | a0001 | c0001 | t0003 | g0170 | AFR | GWD | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG02818 | hp1 | a0001 | c0001 | t0012 | g0021 | AFR | GWD | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG02818 | hp2 | a0001 | c0001 | t0007 | g0017 | AFR | GWD | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG02886 | hp2 | a0001 | c0001 | t0012 | g0021 | AFR | GWD | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG02896 | hp1 | a0001 | c0001 | t0016 | g0044 | AFR | GWD | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | GWD | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | GWD | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG02897 | hp2 | a0001 | c0001 | t0016 | g0034 | AFR | GWD | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG02922 | hp1 | a0001 | c0001 | t0004 | g0010 | AFR | ESN | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG02922 | hp2 | a0001 | c0001 | t0026 | g0194 | AFR | ESN | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG02965 | hp1 | a0001 | c0001 | t0004 | g0207 | AFR | ESN | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | ESN | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG02970 | hp1 | a0001 | c0001 | t0005 | g0173 | AFR | ESN | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG02970 | hp2 | a0001 | c0001 | t0007 | g0150 | AFR | ESN | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | ESN | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG02976 | hp2 | a0001 | c0001 | t0010 | g0009 | AFR | ESN | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG03017 | hp1 | a0001 | c0001 | t0003 | g0164 | SAS | PJL | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG03041 | hp2 | a0001 | c0001 | t0005 | g0155 | AFR | GWD | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG03098 | hp1 | a0001 | c0001 | t0006 | g0203 | AFR | MSL | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG03098 | hp2 | a0001 | c0001 | t0006 | g0202 | AFR | MSL | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG03130 | hp1 | a0001 | c0001 | t0014 | g0198 | AFR | ESN | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | ESN | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG03139 | hp1 | a0001 | c0001 | t0017 | g0023 | AFR | ESN | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG03139 | hp2 | a0001 | c0001 | t0004 | g0010 | AFR | ESN | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | ESN | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG03195 | hp2 | a0001 | c0001 | t0010 | g0009 | AFR | ESN | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG03209 | hp1 | a0001 | c0001 | t0003 | g0161 | AFR | MSL | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | MSL | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG03225 | hp1 | a0001 | c0001 | t0003 | g0004 | AFR | MSL | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG03225 | hp2 | a0001 | c0001 | t0004 | g0210 | AFR | MSL | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG03239 | hp1 | a0001 | c0001 | t0027 | g0168 | SAS | PJL | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0019 | SAS | PJL | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | MSL | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | MSL | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG03486 | hp1 | a0001 | c0001 | t0007 | g0017 | AFR | MSL | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG03486 | hp2 | a0001 | c0001 | t0003 | g0157 | AFR | MSL | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | ESN | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG03516 | hp2 | a0001 | c0001 | t0008 | g0054 | AFR | ESN | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | MSL | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG03579 | hp2 | a0001 | c0001 | t0003 | g0004 | AFR | MSL | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0051 | SAS | PJL | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0052 | SAS | PJL | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG03704 | hp2 | a0001 | c0001 | t0019 | g0154 | SAS | PJL | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0049 | SAS | PJL | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0094 | SAS | PJL | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0121 | SAS | BEB | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | BEB | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0190 | SAS | BEB | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0117 | SAS | BEB | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0192 | SAS | STU | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0087 | SAS | STU | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | STU | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0075 | SAS | STU | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
NA18522 | hp1 | a0001 | c0001 | t0017 | g0023 | AFR | YRI | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | YRI | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0181 | EAS | CHB | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | CHB | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | CHB | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
NA18953 | hp1 | a0001 | c0001 | t0003 | g0165 | EAS | JPT | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
NA18957 | hp1 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
NA18968 | hp1 | a0001 | c0001 | t0021 | g0186 | EAS | JPT | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
NA18971 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
NA18988 | hp2 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
NA18992 | hp1 | a0001 | c0001 | t0018 | g0176 | EAS | JPT | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
NA18993 | hp1 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
NA18993 | hp2 | a0001 | c0001 | t0033 | g0113 | EAS | JPT | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
NA18995 | hp1 | a0001 | c0001 | t0029 | g0112 | EAS | JPT | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
NA18999 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
NA19009 | hp2 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
NA19030 | hp1 | a0001 | c0001 | t0025 | g0134 | AFR | LWK | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | LWK | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
NA19043 | hp1 | a0001 | c0001 | t0003 | g0016 | AFR | LWK | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
NA19043 | hp2 | a0001 | c0001 | t0005 | g0163 | AFR | LWK | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
NA19060 | hp2 | a0001 | c0001 | t0035 | g0160 | EAS | JPT | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
NA19064 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
NA19070 | hp2 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
NA19085 | hp1 | a0001 | c0001 | t0022 | g0064 | EAS | JPT | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
NA19091 | hp2 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | YRI | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
NA19240 | hp2 | a0001 | c0001 | t0008 | g0055 | AFR | YRI | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
NA20129 | hp1 | a0001 | c0001 | t0003 | g0159 | AFR | ASW | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
NA20129 | hp2 | a0001 | c0001 | t0007 | g0149 | AFR | ASW | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0125 | EUR | TSI | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
NA20805 | hp2 | a0001 | c0001 | t0015 | g0166 | EUR | TSI | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0081 | SAS | GIH | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0048 | SAS | GIH | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG02109 | hp1 | a0001 | c0001 | t0004 | g0010 | AFR | ACB | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG02109 | hp2 | a0001 | c0001 | t0013 | g0175 | AFR | ACB | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG02559 | hp1 | a0001 | c0001 | t0004 | g0211 | AFR | ACB | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG02559 | hp2 | a0001 | c0001 | t0003 | g0158 | AFR | ACB | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | MSL | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | MSL | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG06807 | hp1 | a0001 | c0001 | t0024 | g0206 | AFR | USA | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
HG06807 | hp2 | a0001 | c0001 | t0005 | g0018 | AFR | USA | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | USA | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | USA | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
NA21309 | hp1 | a0001 | c0001 | t0002 | g0187 | AFR | LWK | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | LWK | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0011 | g0008 | REF | REF | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0046 | REF | REF | FAM168B_chr2_131042876_131098460 | FAM168B | chr2 | 131042876 | 131098460 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:131047985
|
G | A | 1 | a0001c0001t0027 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4480C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 7/7 | 4918 | chr2 | 131047985 | |||||
chr2:131048004
|
T | C | 1 | a0001c0001t0015 | 2 | HG00741.hp2 NA20805.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4461A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 7/7 | 4899 | chr2 | 131048004 | |||||
chr2:131048052
|
T | A | 1 | a0001c0001t0023 | 1 | HG01943.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4413A>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 7/7 | 4851 | chr2 | 131048052 | |||||
chr2:131048185
|
C | A | 1 | a0001c0001t0019 | 1 | HG03704.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4280G>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 7/7 | 4718 | chr2 | 131048185 | |||||
chr2:131048325
|
A | G | 1 | a0001c0001t0013 | 3 | HG02055.hp1 HG02109.hp2 HG02451.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4140T>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 7/7 | 4578 | chr2 | 131048325 | |||||
chr2:131048411
|
G | T | 13 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(10): Show | 67 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*4054C>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 7/7 | 4492 | chr2 | 131048411 | |||||
chr2:131048432
|
G | A | 1 | a0001c0001t0026 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4033C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 7/7 | 4471 | chr2 | 131048432 | |||||
chr2:131048540
|
G | A | 1 | a0001c0001t0017 | 2 | HG03139.hp1 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3925C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 7/7 | 4363 | chr2 | 131048540 | |||||
chr2:131048840
|
A | G | 1 | a0001c0001t0025 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3625T>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 7/7 | 4063 | chr2 | 131048840 | |||||
chr2:131048878
|
T | G | 1 | a0001c0001t0033 | 1 | NA18993.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3587A>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 7/7 | 4025 | chr2 | 131048878 | |||||
chr2:131049004
|
G | C | 2 | a0001c0001t0012a0001c0001t0014 | 5 | HG02257.hp2 HG02622.hp2 HG02818.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3461C>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 7/7 | 3899 | chr2 | 131049004 | |||||
chr2:131049240
|
C | T | 1 | a0001c0001t0005 | 7 | HG01243.hp1 HG01891.hp1 HG02630.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3225G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 7/7 | 3663 | chr2 | 131049240 | |||||
chr2:131049259
|
C | T | 1 | a0001c0001t0025 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3206G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 7/7 | 3644 | chr2 | 131049259 | |||||
chr2:131049332
|
T | C | 2 | a0001c0001t0004a0001c0001t0017 | 11 | HG02109.hp1 HG02280.hp1 HG02451.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*3133A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 7/7 | 3571 | chr2 | 131049332 | |||||
chr2:131049526
|
C | T | 1 | a0001c0001t0032 | 1 | HG00639.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2939G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 7/7 | 3377 | chr2 | 131049526 | |||||
chr2:131049555
|
A | G | 2 | a0001c0001t0004a0001c0001t0017 | 11 | HG02109.hp1 HG02280.hp1 HG02451.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2910T>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 7/7 | 3348 | chr2 | 131049555 | |||||
chr2:131049673
|
AT | A | 1 | a0001c0001t0013 | 3 | HG02055.hp1 HG02109.hp2 HG02451.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2791delA | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 7/7 | 3229 | chr2 | 131049673 | |||||
chr2:131049788
|
C | T | 1 | a0001c0001t0018 | 1 | NA18992.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2677G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 7/7 | 3115 | chr2 | 131049788 | |||||
chr2:131049887
|
C | T | 1 | a0001c0001t0011 | 3 | HG00099.hp1 HG00642.hp1 homoSapiens_chm13v2.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2578G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 7/7 | 3016 | chr2 | 131049887 | |||||
chr2:131049982
|
C | T | 1 | a0001c0001t0025 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2483G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 7/7 | 2921 | chr2 | 131049982 | |||||
chr2:131050265
|
T | C | 1 | a0001c0001t0016 | 2 | HG02896.hp1 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2200A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 7/7 | 2638 | chr2 | 131050265 | |||||
chr2:131050409
|
C | A | 4 | a0001c0001t0009a0001c0001t0012a0001c0001t0014others(1): Show | 9 | HG01175.hp2 HG01261.hp2 HG02257.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2056G>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 7/7 | 2494 | chr2 | 131050409 | |||||
chr2:131050666
|
A | G | 1 | a0001c0001t0025 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1799T>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 7/7 | 2237 | chr2 | 131050666 | |||||
chr2:131050826
|
C | G | 1 | a0001c0001t0031 | 1 | HG01109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1639G>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 7/7 | 2077 | chr2 | 131050826 | |||||
chr2:131050870
|
C | T | 1 | a0001c0001t0007 | 5 | HG01243.hp2 HG02818.hp2 HG02970.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1595G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 7/7 | 2033 | chr2 | 131050870 | |||||
chr2:131050877
|
T | C | 1 | a0001c0001t0020 | 1 | HG02738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1588A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 7/7 | 2026 | chr2 | 131050877 | |||||
chr2:131050896
|
G | C | 1 | a0001c0001t0013 | 3 | HG02055.hp1 HG02109.hp2 HG02451.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1569C>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 7/7 | 2007 | chr2 | 131050896 | |||||
chr2:131050951
|
G | A | 1 | a0001c0001t0034 | 1 | HG01106.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1514C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 7/7 | 1952 | chr2 | 131050951 | |||||
chr2:131050976
|
C | T | 2 | a0001c0001t0010a0001c0001t0030 | 4 | HG01099.hp1 HG02615.hp1 HG02976.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1489G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 7/7 | 1927 | chr2 | 131050976 | |||||
chr2:131050983
|
A | AT | 2 | a0001c0001t0004a0001c0001t0017 | 11 | HG02109.hp1 HG02280.hp1 HG02451.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1481dupA | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 7/7 | 1919 | chr2 | 131050983 | |||||
chr2:131051082
|
C | T | 10 | a0001c0001t0004a0001c0001t0006a0001c0001t0009others(7): Show | 29 | HG01175.hp2 HG01257.hp1 HG01258.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*1383G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 7/7 | 1821 | chr2 | 131051082 | |||||
chr2:131051205
|
A | T | 1 | a0001c0001t0025 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1260T>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 7/7 | 1698 | chr2 | 131051205 | |||||
chr2:131051473
|
A | G | 1 | a0001c0001t0029 | 1 | NA18995.hp1 | 3_prime_UTR_variant | MODIFIER | c.*992T>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 7/7 | 1430 | chr2 | 131051473 | |||||
chr2:131051483
|
GA | G | 21 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(18): Show | 97 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(94): Show |
3_prime_UTR_variant | MODIFIER | c.*981delT | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 7/7 | 1419 | chr2 | 131051483 | |||||
chr2:131051486
|
A | T | 1 | a0001c0001t0024 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*979T>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 7/7 | 1417 | chr2 | 131051486 | |||||
chr2:131051552
|
G | T | 1 | a0001c0001t0023 | 1 | HG01943.hp1 | 3_prime_UTR_variant | MODIFIER | c.*913C>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 7/7 | 1351 | chr2 | 131051552 | |||||
chr2:131051624
|
C | T | 24 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(21): Show | 103 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(100): Show |
3_prime_UTR_variant | MODIFIER | c.*841G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 7/7 | 1279 | chr2 | 131051624 | |||||
chr2:131051739
|
C | T | 1 | a0001c0001t0022 | 1 | NA19085.hp1 | 3_prime_UTR_variant | MODIFIER | c.*726G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 7/7 | 1164 | chr2 | 131051739 | |||||
chr2:131051825
|
T | C | 1 | a0001c0001t0013 | 3 | HG02055.hp1 HG02109.hp2 HG02451.hp1 |
3_prime_UTR_variant | MODIFIER | c.*640A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 7/7 | 1078 | chr2 | 131051825 | |||||
chr2:131051863
|
A | T | 5 | a0001c0001t0002a0001c0001t0018a0001c0001t0019others(2): Show | 36 | HG00280.hp1 HG00544.hp2 HG00673.hp1 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*602T>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 7/7 | 1040 | chr2 | 131051863 | |||||
chr2:131052152
|
T | G | 1 | a0001c0001t0035 | 1 | NA19060.hp2 | 3_prime_UTR_variant | MODIFIER | c.*313A>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 7/7 | 751 | chr2 | 131052152 | |||||
chr2:131093249
|
C | A | 2 | a0001c0001t0004a0001c0001t0017 | 11 | HG02109.hp1 HG02280.hp1 HG02451.hp2 others(8): Show |
5_prime_UTR_variant | MODIFIER | c.-47G>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/7 | 10603 | chr2 | 131093249 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:131052474
|
C | G | 7 | a0001c0001t0009g0020a0001c0001t0009g0195a0001c0001t0012g0021others(4): Show | 9 | HG01175.hp2 HG01261.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.*13-22G>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 6/6 | chr2 | 131052474 | ||||||
chr2:131052475
|
T | A | 7 | a0001c0001t0009g0020a0001c0001t0009g0195a0001c0001t0012g0021others(4): Show | 9 | HG01175.hp2 HG01261.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.*13-23A>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 6/6 | chr2 | 131052475 | ||||||
chr2:131052543
|
G | A | 7 | a0001c0001t0006g0022a0001c0001t0006g0201a0001c0001t0006g0202others(4): Show | 8 | HG01257.hp1 HG01258.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.*13-91C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 6/6 | chr2 | 131052543 | ||||||
chr2:131052694
|
T | G | 51 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0019others(48): Show | 66 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.*12+197A>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 6/6 | chr2 | 131052694 | ||||||
chr2:131052776
|
G | C | 1 | a0001c0001t0024g0206 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.*12+115C>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 6/6 | chr2 | 131052776 | ||||||
chr2:131052807
|
T | C | 8 | a0001c0001t0004g0010a0001c0001t0004g0207a0001c0001t0004g0208others(5): Show | 11 | HG02109.hp1 HG02280.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.*12+84A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 6/6 | chr2 | 131052807 | ||||||
chr2:131053174
|
C | T | 4 | a0001c0001t0007g0017a0001c0001t0007g0149a0001c0001t0007g0150others(1): Show | 5 | HG01243.hp2 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.476-159G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 5/6 | chr2 | 131053174 | ||||||
chr2:131053187
|
T | C | 2 | a0001c0001t0001g0035a0001c0001t0001g0037 | 2 | HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.476-172A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 5/6 | chr2 | 131053187 | ||||||
chr2:131053189
|
G | A | 1 | a0001c0001t0025g0134 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.476-174C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 5/6 | chr2 | 131053189 | ||||||
chr2:131053655
|
T | C | 1 | a0001c0001t0010g0009 | 3 | HG02615.hp1 HG02976.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.476-640A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 5/6 | chr2 | 131053655 | ||||||
chr2:131053670
|
A | T | 1 | a0001c0001t0006g0203 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.476-655T>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 5/6 | chr2 | 131053670 | ||||||
chr2:131053747
|
T | C | 82 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(79): Show | 106 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(103): Show |
intron_variant | MODIFIER | c.476-732A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 5/6 | chr2 | 131053747 | ||||||
chr2:131053960
|
C | G | 2 | a0001c0001t0001g0061a0001c0001t0001g0068 | 2 | HG02976.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.476-945G>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 5/6 | chr2 | 131053960 | ||||||
chr2:131054070
|
A | G | 23 | a0001c0001t0004g0010a0001c0001t0004g0207a0001c0001t0004g0208others(20): Show | 29 | HG01175.hp2 HG01257.hp1 HG01258.hp2 others(26): Show |
intron_variant | MODIFIER | c.476-1055T>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 5/6 | chr2 | 131054070 | ||||||
chr2:131054095
|
G | A | 2 | a0001c0001t0001g0012a0001c0001t0001g0111 | 3 | HG00735.hp1 HG01928.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.476-1080C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 5/6 | chr2 | 131054095 | ||||||
chr2:131054134
|
A | C | 1 | a0001c0001t0001g0059 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.476-1119T>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 5/6 | chr2 | 131054134 | ||||||
chr2:131054236
|
T | TA | 4 | a0001c0001t0007g0017a0001c0001t0007g0149a0001c0001t0007g0150others(1): Show | 5 | HG01243.hp2 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.475+1035dupT | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 5/6 | chr2 | 131054236 | ||||||
chr2:131054236
|
TA | T | 12 | a0001c0001t0001g0089a0001c0001t0001g0147a0001c0001t0002g0183others(9): Show | 14 | HG01175.hp2 HG01261.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.475+1035delT | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 5/6 | chr2 | 131054236 | ||||||
chr2:131054322
|
A | C | 1 | a0001c0001t0001g0052 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.475+950T>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 5/6 | chr2 | 131054322 | ||||||
chr2:131054525
|
T | C | 1 | a0001c0001t0001g0133 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.475+747A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 5/6 | chr2 | 131054525 | ||||||
chr2:131054806
|
T | C | 1 | a0001c0001t0003g0159 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.475+466A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 5/6 | chr2 | 131054806 | ||||||
chr2:131054811
|
G | C | 3 | a0001c0001t0001g0096a0001c0001t0001g0110a0001c0001t0001g0130 | 3 | HG02723.hp1 HG03130.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.475+461C>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 5/6 | chr2 | 131054811 | ||||||
chr2:131054854
|
G | A | 1 | a0001c0001t0001g0066 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.475+418C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 5/6 | chr2 | 131054854 | ||||||
chr2:131054989
|
A | G | 3 | a0001c0001t0008g0053a0001c0001t0008g0054a0001c0001t0008g0055 | 3 | HG02258.hp1 HG03516.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.475+283T>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 5/6 | chr2 | 131054989 | ||||||
chr2:131054999
|
G | T | 12 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(9): Show | 12 | HG01109.hp2 HG01884.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.475+273C>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 5/6 | chr2 | 131054999 | ||||||
chr2:131055119
|
T | C | 3 | a0001c0001t0013g0024a0001c0001t0013g0174a0001c0001t0013g0175 | 3 | HG02055.hp1 HG02109.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.475+153A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 5/6 | chr2 | 131055119 | ||||||
chr2:131055165
|
C | T | 52 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0019others(49): Show | 69 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.475+107G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 5/6 | chr2 | 131055165 | ||||||
chr2:131055204
|
C | T | 2 | a0001c0001t0003g0165a0001c0001t0035g0160 | 2 | NA18953.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.475+68G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 5/6 | chr2 | 131055204 | ||||||
chr2:131055219
|
C | T | 2 | a0001c0001t0014g0197a0001c0001t0014g0198 | 2 | HG02257.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.475+53G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 5/6 | chr2 | 131055219 | ||||||
chr2:131055744
|
G | A | 7 | a0001c0001t0009g0020a0001c0001t0009g0195a0001c0001t0012g0021others(4): Show | 9 | HG01175.hp2 HG01261.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.155-49C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131055744 | ||||||
chr2:131055869
|
A | G | 209 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(206): Show | 257 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(254): Show |
intron_variant | MODIFIER | c.155-174T>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131055869 | ||||||
chr2:131055959
|
A | C | 7 | a0001c0001t0009g0020a0001c0001t0009g0195a0001c0001t0012g0021others(4): Show | 9 | HG01175.hp2 HG01261.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.155-264T>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131055959 | ||||||
chr2:131056199
|
T | C | 52 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0019others(49): Show | 69 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.155-504A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131056199 | ||||||
chr2:131056503
|
A | C | 1 | a0001c0001t0025g0134 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.155-808T>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131056503 | ||||||
chr2:131056557
|
G | A | 8 | a0001c0001t0004g0010a0001c0001t0004g0207a0001c0001t0004g0208others(5): Show | 11 | HG02109.hp1 HG02280.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.155-862C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131056557 | ||||||
chr2:131056659
|
A | G | 4 | a0001c0001t0001g0129a0001c0001t0008g0053a0001c0001t0008g0054others(1): Show | 4 | HG02258.hp1 HG03209.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.155-964T>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131056659 | ||||||
chr2:131056685
|
C | T | 1 | a0001c0001t0001g0065 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.155-990G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131056685 | ||||||
chr2:131056692
|
C | T | 1 | a0001c0001t0001g0108 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.155-997G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131056692 | ||||||
chr2:131056847
|
CAGA | C | 8 | a0001c0001t0004g0010a0001c0001t0004g0207a0001c0001t0004g0208others(5): Show | 11 | HG02109.hp1 HG02280.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.155-1155_155-1153d others(5): Show |
FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131056847 | ||||||
chr2:131056891
|
C | G | 1 | a0001c0001t0002g0182 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.155-1196G>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131056891 | ||||||
chr2:131056891
|
C | T | 1 | a0001c0001t0001g0108 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.155-1196G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131056891 | ||||||
chr2:131056981
|
T | C | 1 | a0001c0001t0001g0099 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.155-1286A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131056981 | ||||||
chr2:131057011
|
C | T | 1 | a0001c0001t0025g0134 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.155-1316G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131057011 | ||||||
chr2:131057275
|
A | G | 5 | a0001c0001t0006g0022a0001c0001t0006g0201a0001c0001t0006g0202others(2): Show | 6 | HG01257.hp1 HG01258.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.155-1580T>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131057275 | ||||||
chr2:131057572
|
C | T | 1 | a0001c0001t0031g0045 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.155-1877G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131057572 | ||||||
chr2:131057817
|
G | A | 7 | a0001c0001t0009g0020a0001c0001t0009g0195a0001c0001t0012g0021others(4): Show | 9 | HG01175.hp2 HG01261.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.155-2122C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131057817 | ||||||
chr2:131057883
|
T | C | 4 | a0001c0001t0007g0017a0001c0001t0007g0149a0001c0001t0007g0150others(1): Show | 5 | HG01243.hp2 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.155-2188A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131057883 | ||||||
chr2:131058120
|
GTA | G | 75 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0019others(72): Show | 98 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.155-2427_155-2426d others(4): Show |
FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131058120 | ||||||
chr2:131058297
|
C | T | 3 | a0001c0001t0001g0006a0001c0001t0001g0072a0001c0001t0001g0099 | 5 | HG01255.hp1 HG01934.hp2 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.155-2602G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131058297 | ||||||
chr2:131058329
|
A | G | 1 | a0001c0001t0002g0187 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.155-2634T>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131058329 | ||||||
chr2:131058405
|
C | T | 1 | a0001c0001t0001g0121 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.155-2710G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131058405 | ||||||
chr2:131058709
|
A | T | 1 | a0001c0001t0001g0109 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.155-3014T>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131058709 | ||||||
chr2:131058826
|
C | T | 2 | a0001c0001t0001g0039a0001c0001t0001g0040 | 2 | HG02895.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.155-3131G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131058826 | ||||||
chr2:131058900
|
T | A | 1 | a0001c0001t0007g0150 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.155-3205A>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131058900 | ||||||
chr2:131058915
|
A | C | 1 | a0001c0001t0012g0021 | 2 | HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.155-3220T>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131058915 | ||||||
chr2:131058943
|
T | C | 11 | a0001c0001t0003g0004a0001c0001t0003g0157a0001c0001t0003g0158others(8): Show | 15 | HG01243.hp1 HG01891.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.155-3248A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131058943 | ||||||
chr2:131059479
|
T | C | 1 | a0001c0001t0010g0009 | 3 | HG02615.hp1 HG02976.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.155-3784A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131059479 | ||||||
chr2:131059517
|
A | G | 4 | a0001c0001t0007g0017a0001c0001t0007g0149a0001c0001t0007g0150others(1): Show | 5 | HG01243.hp2 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.155-3822T>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131059517 | ||||||
chr2:131059615
|
C | A | 50 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0019others(47): Show | 65 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.155-3920G>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131059615 | ||||||
chr2:131059615
|
CCCTCTGT others(6): Show |
C | 1 | a0001c0001t0001g0122 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.155-3933_155-3921d others(15): Show |
FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131059615 | ||||||
chr2:131059695
|
A | G | 211 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(208): Show | 259 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.155-4000T>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131059695 | ||||||
chr2:131059797
|
A | T | 101 | a0001c0001t0001g0043a0001c0001t0001g0108a0001c0001t0001g0138others(98): Show | 125 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(122): Show |
intron_variant | MODIFIER | c.155-4102T>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131059797 | ||||||
chr2:131059807
|
G | T | 1 | a0001c0001t0001g0066 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.155-4112C>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131059807 | ||||||
chr2:131059879
|
T | C | 3 | a0001c0001t0009g0020a0001c0001t0009g0195a0001c0001t0026g0194 | 4 | HG01175.hp2 HG01261.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.155-4184A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131059879 | ||||||
chr2:131059896
|
C | G | 1 | a0001c0001t0001g0133 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.155-4201G>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131059896 | ||||||
chr2:131060198
|
G | A | 8 | a0001c0001t0004g0010a0001c0001t0004g0207a0001c0001t0004g0208others(5): Show | 11 | HG02109.hp1 HG02280.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.155-4503C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131060198 | ||||||
chr2:131060267
|
G | A | 1 | a0001c0001t0008g0053 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.155-4572C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131060267 | ||||||
chr2:131060284
|
A | G | 52 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0019others(49): Show | 69 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.155-4589T>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131060284 | ||||||
chr2:131060487
|
A | G | 1 | a0001c0001t0001g0065 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.155-4792T>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131060487 | ||||||
chr2:131060913
|
G | A | 4 | a0001c0001t0007g0017a0001c0001t0007g0149a0001c0001t0007g0150others(1): Show | 5 | HG01243.hp2 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.155-5218C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131060913 | ||||||
chr2:131061063
|
G | T | 1 | a0001c0001t0001g0130 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.155-5368C>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131061063 | ||||||
chr2:131061149
|
C | A | 52 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0019others(49): Show | 69 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.155-5454G>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131061149 | ||||||
chr2:131061177
|
G | A | 52 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0019others(49): Show | 69 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.155-5482C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131061177 | ||||||
chr2:131061247
|
G | A | 1 | a0001c0001t0001g0041 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.155-5552C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131061247 | ||||||
chr2:131061292
|
AT | A | 6 | a0001c0001t0006g0022a0001c0001t0006g0202a0001c0001t0006g0203others(3): Show | 7 | HG01258.hp2 HG02615.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.155-5598delA | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131061292 | ||||||
chr2:131061295
|
T | TA | 6 | a0001c0001t0001g0088a0001c0001t0007g0017a0001c0001t0007g0149others(3): Show | 7 | HG01243.hp2 HG02818.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.155-5601dupT | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131061295 | ||||||
chr2:131061295
|
TA | T | 5 | a0001c0001t0001g0072a0001c0001t0001g0089a0001c0001t0001g0128others(2): Show | 5 | HG01943.hp2 HG02895.hp2 NA18951.hp1 others(2): Show |
intron_variant | MODIFIER | c.155-5601delT | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131061295 | ||||||
chr2:131061482
|
C | G | 1 | a0001c0001t0003g0156 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.155-5787G>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131061482 | ||||||
chr2:131061782
|
GA | G | 63 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0019others(60): Show | 83 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.155-6088delT | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131061782 | ||||||
chr2:131062078
|
C | T | 184 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0011others(181): Show | 224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.155-6383G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131062078 | ||||||
chr2:131062180
|
A | T | 3 | a0001c0001t0008g0053a0001c0001t0008g0054a0001c0001t0008g0055 | 3 | HG02258.hp1 HG03516.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.155-6485T>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131062180 | ||||||
chr2:131062270
|
T | C | 1 | a0001c0001t0001g0058 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.155-6575A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131062270 | ||||||
chr2:131062292
|
T | C | 1 | a0001c0001t0031g0045 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.155-6597A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131062292 | ||||||
chr2:131062464
|
T | C | 3 | a0001c0001t0001g0079a0001c0001t0001g0101a0001c0001t0001g0118 | 3 | HG01934.hp1 HG01975.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.155-6769A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131062464 | ||||||
chr2:131062479
|
G | A | 1 | a0001c0001t0002g0180 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.155-6784C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131062479 | ||||||
chr2:131062524
|
T | C | 6 | a0001c0001t0002g0005a0001c0001t0002g0178a0001c0001t0002g0179others(3): Show | 9 | HG00544.hp2 HG00673.hp1 HG02155.hp2 others(6): Show |
intron_variant | MODIFIER | c.155-6829A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131062524 | ||||||
chr2:131062636
|
C | A | 1 | a0001c0001t0010g0009 | 3 | HG02615.hp1 HG02976.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.155-6941G>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131062636 | ||||||
chr2:131062663
|
G | A | 1 | a0001c0001t0001g0094 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.155-6968C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131062663 | ||||||
chr2:131062744
|
G | A | 1 | a0001c0001t0025g0134 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.155-7049C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131062744 | ||||||
chr2:131062869
|
G | A | 52 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0019others(49): Show | 69 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.155-7174C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131062869 | ||||||
chr2:131062926
|
A | G | 1 | a0001c0001t0001g0083 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.155-7231T>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131062926 | ||||||
chr2:131062941
|
C | G | 1 | a0001c0001t0001g0048 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.155-7246G>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131062941 | ||||||
chr2:131063242
|
C | A | 1 | a0001c0001t0001g0083 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.155-7547G>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131063242 | ||||||
chr2:131063304
|
C | CAACAATG others(220): Show |
1 | a0001c0001t0002g0187 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.155-7610_155-7609i others(229): Show |
FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131063304 | ||||||
chr2:131063405
|
T | C | 52 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0019others(49): Show | 69 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.155-7710A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131063405 | ||||||
chr2:131063639
|
G | C | 1 | a0001c0001t0001g0077 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.155-7944C>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131063639 | ||||||
chr2:131063725
|
G | A | 1 | a0001c0001t0014g0198 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.155-8030C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131063725 | ||||||
chr2:131064156
|
G | A | 1 | a0001c0001t0006g0205 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.154+7699C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131064156 | ||||||
chr2:131064204
|
G | A | 1 | a0001c0001t0001g0084 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.154+7651C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131064204 | ||||||
chr2:131064486
|
G | A | 7 | a0001c0001t0009g0020a0001c0001t0009g0195a0001c0001t0012g0021others(4): Show | 9 | HG01175.hp2 HG01261.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.154+7369C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131064486 | ||||||
chr2:131064565
|
A | G | 1 | a0001c0001t0004g0207 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.154+7290T>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131064565 | ||||||
chr2:131064749
|
T | C | 4 | a0001c0001t0007g0017a0001c0001t0007g0149a0001c0001t0007g0150others(1): Show | 5 | HG01243.hp2 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.154+7106A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131064749 | ||||||
chr2:131064879
|
T | A | 28 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0019others(25): Show | 36 | HG00280.hp1 HG00544.hp2 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.154+6976A>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131064879 | ||||||
chr2:131064935
|
T | G | 1 | a0001c0001t0024g0206 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.154+6920A>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131064935 | ||||||
chr2:131064976
|
C | T | 1 | a0001c0001t0002g0181 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.154+6879G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131064976 | ||||||
chr2:131064993
|
A | G | 3 | a0001c0001t0009g0020a0001c0001t0009g0195a0001c0001t0026g0194 | 4 | HG01175.hp2 HG01261.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.154+6862T>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131064993 | ||||||
chr2:131065034
|
A | G | 79 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0019others(76): Show | 103 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.154+6821T>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131065034 | ||||||
chr2:131065055
|
T | C | 1 | a0001c0001t0002g0185 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.154+6800A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131065055 | ||||||
chr2:131065085
|
G | A | 2 | a0001c0001t0002g0136a0001c0001t0002g0137 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.154+6770C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131065085 | ||||||
chr2:131065295
|
A | AT | 8 | a0001c0001t0004g0010a0001c0001t0004g0207a0001c0001t0004g0208others(5): Show | 11 | HG02109.hp1 HG02280.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.154+6559dupA | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131065295 | ||||||
chr2:131065420
|
C | T | 2 | a0001c0001t0001g0074a0001c0001t0001g0086 | 2 | HG00741.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.154+6435G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131065420 | ||||||
chr2:131065511
|
G | A | 2 | a0001c0001t0001g0085a0001c0001t0001g0100 | 2 | HG00642.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.154+6344C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131065511 | ||||||
chr2:131065563
|
C | T | 9 | a0001c0001t0004g0010a0001c0001t0004g0207a0001c0001t0004g0208others(6): Show | 12 | HG02109.hp1 HG02280.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.154+6292G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131065563 | ||||||
chr2:131065564
|
G | A | 2 | a0001c0001t0005g0018a0001c0001t0005g0163 | 3 | HG02630.hp2 HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.154+6291C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131065564 | ||||||
chr2:131065619
|
G | A | 1 | a0001c0001t0001g0071 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.154+6236C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131065619 | ||||||
chr2:131065650
|
G | A | 2 | a0001c0001t0001g0069a0001c0001t0001g0070 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.154+6205C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131065650 | ||||||
chr2:131065703
|
C | T | 1 | a0001c0001t0001g0014 | 2 | HG00738.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.154+6152G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131065703 | ||||||
chr2:131065759
|
A | G | 1 | a0001c0001t0001g0094 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.154+6096T>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131065759 | ||||||
chr2:131065807
|
G | GA | 7 | a0001c0001t0001g0073a0001c0001t0003g0165a0001c0001t0007g0017others(4): Show | 8 | HG01243.hp2 HG01258.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.154+6047dupT | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131065807 | ||||||
chr2:131065878
|
C | G | 6 | a0001c0001t0006g0022a0001c0001t0006g0201a0001c0001t0006g0202others(3): Show | 7 | HG01257.hp1 HG01258.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.154+5977G>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131065878 | ||||||
chr2:131065955
|
C | T | 1 | a0001c0001t0005g0155 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.154+5900G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131065955 | ||||||
chr2:131066017
|
G | A | 1 | a0001c0001t0001g0133 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.154+5838C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131066017 | ||||||
chr2:131066050
|
T | C | 52 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0019others(49): Show | 69 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.154+5805A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131066050 | ||||||
chr2:131066161
|
C | CT | 70 | a0001c0001t0001g0062a0001c0001t0001g0129a0001c0001t0001g0130others(67): Show | 86 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.154+5693dupA | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131066161 | ||||||
chr2:131066161
|
CT | C | 5 | a0001c0001t0001g0013a0001c0001t0001g0061a0001c0001t0001g0068others(2): Show | 6 | HG02717.hp2 HG02886.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.154+5693delA | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131066161 | ||||||
chr2:131066205
|
G | A | 1 | a0001c0001t0005g0162 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.154+5650C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131066205 | ||||||
chr2:131066337
|
G | A | 7 | a0001c0001t0006g0022a0001c0001t0006g0201a0001c0001t0006g0202others(4): Show | 8 | HG01257.hp1 HG01258.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.154+5518C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131066337 | ||||||
chr2:131066471
|
G | A | 4 | a0001c0001t0001g0103a0001c0001t0001g0128a0001c0001t0008g0054others(1): Show | 4 | HG02080.hp2 HG03516.hp2 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.154+5384C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131066471 | ||||||
chr2:131066520
|
A | C | 1 | a0001c0001t0001g0058 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.154+5335T>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131066520 | ||||||
chr2:131066567
|
C | G | 1 | a0001c0001t0031g0045 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.154+5288G>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131066567 | ||||||
chr2:131066661
|
T | C | 1 | a0001c0001t0001g0140 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.154+5194A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131066661 | ||||||
chr2:131066712
|
G | T | 1 | a0001c0001t0006g0203 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.154+5143C>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131066712 | ||||||
chr2:131066917
|
T | C | 2 | a0001c0001t0001g0074a0001c0001t0001g0086 | 2 | HG00741.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.154+4938A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131066917 | ||||||
chr2:131067285
|
C | T | 3 | a0001c0001t0013g0024a0001c0001t0013g0174a0001c0001t0013g0175 | 3 | HG02055.hp1 HG02109.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.154+4570G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131067285 | ||||||
chr2:131067315
|
T | A | 1 | a0001c0001t0001g0039 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.154+4540A>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131067315 | ||||||
chr2:131067346
|
C | T | 1 | a0001c0001t0010g0009 | 3 | HG02615.hp1 HG02976.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.154+4509G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131067346 | ||||||
chr2:131067358
|
A | G | 1 | a0001c0001t0001g0076 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.154+4497T>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131067358 | ||||||
chr2:131067523
|
T | C | 5 | a0001c0001t0001g0079a0001c0001t0001g0088a0001c0001t0001g0101others(2): Show | 5 | HG01934.hp1 HG01975.hp1 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.154+4332A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131067523 | ||||||
chr2:131067723
|
T | TCA | 3 | a0001c0001t0002g0187a0001c0001t0007g0017a0001c0001t0021g0186 | 4 | HG02818.hp2 HG03486.hp1 NA18968.hp1 others(1): Show |
intron_variant | MODIFIER | c.154+4130_154+4131d others(4): Show |
FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131067723 | ||||||
chr2:131067770
|
G | A | 7 | a0001c0001t0009g0020a0001c0001t0009g0195a0001c0001t0012g0021others(4): Show | 9 | HG01175.hp2 HG01261.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.154+4085C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131067770 | ||||||
chr2:131067947
|
G | T | 7 | a0001c0001t0009g0020a0001c0001t0009g0195a0001c0001t0012g0021others(4): Show | 9 | HG01175.hp2 HG01261.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.154+3908C>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131067947 | ||||||
chr2:131067988
|
G | A | 1 | a0001c0001t0001g0080 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.154+3867C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131067988 | ||||||
chr2:131068080
|
C | G | 6 | a0001c0001t0006g0022a0001c0001t0006g0201a0001c0001t0006g0202others(3): Show | 7 | HG01257.hp1 HG01258.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.154+3775G>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131068080 | ||||||
chr2:131068305
|
T | A | 1 | a0001c0001t0001g0139 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.154+3550A>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131068305 | ||||||
chr2:131068457
|
G | A | 1 | a0001c0001t0025g0134 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.154+3398C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131068457 | ||||||
chr2:131068522
|
T | C | 1 | a0001c0001t0001g0140 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.154+3333A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131068522 | ||||||
chr2:131068742
|
A | G | 1 | a0001c0001t0001g0088 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.154+3113T>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131068742 | ||||||
chr2:131068825
|
A | G | 8 | a0001c0001t0004g0010a0001c0001t0004g0207a0001c0001t0004g0208others(5): Show | 11 | HG02109.hp1 HG02280.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.154+3030T>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131068825 | ||||||
chr2:131068886
|
T | C | 5 | a0001c0001t0007g0017a0001c0001t0007g0149a0001c0001t0007g0150others(2): Show | 6 | HG01243.hp2 HG02258.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.154+2969A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131068886 | ||||||
chr2:131068983
|
T | C | 9 | a0001c0001t0004g0010a0001c0001t0004g0207a0001c0001t0004g0208others(6): Show | 12 | HG02109.hp1 HG02280.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.154+2872A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131068983 | ||||||
chr2:131068999
|
G | C | 7 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0144others(4): Show | 7 | HG01884.hp2 HG02630.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.154+2856C>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131068999 | ||||||
chr2:131069307
|
G | A | 7 | a0001c0001t0009g0020a0001c0001t0009g0195a0001c0001t0012g0021others(4): Show | 9 | HG01175.hp2 HG01261.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.154+2548C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131069307 | ||||||
chr2:131069320
|
C | T | 7 | a0001c0001t0009g0020a0001c0001t0009g0195a0001c0001t0012g0021others(4): Show | 9 | HG01175.hp2 HG01261.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.154+2535G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131069320 | ||||||
chr2:131069510
|
T | G | 52 | a0001c0001t0001g0051a0001c0001t0002g0003a0001c0001t0002g0005others(49): Show | 69 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.154+2345A>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131069510 | ||||||
chr2:131069511
|
G | T | 1 | a0001c0001t0001g0081 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.154+2344C>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131069511 | ||||||
chr2:131069524
|
T | C | 79 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0019others(76): Show | 103 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.154+2331A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131069524 | ||||||
chr2:131069555
|
G | A | 1 | a0001c0001t0001g0074 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.154+2300C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131069555 | ||||||
chr2:131069784
|
C | T | 1 | a0001c0001t0002g0180 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.154+2071G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131069784 | ||||||
chr2:131069903
|
G | C | 1 | a0001c0001t0001g0059 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.154+1952C>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131069903 | ||||||
chr2:131070000
|
C | T | 2 | a0001c0001t0001g0048a0001c0001t0001g0097 | 2 | HG03831.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.154+1855G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131070000 | ||||||
chr2:131070041
|
T | C | 1 | a0001c0001t0001g0110 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.154+1814A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131070041 | ||||||
chr2:131071023
|
A | G | 1 | a0001c0001t0008g0053 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.154+832T>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131071023 | ||||||
chr2:131071065
|
C | T | 13 | a0001c0001t0003g0004a0001c0001t0003g0016a0001c0001t0003g0157others(10): Show | 18 | HG01243.hp1 HG01891.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.154+790G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131071065 | ||||||
chr2:131071337
|
G | A | 1 | a0001c0001t0005g0163 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.154+518C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131071337 | ||||||
chr2:131071379
|
G | A | 7 | a0001c0001t0009g0020a0001c0001t0009g0195a0001c0001t0012g0021others(4): Show | 9 | HG01175.hp2 HG01261.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.154+476C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131071379 | ||||||
chr2:131071469
|
C | T | 5 | a0001c0001t0001g0079a0001c0001t0001g0088a0001c0001t0001g0101others(2): Show | 5 | HG01934.hp1 HG01975.hp1 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.154+386G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131071469 | ||||||
chr2:131071476
|
A | T | 4 | a0001c0001t0007g0017a0001c0001t0007g0149a0001c0001t0007g0150others(1): Show | 5 | HG01243.hp2 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.154+379T>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131071476 | ||||||
chr2:131071522
|
C | G | 2 | a0001c0001t0001g0050a0001c0001t0029g0112 | 2 | NA18995.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.154+333G>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131071522 | ||||||
chr2:131071576
|
T | C | 1 | a0001c0001t0002g0192 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.154+279A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131071576 | ||||||
chr2:131071579
|
C | G | 1 | a0001c0001t0001g0068 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.154+276G>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131071579 | ||||||
chr2:131071815
|
C | A | 4 | a0001c0001t0001g0073a0001c0001t0001g0095a0001c0001t0001g0104others(1): Show | 4 | HG01258.hp1 HG03492.hp1 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.154+40G>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131071815 | ||||||
chr2:131071841
|
C | T | 2 | a0001c0001t0001g0146a0001c0001t0001g0147 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.154+14G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 3/6 | chr2 | 131071841 | ||||||
chr2:131071984
|
G | GACAC | 24 | a0001c0001t0004g0010a0001c0001t0004g0207a0001c0001t0004g0208others(21): Show | 32 | HG01175.hp2 HG01257.hp1 HG01258.hp2 others(29): Show |
intron_variant | MODIFIER | c.71-47_71-46insGTGT | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131071984 | ||||||
chr2:131071987
|
A | ACACC | 51 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0019others(48): Show | 66 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.71-50_71-49insGGTG | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131071987 | ||||||
chr2:131072267
|
G | A | 1 | a0001c0001t0015g0166 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.71-329C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131072267 | ||||||
chr2:131072307
|
A | G | 4 | a0001c0001t0012g0021a0001c0001t0012g0196a0001c0001t0014g0197others(1): Show | 5 | HG02257.hp2 HG02622.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.71-369T>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131072307 | ||||||
chr2:131072346
|
A | C | 6 | a0001c0001t0006g0022a0001c0001t0006g0201a0001c0001t0006g0202others(3): Show | 7 | HG01257.hp1 HG01258.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.71-408T>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131072346 | ||||||
chr2:131072393
|
G | C | 7 | a0001c0001t0006g0022a0001c0001t0006g0201a0001c0001t0006g0202others(4): Show | 8 | HG01257.hp1 HG01258.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.71-455C>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131072393 | ||||||
chr2:131072464
|
T | A | 7 | a0001c0001t0006g0022a0001c0001t0006g0201a0001c0001t0006g0202others(4): Show | 8 | HG01257.hp1 HG01258.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.71-526A>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131072464 | ||||||
chr2:131072601
|
G | C | 7 | a0001c0001t0006g0022a0001c0001t0006g0201a0001c0001t0006g0202others(4): Show | 8 | HG01257.hp1 HG01258.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.71-663C>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131072601 | ||||||
chr2:131072626
|
T | A | 4 | a0001c0001t0007g0017a0001c0001t0007g0149a0001c0001t0007g0150others(1): Show | 5 | HG01243.hp2 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.71-688A>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131072626 | ||||||
chr2:131072741
|
G | A | 52 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0019others(49): Show | 69 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.71-803C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131072741 | ||||||
chr2:131072749
|
G | A | 3 | a0001c0001t0013g0024a0001c0001t0013g0174a0001c0001t0013g0175 | 3 | HG02055.hp1 HG02109.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.71-811C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131072749 | ||||||
chr2:131073086
|
C | T | 23 | a0001c0001t0004g0010a0001c0001t0004g0207a0001c0001t0004g0208others(20): Show | 29 | HG01175.hp2 HG01257.hp1 HG01258.hp2 others(26): Show |
intron_variant | MODIFIER | c.71-1148G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131073086 | ||||||
chr2:131073137
|
C | T | 1 | a0001c0001t0025g0134 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.71-1199G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131073137 | ||||||
chr2:131073431
|
C | T | 9 | a0001c0001t0004g0010a0001c0001t0004g0207a0001c0001t0004g0208others(6): Show | 12 | HG02109.hp1 HG02280.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.71-1493G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131073431 | ||||||
chr2:131073585
|
G | A | 1 | a0001c0001t0001g0052 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.71-1647C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131073585 | ||||||
chr2:131073661
|
T | C | 1 | a0001c0001t0006g0203 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.71-1723A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131073661 | ||||||
chr2:131073802
|
T | C | 1 | a0001c0001t0002g0190 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.71-1864A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131073802 | ||||||
chr2:131073966
|
A | G | 1 | a0001c0001t0001g0129 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.71-2028T>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131073966 | ||||||
chr2:131073974
|
T | C | 1 | a0001c0001t0001g0108 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.71-2036A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131073974 | ||||||
chr2:131074005
|
G | A | 2 | a0001c0001t0008g0054a0001c0001t0008g0055 | 2 | HG03516.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.71-2067C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131074005 | ||||||
chr2:131074030
|
G | A | 1 | a0001c0001t0031g0045 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.71-2092C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131074030 | ||||||
chr2:131074094
|
G | A | 3 | a0001c0001t0009g0020a0001c0001t0009g0195a0001c0001t0026g0194 | 4 | HG01175.hp2 HG01261.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.71-2156C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131074094 | ||||||
chr2:131074138
|
C | CT | 8 | a0001c0001t0001g0043a0001c0001t0001g0108a0001c0001t0007g0017others(5): Show | 9 | HG01243.hp2 HG01891.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.71-2201dupA | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131074138 | ||||||
chr2:131074178
|
G | C | 2 | a0001c0001t0008g0054a0001c0001t0008g0055 | 2 | HG03516.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.71-2240C>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131074178 | ||||||
chr2:131074246
|
A | G | 1 | a0001c0001t0001g0129 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.71-2308T>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131074246 | ||||||
chr2:131074270
|
G | A | 1 | a0001c0001t0015g0166 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.71-2332C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131074270 | ||||||
chr2:131074379
|
G | A | 6 | a0001c0001t0006g0022a0001c0001t0006g0201a0001c0001t0006g0202others(3): Show | 7 | HG01257.hp1 HG01258.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.71-2441C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131074379 | ||||||
chr2:131074410
|
A | G | 52 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0019others(49): Show | 69 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.71-2472T>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131074410 | ||||||
chr2:131074433
|
C | T | 7 | a0001c0001t0009g0020a0001c0001t0009g0195a0001c0001t0012g0021others(4): Show | 9 | HG01175.hp2 HG01261.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.71-2495G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131074433 | ||||||
chr2:131074434
|
G | A | 2 | a0001c0001t0001g0069a0001c0001t0001g0070 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.71-2496C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131074434 | ||||||
chr2:131074596
|
G | A | 1 | a0001c0001t0001g0090 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.71-2658C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131074596 | ||||||
chr2:131074647
|
A | C | 4 | a0001c0001t0004g0010a0001c0001t0004g0210a0001c0001t0004g0211others(1): Show | 6 | HG02109.hp1 HG02559.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.71-2709T>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131074647 | ||||||
chr2:131074686
|
A | G | 1 | a0001c0001t0031g0045 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.71-2748T>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131074686 | ||||||
chr2:131074812
|
C | T | 1 | a0001c0001t0001g0080 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.71-2874G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131074812 | ||||||
chr2:131074813
|
G | C | 3 | a0001c0001t0013g0024a0001c0001t0013g0174a0001c0001t0013g0175 | 3 | HG02055.hp1 HG02109.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.71-2875C>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131074813 | ||||||
chr2:131074826
|
T | A | 1 | a0001c0001t0024g0206 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.71-2888A>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131074826 | ||||||
chr2:131075015
|
C | T | 4 | a0001c0001t0007g0017a0001c0001t0007g0149a0001c0001t0007g0150others(1): Show | 5 | HG01243.hp2 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.71-3077G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131075015 | ||||||
chr2:131075076
|
G | C | 8 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(5): Show | 8 | HG01884.hp2 HG02630.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.71-3138C>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131075076 | ||||||
chr2:131075213
|
TG | T | 8 | a0001c0001t0004g0010a0001c0001t0004g0207a0001c0001t0004g0208others(5): Show | 11 | HG02109.hp1 HG02280.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.71-3276delC | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131075213 | ||||||
chr2:131075275
|
T | A | 32 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0032others(29): Show | 42 | HG00558.hp1 HG00639.hp2 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.71-3337A>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131075275 | ||||||
chr2:131075275
|
T | TA | 51 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0019others(48): Show | 68 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.71-3338dupT | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131075275 | ||||||
chr2:131075275
|
TA | T | 6 | a0001c0001t0001g0013a0001c0001t0001g0039a0001c0001t0001g0061others(3): Show | 7 | HG01069.hp1 HG01884.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.71-3338delT | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131075275 | ||||||
chr2:131075499
|
C | CT | 14 | a0001c0001t0001g0108a0001c0001t0004g0010a0001c0001t0004g0207others(11): Show | 18 | HG01257.hp1 HG01258.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.71-3562dupA | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131075499 | ||||||
chr2:131075499
|
CT | C | 7 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0038others(4): Show | 7 | HG02055.hp2 HG02895.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.71-3562delA | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131075499 | ||||||
chr2:131075536
|
CCA | C | 8 | a0001c0001t0004g0010a0001c0001t0004g0207a0001c0001t0004g0208others(5): Show | 11 | HG02109.hp1 HG02280.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.71-3600_71-3599del others(2): Show |
FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131075536 | ||||||
chr2:131075627
|
T | C | 7 | a0001c0001t0009g0020a0001c0001t0009g0195a0001c0001t0012g0021others(4): Show | 9 | HG01175.hp2 HG01261.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.71-3689A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131075627 | ||||||
chr2:131075644
|
G | A | 1 | a0001c0001t0001g0087 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.71-3706C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131075644 | ||||||
chr2:131075706
|
T | G | 1 | a0001c0001t0001g0038 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.71-3768A>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131075706 | ||||||
chr2:131075731
|
G | A | 7 | a0001c0001t0006g0022a0001c0001t0006g0201a0001c0001t0006g0202others(4): Show | 8 | HG01257.hp1 HG01258.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.71-3793C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131075731 | ||||||
chr2:131075783
|
C | T | 3 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140 | 3 | HG00735.hp2 HG02717.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.71-3845G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131075783 | ||||||
chr2:131075816
|
T | C | 1 | a0001c0001t0001g0015 | 2 | HG03017.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.71-3878A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131075816 | ||||||
chr2:131075843
|
G | A | 1 | a0001c0001t0004g0209 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.71-3905C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131075843 | ||||||
chr2:131075967
|
C | T | 1 | a0001c0001t0024g0206 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.71-4029G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131075967 | ||||||
chr2:131076050
|
G | A | 9 | a0001c0001t0003g0156a0001c0001t0003g0164a0001c0001t0003g0165others(6): Show | 11 | HG00099.hp1 HG00642.hp1 HG00741.hp2 others(8): Show |
intron_variant | MODIFIER | c.71-4112C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131076050 | ||||||
chr2:131076130
|
C | T | 7 | a0001c0001t0009g0020a0001c0001t0009g0195a0001c0001t0012g0021others(4): Show | 9 | HG01175.hp2 HG01261.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.71-4192G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131076130 | ||||||
chr2:131076185
|
T | C | 95 | a0001c0001t0001g0129a0001c0001t0001g0138a0001c0001t0001g0139others(92): Show | 119 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(116): Show |
intron_variant | MODIFIER | c.71-4247A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131076185 | ||||||
chr2:131076249
|
C | T | 5 | a0001c0001t0006g0022a0001c0001t0006g0201a0001c0001t0006g0202others(2): Show | 6 | HG01257.hp1 HG01258.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.71-4311G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131076249 | ||||||
chr2:131076319
|
CCTACATC others(4): Show |
C | 7 | a0001c0001t0009g0020a0001c0001t0009g0195a0001c0001t0012g0021others(4): Show | 9 | HG01175.hp2 HG01261.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.71-4392_71-4382del others(11): Show |
FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131076319 | ||||||
chr2:131076457
|
T | C | 79 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0019others(76): Show | 103 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.71-4519A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131076457 | ||||||
chr2:131076563
|
G | A | 1 | a0001c0001t0024g0206 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.71-4625C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131076563 | ||||||
chr2:131076652
|
T | TA | 32 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(29): Show | 38 | HG01257.hp1 HG01258.hp2 HG01261.hp2 others(35): Show |
intron_variant | MODIFIER | c.71-4715dupT | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131076652 | ||||||
chr2:131076652
|
TA | T | 7 | a0001c0001t0001g0079a0001c0001t0001g0200a0001c0001t0002g0179others(4): Show | 8 | HG01975.hp1 HG02040.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.71-4715delT | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131076652 | ||||||
chr2:131076690
|
A | T | 1 | a0001c0001t0001g0121 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.71-4752T>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131076690 | ||||||
chr2:131076707
|
A | T | 1 | a0001c0001t0022g0064 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.71-4769T>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131076707 | ||||||
chr2:131076716
|
T | A | 7 | a0001c0001t0006g0022a0001c0001t0006g0201a0001c0001t0006g0202others(4): Show | 8 | HG01257.hp1 HG01258.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.71-4778A>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131076716 | ||||||
chr2:131076834
|
C | T | 1 | a0001c0001t0001g0078 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.71-4896G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131076834 | ||||||
chr2:131076956
|
G | A | 2 | a0001c0001t0001g0088a0001c0001t0033g0113 | 2 | NA18951.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.71-5018C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131076956 | ||||||
chr2:131077003
|
C | A | 1 | a0001c0001t0002g0187 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.71-5065G>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131077003 | ||||||
chr2:131077045
|
G | A | 52 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0019others(49): Show | 69 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.71-5107C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131077045 | ||||||
chr2:131077058
|
G | A | 2 | a0001c0001t0001g0089a0001c0001t0001g0090 | 2 | NA18992.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.71-5120C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131077058 | ||||||
chr2:131077175
|
A | C | 5 | a0001c0001t0001g0129a0001c0001t0008g0053a0001c0001t0008g0054others(2): Show | 5 | HG01109.hp2 HG02258.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.71-5237T>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131077175 | ||||||
chr2:131077212
|
T | TA | 9 | a0001c0001t0001g0071a0001c0001t0001g0091a0001c0001t0001g0121others(6): Show | 12 | HG01243.hp2 HG02055.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.71-5275dupT | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131077212 | ||||||
chr2:131077212
|
TA | T | 67 | a0001c0001t0001g0033a0001c0001t0001g0063a0001c0001t0001g0069others(64): Show | 85 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.71-5275delT | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131077212 | ||||||
chr2:131077212
|
TAAAAAAA others(3): Show |
T | 1 | a0001c0001t0001g0037 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.71-5284_71-5275del others(10): Show |
FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131077212 | ||||||
chr2:131077213
|
A | G | 6 | a0001c0001t0006g0022a0001c0001t0006g0201a0001c0001t0006g0202others(3): Show | 7 | HG01257.hp1 HG01258.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.71-5275T>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131077213 | ||||||
chr2:131077333
|
G | A | 1 | a0001c0001t0024g0206 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.70+5244C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131077333 | ||||||
chr2:131077346
|
T | G | 1 | a0001c0001t0002g0153 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.70+5231A>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131077346 | ||||||
chr2:131077555
|
C | A | 1 | a0001c0001t0001g0114 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.70+5022G>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131077555 | ||||||
chr2:131077741
|
A | T | 2 | a0001c0001t0014g0197a0001c0001t0014g0198 | 2 | HG02257.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.70+4836T>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131077741 | ||||||
chr2:131077853
|
T | C | 4 | a0001c0001t0007g0017a0001c0001t0007g0149a0001c0001t0007g0150others(1): Show | 5 | HG01243.hp2 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.70+4724A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131077853 | ||||||
chr2:131077981
|
A | G | 7 | a0001c0001t0006g0022a0001c0001t0006g0201a0001c0001t0006g0202others(4): Show | 8 | HG01257.hp1 HG01258.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.70+4596T>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131077981 | ||||||
chr2:131078023
|
T | C | 1 | a0001c0001t0031g0045 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.70+4554A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131078023 | ||||||
chr2:131078082
|
A | T | 7 | a0001c0001t0009g0020a0001c0001t0009g0195a0001c0001t0012g0021others(4): Show | 9 | HG01175.hp2 HG01261.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.70+4495T>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131078082 | ||||||
chr2:131078202
|
G | A | 1 | a0001c0001t0003g0170 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.70+4375C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131078202 | ||||||
chr2:131078236
|
G | C | 7 | a0001c0001t0009g0020a0001c0001t0009g0195a0001c0001t0012g0021others(4): Show | 9 | HG01175.hp2 HG01261.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.70+4341C>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131078236 | ||||||
chr2:131078320
|
T | C | 9 | a0001c0001t0004g0010a0001c0001t0004g0207a0001c0001t0004g0208others(6): Show | 12 | HG02109.hp1 HG02280.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.70+4257A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131078320 | ||||||
chr2:131078543
|
C | G | 5 | a0001c0001t0001g0129a0001c0001t0008g0053a0001c0001t0008g0054others(2): Show | 5 | HG01109.hp2 HG02258.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.70+4034G>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131078543 | ||||||
chr2:131078700
|
T | C | 1 | a0001c0001t0001g0117 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.70+3877A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131078700 | ||||||
chr2:131078706
|
A | G | 98 | a0001c0001t0001g0129a0001c0001t0001g0138a0001c0001t0001g0139others(95): Show | 122 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(119): Show |
intron_variant | MODIFIER | c.70+3871T>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131078706 | ||||||
chr2:131078787
|
C | G | 1 | a0001c0001t0003g0170 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.70+3790G>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131078787 | ||||||
chr2:131078841
|
T | C | 1 | a0001c0001t0001g0056 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.70+3736A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131078841 | ||||||
chr2:131078925
|
T | C | 1 | a0001c0001t0001g0075 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.70+3652A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131078925 | ||||||
chr2:131078988
|
A | C | 1 | a0001c0001t0025g0134 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.70+3589T>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131078988 | ||||||
chr2:131079022
|
G | A | 3 | a0001c0001t0009g0020a0001c0001t0009g0195a0001c0001t0026g0194 | 4 | HG01175.hp2 HG01261.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.70+3555C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131079022 | ||||||
chr2:131079036
|
T | A | 1 | a0001c0001t0001g0073 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.70+3541A>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131079036 | ||||||
chr2:131079222
|
A | C | 1 | a0001c0001t0001g0107 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.70+3355T>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131079222 | ||||||
chr2:131079251
|
T | C | 1 | a0001c0001t0005g0173 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.70+3326A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131079251 | ||||||
chr2:131079339
|
G | A | 1 | a0001c0001t0024g0206 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.70+3238C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131079339 | ||||||
chr2:131079346
|
A | G | 82 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(79): Show | 106 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(103): Show |
intron_variant | MODIFIER | c.70+3231T>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131079346 | ||||||
chr2:131079507
|
G | A | 1 | a0001c0001t0001g0115 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.70+3070C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131079507 | ||||||
chr2:131079657
|
G | A | 1 | a0001c0001t0003g0167 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.70+2920C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131079657 | ||||||
chr2:131079669
|
C | A | 184 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0011others(181): Show | 224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.70+2908G>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131079669 | ||||||
chr2:131079990
|
G | A | 1 | a0001c0001t0002g0189 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.70+2587C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131079990 | ||||||
chr2:131080327
|
C | T | 4 | a0001c0001t0007g0017a0001c0001t0007g0149a0001c0001t0007g0150others(1): Show | 5 | HG01243.hp2 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.70+2250G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131080327 | ||||||
chr2:131080543
|
G | A | 1 | a0001c0001t0019g0154 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.70+2034C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131080543 | ||||||
chr2:131080762
|
C | T | 7 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0038others(4): Show | 7 | HG02055.hp2 HG02895.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.70+1815G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131080762 | ||||||
chr2:131080800
|
G | A | 1 | a0001c0001t0001g0108 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.70+1777C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131080800 | ||||||
chr2:131080801
|
C | G | 1 | a0001c0001t0008g0055 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.70+1776G>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131080801 | ||||||
chr2:131080879
|
C | A | 7 | a0001c0001t0009g0020a0001c0001t0009g0195a0001c0001t0012g0021others(4): Show | 9 | HG01175.hp2 HG01261.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.70+1698G>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131080879 | ||||||
chr2:131080934
|
T | C | 4 | a0001c0001t0007g0017a0001c0001t0007g0149a0001c0001t0007g0150others(1): Show | 5 | HG01243.hp2 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.70+1643A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131080934 | ||||||
chr2:131081005
|
C | G | 1 | a0001c0001t0001g0062 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.70+1572G>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131081005 | ||||||
chr2:131081338
|
T | G | 1 | a0001c0001t0001g0108 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.70+1239A>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131081338 | ||||||
chr2:131081417
|
C | T | 50 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0019others(47): Show | 65 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.70+1160G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131081417 | ||||||
chr2:131081889
|
A | T | 1 | a0001c0001t0002g0192 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.70+688T>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131081889 | ||||||
chr2:131082027
|
C | T | 2 | a0001c0001t0012g0021a0001c0001t0012g0196 | 3 | HG02622.hp2 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.70+550G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131082027 | ||||||
chr2:131082254
|
T | C | 1 | a0001c0001t0025g0134 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.70+323A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131082254 | ||||||
chr2:131082257
|
T | A | 1 | a0001c0001t0001g0074 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.70+320A>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131082257 | ||||||
chr2:131082347
|
G | A | 1 | a0001c0001t0002g0190 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.70+230C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131082347 | ||||||
chr2:131082389
|
A | G | 7 | a0001c0001t0009g0020a0001c0001t0009g0195a0001c0001t0012g0021others(4): Show | 9 | HG01175.hp2 HG01261.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.70+188T>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131082389 | ||||||
chr2:131082489
|
C | T | 2 | a0001c0001t0001g0039a0001c0001t0001g0040 | 2 | HG02895.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.70+88G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131082489 | ||||||
chr2:131082490
|
G | A | 1 | a0001c0001t0027g0168 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.70+87C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 2/6 | chr2 | 131082490 | ||||||
chr2:131082820
|
G | A | 1 | a0001c0001t0020g0193 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-11-163C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131082820 | ||||||
chr2:131082835
|
G | A | 1 | a0001c0001t0006g0203 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-11-178C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131082835 | ||||||
chr2:131083183
|
G | A | 9 | a0001c0001t0004g0010a0001c0001t0004g0207a0001c0001t0004g0208others(6): Show | 12 | HG02109.hp1 HG02280.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.-11-526C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131083183 | ||||||
chr2:131083197
|
T | C | 1 | a0001c0001t0031g0045 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-11-540A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131083197 | ||||||
chr2:131083348
|
G | A | 4 | a0001c0001t0007g0017a0001c0001t0007g0149a0001c0001t0007g0150others(1): Show | 5 | HG01243.hp2 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.-11-691C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131083348 | ||||||
chr2:131083358
|
A | C | 2 | a0001c0001t0001g0061a0001c0001t0001g0068 | 2 | HG02976.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-11-701T>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131083358 | ||||||
chr2:131083486
|
AGCCAAGC others(4): Show |
A | 1 | a0001c0001t0001g0116 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-11-840_-11-830del others(11): Show |
FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131083486 | ||||||
chr2:131083539
|
G | A | 3 | a0001c0001t0009g0020a0001c0001t0009g0195a0001c0001t0026g0194 | 4 | HG01175.hp2 HG01261.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.-11-882C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131083539 | ||||||
chr2:131083654
|
A | T | 1 | a0001c0001t0001g0075 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-11-997T>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131083654 | ||||||
chr2:131083845
|
T | A | 1 | a0001c0001t0001g0138 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-11-1188A>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131083845 | ||||||
chr2:131083874
|
G | GTATT | 7 | a0001c0001t0001g0025a0001c0001t0001g0031a0001c0001t0001g0059others(4): Show | 7 | HG01261.hp1 HG01517.hp2 HG02129.hp1 others(4): Show |
intron_variant | MODIFIER | c.-11-1221_-11-1218d others(6): Show |
FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131083874 | ||||||
chr2:131083874
|
GTATT | G | 37 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0035others(34): Show | 44 | HG00735.hp2 HG01069.hp2 HG01071.hp2 others(41): Show |
intron_variant | MODIFIER | c.-11-1221_-11-1218d others(6): Show |
FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131083874 | ||||||
chr2:131083874
|
GTATTTAT others(1): Show |
G | 64 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0094others(61): Show | 78 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.-11-1225_-11-1218d others(10): Show |
FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131083874 | ||||||
chr2:131083874
|
GTATTTAT others(5): Show |
G | 6 | a0001c0001t0006g0022a0001c0001t0006g0201a0001c0001t0006g0202others(3): Show | 7 | HG01257.hp1 HG01258.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.-11-1229_-11-1218d others(14): Show |
FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131083874 | ||||||
chr2:131083874
|
GTATTTAT others(9): Show |
G | 8 | a0001c0001t0009g0020a0001c0001t0009g0195a0001c0001t0012g0021others(5): Show | 10 | HG01175.hp2 HG01261.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.-11-1233_-11-1218d others(18): Show |
FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131083874 | ||||||
chr2:131083930
|
A | C | 4 | a0001c0001t0001g0129a0001c0001t0008g0053a0001c0001t0008g0054others(1): Show | 4 | HG02258.hp1 HG03209.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11-1273T>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131083930 | ||||||
chr2:131083998
|
G | C | 1 | a0001c0001t0024g0206 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-11-1341C>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131083998 | ||||||
chr2:131084052
|
G | A | 1 | a0001c0001t0001g0117 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-11-1395C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131084052 | ||||||
chr2:131084127
|
C | T | 1 | a0001c0001t0025g0134 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-11-1470G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131084127 | ||||||
chr2:131084143
|
G | A | 2 | a0001c0001t0001g0073a0001c0001t0001g0125 | 2 | HG01258.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-11-1486C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131084143 | ||||||
chr2:131084191
|
C | G | 1 | a0001c0001t0001g0035 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-11-1534G>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131084191 | ||||||
chr2:131084197
|
C | A | 9 | a0001c0001t0001g0099a0001c0001t0003g0159a0001c0001t0006g0022others(6): Show | 10 | HG01257.hp1 HG01258.hp2 HG02148.hp2 others(7): Show |
intron_variant | MODIFIER | c.-11-1540G>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131084197 | ||||||
chr2:131084198
|
A | C | 2 | a0001c0001t0001g0029a0001c0001t0001g0030 | 2 | NA18971.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.-11-1541T>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131084198 | ||||||
chr2:131084235
|
G | A | 1 | a0001c0001t0008g0055 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-11-1578C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131084235 | ||||||
chr2:131084239
|
G | A | 1 | a0001c0001t0005g0173 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-11-1582C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131084239 | ||||||
chr2:131084378
|
T | A | 7 | a0001c0001t0006g0022a0001c0001t0006g0201a0001c0001t0006g0202others(4): Show | 8 | HG01257.hp1 HG01258.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.-11-1721A>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131084378 | ||||||
chr2:131084448
|
C | A | 54 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0019others(51): Show | 71 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.-11-1791G>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131084448 | ||||||
chr2:131084500
|
A | G | 1 | a0001c0001t0003g0016 | 2 | HG02257.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-11-1843T>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131084500 | ||||||
chr2:131084581
|
A | G | 8 | a0001c0001t0004g0010a0001c0001t0004g0207a0001c0001t0004g0208others(5): Show | 11 | HG02109.hp1 HG02280.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.-11-1924T>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131084581 | ||||||
chr2:131084606
|
G | T | 5 | a0001c0001t0006g0022a0001c0001t0006g0201a0001c0001t0006g0202others(2): Show | 6 | HG01257.hp1 HG01258.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-11-1949C>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131084606 | ||||||
chr2:131084880
|
G | T | 2 | a0001c0001t0002g0019a0001c0001t0002g0177 | 3 | HG00280.hp1 HG01192.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.-11-2223C>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131084880 | ||||||
chr2:131085297
|
A | G | 4 | a0001c0001t0001g0073a0001c0001t0001g0095a0001c0001t0001g0104others(1): Show | 4 | HG01258.hp1 HG03492.hp1 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11-2640T>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131085297 | ||||||
chr2:131085408
|
A | G | 3 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140 | 3 | HG00735.hp2 HG02717.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-11-2751T>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131085408 | ||||||
chr2:131085522
|
C | T | 1 | a0001c0001t0001g0058 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-11-2865G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131085522 | ||||||
chr2:131085585
|
C | T | 1 | a0001c0001t0001g0049 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-11-2928G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131085585 | ||||||
chr2:131085686
|
C | T | 1 | a0001c0001t0025g0134 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-11-3029G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131085686 | ||||||
chr2:131085706
|
ACTGT | A | 9 | a0001c0001t0004g0010a0001c0001t0004g0207a0001c0001t0004g0208others(6): Show | 12 | HG02109.hp1 HG02280.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.-11-3053_-11-3050d others(6): Show |
FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131085706 | ||||||
chr2:131086038
|
T | C | 7 | a0001c0001t0006g0022a0001c0001t0006g0201a0001c0001t0006g0202others(4): Show | 8 | HG01257.hp1 HG01258.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.-11-3381A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131086038 | ||||||
chr2:131086312
|
A | G | 3 | a0001c0001t0001g0006a0001c0001t0001g0072a0001c0001t0001g0099 | 5 | HG01255.hp1 HG01934.hp2 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.-11-3655T>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131086312 | ||||||
chr2:131086551
|
G | A | 1 | a0001c0001t0025g0134 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-11-3894C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131086551 | ||||||
chr2:131086578
|
T | C | 2 | a0001c0001t0001g0095a0001c0001t0001g0104 | 2 | HG03492.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.-11-3921A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131086578 | ||||||
chr2:131086644
|
A | C | 2 | a0001c0001t0001g0029a0001c0001t0001g0030 | 2 | NA18971.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.-11-3987T>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131086644 | ||||||
chr2:131086647
|
T | A | 69 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0011others(66): Show | 84 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.-11-3990A>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131086647 | ||||||
chr2:131086721
|
T | C | 1 | a0001c0001t0001g0108 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-11-4064A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131086721 | ||||||
chr2:131086766
|
TAAGAGTC others(310): Show |
T | 27 | a0001c0001t0004g0010a0001c0001t0004g0207a0001c0001t0004g0208others(24): Show | 34 | HG01175.hp2 HG01243.hp2 HG01257.hp1 others(31): Show |
intron_variant | MODIFIER | c.-11-4426_-11-4110d others(2): Show |
FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131086766 | ||||||
chr2:131086781
|
AAAGGCCG others(312): Show |
A | 55 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0019others(52): Show | 72 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.-11-4443_-11-4125d others(2): Show |
FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131086781 | ||||||
chr2:131086838
|
G | T | 3 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140 | 3 | HG00735.hp2 HG02717.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-11-4181C>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131086838 | ||||||
chr2:131086858
|
G | A | 1 | a0001c0001t0001g0050 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.-11-4201C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131086858 | ||||||
chr2:131086981
|
T | C | 19 | a0001c0001t0001g0043a0001c0001t0001g0108a0001c0001t0001g0138others(16): Show | 19 | HG00735.hp2 HG01109.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.-11-4324A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131086981 | ||||||
chr2:131087030
|
C | A | 2 | a0001c0001t0001g0096a0001c0001t0001g0110 | 2 | HG02723.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-11-4373G>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131087030 | ||||||
chr2:131087044
|
C | T | 1 | a0001c0001t0001g0118 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-11-4387G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131087044 | ||||||
chr2:131087045
|
G | A | 1 | a0001c0001t0001g0033 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.-11-4388C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131087045 | ||||||
chr2:131087063
|
C | CA | 93 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(90): Show | 117 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.-11-4407dupT | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131087063 | ||||||
chr2:131087063
|
C | CAA | 18 | a0001c0001t0001g0027a0001c0001t0001g0031a0001c0001t0001g0042others(15): Show | 18 | HG01261.hp1 HG01884.hp1 HG01934.hp1 others(15): Show |
intron_variant | MODIFIER | c.-11-4408_-11-4407d others(4): Show |
FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131087063 | ||||||
chr2:131087063
|
C | CAAAAAAA others(6): Show |
1 | a0001c0001t0001g0143 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-11-4419_-11-4407d others(15): Show |
FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131087063 | ||||||
chr2:131087063
|
C | CAAAAAAA others(10): Show |
1 | a0001c0001t0008g0053 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-11-4423_-11-4407d others(19): Show |
FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131087063 | ||||||
chr2:131087063
|
C | CAAAAAAA others(11): Show |
3 | a0001c0001t0001g0144a0001c0001t0008g0054a0001c0001t0008g0055 | 3 | HG01884.hp2 HG03516.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-11-4424_-11-4407d others(20): Show |
FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131087063 | ||||||
chr2:131087063
|
C | CAAAAAAA others(12): Show |
1 | a0001c0001t0001g0145 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-11-4425_-11-4407d others(21): Show |
FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131087063 | ||||||
chr2:131087063
|
C | CAAAAAAA others(15): Show |
2 | a0001c0001t0001g0146a0001c0001t0001g0147 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-11-4428_-11-4407d others(24): Show |
FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131087063 | ||||||
chr2:131087063
|
C | CAAAAAAA others(16): Show |
1 | a0001c0001t0001g0141 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-11-4407_-11-4406i others(25): Show |
FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131087063 | ||||||
chr2:131087063
|
C | CAAAAAAA others(17): Show |
1 | a0001c0001t0001g0148 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-11-4407_-11-4406i others(26): Show |
FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131087063 | ||||||
chr2:131087102
|
A | T | 55 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0019others(52): Show | 72 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.-11-4445T>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131087102 | ||||||
chr2:131087177
|
G | A | 1 | a0001c0001t0001g0105 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-11-4520C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131087177 | ||||||
chr2:131087183
|
G | A | 1 | a0001c0001t0004g0212 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-11-4526C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131087183 | ||||||
chr2:131087199
|
C | T | 1 | a0001c0001t0001g0108 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-11-4542G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131087199 | ||||||
chr2:131087367
|
G | A | 1 | a0001c0001t0025g0134 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-11-4710C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131087367 | ||||||
chr2:131087467
|
G | A | 4 | a0001c0001t0007g0017a0001c0001t0007g0149a0001c0001t0007g0150others(1): Show | 5 | HG01243.hp2 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.-11-4810C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131087467 | ||||||
chr2:131087697
|
A | C | 1 | a0001c0001t0008g0053 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-11-5040T>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131087697 | ||||||
chr2:131087814
|
C | T | 1 | a0001c0001t0001g0056 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-11-5157G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131087814 | ||||||
chr2:131087982
|
A | C | 7 | a0001c0001t0009g0020a0001c0001t0009g0195a0001c0001t0012g0021others(4): Show | 9 | HG01175.hp2 HG01261.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.-12+5232T>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131087982 | ||||||
chr2:131088020
|
C | T | 7 | a0001c0001t0006g0022a0001c0001t0006g0201a0001c0001t0006g0202others(4): Show | 8 | HG01257.hp1 HG01258.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.-12+5194G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131088020 | ||||||
chr2:131088118
|
C | T | 4 | a0001c0001t0012g0021a0001c0001t0012g0196a0001c0001t0014g0197others(1): Show | 5 | HG02257.hp2 HG02622.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.-12+5096G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131088118 | ||||||
chr2:131088199
|
T | A | 2 | a0001c0001t0001g0106a0001c0001t0001g0107 | 2 | HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.-12+5015A>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131088199 | ||||||
chr2:131088226
|
A | G | 1 | a0001c0001t0024g0206 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-12+4988T>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131088226 | ||||||
chr2:131088250
|
GA | G | 97 | a0001c0001t0001g0130a0001c0001t0001g0138a0001c0001t0001g0139others(94): Show | 121 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(118): Show |
intron_variant | MODIFIER | c.-12+4963delT | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131088250 | ||||||
chr2:131088328
|
T | C | 9 | a0001c0001t0004g0010a0001c0001t0004g0207a0001c0001t0004g0208others(6): Show | 12 | HG02109.hp1 HG02280.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.-12+4886A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131088328 | ||||||
chr2:131088605
|
G | A | 1 | a0001c0001t0007g0017 | 2 | HG02818.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-12+4609C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131088605 | ||||||
chr2:131088629
|
G | A | 82 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0019others(79): Show | 106 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(103): Show |
intron_variant | MODIFIER | c.-12+4585C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131088629 | ||||||
chr2:131088802
|
G | A | 4 | a0001c0001t0001g0043a0001c0001t0001g0108a0001c0001t0016g0034others(1): Show | 4 | HG01891.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-12+4412C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131088802 | ||||||
chr2:131088802
|
G | C | 51 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0019others(48): Show | 66 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.-12+4412C>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131088802 | ||||||
chr2:131088959
|
G | A | 1 | a0001c0001t0001g0109 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-12+4255C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131088959 | ||||||
chr2:131088965
|
C | CT | 85 | a0001c0001t0001g0035a0001c0001t0001g0051a0001c0001t0001g0052others(82): Show | 109 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.-12+4248dupA | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131088965 | ||||||
chr2:131089029
|
C | T | 1 | a0001c0001t0003g0170 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-12+4185G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131089029 | ||||||
chr2:131089030
|
G | C | 1 | a0001c0001t0001g0110 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-12+4184C>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131089030 | ||||||
chr2:131089154
|
C | T | 1 | a0001c0001t0001g0140 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-12+4060G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131089154 | ||||||
chr2:131089471
|
G | A | 1 | a0001c0001t0007g0149 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-12+3743C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131089471 | ||||||
chr2:131089701
|
G | C | 1 | a0001c0001t0001g0032 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-12+3513C>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131089701 | ||||||
chr2:131089704
|
C | T | 1 | a0001c0001t0001g0050 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.-12+3510G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131089704 | ||||||
chr2:131089847
|
C | T | 9 | a0001c0001t0004g0010a0001c0001t0004g0207a0001c0001t0004g0208others(6): Show | 12 | HG02109.hp1 HG02280.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.-12+3367G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131089847 | ||||||
chr2:131089892
|
G | A | 50 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0019others(47): Show | 65 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.-12+3322C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131089892 | ||||||
chr2:131089933
|
G | A | 1 | a0001c0001t0003g0170 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-12+3281C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131089933 | ||||||
chr2:131090086
|
G | A | 55 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0019others(52): Show | 72 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.-12+3128C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131090086 | ||||||
chr2:131090088
|
C | T | 3 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0049 | 3 | HG03710.hp1 NA18971.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.-12+3126G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131090088 | ||||||
chr2:131090112
|
G | C | 1 | a0001c0001t0007g0017 | 2 | HG02818.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-12+3102C>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131090112 | ||||||
chr2:131090135
|
G | A | 2 | a0001c0001t0001g0111a0001c0001t0001g0122 | 2 | HG00735.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.-12+3079C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131090135 | ||||||
chr2:131090151
|
C | CA | 165 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(162): Show | 204 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.-12+3062dupT | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131090151 | ||||||
chr2:131090151
|
C | CAA | 26 | a0001c0001t0001g0007a0001c0001t0001g0114a0001c0001t0001g0115others(23): Show | 30 | HG00544.hp1 HG00741.hp2 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.-12+3061_-12+3062d others(4): Show |
FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131090151 | ||||||
chr2:131090319
|
C | CA | 14 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0142others(11): Show | 15 | HG00733.hp2 HG01258.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.-12+2894dupT | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131090319 | ||||||
chr2:131090319
|
CA | C | 81 | a0001c0001t0001g0029a0001c0001t0001g0035a0001c0001t0001g0036others(78): Show | 103 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.-12+2894delT | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131090319 | ||||||
chr2:131090319
|
CAA | C | 5 | a0001c0001t0003g0016a0001c0001t0003g0156a0001c0001t0007g0149others(2): Show | 6 | HG02257.hp1 HG02698.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.-12+2893_-12+2894d others(4): Show |
FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131090319 | ||||||
chr2:131090418
|
C | A | 1 | a0001c0001t0001g0125 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-12+2796G>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131090418 | ||||||
chr2:131090486
|
T | C | 8 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(5): Show | 8 | HG01884.hp2 HG02630.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.-12+2728A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131090486 | ||||||
chr2:131090713
|
A | C | 1 | a0001c0001t0001g0033 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.-12+2501T>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131090713 | ||||||
chr2:131090736
|
A | G | 1 | a0001c0001t0001g0032 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-12+2478T>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131090736 | ||||||
chr2:131090890
|
C | T | 1 | a0001c0001t0005g0155 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-12+2324G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131090890 | ||||||
chr2:131090974
|
C | G | 1 | a0001c0001t0001g0031 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-12+2240G>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131090974 | ||||||
chr2:131091059
|
T | C | 82 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0019others(79): Show | 106 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(103): Show |
intron_variant | MODIFIER | c.-12+2155A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131091059 | ||||||
chr2:131091318
|
G | A | 2 | a0001c0001t0001g0126a0001c0001t0008g0127 | 2 | HG01069.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.-12+1896C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131091318 | ||||||
chr2:131091318
|
G | C | 1 | a0001c0001t0025g0134 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-12+1896C>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131091318 | ||||||
chr2:131091516
|
G | C | 4 | a0001c0001t0010g0009a0001c0001t0013g0024a0001c0001t0013g0174others(1): Show | 6 | HG02055.hp1 HG02109.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12+1698C>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131091516 | ||||||
chr2:131091591
|
G | C | 28 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0019others(25): Show | 36 | HG00280.hp1 HG00544.hp2 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.-12+1623C>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131091591 | ||||||
chr2:131091595
|
C | G | 7 | a0001c0001t0009g0020a0001c0001t0009g0195a0001c0001t0012g0021others(4): Show | 9 | HG01175.hp2 HG01261.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.-12+1619G>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131091595 | ||||||
chr2:131091686
|
C | T | 2 | a0001c0001t0001g0029a0001c0001t0001g0030 | 2 | NA18971.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.-12+1528G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131091686 | ||||||
chr2:131091861
|
G | A | 1 | a0001c0001t0001g0128 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-12+1353C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131091861 | ||||||
chr2:131091965
|
T | TAA | 51 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0019others(48): Show | 67 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(64): Show |
intron_variant | MODIFIER | c.-12+1247_-12+1248d others(4): Show |
FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131091965 | ||||||
chr2:131091965
|
TA | T | 7 | a0001c0001t0009g0020a0001c0001t0009g0195a0001c0001t0012g0021others(4): Show | 9 | HG01175.hp2 HG01261.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.-12+1248delT | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131091965 | ||||||
chr2:131092004
|
C | A | 8 | a0001c0001t0004g0010a0001c0001t0004g0207a0001c0001t0004g0208others(5): Show | 11 | HG02109.hp1 HG02280.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.-12+1210G>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131092004 | ||||||
chr2:131092036
|
T | C | 4 | a0001c0001t0012g0021a0001c0001t0012g0196a0001c0001t0014g0197others(1): Show | 5 | HG02257.hp2 HG02622.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.-12+1178A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131092036 | ||||||
chr2:131092062
|
T | G | 1 | a0001c0001t0001g0129 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-12+1152A>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131092062 | ||||||
chr2:131092143
|
C | CA | 5 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0004g0210others(2): Show | 5 | HG02559.hp1 HG02572.hp1 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.-12+1070dupT | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131092143 | ||||||
chr2:131092143
|
CA | C | 5 | a0001c0001t0001g0028a0001c0001t0002g0135a0001c0001t0002g0136others(2): Show | 6 | HG01433.hp1 HG01515.hp2 HG01517.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12+1070delT | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131092143 | ||||||
chr2:131092210
|
T | C | 1 | a0001c0001t0001g0131 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-12+1004A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131092210 | ||||||
chr2:131092285
|
T | A | 1 | a0001c0001t0001g0132 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-12+929A>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131092285 | ||||||
chr2:131092366
|
C | CTTT | 23 | a0001c0001t0004g0010a0001c0001t0004g0207a0001c0001t0004g0208others(20): Show | 29 | HG01175.hp2 HG01257.hp1 HG01258.hp2 others(26): Show |
intron_variant | MODIFIER | c.-12+847_-12+848ins others(3): Show |
FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131092366 | ||||||
chr2:131092555
|
C | T | 3 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0008g0026 | 3 | HG01517.hp2 HG01884.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.-12+659G>A | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131092555 | ||||||
chr2:131092680
|
T | C | 1 | a0001c0001t0001g0133 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-12+534A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131092680 | ||||||
chr2:131092806
|
C | CA | 8 | a0001c0001t0002g0199a0001c0001t0009g0020a0001c0001t0009g0195others(5): Show | 10 | HG01175.hp2 HG01261.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.-12+407dupT | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131092806 | ||||||
chr2:131092814
|
T | A | 93 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(90): Show | 117 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(114): Show |
intron_variant | MODIFIER | c.-12+400A>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131092814 | ||||||
chr2:131092821
|
A | G | 1 | a0001c0001t0013g0024 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-12+393T>C | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131092821 | ||||||
chr2:131092863
|
C | A | 1 | a0001c0001t0001g0200 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-12+351G>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131092863 | ||||||
chr2:131092867
|
T | C | 1 | a0001c0001t0024g0206 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-12+347A>G | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131092867 | ||||||
chr2:131092962
|
G | A | 7 | a0001c0001t0006g0022a0001c0001t0006g0201a0001c0001t0006g0202others(4): Show | 8 | HG01257.hp1 HG01258.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.-12+252C>T | FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | 131092962 |