geneid | 57596 |
---|---|
ensemblid | ENSG00000183092.18 |
hgncid | 24163 |
symbol | BEGAIN |
name | brain enriched guanylate kinase associated |
refseq_nuc | NM_001385089.1 |
refseq_prot | NP_001372018.1 |
ensembl_nuc | ENST00000554140.3 |
ensembl_prot | ENSP00000451125.2 |
mane_status | MANE Select |
chr | chr14 |
start | 100537147 |
end | 100587417 |
strand | - |
ver | v1.2 |
region | chr14:100537147-100587417 |
region5000 | chr14:100532147-100592417 |
regionname0 | BEGAIN_chr14_100537147_100587417 |
regionname5000 | BEGAIN_chr14_100532147_100592417 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 612 | 320 | 96 | 57 | 128 | 9 | 28 | 85 | BEGAIN_chr14_100532147_100592417 | BEGAIN | copy fasta | chr14 | 100532147 | 100592417 |
a0002 | 0/0 | 612 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | BEGAIN_chr14_100532147_100592417 | BEGAIN | copy fasta | chr14 | 100532147 | 100592417 |
a0003 | 0/0 | 612 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | BEGAIN_chr14_100532147_100592417 | BEGAIN | copy fasta | chr14 | 100532147 | 100592417 |
a0004 | 0/0 | 616 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | BEGAIN_chr14_100532147_100592417 | BEGAIN | copy fasta | chr14 | 100532147 | 100592417 |
a0005 | 0/0 | 612 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | copy fasta | chr14 | 100532147 | 100592417 |
a0006 | 0/0 | 612 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | copy fasta | chr14 | 100532147 | 100592417 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 1839 | 157 | 39 | 36 | 72 | 2 | 8 | BEGAIN_chr14_100532147_100592417 | BEGAIN | copy fasta | chr14 | 100532147 | 100592417 |
c0002 | 1/1 | 1839 | 93 | 4 | 20 | 41 | 6 | 20 | BEGAIN_chr14_100532147_100592417 | BEGAIN | copy fasta | chr14 | 100532147 | 100592417 |
c0003 | 0/0 | 1839 | 31 | 29 | 0 | 2 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | copy fasta | chr14 | 100532147 | 100592417 |
c0004 | 0/0 | 1839 | 18 | 6 | 0 | 12 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | copy fasta | chr14 | 100532147 | 100592417 |
c0005 | 0/0 | 1839 | 13 | 13 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | copy fasta | chr14 | 100532147 | 100592417 |
c0006 | 0/0 | 1839 | 2 | 2 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | copy fasta | chr14 | 100532147 | 100592417 |
c0007 | 0/0 | 1839 | 2 | 0 | 0 | 2 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | copy fasta | chr14 | 100532147 | 100592417 |
c0008 | 0/0 | 1839 | 2 | 2 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | copy fasta | chr14 | 100532147 | 100592417 |
c0009 | 0/0 | 1839 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | copy fasta | chr14 | 100532147 | 100592417 |
c0010 | 0/0 | 1839 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | copy fasta | chr14 | 100532147 | 100592417 |
c0011 | 0/0 | 1839 | 1 | 0 | 0 | 0 | 1 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | copy fasta | chr14 | 100532147 | 100592417 |
c0012 | 0/0 | 1839 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | copy fasta | chr14 | 100532147 | 100592417 |
c0013 | 0/0 | 1839 | 1 | 0 | 0 | 0 | 1 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | copy fasta | chr14 | 100532147 | 100592417 |
c0014 | 0/0 | 1851 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | copy fasta | chr14 | 100532147 | 100592417 |
c0015 | 0/0 | 1839 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | copy fasta | chr14 | 100532147 | 100592417 |
c0016 | 0/0 | 1839 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | copy fasta | chr14 | 100532147 | 100592417 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 950 | 277 | 77 | 57 | 112 | 9 | 21 | BEGAIN_chr14_100532147_100592417 | BEGAIN | copy fasta | chr14 | 100532147 | 100592417 |
t0002 | 0/0 | 950 | 12 | 12 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | copy fasta | chr14 | 100532147 | 100592417 |
t0003 | 0/0 | 950 | 9 | 0 | 0 | 9 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | copy fasta | chr14 | 100532147 | 100592417 |
t0004 | 1/0 | 950 | 5 | 0 | 0 | 2 | 0 | 2 | BEGAIN_chr14_100532147_100592417 | BEGAIN | copy fasta | chr14 | 100532147 | 100592417 |
t0005 | 0/0 | 951 | 5 | 1 | 1 | 2 | 0 | 1 | BEGAIN_chr14_100532147_100592417 | BEGAIN | copy fasta | chr14 | 100532147 | 100592417 |
t0006 | 0/0 | 950 | 5 | 3 | 0 | 0 | 0 | 2 | BEGAIN_chr14_100532147_100592417 | BEGAIN | copy fasta | chr14 | 100532147 | 100592417 |
t0007 | 0/0 | 950 | 2 | 0 | 0 | 2 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | copy fasta | chr14 | 100532147 | 100592417 |
t0008 | 0/0 | 950 | 2 | 0 | 0 | 0 | 0 | 2 | BEGAIN_chr14_100532147_100592417 | BEGAIN | copy fasta | chr14 | 100532147 | 100592417 |
t0009 | 0/0 | 950 | 1 | 0 | 0 | 0 | 1 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | copy fasta | chr14 | 100532147 | 100592417 |
t0010 | 0/0 | 950 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | copy fasta | chr14 | 100532147 | 100592417 |
t0011 | 0/0 | 950 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | copy fasta | chr14 | 100532147 | 100592417 |
t0012 | 0/0 | 950 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | copy fasta | chr14 | 100532147 | 100592417 |
t0013 | 0/0 | 950 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | copy fasta | chr14 | 100532147 | 100592417 |
t0014 | 0/0 | 950 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | copy fasta | chr14 | 100532147 | 100592417 |
t0015 | 0/0 | 951 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | copy fasta | chr14 | 100532147 | 100592417 |
t0016 | 0/0 | 950 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | copy fasta | chr14 | 100532147 | 100592417 |
t0017 | 0/0 | 950 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | copy fasta | chr14 | 100532147 | 100592417 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 6 | 0 | 2 | 4 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0002 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0008 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0011 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0128 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0223 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 1839 | 157 | 39 | 36 | 72 | 2 | 8 | BEGAIN_chr14_100532147_100592417 | BEGAIN | copy fasta | chr14 | 100532147 | 100592417 |
a0001c0002 | 1/1 | 1839 | 93 | 4 | 20 | 41 | 6 | 20 | BEGAIN_chr14_100532147_100592417 | BEGAIN | copy fasta | chr14 | 100532147 | 100592417 |
a0001c0003 | 0/0 | 1839 | 31 | 29 | 0 | 2 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | copy fasta | chr14 | 100532147 | 100592417 |
a0001c0004 | 0/0 | 1839 | 18 | 6 | 0 | 12 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | copy fasta | chr14 | 100532147 | 100592417 |
a0001c0005 | 0/0 | 1839 | 13 | 13 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | copy fasta | chr14 | 100532147 | 100592417 |
a0001c0006 | 0/0 | 1839 | 2 | 2 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | copy fasta | chr14 | 100532147 | 100592417 |
a0001c0008 | 0/0 | 1839 | 2 | 2 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | copy fasta | chr14 | 100532147 | 100592417 |
a0001c0009 | 0/0 | 1839 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | copy fasta | chr14 | 100532147 | 100592417 |
a0001c0012 | 0/0 | 1839 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | copy fasta | chr14 | 100532147 | 100592417 |
a0001c0013 | 0/0 | 1839 | 1 | 0 | 0 | 0 | 1 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | copy fasta | chr14 | 100532147 | 100592417 |
a0001c0016 | 0/0 | 1839 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | copy fasta | chr14 | 100532147 | 100592417 |
a0002c0007 | 0/0 | 1839 | 2 | 0 | 0 | 2 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | copy fasta | chr14 | 100532147 | 100592417 |
a0003c0010 | 0/0 | 1839 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | copy fasta | chr14 | 100532147 | 100592417 |
a0004c0014 | 0/0 | 1851 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | copy fasta | chr14 | 100532147 | 100592417 |
a0005c0011 | 0/0 | 1839 | 1 | 0 | 0 | 0 | 1 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | copy fasta | chr14 | 100532147 | 100592417 |
a0006c0015 | 0/0 | 1839 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | copy fasta | chr14 | 100532147 | 100592417 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 2788 | 148 | 39 | 36 | 65 | 2 | 6 | BEGAIN_chr14_100532147_100592417 | BEGAIN | copy fasta | chr14 | 100532147 | 100592417 |
a0001c0001t0005 | 0/0 | 2789 | 2 | 0 | 0 | 2 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | copy fasta | chr14 | 100532147 | 100592417 |
a0001c0001t0007 | 0/0 | 2788 | 2 | 0 | 0 | 2 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | copy fasta | chr14 | 100532147 | 100592417 |
a0001c0001t0008 | 0/0 | 2788 | 2 | 0 | 0 | 0 | 0 | 2 | BEGAIN_chr14_100532147_100592417 | BEGAIN | copy fasta | chr14 | 100532147 | 100592417 |
a0001c0001t0011 | 0/0 | 2788 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | copy fasta | chr14 | 100532147 | 100592417 |
a0001c0001t0013 | 0/0 | 2788 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | copy fasta | chr14 | 100532147 | 100592417 |
a0001c0001t0014 | 0/0 | 2788 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | copy fasta | chr14 | 100532147 | 100592417 |
a0001c0002t0001 | 0/1 | 2788 | 82 | 4 | 19 | 37 | 6 | 15 | BEGAIN_chr14_100532147_100592417 | BEGAIN | copy fasta | chr14 | 100532147 | 100592417 |
a0001c0002t0004 | 1/0 | 2788 | 5 | 0 | 0 | 2 | 0 | 2 | BEGAIN_chr14_100532147_100592417 | BEGAIN | copy fasta | chr14 | 100532147 | 100592417 |
a0001c0002t0005 | 0/0 | 2789 | 2 | 0 | 1 | 0 | 0 | 1 | BEGAIN_chr14_100532147_100592417 | BEGAIN | copy fasta | chr14 | 100532147 | 100592417 |
a0001c0002t0006 | 0/0 | 2788 | 2 | 0 | 0 | 0 | 0 | 2 | BEGAIN_chr14_100532147_100592417 | BEGAIN | copy fasta | chr14 | 100532147 | 100592417 |
a0001c0002t0012 | 0/0 | 2788 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | copy fasta | chr14 | 100532147 | 100592417 |
a0001c0002t0015 | 0/0 | 2789 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | copy fasta | chr14 | 100532147 | 100592417 |
a0001c0003t0001 | 0/0 | 2788 | 27 | 25 | 0 | 2 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | copy fasta | chr14 | 100532147 | 100592417 |
a0001c0003t0005 | 0/0 | 2789 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | copy fasta | chr14 | 100532147 | 100592417 |
a0001c0003t0006 | 0/0 | 2788 | 3 | 3 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | copy fasta | chr14 | 100532147 | 100592417 |
a0001c0004t0001 | 0/0 | 2788 | 4 | 1 | 0 | 3 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | copy fasta | chr14 | 100532147 | 100592417 |
a0001c0004t0002 | 0/0 | 2788 | 4 | 4 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | copy fasta | chr14 | 100532147 | 100592417 |
a0001c0004t0003 | 0/0 | 2788 | 9 | 0 | 0 | 9 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | copy fasta | chr14 | 100532147 | 100592417 |
a0001c0004t0017 | 0/0 | 2788 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | copy fasta | chr14 | 100532147 | 100592417 |
a0001c0005t0001 | 0/0 | 2788 | 3 | 3 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | copy fasta | chr14 | 100532147 | 100592417 |
a0001c0005t0002 | 0/0 | 2788 | 8 | 8 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | copy fasta | chr14 | 100532147 | 100592417 |
a0001c0005t0010 | 0/0 | 2788 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | copy fasta | chr14 | 100532147 | 100592417 |
a0001c0005t0016 | 0/0 | 2788 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | copy fasta | chr14 | 100532147 | 100592417 |
a0001c0006t0001 | 0/0 | 2788 | 2 | 2 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | copy fasta | chr14 | 100532147 | 100592417 |
a0001c0008t0001 | 0/0 | 2788 | 2 | 2 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | copy fasta | chr14 | 100532147 | 100592417 |
a0001c0009t0001 | 0/0 | 2788 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | copy fasta | chr14 | 100532147 | 100592417 |
a0001c0012t0001 | 0/0 | 2788 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | copy fasta | chr14 | 100532147 | 100592417 |
a0001c0013t0001 | 0/0 | 2788 | 1 | 0 | 0 | 0 | 1 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | copy fasta | chr14 | 100532147 | 100592417 |
a0001c0016t0001 | 0/0 | 2788 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | copy fasta | chr14 | 100532147 | 100592417 |
a0002c0007t0001 | 0/0 | 2788 | 2 | 0 | 0 | 2 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | copy fasta | chr14 | 100532147 | 100592417 |
a0003c0010t0001 | 0/0 | 2788 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | copy fasta | chr14 | 100532147 | 100592417 |
a0004c0014t0001 | 0/0 | 2800 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | copy fasta | chr14 | 100532147 | 100592417 |
a0005c0011t0009 | 0/0 | 2788 | 1 | 0 | 0 | 0 | 1 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | copy fasta | chr14 | 100532147 | 100592417 |
a0006c0015t0001 | 0/0 | 2788 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | copy fasta | chr14 | 100532147 | 100592417 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 6 | 0 | 2 | 4 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0002 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0008 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0005g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0005g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0007g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0007g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0008g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0008g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0011g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0013g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0001t0014g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0223 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0004g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0004g0128 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0004g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0004g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0004g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0005g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0005g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0006g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0006g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0012g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0002t0015g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0003t0001g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0003t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0003t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0003t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0003t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0003t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0003t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0003t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0003t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0003t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0003t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0003t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0003t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0003t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0003t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0003t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0003t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0003t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0003t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0003t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0003t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0003t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0003t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0003t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0003t0005g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0003t0006g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0003t0006g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0003t0006g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0004t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0004t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0004t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0004t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0004t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0004t0002g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0004t0002g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0004t0003g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0004t0003g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0004t0003g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0004t0003g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0004t0003g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0004t0003g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0004t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0004t0003g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0004t0003g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0004t0017g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0005t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0005t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0005t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0005t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0005t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0005t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0005t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0005t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0005t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0005t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0005t0002g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0005t0010g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0005t0016g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0006t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0006t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0008t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0008t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0009t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0012t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0013t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0001c0016t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0002c0007t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0002c0007t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0003c0010t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0004c0014t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0005c0011t0009g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
a0006c0015t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0013 | t0001 | g0189 | EUR | GBR | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG00099 | hp2 | a0001 | c0002 | t0001 | g0130 | EUR | GBR | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG00140 | hp1 | a0001 | c0002 | t0001 | g0253 | EUR | GBR | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG00140 | hp2 | a0001 | c0002 | t0001 | g0211 | EUR | GBR | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | CHS | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG00408 | hp2 | a0001 | c0002 | t0001 | g0236 | EAS | CHS | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG00423 | hp1 | a0002 | c0007 | t0001 | g0029 | EAS | CHS | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | CHS | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | CHS | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG00438 | hp2 | a0001 | c0002 | t0001 | g0282 | EAS | CHS | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG00544 | hp1 | a0001 | c0016 | t0001 | g0257 | EAS | CHS | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG00558 | hp2 | a0001 | c0002 | t0004 | g0258 | EAS | CHS | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | CHS | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | CHS | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | CHS | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | CHS | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | CHS | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | CHS | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | PUR | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG00642 | hp1 | a0001 | c0002 | t0001 | g0235 | AMR | PUR | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG00642 | hp2 | a0001 | c0002 | t0001 | g0026 | AMR | PUR | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | CHS | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0266 | AMR | PUR | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | PUR | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG00741 | hp2 | a0001 | c0002 | t0001 | g0145 | AMR | PUR | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0250 | AMR | PUR | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0290 | AMR | PUR | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG01081 | hp1 | a0001 | c0002 | t0001 | g0233 | AMR | PUR | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG01081 | hp2 | a0001 | c0012 | t0001 | g0224 | AMR | PUR | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG01106 | hp2 | a0001 | c0002 | t0001 | g0218 | AMR | PUR | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG01109 | hp1 | a0001 | c0002 | t0001 | g0024 | AMR | PUR | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG01167 | hp1 | a0001 | c0002 | t0001 | g0097 | AMR | PUR | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG01169 | hp1 | a0001 | c0002 | t0001 | g0123 | AMR | PUR | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0255 | AMR | PUR | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG01175 | hp2 | a0001 | c0002 | t0001 | g0153 | AMR | PUR | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG01192 | hp1 | a0001 | c0002 | t0005 | g0300 | AMR | PUR | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG01243 | hp1 | a0001 | c0002 | t0001 | g0256 | AMR | PUR | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG01243 | hp2 | a0001 | c0002 | t0001 | g0249 | AMR | PUR | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | CLM | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG01261 | hp1 | a0001 | c0002 | t0001 | g0240 | AMR | CLM | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG01261 | hp2 | a0006 | c0015 | t0001 | g0226 | AMR | CLM | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | CLM | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | CLM | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG01358 | hp2 | a0001 | c0002 | t0001 | g0220 | AMR | CLM | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG01433 | hp1 | a0001 | c0002 | t0001 | g0241 | AMR | CLM | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | CLM | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | CLM | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | CLM | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG01517 | hp1 | a0005 | c0011 | t0009 | g0014 | EUR | IBS | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0234 | EUR | IBS | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG01884 | hp1 | a0001 | c0005 | t0001 | g0069 | AFR | ACB | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | ACB | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG01891 | hp1 | a0001 | c0003 | t0001 | g0042 | AFR | ACB | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG01891 | hp2 | a0001 | c0005 | t0002 | g0068 | AFR | ACB | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PEL | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG01934 | hp1 | a0001 | c0002 | t0001 | g0242 | AMR | PEL | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG01934 | hp2 | a0001 | c0002 | t0001 | g0111 | AMR | PEL | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PEL | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG01952 | hp1 | a0001 | c0002 | t0001 | g0245 | AMR | PEL | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PEL | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | PEL | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | PEL | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG01978 | hp2 | a0001 | c0002 | t0001 | g0231 | AMR | PEL | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PEL | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | PEL | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02015 | hp1 | a0001 | c0002 | t0001 | g0075 | EAS | KHV | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02015 | hp2 | a0001 | c0002 | t0001 | g0070 | EAS | KHV | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | KHV | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | KHV | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02055 | hp1 | a0001 | c0008 | t0001 | g0167 | AFR | ACB | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02055 | hp2 | a0001 | c0005 | t0002 | g0139 | AFR | ACB | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | KHV | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02056 | hp2 | a0001 | c0004 | t0003 | g0291 | EAS | KHV | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | KHV | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | KHV | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02080 | hp1 | a0001 | c0002 | t0001 | g0197 | EAS | KHV | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | KHV | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | KHV | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02129 | hp1 | a0001 | c0001 | t0011 | g0098 | EAS | KHV | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | KHV | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | KHV | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | KHV | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | KHV | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02145 | hp1 | a0001 | c0002 | t0001 | g0247 | AFR | ACB | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02145 | hp2 | a0001 | c0002 | t0001 | g0156 | AFR | ACB | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02165 | hp1 | a0001 | c0002 | t0001 | g0215 | EAS | CDX | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02165 | hp2 | a0001 | c0002 | t0001 | g0293 | EAS | CDX | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02257 | hp1 | a0001 | c0002 | t0001 | g0217 | AFR | ACB | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | ACB | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02258 | hp1 | a0001 | c0005 | t0010 | g0289 | AFR | ACB | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | ACB | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02280 | hp1 | a0001 | c0005 | t0002 | g0051 | AFR | ACB | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02280 | hp2 | a0001 | c0003 | t0001 | g0064 | AFR | ACB | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | PEL | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02300 | hp2 | a0001 | c0002 | t0001 | g0133 | AMR | PEL | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02451 | hp1 | a0001 | c0003 | t0001 | g0003 | AFR | ACB | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02523 | hp1 | a0001 | c0002 | t0001 | g0117 | EAS | KHV | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02523 | hp2 | a0001 | c0002 | t0001 | g0030 | EAS | KHV | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | GWD | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02572 | hp2 | a0001 | c0003 | t0001 | g0292 | AFR | GWD | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02602 | hp1 | a0001 | c0001 | t0008 | g0182 | SAS | PJL | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02615 | hp1 | a0001 | c0003 | t0005 | g0297 | AFR | GWD | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02615 | hp2 | a0001 | c0003 | t0001 | g0272 | AFR | GWD | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02622 | hp2 | a0001 | c0005 | t0001 | g0138 | AFR | GWD | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | GWD | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02630 | hp2 | a0001 | c0003 | t0001 | g0274 | AFR | GWD | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02647 | hp1 | a0001 | c0003 | t0001 | g0142 | AFR | GWD | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02647 | hp2 | a0001 | c0005 | t0001 | g0047 | AFR | GWD | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02683 | hp1 | a0001 | c0002 | t0001 | g0044 | SAS | PJL | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02698 | hp1 | a0001 | c0002 | t0001 | g0020 | SAS | PJL | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02698 | hp2 | a0001 | c0002 | t0001 | g0251 | SAS | PJL | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02717 | hp1 | a0001 | c0002 | t0001 | g0152 | AFR | GWD | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02717 | hp2 | a0001 | c0003 | t0006 | g0306 | AFR | GWD | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02723 | hp2 | a0001 | c0005 | t0002 | g0076 | AFR | GWD | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02735 | hp1 | a0001 | c0002 | t0006 | g0302 | SAS | PJL | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02735 | hp2 | a0001 | c0002 | t0001 | g0043 | SAS | PJL | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02738 | hp2 | a0001 | c0002 | t0005 | g0296 | SAS | PJL | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | GWD | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02809 | hp2 | a0001 | c0004 | t0002 | g0268 | AFR | GWD | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02818 | hp1 | a0001 | c0003 | t0001 | g0275 | AFR | GWD | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | GWD | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02886 | hp1 | a0001 | c0006 | t0001 | g0204 | AFR | GWD | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | GWD | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02895 | hp2 | a0001 | c0003 | t0001 | g0294 | AFR | GWD | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0271 | AFR | GWD | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0277 | AFR | GWD | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02922 | hp1 | a0001 | c0003 | t0001 | g0172 | AFR | ESN | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | ESN | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | ESN | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02965 | hp2 | a0001 | c0003 | t0001 | g0177 | AFR | ESN | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02976 | hp1 | a0001 | c0003 | t0001 | g0003 | AFR | ESN | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | ESN | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG03041 | hp1 | a0001 | c0004 | t0002 | g0288 | AFR | GWD | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG03041 | hp2 | a0001 | c0003 | t0001 | g0174 | AFR | GWD | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG03098 | hp1 | a0001 | c0003 | t0001 | g0013 | AFR | MSL | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG03098 | hp2 | a0001 | c0003 | t0001 | g0202 | AFR | MSL | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG03130 | hp1 | a0001 | c0005 | t0002 | g0077 | AFR | ESN | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG03130 | hp2 | a0001 | c0003 | t0001 | g0054 | AFR | ESN | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | ESN | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG03139 | hp2 | a0001 | c0006 | t0001 | g0267 | AFR | ESN | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG03195 | hp1 | a0001 | c0009 | t0001 | g0136 | AFR | ESN | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | ESN | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG03209 | hp1 | a0001 | c0003 | t0006 | g0303 | AFR | MSL | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG03209 | hp2 | a0001 | c0003 | t0001 | g0171 | AFR | MSL | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | MSL | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG03239 | hp1 | a0001 | c0002 | t0001 | g0252 | SAS | PJL | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG03239 | hp2 | a0001 | c0002 | t0001 | g0278 | SAS | PJL | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG03453 | hp1 | a0001 | c0003 | t0001 | g0140 | AFR | MSL | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG03453 | hp2 | a0001 | c0004 | t0001 | g0273 | AFR | MSL | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | MSL | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | MSL | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG03516 | hp2 | a0001 | c0003 | t0001 | g0003 | AFR | ESN | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | GWD | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG03540 | hp2 | a0001 | c0005 | t0002 | g0052 | AFR | GWD | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG03579 | hp1 | a0001 | c0003 | t0001 | g0276 | AFR | MSL | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG03579 | hp2 | a0001 | c0004 | t0002 | g0045 | AFR | MSL | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG03704 | hp1 | a0001 | c0002 | t0001 | g0184 | SAS | PJL | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG03704 | hp2 | a0001 | c0002 | t0004 | g0161 | SAS | PJL | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG03831 | hp1 | a0001 | c0002 | t0001 | g0214 | SAS | BEB | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG03831 | hp2 | a0001 | c0002 | t0001 | g0154 | SAS | BEB | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG03942 | hp1 | a0001 | c0002 | t0006 | g0307 | SAS | BEB | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG03942 | hp2 | a0001 | c0002 | t0001 | g0264 | SAS | BEB | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG04184 | hp1 | a0001 | c0002 | t0001 | g0144 | SAS | BEB | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG04184 | hp2 | a0001 | c0002 | t0001 | g0269 | SAS | BEB | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG04199 | hp1 | a0001 | c0001 | t0008 | g0228 | SAS | STU | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0210 | SAS | STU | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG04204 | hp1 | a0001 | c0002 | t0001 | g0183 | SAS | STU | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG04204 | hp2 | a0001 | c0002 | t0001 | g0229 | SAS | STU | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG04228 | hp1 | a0001 | c0002 | t0004 | g0040 | SAS | STU | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0050 | SAS | STU | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA18522 | hp1 | a0001 | c0005 | t0016 | g0301 | AFR | YRI | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | YRI | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | CHB | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | CHB | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA18747 | hp1 | a0001 | c0002 | t0004 | g0212 | EAS | CHB | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA18747 | hp2 | a0001 | c0002 | t0001 | g0287 | EAS | CHB | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA18906 | hp1 | a0001 | c0005 | t0002 | g0180 | AFR | YRI | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA18906 | hp2 | a0001 | c0003 | t0006 | g0304 | AFR | YRI | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA18940 | hp2 | a0001 | c0002 | t0012 | g0150 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA18942 | hp2 | a0004 | c0014 | t0001 | g0079 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA18945 | hp1 | a0001 | c0002 | t0001 | g0238 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA18945 | hp2 | a0001 | c0002 | t0001 | g0159 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA18947 | hp2 | a0001 | c0002 | t0001 | g0225 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA18948 | hp1 | a0001 | c0002 | t0015 | g0295 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA18950 | hp2 | a0001 | c0002 | t0001 | g0285 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA18959 | hp1 | a0001 | c0002 | t0001 | g0239 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA18959 | hp2 | a0003 | c0010 | t0001 | g0259 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA18962 | hp1 | a0001 | c0002 | t0001 | g0132 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA18964 | hp1 | a0001 | c0002 | t0001 | g0135 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA18964 | hp2 | a0001 | c0004 | t0003 | g0265 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA18969 | hp1 | a0001 | c0002 | t0001 | g0222 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA18969 | hp2 | a0001 | c0002 | t0001 | g0179 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA18970 | hp1 | a0001 | c0002 | t0001 | g0262 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA18971 | hp1 | a0001 | c0002 | t0001 | g0237 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA18973 | hp1 | a0001 | c0004 | t0001 | g0034 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA18973 | hp2 | a0001 | c0002 | t0001 | g0083 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA18977 | hp2 | a0001 | c0001 | t0007 | g0016 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA18979 | hp1 | a0001 | c0002 | t0001 | g0158 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA18979 | hp2 | a0001 | c0004 | t0003 | g0032 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA18981 | hp2 | a0001 | c0002 | t0001 | g0283 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA18984 | hp2 | a0001 | c0004 | t0003 | g0035 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA18985 | hp1 | a0001 | c0004 | t0001 | g0004 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA18985 | hp2 | a0001 | c0002 | t0001 | g0280 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA18995 | hp2 | a0001 | c0004 | t0003 | g0031 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA18998 | hp1 | a0001 | c0003 | t0001 | g0187 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA18998 | hp2 | a0001 | c0002 | t0001 | g0060 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA18999 | hp1 | a0001 | c0002 | t0001 | g0087 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA19000 | hp1 | a0001 | c0001 | t0005 | g0299 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA19000 | hp2 | a0001 | c0002 | t0001 | g0018 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA19003 | hp1 | a0002 | c0007 | t0001 | g0025 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA19003 | hp2 | a0001 | c0004 | t0003 | g0147 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA19009 | hp2 | a0001 | c0002 | t0001 | g0230 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA19010 | hp2 | a0001 | c0002 | t0001 | g0219 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA19012 | hp2 | a0001 | c0002 | t0001 | g0263 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA19030 | hp1 | a0001 | c0005 | t0002 | g0078 | AFR | LWK | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | LWK | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA19043 | hp1 | a0001 | c0003 | t0001 | g0143 | AFR | LWK | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | LWK | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA19060 | hp1 | a0001 | c0004 | t0003 | g0033 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA19060 | hp2 | a0001 | c0001 | t0013 | g0124 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA19064 | hp2 | a0001 | c0002 | t0001 | g0095 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA19068 | hp2 | a0001 | c0004 | t0003 | g0134 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA19074 | hp1 | a0001 | c0002 | t0001 | g0284 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA19079 | hp2 | a0001 | c0003 | t0001 | g0194 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA19080 | hp1 | a0001 | c0002 | t0001 | g0201 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA19081 | hp1 | a0001 | c0002 | t0001 | g0148 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA19083 | hp1 | a0001 | c0001 | t0007 | g0015 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA19083 | hp2 | a0001 | c0001 | t0005 | g0298 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA19084 | hp2 | a0001 | c0004 | t0003 | g0028 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA19085 | hp1 | a0001 | c0001 | t0014 | g0048 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA19085 | hp2 | a0001 | c0002 | t0001 | g0232 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA19087 | hp1 | a0001 | c0002 | t0001 | g0160 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA19088 | hp2 | a0001 | c0004 | t0001 | g0004 | EAS | JPT | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA19240 | hp1 | a0001 | c0008 | t0001 | g0066 | AFR | YRI | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | YRI | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | ASW | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | ASW | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA20752 | hp1 | a0001 | c0002 | t0001 | g0246 | EUR | TSI | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA20752 | hp2 | a0001 | c0002 | t0001 | g0243 | EUR | TSI | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA20805 | hp1 | a0001 | c0002 | t0001 | g0155 | EUR | TSI | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0011 | EUR | TSI | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA20905 | hp1 | a0001 | c0002 | t0001 | g0261 | SAS | GIH | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0270 | SAS | GIH | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02109 | hp1 | a0001 | c0003 | t0001 | g0279 | AFR | ACB | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | ACB | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG02486 | hp2 | a0001 | c0004 | t0002 | g0170 | AFR | ACB | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG03471 | hp1 | a0001 | c0004 | t0017 | g0305 | AFR | MSL | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | MSL | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG06807 | hp1 | a0001 | c0003 | t0001 | g0141 | AFR | USA | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | USA | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA20300 | hp1 | a0001 | c0003 | t0001 | g0013 | AFR | USA | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0244 | AFR | USA | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA21309 | hp1 | a0001 | c0003 | t0001 | g0067 | AFR | LWK | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | LWK | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0001 | g0223 | REF | REF | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
homoSapiens_grch38 | hp1 | a0001 | c0002 | t0004 | g0128 | REF | REF | BEGAIN_chr14_100532147_100592417 | BEGAIN | chr14 | 100532147 | 100592417 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:100538045
|
G | A | 1 | a0002 | 2 | HG00423.hp1 NA19003.hp1 |
missense_variant | MODERATE | c.1763C>T | p.Pro588Leu | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 7/7 | 1890/2788 | 1763/1839 | 588/612 | chr14 | 100538045 | ||
chr14:100538903
|
T | TGGAAGCC others(5): Show |
1 | a0004 | 1 | NA18942.hp2 | conservative_inframe_insertion | MODERATE | c.893_904dupCGGCGGGC others(4): Show |
p.Pro298_Phe301dup | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 7/7 | 1031/2788 | 904/1839 | 302/612 | chr14 | 100538903 | ||
chr14:100539098
|
G | T | 1 | a0005 | 1 | HG01517.hp1 | missense_variant | MODERATE | c.710C>A | p.Pro237Gln | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 7/7 | 837/2788 | 710/1839 | 237/612 | chr14 | 100539098 | ||
chr14:100539168
|
G | C | 1 | a0006 | 1 | HG01261.hp2 | missense_variant | MODERATE | c.640C>G | p.Leu214Val | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 7/7 | 767/2788 | 640/1839 | 214/612 | chr14 | 100539168 | ||
chr14:100539219
|
C | T | 1 | a0003 | 1 | NA18959.hp2 | missense_variant | MODERATE | c.589G>A | p.Val197Ile | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 7/7 | 716/2788 | 589/1839 | 197/612 | chr14 | 100539219 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:100538095
|
G | A | 2 | a0001c0004a0001c0005 | 31 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(28): Show |
synonymous_variant | LOW | c.1713C>T | p.Ala571Ala | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 7/7 | 1840/2788 | 1713/1839 | 571/612 | chr14 | 100538095 | ||
chr14:100538218
|
G | A | 1 | a0001c0008 | 2 | HG02055.hp1 NA19240.hp1 |
synonymous_variant | LOW | c.1590C>T | p.Pro530Pro | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 7/7 | 1717/2788 | 1590/1839 | 530/612 | chr14 | 100538218 | ||
chr14:100538344
|
G | A | 1 | a0001c0012 | 1 | HG01081.hp2 | synonymous_variant | LOW | c.1464C>T | p.Ala488Ala | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 7/7 | 1591/2788 | 1464/1839 | 488/612 | chr14 | 100538344 | ||
chr14:100538878
|
T | C | 10 | a0001c0001a0001c0003a0001c0004others(7): Show | 227 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(224): Show |
synonymous_variant | LOW | c.930A>G | p.Ala310Ala | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 7/7 | 1057/2788 | 930/1839 | 310/612 | chr14 | 100538878 | ||
chr14:100538899
|
A | G | 9 | a0001c0001a0001c0003a0001c0004others(6): Show | 226 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(223): Show |
synonymous_variant | LOW | c.909T>C | p.His303His | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 7/7 | 1036/2788 | 909/1839 | 303/612 | chr14 | 100538899 | ||
chr14:100538902
|
C | T | 1 | a0001c0016 | 1 | HG00544.hp1 | synonymous_variant | LOW | c.906G>A | p.Gln302Gln | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 7/7 | 1033/2788 | 906/1839 | 302/612 | chr14 | 100538902 | ||
chr14:100539094
|
C | T | 1 | a0001c0006 | 2 | HG02886.hp1 HG03139.hp2 |
synonymous_variant | LOW | c.714G>A | p.Arg238Arg | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 7/7 | 841/2788 | 714/1839 | 238/612 | chr14 | 100539094 | ||
chr14:100543867
|
T | C | 4 | a0001c0003a0001c0004a0001c0008others(1): Show | 52 | HG00544.hp1 HG01891.hp1 HG02055.hp1 others(49): Show |
synonymous_variant | LOW | c.399A>G | p.Ser133Ser | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 5/7 | 526/2788 | 399/1839 | 133/612 | chr14 | 100543867 | ||
chr14:100543918
|
A | C | 1 | a0001c0009 | 1 | HG03195.hp1 | synonymous_variant | LOW | c.348T>G | p.Val116Val | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 5/7 | 475/2788 | 348/1839 | 116/612 | chr14 | 100543918 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:100537308
|
G | A | 1 | a0001c0001t0011 | 1 | HG02129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*661C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 7/7 | 661 | chr14 | 100537308 | |||||
chr14:100537341
|
C | A | 1 | a0001c0001t0008 | 2 | HG02602.hp1 HG04199.hp1 |
3_prime_UTR_variant | MODIFIER | c.*628G>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 7/7 | 628 | chr14 | 100537341 | |||||
chr14:100537557
|
C | T | 1 | a0001c0005t0010 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*412G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 7/7 | 412 | chr14 | 100537557 | |||||
chr14:100537619
|
A | G | 1 | a0001c0004t0003 | 9 | HG02056.hp2 NA18964.hp2 NA18979.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*350T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 7/7 | 350 | chr14 | 100537619 | |||||
chr14:100537664
|
C | A | 1 | a0001c0002t0015 | 1 | NA18948.hp1 | 3_prime_UTR_variant | MODIFIER | c.*305G>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 7/7 | 305 | chr14 | 100537664 | |||||
chr14:100537667
|
T | G | 1 | a0001c0002t0012 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*302A>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 7/7 | 302 | chr14 | 100537667 | |||||
chr14:100537765
|
C | G | 33 | a0001c0001t0001a0001c0001t0005a0001c0001t0007others(30): Show | 320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
3_prime_UTR_variant | MODIFIER | c.*204G>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 7/7 | 204 | chr14 | 100537765 | |||||
chr14:100537839
|
G | A | 1 | a0001c0001t0013 | 1 | NA19060.hp2 | 3_prime_UTR_variant | MODIFIER | c.*130C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 7/7 | 130 | chr14 | 100537839 | |||||
chr14:100537947
|
G | A | 1 | a0001c0001t0014 | 1 | NA19085.hp1 | 3_prime_UTR_variant | MODIFIER | c.*22C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 7/7 | 22 | chr14 | 100537947 | |||||
chr14:100537956
|
T | C | 3 | a0001c0004t0002a0001c0004t0017a0001c0005t0002 | 13 | HG01891.hp2 HG02055.hp2 HG02280.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*13A>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 7/7 | 13 | chr14 | 100537956 | |||||
chr14:100587336
|
G | GC | 4 | a0001c0001t0005a0001c0002t0005a0001c0002t0015others(1): Show | 6 | HG01192.hp1 HG02615.hp1 HG02738.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-47dupG | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/7 | 47 | chr14 | 100587336 | |||||
chr14:100587339
|
C | T | 1 | a0001c0001t0007 | 2 | NA18977.hp2 NA19083.hp1 |
5_prime_UTR_variant | MODIFIER | c.-49G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/7 | 49 | chr14 | 100587339 | |||||
chr14:100587348
|
C | T | 1 | a0005c0011t0009 | 1 | HG01517.hp1 | 5_prime_UTR_variant | MODIFIER | c.-58G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/7 | 58 | chr14 | 100587348 | |||||
chr14:100587360
|
G | C | 1 | a0001c0005t0016 | 1 | NA18522.hp1 | 5_prime_UTR_variant | MODIFIER | c.-70C>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/7 | 70 | chr14 | 100587360 | |||||
chr14:100587397
|
G | A | 3 | a0001c0002t0006a0001c0003t0006a0001c0004t0017 | 6 | HG02717.hp2 HG02735.hp1 HG03209.hp1 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-107C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/7 | 107 | chr14 | 100587397 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:100539329
|
G | A | 2 | a0001c0004t0001g0004a0001c0004t0001g0034 | 3 | NA18973.hp1 NA18985.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.493-14C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 6/6 | chr14 | 100539329 | ||||||
chr14:100539554
|
C | T | 1 | a0001c0001t0001g0091 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.493-239G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 6/6 | chr14 | 100539554 | ||||||
chr14:100539558
|
C | T | 137 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(134): Show | 151 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.493-243G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 6/6 | chr14 | 100539558 | ||||||
chr14:100539612
|
G | A | 1 | a0001c0004t0001g0273 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.493-297C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 6/6 | chr14 | 100539612 | ||||||
chr14:100539649
|
C | A | 11 | a0001c0004t0001g0004a0001c0004t0001g0034a0001c0004t0003g0028others(8): Show | 12 | HG02056.hp2 NA18964.hp2 NA18973.hp1 others(9): Show |
intron_variant | MODIFIER | c.493-334G>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 6/6 | chr14 | 100539649 | ||||||
chr14:100539763
|
A | G | 3 | a0001c0003t0001g0003a0001c0003t0001g0171a0001c0003t0001g0294 | 5 | HG02451.hp1 HG02895.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.493-448T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 6/6 | chr14 | 100539763 | ||||||
chr14:100539780
|
G | C | 23 | a0001c0001t0001g0005a0001c0001t0001g0037a0001c0001t0001g0041others(20): Show | 24 | HG00639.hp1 HG01884.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.493-465C>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 6/6 | chr14 | 100539780 | ||||||
chr14:100539900
|
C | G | 139 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(136): Show | 153 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.493-585G>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 6/6 | chr14 | 100539900 | ||||||
chr14:100539929
|
C | T | 2 | a0001c0006t0001g0204a0001c0006t0001g0267 | 2 | HG02886.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.492+567G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 6/6 | chr14 | 100539929 | ||||||
chr14:100539969
|
G | A | 10 | a0001c0001t0001g0176a0001c0005t0001g0069a0001c0005t0002g0051others(7): Show | 10 | HG00733.hp2 HG01884.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.492+527C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 6/6 | chr14 | 100539969 | ||||||
chr14:100539985
|
G | A | 5 | a0001c0004t0002g0045a0001c0004t0002g0170a0001c0004t0002g0268others(2): Show | 5 | HG02486.hp2 HG02809.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.492+511C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 6/6 | chr14 | 100539985 | ||||||
chr14:100539998
|
G | C | 1 | a0001c0001t0001g0186 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.492+498C>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 6/6 | chr14 | 100539998 | ||||||
chr14:100540026
|
C | G | 2 | a0001c0001t0001g0009a0001c0001t0001g0027 | 3 | HG02109.hp2 HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.492+470G>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 6/6 | chr14 | 100540026 | ||||||
chr14:100540166
|
C | T | 4 | a0001c0003t0001g0187a0001c0003t0001g0194a0001c0004t0001g0273others(1): Show | 4 | HG00544.hp1 HG03453.hp2 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.492+330G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 6/6 | chr14 | 100540166 | ||||||
chr14:100540208
|
G | T | 3 | a0001c0003t0001g0187a0001c0003t0001g0194a0001c0016t0001g0257 | 3 | HG00544.hp1 NA18998.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.492+288C>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 6/6 | chr14 | 100540208 | ||||||
chr14:100540363
|
G | T | 1 | a0001c0001t0001g0022 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.492+133C>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 6/6 | chr14 | 100540363 | ||||||
chr14:100540641
|
C | T | 2 | a0001c0002t0001g0026a0001c0002t0001g0253 | 2 | HG00140.hp1 HG00642.hp2 |
intron_variant | MODIFIER | c.409-62G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 5/6 | chr14 | 100540641 | ||||||
chr14:100540735
|
C | G | 305 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(302): Show | 324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.409-156G>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 5/6 | chr14 | 100540735 | ||||||
chr14:100540786
|
C | T | 10 | a0001c0001t0001g0176a0001c0005t0001g0069a0001c0005t0002g0051others(7): Show | 10 | HG00733.hp2 HG01884.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.409-207G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 5/6 | chr14 | 100540786 | ||||||
chr14:100540934
|
C | G | 33 | a0001c0003t0001g0003a0001c0003t0001g0013a0001c0003t0001g0042others(30): Show | 36 | HG01891.hp1 HG02055.hp1 HG02109.hp1 others(33): Show |
intron_variant | MODIFIER | c.409-355G>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 5/6 | chr14 | 100540934 | ||||||
chr14:100541007
|
C | A | 3 | a0001c0001t0001g0094a0001c0001t0001g0109a0001c0001t0001g0113 | 3 | HG00673.hp1 NA18989.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.409-428G>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 5/6 | chr14 | 100541007 | ||||||
chr14:100541014
|
A | G | 33 | a0001c0003t0001g0003a0001c0003t0001g0013a0001c0003t0001g0042others(30): Show | 36 | HG01891.hp1 HG02055.hp1 HG02109.hp1 others(33): Show |
intron_variant | MODIFIER | c.409-435T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 5/6 | chr14 | 100541014 | ||||||
chr14:100541037
|
C | T | 1 | a0001c0004t0002g0288 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.409-458G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 5/6 | chr14 | 100541037 | ||||||
chr14:100541049
|
G | C | 1 | a0001c0001t0001g0200 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.409-470C>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 5/6 | chr14 | 100541049 | ||||||
chr14:100541106
|
G | A | 1 | a0001c0002t0001g0249 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.409-527C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 5/6 | chr14 | 100541106 | ||||||
chr14:100541111
|
G | T | 1 | a0001c0001t0001g0085 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.409-532C>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 5/6 | chr14 | 100541111 | ||||||
chr14:100541194
|
C | T | 10 | a0001c0001t0001g0176a0001c0005t0001g0069a0001c0005t0002g0051others(7): Show | 10 | HG00733.hp2 HG01884.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.409-615G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 5/6 | chr14 | 100541194 | ||||||
chr14:100541232
|
T | C | 1 | a0001c0003t0001g0177 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.409-653A>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 5/6 | chr14 | 100541232 | ||||||
chr14:100541267
|
C | T | 1 | a0001c0001t0001g0221 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.409-688G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 5/6 | chr14 | 100541267 | ||||||
chr14:100541326
|
A | G | 2 | a0001c0002t0001g0211a0001c0002t0001g0246 | 2 | HG00140.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.409-747T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 5/6 | chr14 | 100541326 | ||||||
chr14:100541454
|
C | T | 10 | a0001c0001t0001g0176a0001c0005t0001g0069a0001c0005t0002g0051others(7): Show | 10 | HG00733.hp2 HG01884.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.409-875G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 5/6 | chr14 | 100541454 | ||||||
chr14:100541518
|
C | T | 36 | a0001c0003t0001g0003a0001c0003t0001g0013a0001c0003t0001g0042others(33): Show | 39 | HG00544.hp1 HG01891.hp1 HG02055.hp1 others(36): Show |
intron_variant | MODIFIER | c.409-939G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 5/6 | chr14 | 100541518 | ||||||
chr14:100541574
|
C | T | 2 | a0001c0002t0001g0219a0001c0002t0001g0232 | 2 | NA19010.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.409-995G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 5/6 | chr14 | 100541574 | ||||||
chr14:100541607
|
A | G | 207 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(204): Show | 226 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(223): Show |
intron_variant | MODIFIER | c.409-1028T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 5/6 | chr14 | 100541607 | ||||||
chr14:100541702
|
G | C | 2 | a0001c0001t0001g0062a0001c0009t0001g0136 | 2 | HG02809.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.409-1123C>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 5/6 | chr14 | 100541702 | ||||||
chr14:100541848
|
C | T | 1 | a0001c0004t0001g0273 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.409-1269G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 5/6 | chr14 | 100541848 | ||||||
chr14:100541866
|
G | A | 1 | a0001c0004t0001g0273 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.409-1287C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 5/6 | chr14 | 100541866 | ||||||
chr14:100541937
|
G | C | 1 | a0001c0001t0001g0200 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.409-1358C>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 5/6 | chr14 | 100541937 | ||||||
chr14:100542139
|
C | A | 1 | a0001c0004t0001g0273 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.409-1560G>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 5/6 | chr14 | 100542139 | ||||||
chr14:100542217
|
C | T | 1 | a0001c0004t0001g0273 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.409-1638G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 5/6 | chr14 | 100542217 | ||||||
chr14:100542315
|
G | T | 6 | a0001c0004t0001g0273a0001c0004t0002g0045a0001c0004t0002g0170others(3): Show | 6 | HG02486.hp2 HG02809.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.408+1543C>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 5/6 | chr14 | 100542315 | ||||||
chr14:100542446
|
G | A | 1 | a0001c0005t0002g0068 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.408+1412C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 5/6 | chr14 | 100542446 | ||||||
chr14:100542481
|
C | A | 1 | a0001c0001t0001g0116 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.408+1377G>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 5/6 | chr14 | 100542481 | ||||||
chr14:100542482
|
G | A | 10 | a0001c0001t0001g0176a0001c0005t0001g0069a0001c0005t0002g0051others(7): Show | 10 | HG00733.hp2 HG01884.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.408+1376C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 5/6 | chr14 | 100542482 | ||||||
chr14:100542510
|
C | T | 3 | a0001c0003t0001g0187a0001c0003t0001g0194a0001c0016t0001g0257 | 3 | HG00544.hp1 NA18998.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.408+1348G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 5/6 | chr14 | 100542510 | ||||||
chr14:100542528
|
G | A | 36 | a0001c0003t0001g0003a0001c0003t0001g0013a0001c0003t0001g0042others(33): Show | 39 | HG00544.hp1 HG01891.hp1 HG02055.hp1 others(36): Show |
intron_variant | MODIFIER | c.408+1330C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 5/6 | chr14 | 100542528 | ||||||
chr14:100542596
|
G | A | 1 | a0001c0001t0013g0124 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.408+1262C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 5/6 | chr14 | 100542596 | ||||||
chr14:100542632
|
GC | G | 4 | a0001c0005t0001g0047a0001c0005t0001g0138a0001c0005t0010g0289others(1): Show | 4 | HG02258.hp1 HG02622.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.408+1225delG | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 5/6 | chr14 | 100542632 | ||||||
chr14:100542790
|
T | G | 11 | a0001c0004t0001g0004a0001c0004t0001g0034a0001c0004t0003g0028others(8): Show | 12 | HG02056.hp2 NA18964.hp2 NA18973.hp1 others(9): Show |
intron_variant | MODIFIER | c.408+1068A>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 5/6 | chr14 | 100542790 | ||||||
chr14:100542832
|
C | T | 1 | a0001c0004t0001g0273 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.408+1026G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 5/6 | chr14 | 100542832 | ||||||
chr14:100542949
|
T | C | 3 | a0001c0002t0001g0145a0001c0002t0001g0155a0001c0002t0001g0156 | 3 | HG00741.hp2 HG02145.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.408+909A>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 5/6 | chr14 | 100542949 | ||||||
chr14:100542995
|
GCTGGGCG others(3): Show |
G | 5 | a0001c0004t0002g0045a0001c0004t0002g0170a0001c0004t0002g0268others(2): Show | 5 | HG02486.hp2 HG02809.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.408+853_408+862del others(10): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 5/6 | chr14 | 100542995 | ||||||
chr14:100543043
|
A | G | 1 | a0001c0004t0001g0273 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.408+815T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 5/6 | chr14 | 100543043 | ||||||
chr14:100543141
|
C | T | 1 | a0001c0001t0001g0163 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.408+717G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 5/6 | chr14 | 100543141 | ||||||
chr14:100543162
|
G | GA | 4 | a0001c0005t0001g0047a0001c0005t0001g0138a0001c0005t0010g0289others(1): Show | 4 | HG02258.hp1 HG02622.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.408+695dupT | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 5/6 | chr14 | 100543162 | ||||||
chr14:100543292
|
GTGTTTTT others(5): Show |
G | 1 | a0001c0006t0001g0204 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.408+554_408+565del others(12): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 5/6 | chr14 | 100543292 | ||||||
chr14:100543295
|
T | G | 7 | a0001c0001t0001g0039a0001c0001t0001g0061a0001c0001t0001g0118others(4): Show | 7 | HG01346.hp1 HG01928.hp2 HG01975.hp1 others(4): Show |
intron_variant | MODIFIER | c.408+563A>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 5/6 | chr14 | 100543295 | ||||||
chr14:100543306
|
G | GT | 24 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0104others(21): Show | 27 | HG02109.hp1 HG02280.hp2 HG02451.hp1 others(24): Show |
intron_variant | MODIFIER | c.408+551dupA | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 5/6 | chr14 | 100543306 | ||||||
chr14:100543306
|
G | T | 1 | a0001c0002t0012g0150 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.408+552C>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 5/6 | chr14 | 100543306 | ||||||
chr14:100543311
|
T | G | 1 | a0001c0005t0002g0180 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.408+547A>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 5/6 | chr14 | 100543311 | ||||||
chr14:100543318
|
G | T | 1 | a0001c0006t0001g0267 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.408+540C>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 5/6 | chr14 | 100543318 | ||||||
chr14:100543530
|
A | G | 5 | a0001c0004t0001g0273a0001c0005t0001g0047a0001c0005t0001g0138others(2): Show | 5 | HG02258.hp1 HG02622.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.408+328T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 5/6 | chr14 | 100543530 | ||||||
chr14:100543618
|
G | T | 9 | a0001c0001t0001g0176a0001c0005t0002g0051a0001c0005t0002g0052others(6): Show | 9 | HG00733.hp2 HG01891.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.408+240C>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 5/6 | chr14 | 100543618 | ||||||
chr14:100543834
|
G | A | 1 | a0001c0001t0001g0027 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.408+24C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 5/6 | chr14 | 100543834 | ||||||
chr14:100543978
|
C | T | 1 | a0001c0001t0001g0053 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.301-13G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 4/6 | chr14 | 100543978 | ||||||
chr14:100544027
|
G | A | 92 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(89): Show | 103 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.301-62C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 4/6 | chr14 | 100544027 | ||||||
chr14:100544042
|
C | A | 4 | a0001c0001t0001g0005a0001c0001t0001g0037a0001c0001t0001g0041others(1): Show | 5 | HG00639.hp1 HG01884.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.301-77G>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 4/6 | chr14 | 100544042 | ||||||
chr14:100544082
|
A | T | 7 | a0001c0003t0001g0003a0001c0003t0001g0067a0001c0003t0001g0171others(4): Show | 9 | HG02451.hp1 HG02615.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.301-117T>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 4/6 | chr14 | 100544082 | ||||||
chr14:100544393
|
T | C | 150 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(147): Show | 165 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(162): Show |
intron_variant | MODIFIER | c.301-428A>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 4/6 | chr14 | 100544393 | ||||||
chr14:100544439
|
G | C | 10 | a0001c0001t0001g0176a0001c0005t0001g0069a0001c0005t0002g0051others(7): Show | 10 | HG00733.hp2 HG01884.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.301-474C>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 4/6 | chr14 | 100544439 | ||||||
chr14:100544478
|
C | T | 2 | a0001c0001t0001g0146a0001c0001t0001g0157 | 2 | HG01099.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.301-513G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 4/6 | chr14 | 100544478 | ||||||
chr14:100544522
|
G | A | 10 | a0001c0001t0001g0176a0001c0005t0001g0069a0001c0005t0002g0051others(7): Show | 10 | HG00733.hp2 HG01884.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.300+478C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 4/6 | chr14 | 100544522 | ||||||
chr14:100544665
|
T | A | 1 | a0001c0006t0001g0267 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.300+335A>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 4/6 | chr14 | 100544665 | ||||||
chr14:100544671
|
C | T | 139 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(136): Show | 153 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.300+329G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 4/6 | chr14 | 100544671 | ||||||
chr14:100544689
|
C | T | 14 | a0001c0003t0001g0003a0001c0003t0001g0013a0001c0003t0001g0064others(11): Show | 17 | HG02109.hp1 HG02280.hp2 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.300+311G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 4/6 | chr14 | 100544689 | ||||||
chr14:100544835
|
C | T | 2 | a0001c0001t0001g0221a0001c0001t0001g0254 | 2 | NA19067.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.300+165G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 4/6 | chr14 | 100544835 | ||||||
chr14:100544872
|
A | G | 207 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(204): Show | 226 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(223): Show |
intron_variant | MODIFIER | c.300+128T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 4/6 | chr14 | 100544872 | ||||||
chr14:100544982
|
G | A | 8 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0164others(5): Show | 8 | HG01099.hp2 HG02922.hp2 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.300+18C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 4/6 | chr14 | 100544982 | ||||||
chr14:100545439
|
C | G | 1 | a0001c0001t0001g0190 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.234-373G>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 3/6 | chr14 | 100545439 | ||||||
chr14:100545607
|
G | A | 1 | a0001c0006t0001g0267 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.234-541C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 3/6 | chr14 | 100545607 | ||||||
chr14:100545863
|
C | T | 3 | a0001c0002t0001g0043a0001c0002t0001g0130a0001c0002t0001g0231 | 3 | HG00099.hp2 HG01978.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.233+638G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 3/6 | chr14 | 100545863 | ||||||
chr14:100545879
|
C | T | 1 | a0001c0002t0001g0261 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.233+622G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 3/6 | chr14 | 100545879 | ||||||
chr14:100546080
|
G | T | 306 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(303): Show | 325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.233+421C>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 3/6 | chr14 | 100546080 | ||||||
chr14:100546082
|
G | A | 2 | a0001c0006t0001g0204a0001c0006t0001g0267 | 2 | HG02886.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.233+419C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 3/6 | chr14 | 100546082 | ||||||
chr14:100546117
|
C | G | 4 | a0001c0005t0001g0047a0001c0005t0001g0138a0001c0005t0010g0289others(1): Show | 4 | HG02258.hp1 HG02622.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.233+384G>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 3/6 | chr14 | 100546117 | ||||||
chr14:100546192
|
C | A | 1 | a0001c0002t0001g0111 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.233+309G>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 3/6 | chr14 | 100546192 | ||||||
chr14:100546272
|
G | A | 26 | a0001c0001t0001g0005a0001c0001t0001g0037a0001c0001t0001g0041others(23): Show | 27 | HG00544.hp1 HG00639.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.233+229C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 3/6 | chr14 | 100546272 | ||||||
chr14:100546276
|
A | G | 209 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(206): Show | 228 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(225): Show |
intron_variant | MODIFIER | c.233+225T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 3/6 | chr14 | 100546276 | ||||||
chr14:100546290
|
G | A | 1 | a0001c0004t0001g0273 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.233+211C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 3/6 | chr14 | 100546290 | ||||||
chr14:100546333
|
T | TGCCCCGC others(44): Show |
2 | a0001c0002t0001g0160a0001c0002t0001g0211 | 2 | HG00140.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.233+167_233+168ins others(51): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 3/6 | chr14 | 100546333 | ||||||
chr14:100546333
|
T | TGCCCCGC others(61): Show |
2 | a0001c0002t0001g0179a0001c0004t0003g0147 | 2 | NA18969.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.233+167_233+168ins others(68): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 3/6 | chr14 | 100546333 | ||||||
chr14:100546339
|
A | ACCCCGGC others(10): Show |
18 | a0001c0002t0001g0020a0001c0002t0001g0030a0001c0002t0001g0043others(15): Show | 18 | HG00558.hp2 HG01517.hp1 HG01952.hp1 others(15): Show |
intron_variant | MODIFIER | c.233+145_233+161dup others(17): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 3/6 | chr14 | 100546339 | ||||||
chr14:100546339
|
A | ACCCCGGC others(45): Show |
1 | a0001c0002t0001g0026 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.233+161_233+162ins others(52): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 3/6 | chr14 | 100546339 | ||||||
chr14:100546339
|
A | ACCCCGGC others(79): Show |
1 | a0001c0002t0001g0253 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.233+161_233+162ins others(86): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 3/6 | chr14 | 100546339 | ||||||
chr14:100546339
|
A | ACCCCGGC others(96): Show |
1 | a0001c0002t0001g0184 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.233+161_233+162ins others(103): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 3/6 | chr14 | 100546339 | ||||||
chr14:100546339
|
A | ACCCCGGC others(27): Show |
19 | a0001c0001t0001g0244a0001c0002t0001g0024a0001c0002t0001g0111others(16): Show | 19 | HG00408.hp2 HG00423.hp1 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.233+128_233+161dup others(34): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 3/6 | chr14 | 100546339 | ||||||
chr14:100546339
|
A | ACCCCGGC others(44): Show |
19 | a0001c0002t0001g0018a0001c0002t0001g0083a0001c0002t0001g0095others(16): Show | 19 | HG00438.hp2 HG00741.hp2 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.233+111_233+161dup others(51): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 3/6 | chr14 | 100546339 | ||||||
chr14:100546339
|
A | ACCCCGGC others(61): Show |
8 | a0001c0002t0001g0044a0001c0002t0001g0232a0001c0002t0001g0239others(5): Show | 9 | HG01243.hp1 HG02683.hp1 NA18959.hp1 others(6): Show |
intron_variant | MODIFIER | c.233+94_233+161dupC others(67): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 3/6 | chr14 | 100546339 | ||||||
chr14:100546339
|
A | ACCCCGGC others(78): Show |
5 | a0001c0002t0001g0130a0001c0002t0001g0238a0001c0002t0001g0283others(2): Show | 5 | HG00099.hp2 NA18942.hp2 NA18945.hp1 others(2): Show |
intron_variant | MODIFIER | c.233+77_233+161dupC others(84): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 3/6 | chr14 | 100546339 | ||||||
chr14:100546339
|
A | ACCCCGGC others(95): Show |
3 | a0001c0002t0001g0132a0001c0002t0001g0197a0001c0004t0003g0134 | 3 | HG02080.hp1 NA18962.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.233+60_233+161dupC others(101): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 3/6 | chr14 | 100546339 | ||||||
chr14:100546339
|
A | ACCCCGGC others(112): Show |
1 | a0001c0002t0001g0060 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.233+43_233+161dupC others(118): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 3/6 | chr14 | 100546339 | ||||||
chr14:100546339
|
A | ACCCCGGC others(129): Show |
1 | a0001c0002t0001g0225 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.233+26_233+161dupC others(135): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 3/6 | chr14 | 100546339 | ||||||
chr14:100546339
|
A | G | 4 | a0001c0002t0001g0160a0001c0002t0001g0179a0001c0002t0001g0211others(1): Show | 4 | HG00140.hp2 NA18969.hp2 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.233+162T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 3/6 | chr14 | 100546339 | ||||||
chr14:100546339
|
ACCCCGGC others(10): Show |
A | 11 | a0001c0002t0001g0148a0001c0002t0001g0183a0001c0002t0001g0237others(8): Show | 11 | HG01891.hp1 HG02647.hp1 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.233+145_233+161del others(17): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 3/6 | chr14 | 100546339 | ||||||
chr14:100546339
|
ACCCCGGC others(27): Show |
A | 23 | a0001c0001t0001g0062a0001c0001t0001g0266a0001c0002t0001g0230others(20): Show | 23 | HG00642.hp1 HG00733.hp1 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.233+128_233+161del others(34): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 3/6 | chr14 | 100546339 | ||||||
chr14:100546339
|
ACCCCGGC others(44): Show |
A | 33 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0037others(30): Show | 38 | HG00408.hp1 HG00639.hp1 HG01069.hp1 others(35): Show |
intron_variant | MODIFIER | c.233+111_233+161del others(51): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 3/6 | chr14 | 100546339 | ||||||
chr14:100546339
|
ACCCCGGC others(61): Show |
A | 32 | a0001c0001t0001g0011a0001c0001t0001g0021a0001c0001t0001g0022others(29): Show | 33 | HG01070.hp1 HG01099.hp1 HG01099.hp2 others(30): Show |
intron_variant | MODIFIER | c.233+94_233+161delC others(67): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 3/6 | chr14 | 100546339 | ||||||
chr14:100546339
|
ACCCCGGC others(78): Show |
A | 6 | a0001c0001t0001g0009a0001c0001t0001g0126a0001c0005t0001g0069others(3): Show | 7 | HG00544.hp1 HG01884.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.233+77_233+161delC others(84): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 3/6 | chr14 | 100546339 | ||||||
chr14:100546339
|
ACCCCGGC others(95): Show |
A | 95 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(92): Show | 106 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(103): Show |
intron_variant | MODIFIER | c.233+60_233+161del | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 3/6 | chr14 | 100546339 | ||||||
chr14:100546339
|
ACCCCGGC others(112): Show |
A | 7 | a0001c0001t0001g0176a0001c0003t0001g0194a0001c0004t0001g0273others(4): Show | 7 | HG00733.hp2 HG02258.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.233+43_233+161del | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 3/6 | chr14 | 100546339 | ||||||
chr14:100546391
|
C | G | 2 | a0001c0003t0001g0143a0001c0003t0005g0297 | 2 | HG02615.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.233+110G>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 3/6 | chr14 | 100546391 | ||||||
chr14:100546408
|
C | G | 11 | a0001c0001t0001g0046a0001c0001t0001g0062a0001c0001t0001g0173others(8): Show | 11 | HG00733.hp1 HG01891.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.233+93G>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 3/6 | chr14 | 100546408 | ||||||
chr14:100546425
|
C | G | 38 | a0001c0001t0001g0010a0001c0001t0001g0046a0001c0001t0001g0049others(35): Show | 40 | HG00408.hp1 HG00733.hp1 HG01069.hp1 others(37): Show |
intron_variant | MODIFIER | c.233+76G>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 3/6 | chr14 | 100546425 | ||||||
chr14:100546442
|
C | G | 85 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0021others(82): Show | 90 | HG00408.hp1 HG00544.hp1 HG00733.hp1 others(87): Show |
intron_variant | MODIFIER | c.233+59G>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 3/6 | chr14 | 100546442 | ||||||
chr14:100546459
|
C | G | 102 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(99): Show | 109 | HG00408.hp1 HG00544.hp1 HG00639.hp1 others(106): Show |
intron_variant | MODIFIER | c.233+42G>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 3/6 | chr14 | 100546459 | ||||||
chr14:100546476
|
C | CCCCGGCC others(10): Show |
1 | a0001c0002t0001g0159 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.233+24_233+25insCC others(15): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 3/6 | chr14 | 100546476 | ||||||
chr14:100546476
|
C | G | 201 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(198): Show | 219 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(216): Show |
intron_variant | MODIFIER | c.233+25G>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 3/6 | chr14 | 100546476 | ||||||
chr14:100546689
|
G | A | 3 | a0001c0003t0001g0187a0001c0003t0001g0194a0001c0016t0001g0257 | 3 | HG00544.hp1 NA18998.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.72-27C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100546689 | ||||||
chr14:100546763
|
G | GGC | 8 | a0001c0001t0001g0039a0001c0001t0001g0061a0001c0001t0001g0127others(5): Show | 8 | HG01346.hp1 HG01928.hp2 HG01975.hp1 others(5): Show |
intron_variant | MODIFIER | c.72-103_72-102dupGC | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100546763 | ||||||
chr14:100546763
|
GGC | G | 15 | a0001c0001t0001g0053a0001c0001t0001g0056a0001c0001t0001g0089others(12): Show | 15 | HG00438.hp1 HG01099.hp1 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.72-103_72-102delGC | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100546763 | ||||||
chr14:100546763
|
GGCGC | G | 4 | a0001c0001t0001g0114a0001c0001t0001g0176a0001c0001t0001g0185others(1): Show | 4 | HG00621.hp2 HG00733.hp2 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.72-105_72-102delGC others(2): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100546763 | ||||||
chr14:100546767
|
C | G | 4 | a0001c0001t0001g0005a0001c0001t0001g0037a0001c0001t0001g0041others(1): Show | 5 | HG00639.hp1 HG01884.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.72-105G>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100546767 | ||||||
chr14:100546774
|
GCGCGCGC others(3): Show |
G | 15 | a0001c0003t0001g0003a0001c0003t0001g0013a0001c0003t0001g0064others(12): Show | 18 | HG02109.hp1 HG02280.hp2 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.72-122_72-113delTG others(8): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100546774 | ||||||
chr14:100546774
|
GCGCGCGC others(9): Show |
G | 1 | a0001c0004t0001g0273 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.72-128_72-113delTG others(14): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100546774 | ||||||
chr14:100546774
|
GCGCGCGC others(11): Show |
G | 5 | a0001c0005t0001g0047a0001c0005t0001g0138a0001c0005t0010g0289others(2): Show | 5 | HG02258.hp1 HG02622.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.72-130_72-113delTG others(16): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100546774 | ||||||
chr14:100546776
|
G | A | 1 | a0001c0001t0001g0050 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.72-114C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100546776 | ||||||
chr14:100546776
|
G | GCA | 4 | a0001c0001t0001g0071a0001c0001t0001g0149a0001c0001t0001g0175others(1): Show | 4 | HG01167.hp2 HG01346.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.72-115_72-114insTG | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100546776 | ||||||
chr14:100546776
|
G | GCACA | 6 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(3): Show | 6 | HG02258.hp2 HG02809.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.72-115_72-114insTG others(2): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100546776 | ||||||
chr14:100546776
|
GCGCGCAC others(1): Show |
G | 8 | a0001c0001t0001g0049a0001c0001t0001g0195a0001c0003t0005g0297others(5): Show | 8 | HG01978.hp1 HG02615.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.72-122_72-115delTG others(6): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100546776 | ||||||
chr14:100546776
|
GCGCGCAC others(3): Show |
G | 8 | a0001c0001t0001g0005a0001c0001t0001g0037a0001c0001t0001g0041others(5): Show | 9 | HG00639.hp1 HG01884.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.72-124_72-115delTG others(8): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100546776 | ||||||
chr14:100546776
|
GCGCGCAC others(5): Show |
G | 2 | a0001c0003t0001g0202a0001c0008t0001g0066 | 2 | HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.72-126_72-115delTG others(10): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100546776 | ||||||
chr14:100546778
|
G | A | 25 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0021others(22): Show | 27 | HG00408.hp1 HG00733.hp1 HG01069.hp1 others(24): Show |
intron_variant | MODIFIER | c.72-116C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100546778 | ||||||
chr14:100546778
|
GCGCA | G | 66 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(63): Show | 71 | HG00423.hp2 HG00597.hp1 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.72-120_72-117delTG others(2): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100546778 | ||||||
chr14:100546778
|
GCGCACA | G | 16 | a0001c0001t0001g0001a0001c0001t0001g0055a0001c0001t0001g0099others(13): Show | 21 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(18): Show |
intron_variant | MODIFIER | c.72-122_72-117delTG others(4): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100546778 | ||||||
chr14:100546778
|
GCGCACAC others(3): Show |
G | 1 | a0001c0003t0001g0194 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.72-126_72-117delTG others(8): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100546778 | ||||||
chr14:100546778
|
GCGCACAC others(5): Show |
G | 2 | a0001c0001t0001g0080a0001c0001t0001g0081 | 2 | NA19068.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.72-128_72-117delTG others(10): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100546778 | ||||||
chr14:100546778
|
GCGCACAC others(7): Show |
G | 6 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0164others(3): Show | 6 | HG01099.hp2 HG02976.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.72-130_72-117delTG others(12): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100546778 | ||||||
chr14:100546780
|
G | A | 40 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(37): Show | 44 | HG00408.hp1 HG00733.hp1 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.72-118C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100546780 | ||||||
chr14:100546780
|
G | GCA | 13 | a0001c0002t0001g0097a0001c0002t0001g0123a0001c0002t0001g0145others(10): Show | 13 | HG00741.hp2 HG01081.hp2 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.72-120_72-119dupTG | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100546780 | ||||||
chr14:100546780
|
GCA | G | 49 | a0001c0001t0001g0244a0001c0002t0001g0018a0001c0002t0001g0020others(46): Show | 49 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(46): Show |
intron_variant | MODIFIER | c.72-120_72-119delTG | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100546780 | ||||||
chr14:100546780
|
GCACA | G | 7 | a0001c0001t0001g0110a0001c0001t0001g0119a0001c0001t0001g0227others(4): Show | 7 | HG00642.hp2 HG00741.hp1 HG01069.hp2 others(4): Show |
intron_variant | MODIFIER | c.72-122_72-119delTG others(2): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100546780 | ||||||
chr14:100546780
|
GCACACA | G | 4 | a0001c0001t0001g0120a0001c0002t0001g0219a0001c0002t0001g0232others(1): Show | 4 | HG00099.hp1 HG02135.hp2 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.72-124_72-119delTG others(4): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100546780 | ||||||
chr14:100546780
|
GCACACAC others(5): Show |
G | 11 | a0001c0004t0001g0004a0001c0004t0001g0034a0001c0004t0003g0028others(8): Show | 12 | HG02056.hp2 NA18964.hp2 NA18973.hp1 others(9): Show |
intron_variant | MODIFIER | c.72-130_72-119delTG others(10): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100546780 | ||||||
chr14:100546780
|
GCACACAC others(7): Show |
G | 2 | a0001c0001t0001g0166a0001c0001t0001g0169 | 2 | HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.72-132_72-119delTG others(12): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100546780 | ||||||
chr14:100546782
|
A | G | 1 | a0001c0001t0001g0118 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.72-120T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100546782 | ||||||
chr14:100546784
|
A | G | 1 | a0001c0002t0012g0150 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.72-122T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100546784 | ||||||
chr14:100546786
|
A | G | 1 | a0001c0001t0001g0110 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.72-124T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100546786 | ||||||
chr14:100546790
|
A | G | 1 | a0001c0002t0001g0282 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.72-128T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100546790 | ||||||
chr14:100546794
|
A | G | 11 | a0001c0004t0001g0004a0001c0004t0001g0034a0001c0004t0003g0028others(8): Show | 12 | HG02056.hp2 NA18964.hp2 NA18973.hp1 others(9): Show |
intron_variant | MODIFIER | c.72-132T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100546794 | ||||||
chr14:100546806
|
A | G | 1 | a0001c0001t0001g0186 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.72-144T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100546806 | ||||||
chr14:100546810
|
A | T | 16 | a0001c0003t0001g0003a0001c0003t0001g0013a0001c0003t0001g0064others(13): Show | 19 | HG02109.hp1 HG02280.hp2 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.72-148T>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100546810 | ||||||
chr14:100546812
|
ACTCACAC others(4): Show |
A | 1 | a0001c0008t0001g0167 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.72-161_72-151delGT others(9): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100546812 | ||||||
chr14:100546814
|
T | A | 41 | a0001c0001t0001g0005a0001c0001t0001g0037a0001c0001t0001g0041others(38): Show | 45 | HG00544.hp1 HG00639.hp1 HG01884.hp2 others(42): Show |
intron_variant | MODIFIER | c.72-152A>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100546814 | ||||||
chr14:100546823
|
C | A | 1 | a0001c0001t0001g0057 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.72-161G>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100546823 | ||||||
chr14:100546837
|
C | A | 11 | a0001c0004t0001g0004a0001c0004t0001g0034a0001c0004t0003g0028others(8): Show | 12 | HG02056.hp2 NA18964.hp2 NA18973.hp1 others(9): Show |
intron_variant | MODIFIER | c.72-175G>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100546837 | ||||||
chr14:100546852
|
T | C | 207 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(204): Show | 226 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(223): Show |
intron_variant | MODIFIER | c.72-190A>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100546852 | ||||||
chr14:100546885
|
C | T | 4 | a0001c0005t0001g0047a0001c0005t0001g0138a0001c0005t0010g0289others(1): Show | 4 | HG02258.hp1 HG02622.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.72-223G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100546885 | ||||||
chr14:100547059
|
C | G | 10 | a0001c0003t0001g0013a0001c0003t0001g0064a0001c0003t0001g0140others(7): Show | 11 | HG02109.hp1 HG02280.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.72-397G>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100547059 | ||||||
chr14:100547343
|
C | T | 2 | a0001c0001t0001g0196a0001c0001t0001g0281 | 2 | HG00609.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.72-681G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100547343 | ||||||
chr14:100547492
|
T | G | 55 | a0001c0001t0001g0005a0001c0001t0001g0037a0001c0001t0001g0041others(52): Show | 60 | HG00544.hp1 HG00639.hp1 HG01884.hp2 others(57): Show |
intron_variant | MODIFIER | c.72-830A>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100547492 | ||||||
chr14:100547653
|
G | A | 2 | a0001c0006t0001g0204a0001c0006t0001g0267 | 2 | HG02886.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.72-991C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100547653 | ||||||
chr14:100547704
|
G | A | 1 | a0001c0002t0001g0211 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.72-1042C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100547704 | ||||||
chr14:100547712
|
C | T | 1 | a0001c0004t0001g0273 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.72-1050G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100547712 | ||||||
chr14:100547796
|
T | C | 11 | a0001c0001t0001g0001a0001c0001t0001g0055a0001c0001t0001g0080others(8): Show | 16 | HG00544.hp2 HG00558.hp1 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.72-1134A>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100547796 | ||||||
chr14:100547880
|
C | T | 1 | a0001c0002t0001g0243 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.72-1218G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100547880 | ||||||
chr14:100547950
|
A | G | 4 | a0001c0001t0001g0173a0001c0003t0001g0202a0001c0008t0001g0066others(1): Show | 4 | HG02055.hp1 HG02965.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.72-1288T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100547950 | ||||||
chr14:100548081
|
G | C | 197 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(194): Show | 215 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(212): Show |
intron_variant | MODIFIER | c.72-1419C>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100548081 | ||||||
chr14:100548172
|
G | A | 1 | a0001c0001t0001g0195 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.72-1510C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100548172 | ||||||
chr14:100548255
|
A | T | 10 | a0001c0001t0001g0176a0001c0005t0001g0069a0001c0005t0002g0051others(7): Show | 10 | HG00733.hp2 HG01884.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.72-1593T>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100548255 | ||||||
chr14:100548296
|
A | AG | 196 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(193): Show | 214 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(211): Show |
intron_variant | MODIFIER | c.72-1635_72-1634ins others(1): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100548296 | ||||||
chr14:100548364
|
G | A | 4 | a0001c0001t0001g0002a0001c0001t0001g0116a0001c0001t0001g0125others(1): Show | 6 | HG00639.hp2 HG01192.hp2 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.72-1702C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100548364 | ||||||
chr14:100548381
|
T | C | 1 | a0001c0004t0001g0273 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.72-1719A>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100548381 | ||||||
chr14:100548492
|
C | T | 1 | a0001c0006t0001g0204 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.72-1830G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100548492 | ||||||
chr14:100548539
|
C | G | 8 | a0001c0003t0001g0013a0001c0003t0001g0140a0001c0003t0001g0141others(5): Show | 9 | HG02109.hp1 HG02630.hp2 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.72-1877G>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100548539 | ||||||
chr14:100548692
|
G | A | 1 | a0001c0003t0001g0067 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.72-2030C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100548692 | ||||||
chr14:100548734
|
A | G | 3 | a0001c0003t0001g0187a0001c0003t0001g0194a0001c0016t0001g0257 | 3 | HG00544.hp1 NA18998.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.72-2072T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100548734 | ||||||
chr14:100548781
|
C | T | 1 | a0001c0001t0001g0105 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.72-2119G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100548781 | ||||||
chr14:100548824
|
C | A | 4 | a0001c0001t0001g0005a0001c0001t0001g0037a0001c0001t0001g0041others(1): Show | 5 | HG00639.hp1 HG01884.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.72-2162G>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100548824 | ||||||
chr14:100548853
|
C | T | 3 | a0001c0003t0001g0187a0001c0003t0001g0194a0001c0016t0001g0257 | 3 | HG00544.hp1 NA18998.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.72-2191G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100548853 | ||||||
chr14:100548907
|
C | A | 2 | a0001c0001t0001g0053a0001c0001t0001g0181 | 2 | HG02572.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.72-2245G>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100548907 | ||||||
chr14:100549043
|
T | C | 156 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(153): Show | 170 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(167): Show |
intron_variant | MODIFIER | c.72-2381A>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100549043 | ||||||
chr14:100549044
|
C | T | 1 | a0001c0001t0001g0176 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.72-2382G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100549044 | ||||||
chr14:100549099
|
G | A | 11 | a0001c0001t0001g0173a0001c0003t0001g0054a0001c0003t0001g0202others(8): Show | 11 | HG02055.hp1 HG02486.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.72-2437C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100549099 | ||||||
chr14:100549106
|
G | A | 1 | a0001c0002t0001g0159 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.72-2444C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100549106 | ||||||
chr14:100549128
|
A | C | 8 | a0001c0005t0002g0051a0001c0005t0002g0052a0001c0005t0002g0068others(5): Show | 8 | HG01891.hp2 HG02055.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.72-2466T>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100549128 | ||||||
chr14:100549196
|
C | T | 2 | a0001c0002t0001g0026a0001c0002t0001g0253 | 2 | HG00140.hp1 HG00642.hp2 |
intron_variant | MODIFIER | c.72-2534G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100549196 | ||||||
chr14:100549197
|
G | A | 1 | a0001c0002t0001g0236 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.72-2535C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100549197 | ||||||
chr14:100549292
|
G | A | 14 | a0001c0003t0001g0187a0001c0003t0001g0194a0001c0004t0001g0004others(11): Show | 15 | HG00544.hp1 HG02056.hp2 NA18964.hp2 others(12): Show |
intron_variant | MODIFIER | c.72-2630C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100549292 | ||||||
chr14:100549526
|
A | G | 1 | a0001c0001t0014g0048 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.72-2864T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100549526 | ||||||
chr14:100549594
|
G | C | 2 | a0001c0002t0001g0211a0001c0002t0001g0246 | 2 | HG00140.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.72-2932C>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100549594 | ||||||
chr14:100549605
|
C | G | 3 | a0001c0005t0002g0068a0001c0005t0002g0078a0001c0005t0002g0180 | 3 | HG01891.hp2 NA18906.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.72-2943G>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100549605 | ||||||
chr14:100549847
|
A | G | 2 | a0001c0001t0001g0062a0001c0009t0001g0136 | 2 | HG02809.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.72-3185T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100549847 | ||||||
chr14:100549853
|
G | A | 40 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0021others(37): Show | 42 | HG00408.hp1 HG00733.hp1 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.72-3191C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100549853 | ||||||
chr14:100549902
|
A | G | 1 | a0001c0001t0001g0063 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.72-3240T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100549902 | ||||||
chr14:100549906
|
A | G | 1 | a0001c0005t0001g0069 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.72-3244T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100549906 | ||||||
chr14:100549970
|
C | T | 89 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(86): Show | 102 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.72-3308G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100549970 | ||||||
chr14:100550037
|
G | A | 1 | a0001c0001t0001g0118 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.72-3375C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100550037 | ||||||
chr14:100550163
|
G | A | 2 | a0001c0003t0001g0054a0001c0003t0001g0292 | 2 | HG02572.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.72-3501C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100550163 | ||||||
chr14:100550204
|
C | T | 1 | a0001c0003t0001g0292 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.72-3542G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100550204 | ||||||
chr14:100550230
|
A | G | 210 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(207): Show | 229 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(226): Show |
intron_variant | MODIFIER | c.72-3568T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100550230 | ||||||
chr14:100550385
|
C | T | 1 | a0001c0001t0001g0168 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.72-3723G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100550385 | ||||||
chr14:100550483
|
C | G | 1 | a0001c0001t0001g0162 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.72-3821G>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100550483 | ||||||
chr14:100550487
|
A | G | 181 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(178): Show | 196 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(193): Show |
intron_variant | MODIFIER | c.72-3825T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100550487 | ||||||
chr14:100550550
|
G | C | 7 | a0001c0001t0001g0009a0001c0001t0001g0027a0001c0001t0001g0213others(4): Show | 8 | HG01884.hp1 HG01891.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.72-3888C>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100550550 | ||||||
chr14:100550586
|
A | G | 1 | a0001c0005t0001g0138 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.72-3924T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100550586 | ||||||
chr14:100550659
|
C | CTTG | 106 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(103): Show | 118 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.72-4000_72-3998dup others(3): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100550659 | ||||||
chr14:100550763
|
C | T | 1 | a0001c0002t0001g0264 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.72-4101G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100550763 | ||||||
chr14:100550766
|
C | G | 47 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0021others(44): Show | 49 | HG00408.hp1 HG00558.hp2 HG00733.hp1 others(46): Show |
intron_variant | MODIFIER | c.72-4104G>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100550766 | ||||||
chr14:100550855
|
G | A | 1 | a0001c0003t0001g0202 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.72-4193C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100550855 | ||||||
chr14:100550894
|
G | A | 1 | a0001c0005t0001g0069 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.72-4232C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100550894 | ||||||
chr14:100550934
|
G | T | 1 | a0001c0001t0001g0101 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.72-4272C>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100550934 | ||||||
chr14:100551153
|
C | T | 23 | a0001c0001t0001g0005a0001c0001t0001g0037a0001c0001t0001g0041others(20): Show | 25 | HG00544.hp1 HG00639.hp1 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.72-4491G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100551153 | ||||||
chr14:100551229
|
G | A | 3 | a0001c0002t0001g0018a0001c0002t0001g0083a0001c0002t0001g0222 | 3 | NA18969.hp1 NA18973.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.72-4567C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100551229 | ||||||
chr14:100551344
|
C | T | 1 | a0001c0003t0001g0171 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.72-4682G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100551344 | ||||||
chr14:100551345
|
G | T | 5 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(2): Show | 5 | HG02258.hp2 HG02886.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.72-4683C>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100551345 | ||||||
chr14:100551484
|
G | A | 1 | a0001c0001t0001g0286 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.72-4822C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100551484 | ||||||
chr14:100551709
|
A | C | 1 | a0001c0001t0001g0021 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.72-5047T>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100551709 | ||||||
chr14:100551734
|
A | G | 130 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(127): Show | 143 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(140): Show |
intron_variant | MODIFIER | c.72-5072T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100551734 | ||||||
chr14:100552002
|
C | T | 4 | a0001c0001t0001g0005a0001c0001t0001g0037a0001c0001t0001g0041others(1): Show | 5 | HG00639.hp1 HG01884.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.72-5340G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100552002 | ||||||
chr14:100552051
|
C | T | 6 | a0001c0003t0001g0177a0001c0004t0002g0045a0001c0004t0002g0170others(3): Show | 6 | HG02486.hp2 HG02809.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.72-5389G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100552051 | ||||||
chr14:100552159
|
G | A | 5 | a0001c0001t0001g0062a0001c0003t0001g0140a0001c0003t0001g0141others(2): Show | 5 | HG02809.hp1 HG03195.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.72-5497C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100552159 | ||||||
chr14:100552320
|
T | G | 1 | a0001c0003t0001g0294 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.72-5658A>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100552320 | ||||||
chr14:100552491
|
A | C | 4 | a0001c0002t0001g0070a0001c0002t0001g0144a0001c0002t0001g0215others(1): Show | 4 | HG02015.hp2 HG02165.hp1 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.72-5829T>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100552491 | ||||||
chr14:100552526
|
C | T | 5 | a0001c0003t0001g0054a0001c0003t0001g0274a0001c0003t0001g0275others(2): Show | 5 | HG02572.hp2 HG02630.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.72-5864G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100552526 | ||||||
chr14:100552600
|
G | T | 2 | a0001c0001t0001g0188a0001c0001t0001g0250 | 2 | HG01070.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.72-5938C>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100552600 | ||||||
chr14:100552737
|
G | A | 1 | a0001c0003t0001g0276 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.72-6075C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100552737 | ||||||
chr14:100552752
|
C | T | 7 | a0001c0001t0001g0053a0001c0001t0001g0166a0001c0001t0001g0168others(4): Show | 7 | HG01099.hp2 HG02572.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.72-6090G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100552752 | ||||||
chr14:100552959
|
G | T | 1 | a0001c0013t0001g0189 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.72-6297C>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100552959 | ||||||
chr14:100553092
|
C | T | 22 | a0001c0001t0001g0005a0001c0001t0001g0037a0001c0001t0001g0041others(19): Show | 24 | HG00544.hp1 HG00639.hp1 HG00733.hp2 others(21): Show |
intron_variant | MODIFIER | c.72-6430G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100553092 | ||||||
chr14:100553108
|
C | T | 1 | a0001c0001t0001g0110 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.72-6446G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100553108 | ||||||
chr14:100553631
|
G | A | 1 | a0006c0015t0001g0226 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.72-6969C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100553631 | ||||||
chr14:100553895
|
C | T | 1 | a0001c0001t0001g0207 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.72-7233G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100553895 | ||||||
chr14:100554114
|
C | T | 4 | a0001c0002t0001g0070a0001c0002t0001g0144a0001c0002t0001g0215others(1): Show | 4 | HG02015.hp2 HG02165.hp1 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.72-7452G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100554114 | ||||||
chr14:100554182
|
G | A | 11 | a0001c0003t0001g0054a0001c0003t0001g0177a0001c0003t0001g0292others(8): Show | 11 | HG01891.hp2 HG02486.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.72-7520C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100554182 | ||||||
chr14:100554322
|
G | A | 4 | a0001c0001t0001g0005a0001c0001t0001g0037a0001c0001t0001g0041others(1): Show | 5 | HG00639.hp1 HG01884.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.72-7660C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100554322 | ||||||
chr14:100554463
|
C | T | 50 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0021others(47): Show | 54 | HG00140.hp1 HG00408.hp1 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.72-7801G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100554463 | ||||||
chr14:100554532
|
C | T | 15 | a0001c0003t0001g0054a0001c0003t0001g0177a0001c0003t0001g0272others(12): Show | 15 | HG01891.hp2 HG02486.hp2 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.72-7870G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100554532 | ||||||
chr14:100554732
|
C | A | 10 | a0001c0001t0001g0176a0001c0001t0001g0178a0001c0001t0001g0213others(7): Show | 10 | HG00733.hp2 HG01884.hp1 HG02015.hp2 others(7): Show |
intron_variant | MODIFIER | c.72-8070G>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100554732 | ||||||
chr14:100554881
|
C | A | 200 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(197): Show | 218 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(215): Show |
intron_variant | MODIFIER | c.72-8219G>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100554881 | ||||||
chr14:100554908
|
GGCCTTCG others(6): Show |
G | 10 | a0001c0004t0001g0004a0001c0004t0001g0034a0001c0004t0003g0028others(7): Show | 11 | HG02056.hp2 NA18973.hp1 NA18979.hp2 others(8): Show |
intron_variant | MODIFIER | c.72-8259_72-8247del others(13): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100554908 | ||||||
chr14:100555072
|
C | T | 1 | a0001c0005t0001g0138 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.72-8410G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100555072 | ||||||
chr14:100555221
|
C | T | 53 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0021others(50): Show | 57 | HG00140.hp1 HG00408.hp1 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.72-8559G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100555221 | ||||||
chr14:100555520
|
C | T | 2 | a0001c0001t0001g0019a0001c0001t0001g0100 | 2 | HG01952.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.72-8858G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100555520 | ||||||
chr14:100555679
|
G | A | 1 | a0001c0002t0001g0070 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.72-9017C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100555679 | ||||||
chr14:100555713
|
C | T | 3 | a0001c0004t0003g0028a0001c0004t0003g0031a0001c0004t0003g0032 | 3 | NA18979.hp2 NA18995.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.72-9051G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100555713 | ||||||
chr14:100555879
|
A | G | 1 | a0001c0002t0001g0024 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.72-9217T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100555879 | ||||||
chr14:100555940
|
T | G | 4 | a0001c0002t0001g0070a0001c0002t0001g0144a0001c0002t0001g0215others(1): Show | 4 | HG02015.hp2 HG02165.hp1 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.72-9278A>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100555940 | ||||||
chr14:100556004
|
T | G | 8 | a0001c0001t0001g0005a0001c0001t0001g0037a0001c0001t0001g0041others(5): Show | 9 | HG00544.hp1 HG00639.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.72-9342A>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100556004 | ||||||
chr14:100556238
|
C | G | 7 | a0001c0001t0001g0173a0001c0001t0001g0176a0001c0001t0001g0178others(4): Show | 7 | HG00733.hp2 HG02055.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.72-9576G>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100556238 | ||||||
chr14:100556327
|
G | A | 12 | a0001c0002t0001g0020a0001c0002t0001g0070a0001c0002t0001g0144others(9): Show | 12 | HG00544.hp1 HG00558.hp2 HG02015.hp2 others(9): Show |
intron_variant | MODIFIER | c.72-9665C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100556327 | ||||||
chr14:100556335
|
G | GC | 56 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0021others(53): Show | 60 | HG00140.hp1 HG00408.hp1 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.72-9674dupG | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100556335 | ||||||
chr14:100556338
|
C | G | 10 | a0001c0004t0001g0004a0001c0004t0001g0034a0001c0004t0003g0028others(7): Show | 11 | HG02056.hp2 NA18973.hp1 NA18979.hp2 others(8): Show |
intron_variant | MODIFIER | c.72-9676G>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100556338 | ||||||
chr14:100556344
|
C | A | 1 | a0001c0001t0001g0050 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.72-9682G>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100556344 | ||||||
chr14:100556505
|
G | C | 6 | a0001c0001t0001g0009a0001c0001t0001g0027a0001c0001t0001g0213others(3): Show | 7 | HG01884.hp1 HG02109.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.72-9843C>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100556505 | ||||||
chr14:100556857
|
C | T | 5 | a0001c0002t0001g0070a0001c0002t0001g0144a0001c0002t0001g0215others(2): Show | 5 | HG00558.hp2 HG02015.hp2 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.72-10195G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100556857 | ||||||
chr14:100556902
|
C | A | 1 | a0001c0003t0001g0194 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.72-10240G>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100556902 | ||||||
chr14:100556942
|
C | T | 97 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(94): Show | 108 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.72-10280G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100556942 | ||||||
chr14:100556971
|
C | T | 1 | a0001c0005t0001g0069 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.72-10309G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100556971 | ||||||
chr14:100557055
|
TCTGCCGG others(63): Show |
T | 60 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(57): Show | 65 | HG00140.hp1 HG00408.hp1 HG00642.hp2 others(62): Show |
intron_variant | MODIFIER | c.72-10463_72-10394d others(72): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100557055 | ||||||
chr14:100557099
|
G | C | 19 | a0001c0001t0001g0173a0001c0001t0001g0176a0001c0001t0001g0178others(16): Show | 20 | HG00733.hp2 HG01884.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.72-10437C>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100557099 | ||||||
chr14:100557111
|
G | GTCCCAGC others(63): Show |
1 | a0001c0005t0001g0138 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.72-10519_72-10450d others(72): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100557111 | ||||||
chr14:100557125
|
CCTGCCGG others(63): Show |
C | 2 | a0001c0001t0001g0248a0001c0001t0001g0260 | 2 | HG00597.hp1 HG00621.hp1 |
intron_variant | MODIFIER | c.72-10533_72-10464d others(72): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100557125 | ||||||
chr14:100557129
|
C | T | 2 | a0001c0003t0001g0294a0001c0005t0010g0289 | 2 | HG02258.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.72-10467G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100557129 | ||||||
chr14:100557147
|
A | C | 3 | a0001c0004t0003g0028a0001c0004t0003g0031a0001c0004t0003g0032 | 3 | NA18979.hp2 NA18995.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.72-10485T>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100557147 | ||||||
chr14:100557181
|
A | G | 96 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(93): Show | 107 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.72-10519T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100557181 | ||||||
chr14:100557195
|
T | C | 2 | a0001c0001t0001g0009a0001c0001t0001g0027 | 3 | HG02109.hp2 HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.72-10533A>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100557195 | ||||||
chr14:100557201
|
A | G | 2 | a0001c0001t0001g0009a0001c0001t0001g0027 | 3 | HG02109.hp2 HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.72-10539T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100557201 | ||||||
chr14:100557273
|
G | A | 4 | a0001c0001t0001g0213a0001c0003t0001g0294a0001c0005t0001g0069others(1): Show | 4 | HG01884.hp1 HG02258.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.72-10611C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100557273 | ||||||
chr14:100557286
|
G | A | 4 | a0001c0001t0001g0213a0001c0003t0001g0294a0001c0005t0001g0069others(1): Show | 4 | HG01884.hp1 HG02258.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.72-10624C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100557286 | ||||||
chr14:100557287
|
G | A | 4 | a0001c0001t0001g0213a0001c0003t0001g0294a0001c0005t0001g0069others(1): Show | 4 | HG01884.hp1 HG02258.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.71+10624C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100557287 | ||||||
chr14:100557330
|
C | T | 1 | a0001c0005t0001g0138 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.71+10581G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100557330 | ||||||
chr14:100557369
|
C | T | 62 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(59): Show | 67 | HG00140.hp1 HG00408.hp1 HG00642.hp2 others(64): Show |
intron_variant | MODIFIER | c.71+10542G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100557369 | ||||||
chr14:100557458
|
C | T | 57 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(54): Show | 62 | HG00140.hp1 HG00408.hp1 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.71+10453G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100557458 | ||||||
chr14:100557592
|
A | G | 4 | a0001c0001t0001g0005a0001c0001t0001g0037a0001c0001t0001g0041others(1): Show | 5 | HG00639.hp1 HG01884.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.71+10319T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100557592 | ||||||
chr14:100557904
|
C | A | 15 | a0001c0002t0001g0070a0001c0002t0001g0144a0001c0002t0001g0215others(12): Show | 15 | HG00558.hp2 HG01891.hp2 HG02015.hp2 others(12): Show |
intron_variant | MODIFIER | c.71+10007G>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100557904 | ||||||
chr14:100557956
|
G | C | 2 | a0001c0003t0001g0294a0001c0005t0010g0289 | 2 | HG02258.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.71+9955C>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100557956 | ||||||
chr14:100557960
|
C | T | 4 | a0001c0001t0001g0005a0001c0001t0001g0037a0001c0001t0001g0041others(1): Show | 5 | HG00639.hp1 HG01884.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.71+9951G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100557960 | ||||||
chr14:100558075
|
C | G | 3 | a0001c0001t0001g0176a0001c0001t0001g0178a0001c0003t0001g0177 | 3 | HG00733.hp2 HG02818.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.71+9836G>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100558075 | ||||||
chr14:100558191
|
GAA | G | 97 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(94): Show | 108 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.71+9718_71+9719del others(2): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100558191 | ||||||
chr14:100558205
|
T | C | 6 | a0001c0001t0001g0005a0001c0001t0001g0037a0001c0001t0001g0041others(3): Show | 7 | HG00639.hp1 HG01884.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.71+9706A>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100558205 | ||||||
chr14:100558387
|
C | G | 3 | a0001c0002t0001g0148a0001c0002t0001g0230a0001c0002t0001g0237 | 3 | NA18971.hp1 NA19009.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.71+9524G>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100558387 | ||||||
chr14:100558468
|
C | T | 1 | a0001c0004t0001g0273 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.71+9443G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100558468 | ||||||
chr14:100558608
|
G | C | 5 | a0001c0002t0001g0070a0001c0002t0001g0144a0001c0002t0001g0215others(2): Show | 5 | HG00558.hp2 HG02015.hp2 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.71+9303C>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100558608 | ||||||
chr14:100558844
|
C | T | 5 | a0001c0001t0001g0213a0001c0003t0001g0294a0001c0004t0001g0273others(2): Show | 5 | HG01884.hp1 HG02258.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.71+9067G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100558844 | ||||||
chr14:100558921
|
A | G | 11 | a0001c0004t0001g0004a0001c0004t0001g0034a0001c0004t0003g0028others(8): Show | 12 | HG02056.hp2 HG02622.hp2 NA18973.hp1 others(9): Show |
intron_variant | MODIFIER | c.71+8990T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100558921 | ||||||
chr14:100558945
|
C | T | 2 | a0001c0001t0001g0234a0001c0001t0001g0266 | 2 | HG00733.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.71+8966G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100558945 | ||||||
chr14:100559190
|
G | A | 10 | a0001c0004t0001g0004a0001c0004t0001g0034a0001c0004t0003g0028others(7): Show | 11 | HG02056.hp2 NA18973.hp1 NA18979.hp2 others(8): Show |
intron_variant | MODIFIER | c.71+8721C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100559190 | ||||||
chr14:100559210
|
C | T | 7 | a0001c0001t0001g0053a0001c0001t0001g0166a0001c0001t0001g0168others(4): Show | 7 | HG01099.hp2 HG02572.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.71+8701G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100559210 | ||||||
chr14:100559329
|
C | T | 1 | a0001c0002t0001g0215 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.71+8582G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100559329 | ||||||
chr14:100559381
|
T | A | 19 | a0001c0002t0001g0070a0001c0002t0001g0144a0001c0002t0001g0215others(16): Show | 19 | HG00558.hp2 HG01891.hp2 HG02015.hp2 others(16): Show |
intron_variant | MODIFIER | c.71+8530A>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100559381 | ||||||
chr14:100559482
|
C | T | 1 | a0001c0002t0001g0284 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.71+8429G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100559482 | ||||||
chr14:100559563
|
C | T | 1 | a0001c0001t0001g0056 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.71+8348G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100559563 | ||||||
chr14:100559711
|
C | G | 106 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(103): Show | 118 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.71+8200G>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100559711 | ||||||
chr14:100559721
|
A | G | 8 | a0001c0001t0001g0053a0001c0001t0001g0166a0001c0001t0001g0168others(5): Show | 8 | HG01099.hp2 HG02572.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.71+8190T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100559721 | ||||||
chr14:100559799
|
C | G | 2 | a0001c0001t0001g0080a0001c0001t0001g0081 | 2 | NA19068.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.71+8112G>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100559799 | ||||||
chr14:100559811
|
G | A | 58 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(55): Show | 63 | HG00140.hp1 HG00408.hp1 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.71+8100C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100559811 | ||||||
chr14:100559962
|
A | G | 74 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(71): Show | 80 | HG00140.hp1 HG00408.hp1 HG00642.hp2 others(77): Show |
intron_variant | MODIFIER | c.71+7949T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100559962 | ||||||
chr14:100559974
|
G | A | 2 | a0001c0002t0006g0302a0001c0002t0006g0307 | 2 | HG02735.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.71+7937C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100559974 | ||||||
chr14:100560017
|
ATC | A | 10 | a0001c0004t0001g0004a0001c0004t0001g0034a0001c0004t0003g0028others(7): Show | 11 | HG02056.hp2 NA18973.hp1 NA18979.hp2 others(8): Show |
intron_variant | MODIFIER | c.71+7892_71+7893del others(2): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100560017 | ||||||
chr14:100560031
|
C | T | 1 | a0001c0003t0001g0294 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.71+7880G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100560031 | ||||||
chr14:100560259
|
C | T | 78 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(75): Show | 84 | HG00438.hp1 HG00544.hp1 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.71+7652G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100560259 | ||||||
chr14:100560362
|
C | A | 1 | a0001c0001t0001g0290 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.71+7549G>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100560362 | ||||||
chr14:100560453
|
C | T | 3 | a0001c0001t0001g0071a0001c0003t0001g0003a0001c0003t0001g0171 | 5 | HG02451.hp1 HG02976.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.71+7458G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100560453 | ||||||
chr14:100560454
|
G | A | 3 | a0001c0003t0001g0064a0001c0003t0001g0172a0001c0003t0001g0174 | 3 | HG02280.hp2 HG02922.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.71+7457C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100560454 | ||||||
chr14:100560548
|
C | T | 3 | a0001c0004t0003g0028a0001c0004t0003g0031a0001c0004t0003g0032 | 3 | NA18979.hp2 NA18995.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.71+7363G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100560548 | ||||||
chr14:100560688
|
C | T | 6 | a0001c0001t0001g0109a0001c0002t0001g0020a0001c0003t0001g0187others(3): Show | 6 | HG00544.hp1 HG02698.hp1 NA18995.hp1 others(3): Show |
intron_variant | MODIFIER | c.71+7223G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100560688 | ||||||
chr14:100560796
|
T | C | 277 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(274): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.71+7115A>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100560796 | ||||||
chr14:100560820
|
C | T | 30 | a0001c0001t0001g0005a0001c0001t0001g0037a0001c0001t0001g0041others(27): Show | 32 | HG00544.hp1 HG00639.hp1 HG00733.hp2 others(29): Show |
intron_variant | MODIFIER | c.71+7091G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100560820 | ||||||
chr14:100560964
|
C | T | 7 | a0001c0003t0001g0294a0001c0003t0005g0297a0001c0003t0006g0303others(4): Show | 7 | HG02258.hp1 HG02615.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.71+6947G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100560964 | ||||||
chr14:100560988
|
G | A | 94 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(91): Show | 105 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.71+6923C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100560988 | ||||||
chr14:100561001
|
T | C | 1 | a0001c0001t0001g0270 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.71+6910A>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100561001 | ||||||
chr14:100561036
|
TG | T | 203 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(200): Show | 221 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.71+6874delC | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100561036 | ||||||
chr14:100561064
|
G | A | 1 | a0001c0002t0004g0212 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.71+6847C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100561064 | ||||||
chr14:100561104
|
G | A | 5 | a0001c0001t0001g0166a0001c0001t0001g0168a0001c0001t0001g0169others(2): Show | 5 | HG01099.hp2 HG02886.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.71+6807C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100561104 | ||||||
chr14:100561111
|
C | T | 64 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(61): Show | 69 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(66): Show |
intron_variant | MODIFIER | c.71+6800G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100561111 | ||||||
chr14:100561195
|
C | T | 2 | a0001c0001t0001g0255a0006c0015t0001g0226 | 2 | HG01169.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.71+6716G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100561195 | ||||||
chr14:100561423
|
C | G | 1 | a0001c0002t0005g0296 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.71+6488G>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100561423 | ||||||
chr14:100561454
|
G | A | 6 | a0001c0001t0001g0062a0001c0003t0001g0140a0001c0003t0001g0141others(3): Show | 6 | HG02647.hp1 HG02809.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.71+6457C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100561454 | ||||||
chr14:100561497
|
C | G | 4 | a0001c0001t0001g0181a0001c0005t0002g0068a0001c0005t0002g0078others(1): Show | 4 | HG01891.hp2 HG02572.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.71+6414G>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100561497 | ||||||
chr14:100561557
|
T | C | 109 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(106): Show | 121 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.71+6354A>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100561557 | ||||||
chr14:100561558
|
G | C | 87 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(84): Show | 98 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.71+6353C>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100561558 | ||||||
chr14:100561558
|
G | T | 3 | a0001c0001t0001g0084a0001c0001t0001g0088a0001c0001t0001g0089 | 3 | NA19012.hp1 NA19081.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.71+6353C>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100561558 | ||||||
chr14:100561583
|
T | C | 3 | a0001c0001t0001g0096a0001c0001t0001g0122a0001c0001t0001g0151 | 3 | HG01943.hp1 NA18940.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.71+6328A>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100561583 | ||||||
chr14:100561614
|
G | A | 1 | a0001c0003t0005g0297 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.71+6297C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100561614 | ||||||
chr14:100561669
|
T | C | 110 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(107): Show | 122 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.71+6242A>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100561669 | ||||||
chr14:100561716
|
G | GA | 105 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(102): Show | 117 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.71+6194dupT | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100561716 | ||||||
chr14:100561716
|
G | GAA | 9 | a0001c0001t0001g0074a0001c0001t0001g0088a0001c0001t0001g0193others(6): Show | 9 | HG02055.hp2 HG02622.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.71+6193_71+6194dup others(2): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100561716 | ||||||
chr14:100561733
|
G | A | 1 | a0001c0003t0001g0272 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.71+6178C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100561733 | ||||||
chr14:100561891
|
A | G | 1 | a0001c0001t0001g0250 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.71+6020T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100561891 | ||||||
chr14:100562062
|
A | G | 111 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(108): Show | 124 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.71+5849T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100562062 | ||||||
chr14:100562079
|
C | G | 10 | a0001c0002t0001g0135a0001c0004t0001g0004a0001c0004t0001g0034others(7): Show | 11 | HG02056.hp2 NA18964.hp1 NA18973.hp1 others(8): Show |
intron_variant | MODIFIER | c.71+5832G>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100562079 | ||||||
chr14:100562081
|
A | G | 4 | a0001c0001t0001g0181a0001c0005t0002g0068a0001c0005t0002g0078others(1): Show | 4 | HG01891.hp2 HG02572.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.71+5830T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100562081 | ||||||
chr14:100562238
|
G | A | 1 | a0001c0005t0001g0138 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.71+5673C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100562238 | ||||||
chr14:100562283
|
C | T | 1 | a0001c0004t0003g0035 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.71+5628G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100562283 | ||||||
chr14:100562481
|
G | A | 207 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(204): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.71+5430C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100562481 | ||||||
chr14:100562503
|
T | C | 209 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(206): Show | 228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.71+5408A>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100562503 | ||||||
chr14:100562512
|
G | A | 3 | a0001c0001t0001g0176a0001c0001t0001g0178a0001c0003t0001g0177 | 3 | HG00733.hp2 HG02818.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.71+5399C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100562512 | ||||||
chr14:100562562
|
C | G | 20 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(17): Show | 22 | HG01099.hp2 HG02055.hp1 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.71+5349G>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100562562 | ||||||
chr14:100562587
|
G | A | 5 | a0001c0001t0001g0166a0001c0001t0001g0168a0001c0001t0001g0169others(2): Show | 5 | HG01099.hp2 HG02886.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.71+5324C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100562587 | ||||||
chr14:100562637
|
A | G | 1 | a0001c0002t0001g0214 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.71+5274T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100562637 | ||||||
chr14:100562664
|
C | G | 6 | a0001c0001t0001g0071a0001c0003t0001g0272a0001c0003t0001g0274others(3): Show | 6 | HG02615.hp2 HG02630.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.71+5247G>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100562664 | ||||||
chr14:100562694
|
G | A | 1 | a0001c0002t0001g0020 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.71+5217C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100562694 | ||||||
chr14:100562707
|
G | T | 1 | a0001c0003t0001g0272 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.71+5204C>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100562707 | ||||||
chr14:100562812
|
G | A | 7 | a0001c0003t0001g0294a0001c0003t0005g0297a0001c0003t0006g0303others(4): Show | 7 | HG02258.hp1 HG02615.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.71+5099C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100562812 | ||||||
chr14:100562866
|
G | A | 95 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(92): Show | 101 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.71+5045C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100562866 | ||||||
chr14:100562963
|
C | CA | 183 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(180): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.71+4947dupT | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100562963 | ||||||
chr14:100562987
|
A | G | 183 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(180): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.71+4924T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100562987 | ||||||
chr14:100562998
|
G | A | 1 | a0001c0002t0001g0243 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.71+4913C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100562998 | ||||||
chr14:100563412
|
A | G | 180 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(177): Show | 197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.71+4499T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100563412 | ||||||
chr14:100563522
|
G | A | 6 | a0001c0001t0001g0062a0001c0003t0001g0140a0001c0003t0001g0141others(3): Show | 6 | HG02647.hp1 HG02809.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.71+4389C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100563522 | ||||||
chr14:100563544
|
A | G | 28 | a0001c0001t0001g0166a0001c0001t0001g0168a0001c0001t0001g0169others(25): Show | 30 | HG01099.hp2 HG01891.hp2 HG02056.hp2 others(27): Show |
intron_variant | MODIFIER | c.71+4367T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100563544 | ||||||
chr14:100563547
|
C | T | 5 | a0001c0003t0005g0297a0001c0003t0006g0303a0001c0003t0006g0304others(2): Show | 5 | HG02615.hp1 HG02717.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.71+4364G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100563547 | ||||||
chr14:100563610
|
C | T | 1 | a0001c0001t0001g0012 | 2 | HG00673.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.71+4301G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100563610 | ||||||
chr14:100563672
|
A | AC | 4 | a0001c0001t0001g0091a0001c0001t0001g0101a0001c0001t0001g0102others(1): Show | 4 | HG00423.hp2 HG02080.hp2 HG02129.hp2 others(1): Show |
intron_variant | MODIFIER | c.71+4238dupG | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100563672 | ||||||
chr14:100563673
|
C | T | 2 | a0001c0001t0001g0146a0001c0002t0001g0145 | 2 | HG00741.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.71+4238G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100563673 | ||||||
chr14:100563694
|
C | T | 3 | a0001c0001t0001g0227a0001c0001t0001g0234a0001c0001t0001g0266 | 3 | HG00733.hp1 HG00741.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.71+4217G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100563694 | ||||||
chr14:100563849
|
T | C | 1 | a0001c0003t0001g0141 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.71+4062A>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100563849 | ||||||
chr14:100563855
|
C | T | 5 | a0001c0001t0001g0166a0001c0001t0001g0168a0001c0001t0001g0169others(2): Show | 5 | HG01099.hp2 HG02886.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.71+4056G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100563855 | ||||||
chr14:100563860
|
A | G | 35 | a0001c0001t0001g0062a0001c0001t0001g0166a0001c0001t0001g0168others(32): Show | 37 | HG01099.hp2 HG01891.hp2 HG02056.hp2 others(34): Show |
intron_variant | MODIFIER | c.71+4051T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100563860 | ||||||
chr14:100563895
|
T | C | 1 | a0001c0002t0001g0247 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.71+4016A>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100563895 | ||||||
chr14:100564064
|
G | A | 5 | a0001c0001t0001g0166a0001c0001t0001g0168a0001c0001t0001g0169others(2): Show | 5 | HG01099.hp2 HG02886.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.71+3847C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100564064 | ||||||
chr14:100564121
|
G | C | 1 | a0001c0002t0001g0285 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.71+3790C>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100564121 | ||||||
chr14:100564125
|
G | C | 3 | a0001c0001t0001g0221a0001c0001t0001g0254a0001c0002t0001g0222 | 3 | NA18969.hp1 NA19067.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.71+3786C>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100564125 | ||||||
chr14:100564242
|
G | A | 60 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(57): Show | 63 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(60): Show |
intron_variant | MODIFIER | c.71+3669C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100564242 | ||||||
chr14:100564262
|
G | C | 1 | a0001c0002t0001g0264 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.71+3649C>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100564262 | ||||||
chr14:100564393
|
A | G | 1 | a0001c0001t0001g0186 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.71+3518T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100564393 | ||||||
chr14:100564435
|
A | T | 1 | a0001c0002t0001g0278 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.71+3476T>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100564435 | ||||||
chr14:100564473
|
G | A | 1 | a0001c0001t0013g0124 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.71+3438C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100564473 | ||||||
chr14:100564607
|
T | C | 10 | a0001c0002t0001g0135a0001c0004t0001g0004a0001c0004t0001g0034others(7): Show | 11 | HG02056.hp2 NA18964.hp1 NA18973.hp1 others(8): Show |
intron_variant | MODIFIER | c.71+3304A>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100564607 | ||||||
chr14:100564699
|
C | T | 60 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(57): Show | 63 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(60): Show |
intron_variant | MODIFIER | c.71+3212G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100564699 | ||||||
chr14:100564723
|
G | A | 5 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0164others(2): Show | 5 | HG02976.hp2 HG03225.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.71+3188C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100564723 | ||||||
chr14:100564823
|
C | T | 5 | a0001c0003t0005g0297a0001c0003t0006g0303a0001c0003t0006g0304others(2): Show | 5 | HG02615.hp1 HG02717.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.71+3088G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100564823 | ||||||
chr14:100564971
|
A | G | 10 | a0001c0002t0001g0135a0001c0004t0001g0004a0001c0004t0001g0034others(7): Show | 11 | HG02056.hp2 NA18964.hp1 NA18973.hp1 others(8): Show |
intron_variant | MODIFIER | c.71+2940T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100564971 | ||||||
chr14:100565373
|
G | T | 60 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(57): Show | 63 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(60): Show |
intron_variant | MODIFIER | c.71+2538C>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100565373 | ||||||
chr14:100565529
|
C | T | 1 | a0001c0001t0001g0063 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.71+2382G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100565529 | ||||||
chr14:100565659
|
C | A | 5 | a0001c0001t0001g0039a0001c0001t0001g0061a0001c0001t0001g0131others(2): Show | 5 | HG01346.hp1 HG01928.hp2 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.71+2252G>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100565659 | ||||||
chr14:100565696
|
C | T | 1 | a0001c0001t0011g0098 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.71+2215G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100565696 | ||||||
chr14:100565857
|
AG | A | 5 | a0001c0003t0005g0297a0001c0003t0006g0303a0001c0003t0006g0304others(2): Show | 5 | HG02615.hp1 HG02717.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.71+2053delC | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100565857 | ||||||
chr14:100565870
|
T | C | 2 | a0001c0002t0001g0197a0001c0002t0001g0293 | 2 | HG02080.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.71+2041A>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100565870 | ||||||
chr14:100565880
|
T | C | 191 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(188): Show | 208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.71+2031A>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100565880 | ||||||
chr14:100565986
|
T | C | 1 | a0001c0001t0001g0050 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.71+1925A>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100565986 | ||||||
chr14:100566041
|
G | A | 4 | a0001c0004t0002g0045a0001c0004t0002g0170a0001c0004t0002g0268others(1): Show | 4 | HG02486.hp2 HG02809.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.71+1870C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100566041 | ||||||
chr14:100566327
|
C | T | 16 | a0001c0001t0001g0062a0001c0003t0001g0013a0001c0003t0001g0054others(13): Show | 17 | HG02109.hp1 HG02258.hp1 HG02615.hp1 others(14): Show |
intron_variant | MODIFIER | c.71+1584G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100566327 | ||||||
chr14:100566370
|
A | G | 191 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(188): Show | 208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.71+1541T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100566370 | ||||||
chr14:100566494
|
C | A | 10 | a0001c0002t0001g0135a0001c0004t0001g0004a0001c0004t0001g0034others(7): Show | 11 | HG02056.hp2 NA18964.hp1 NA18973.hp1 others(8): Show |
intron_variant | MODIFIER | c.71+1417G>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100566494 | ||||||
chr14:100566519
|
C | A | 4 | a0001c0001t0008g0182a0001c0002t0001g0070a0001c0002t0001g0252others(1): Show | 4 | HG01884.hp1 HG02015.hp2 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.71+1392G>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100566519 | ||||||
chr14:100566521
|
C | G | 1 | a0001c0001t0001g0100 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.71+1390G>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100566521 | ||||||
chr14:100566752
|
G | A | 7 | a0001c0001t0001g0166a0001c0001t0001g0168a0001c0001t0001g0169others(4): Show | 8 | HG01099.hp2 HG02109.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.71+1159C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100566752 | ||||||
chr14:100566951
|
A | G | 206 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(203): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.71+960T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100566951 | ||||||
chr14:100567083
|
C | T | 190 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(187): Show | 207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.71+828G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100567083 | ||||||
chr14:100567098
|
A | G | 191 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(188): Show | 208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.71+813T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100567098 | ||||||
chr14:100567281
|
C | A | 1 | a0001c0001t0001g0071 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.71+630G>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100567281 | ||||||
chr14:100567498
|
T | TGGGGGTG others(10): Show |
1 | a0001c0003t0001g0064 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.71+396_71+412dupGA others(15): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100567498 | ||||||
chr14:100567573
|
G | A | 2 | a0001c0001t0001g0010a0001c0001t0001g0191 | 3 | HG01106.hp1 HG01346.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.71+338C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100567573 | ||||||
chr14:100567579
|
C | G | 1 | a0001c0001t0001g0059 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.71+332G>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100567579 | ||||||
chr14:100567592
|
G | C | 1 | a0001c0002t0012g0150 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.71+319C>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100567592 | ||||||
chr14:100567593
|
G | T | 1 | a0001c0002t0001g0024 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.71+318C>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100567593 | ||||||
chr14:100567627
|
G | C | 1 | a0001c0003t0001g0054 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.71+284C>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100567627 | ||||||
chr14:100567628
|
G | A | 1 | a0001c0003t0001g0054 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.71+283C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100567628 | ||||||
chr14:100567636
|
G | A | 1 | a0001c0002t0001g0132 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.71+275C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100567636 | ||||||
chr14:100567734
|
G | C | 2 | a0001c0002t0001g0026a0001c0002t0001g0253 | 2 | HG00140.hp1 HG00642.hp2 |
intron_variant | MODIFIER | c.71+177C>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100567734 | ||||||
chr14:100567853
|
G | A | 52 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0049others(49): Show | 54 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(51): Show |
intron_variant | MODIFIER | c.71+58C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 2/6 | chr14 | 100567853 | ||||||
chr14:100568073
|
G | C | 4 | a0001c0004t0002g0045a0001c0004t0002g0170a0001c0004t0002g0268others(1): Show | 4 | HG02486.hp2 HG02809.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.43-134C>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100568073 | ||||||
chr14:100568082
|
T | C | 191 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(188): Show | 208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.43-143A>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100568082 | ||||||
chr14:100568088
|
T | C | 5 | a0001c0001t0001g0166a0001c0001t0001g0168a0001c0001t0001g0169others(2): Show | 5 | HG01099.hp2 HG02886.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.43-149A>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100568088 | ||||||
chr14:100568092
|
G | A | 3 | a0001c0001t0001g0244a0001c0002t0001g0133a0001c0002t0001g0245 | 3 | HG01952.hp1 HG02300.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.43-153C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100568092 | ||||||
chr14:100568115
|
G | A | 1 | a0001c0001t0001g0011 | 2 | HG02602.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.43-176C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100568115 | ||||||
chr14:100568621
|
C | G | 1 | a0001c0002t0001g0183 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.43-682G>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100568621 | ||||||
chr14:100568662
|
C | T | 5 | a0001c0001t0001g0166a0001c0001t0001g0168a0001c0001t0001g0169others(2): Show | 5 | HG01099.hp2 HG02886.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.43-723G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100568662 | ||||||
chr14:100568817
|
C | T | 2 | a0001c0003t0001g0140a0001c0003t0001g0141 | 2 | HG03453.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.43-878G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100568817 | ||||||
chr14:100568925
|
C | G | 1 | a0001c0001t0001g0056 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.43-986G>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100568925 | ||||||
chr14:100569065
|
G | A | 14 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(11): Show | 16 | HG02055.hp1 HG02258.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.43-1126C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100569065 | ||||||
chr14:100569165
|
G | C | 2 | a0001c0002t0001g0246a0001c0002t0001g0247 | 2 | HG02145.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.43-1226C>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100569165 | ||||||
chr14:100569179
|
A | G | 110 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(107): Show | 124 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.43-1240T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100569179 | ||||||
chr14:100569209
|
C | G | 84 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0017others(81): Show | 87 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.43-1270G>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100569209 | ||||||
chr14:100569498
|
C | G | 7 | a0001c0001t0001g0157a0001c0001t0008g0228a0001c0002t0001g0217others(4): Show | 7 | HG01081.hp1 HG01099.hp1 HG01106.hp2 others(4): Show |
intron_variant | MODIFIER | c.43-1559G>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100569498 | ||||||
chr14:100569581
|
CCT | C | 10 | a0001c0002t0001g0135a0001c0004t0001g0004a0001c0004t0001g0034others(7): Show | 11 | HG02056.hp2 NA18964.hp1 NA18973.hp1 others(8): Show |
intron_variant | MODIFIER | c.43-1644_43-1643del others(2): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100569581 | ||||||
chr14:100569601
|
C | T | 1 | a0001c0001t0001g0270 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.43-1662G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100569601 | ||||||
chr14:100569715
|
T | C | 190 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(187): Show | 207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.43-1776A>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100569715 | ||||||
chr14:100569737
|
C | G | 98 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(95): Show | 110 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.43-1798G>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100569737 | ||||||
chr14:100569915
|
A | G | 3 | a0001c0005t0002g0051a0001c0005t0002g0052a0001c0005t0016g0301 | 3 | HG02280.hp1 HG03540.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.43-1976T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100569915 | ||||||
chr14:100569931
|
T | C | 1 | a0001c0001t0001g0185 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.43-1992A>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100569931 | ||||||
chr14:100569932
|
A | G | 2 | a0001c0003t0001g0013a0001c0003t0001g0279 | 3 | HG02109.hp1 HG03098.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.43-1993T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100569932 | ||||||
chr14:100569955
|
C | G | 1 | a0001c0002t0001g0249 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.43-2016G>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100569955 | ||||||
chr14:100570052
|
G | A | 1 | a0001c0005t0001g0138 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.43-2113C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100570052 | ||||||
chr14:100570121
|
C | A | 61 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(58): Show | 64 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(61): Show |
intron_variant | MODIFIER | c.43-2182G>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100570121 | ||||||
chr14:100570249
|
G | A | 1 | a0001c0001t0001g0198 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.43-2310C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100570249 | ||||||
chr14:100570303
|
T | C | 15 | a0001c0001t0001g0166a0001c0001t0001g0168a0001c0001t0001g0169others(12): Show | 16 | HG01099.hp2 HG02056.hp2 HG02886.hp1 others(13): Show |
intron_variant | MODIFIER | c.43-2364A>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100570303 | ||||||
chr14:100570360
|
A | G | 7 | a0001c0001t0001g0062a0001c0003t0001g0054a0001c0003t0001g0140others(4): Show | 7 | HG02647.hp1 HG02809.hp1 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.43-2421T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100570360 | ||||||
chr14:100570487
|
A | G | 201 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(198): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.43-2548T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100570487 | ||||||
chr14:100570495
|
T | C | 21 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(18): Show | 23 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.43-2556A>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100570495 | ||||||
chr14:100570496
|
GCGGCCCT others(1): Show |
G | 4 | a0001c0001t0001g0181a0001c0005t0002g0068a0001c0005t0002g0078others(1): Show | 4 | HG01891.hp2 HG02572.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.43-2565_43-2558del others(8): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100570496 | ||||||
chr14:100570505
|
T | A | 4 | a0001c0001t0001g0181a0001c0005t0002g0068a0001c0005t0002g0078others(1): Show | 4 | HG01891.hp2 HG02572.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.43-2566A>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100570505 | ||||||
chr14:100570507
|
T | A | 4 | a0001c0001t0001g0181a0001c0005t0002g0068a0001c0005t0002g0078others(1): Show | 4 | HG01891.hp2 HG02572.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.43-2568A>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100570507 | ||||||
chr14:100570665
|
A | G | 40 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(37): Show | 42 | HG01099.hp2 HG01891.hp2 HG02055.hp1 others(39): Show |
intron_variant | MODIFIER | c.43-2726T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100570665 | ||||||
chr14:100570678
|
G | T | 134 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(131): Show | 149 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(146): Show |
intron_variant | MODIFIER | c.43-2739C>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100570678 | ||||||
chr14:100570687
|
A | G | 128 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(125): Show | 143 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(140): Show |
intron_variant | MODIFIER | c.43-2748T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100570687 | ||||||
chr14:100570691
|
T | C | 129 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(126): Show | 144 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.43-2752A>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100570691 | ||||||
chr14:100570791
|
G | T | 6 | a0001c0001t0001g0151a0001c0001t0001g0281a0001c0002t0001g0232others(3): Show | 6 | HG00438.hp2 HG00609.hp1 NA18952.hp1 others(3): Show |
intron_variant | MODIFIER | c.43-2852C>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100570791 | ||||||
chr14:100570964
|
A | G | 5 | a0001c0001t0001g0166a0001c0001t0001g0168a0001c0001t0001g0169others(2): Show | 5 | HG01099.hp2 HG02886.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.43-3025T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100570964 | ||||||
chr14:100571112
|
C | T | 1 | a0001c0001t0001g0199 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.43-3173G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100571112 | ||||||
chr14:100571136
|
G | A | 2 | a0001c0001t0001g0125a0001c0002t0001g0249 | 2 | HG01243.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.43-3197C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100571136 | ||||||
chr14:100571262
|
A | G | 209 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(206): Show | 228 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.43-3323T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100571262 | ||||||
chr14:100571270
|
C | G | 6 | a0001c0003t0001g0013a0001c0003t0001g0279a0001c0004t0002g0045others(3): Show | 7 | HG02109.hp1 HG02486.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.43-3331G>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100571270 | ||||||
chr14:100571284
|
C | T | 21 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(18): Show | 23 | HG02055.hp1 HG02258.hp2 HG02280.hp2 others(20): Show |
intron_variant | MODIFIER | c.43-3345G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100571284 | ||||||
chr14:100571312
|
C | T | 4 | a0001c0001t0001g0181a0001c0005t0002g0068a0001c0005t0002g0078others(1): Show | 4 | HG01891.hp2 HG02572.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.43-3373G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100571312 | ||||||
chr14:100571346
|
G | A | 2 | a0001c0003t0001g0294a0001c0005t0010g0289 | 2 | HG02258.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.43-3407C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100571346 | ||||||
chr14:100571372
|
C | T | 1 | a0001c0001t0001g0053 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.43-3433G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100571372 | ||||||
chr14:100571389
|
T | C | 208 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(205): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(224): Show |
intron_variant | MODIFIER | c.43-3450A>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100571389 | ||||||
chr14:100571405
|
G | A | 1 | a0001c0001t0001g0125 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.43-3466C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100571405 | ||||||
chr14:100571425
|
C | G | 56 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(53): Show | 59 | HG00099.hp1 HG00408.hp1 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.43-3486G>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100571425 | ||||||
chr14:100571448
|
G | A | 1 | a0001c0002t0001g0264 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.43-3509C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100571448 | ||||||
chr14:100571472
|
C | G | 10 | a0001c0002t0001g0135a0001c0004t0001g0004a0001c0004t0001g0034others(7): Show | 11 | HG02056.hp2 NA18964.hp1 NA18973.hp1 others(8): Show |
intron_variant | MODIFIER | c.43-3533G>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100571472 | ||||||
chr14:100571486
|
A | T | 21 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(18): Show | 23 | HG02055.hp1 HG02258.hp2 HG02280.hp2 others(20): Show |
intron_variant | MODIFIER | c.43-3547T>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100571486 | ||||||
chr14:100571549
|
T | C | 1 | a0001c0005t0002g0077 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.43-3610A>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100571549 | ||||||
chr14:100571694
|
T | C | 1 | a0001c0002t0001g0144 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.43-3755A>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100571694 | ||||||
chr14:100571879
|
C | G | 1 | a0001c0001t0011g0098 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.43-3940G>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100571879 | ||||||
chr14:100571916
|
G | A | 1 | a0001c0001t0001g0050 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.43-3977C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100571916 | ||||||
chr14:100571992
|
C | T | 1 | a0001c0005t0001g0138 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.43-4053G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100571992 | ||||||
chr14:100572102
|
C | T | 1 | a0001c0001t0001g0056 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.43-4163G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100572102 | ||||||
chr14:100572105
|
G | A | 97 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(94): Show | 109 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.43-4166C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100572105 | ||||||
chr14:100572123
|
G | A | 42 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0049others(39): Show | 44 | HG00099.hp1 HG00408.hp1 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.43-4184C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100572123 | ||||||
chr14:100572152
|
G | A | 2 | a0001c0001t0001g0005a0001c0001t0001g0041 | 3 | HG01884.hp2 HG03225.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.43-4213C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100572152 | ||||||
chr14:100572444
|
A | G | 10 | a0001c0002t0001g0135a0001c0004t0001g0004a0001c0004t0001g0034others(7): Show | 11 | HG02056.hp2 NA18964.hp1 NA18973.hp1 others(8): Show |
intron_variant | MODIFIER | c.43-4505T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100572444 | ||||||
chr14:100572651
|
G | A | 104 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(101): Show | 116 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.43-4712C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100572651 | ||||||
chr14:100572817
|
T | A | 1 | a0001c0003t0001g0054 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.43-4878A>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100572817 | ||||||
chr14:100572915
|
G | C | 1 | a0001c0001t0001g0157 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.43-4976C>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100572915 | ||||||
chr14:100573172
|
A | AGGTGAGT others(31): Show |
2 | a0001c0002t0001g0030a0001c0002t0001g0159 | 2 | HG02523.hp2 NA18945.hp2 |
intron_variant | MODIFIER | c.43-5271_43-5234dup others(38): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100573172 | ||||||
chr14:100573172
|
A | AGGTGAGT others(69): Show |
1 | a0001c0005t0001g0138 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.43-5309_43-5234dup others(76): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100573172 | ||||||
chr14:100573172
|
AGGTGAGT others(31): Show |
A | 1 | a0001c0002t0004g0040 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.43-5271_43-5234del others(38): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100573172 | ||||||
chr14:100573187
|
G | A | 2 | a0001c0003t0001g0003a0001c0003t0001g0171 | 4 | HG02451.hp1 HG02976.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.43-5248C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100573187 | ||||||
chr14:100573207
|
G | A | 5 | a0001c0001t0001g0166a0001c0001t0001g0168a0001c0001t0001g0169others(2): Show | 5 | HG01099.hp2 HG02886.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.43-5268C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100573207 | ||||||
chr14:100573221
|
G | A | 2 | a0001c0003t0001g0013a0001c0003t0001g0279 | 3 | HG02109.hp1 HG03098.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.43-5282C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100573221 | ||||||
chr14:100573242
|
GGGGGCTG others(31): Show |
G | 22 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(19): Show | 24 | HG02055.hp1 HG02258.hp2 HG02280.hp2 others(21): Show |
intron_variant | MODIFIER | c.43-5341_43-5304del others(38): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100573242 | ||||||
chr14:100573280
|
C | G | 187 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(184): Show | 204 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.43-5341G>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100573280 | ||||||
chr14:100573297
|
G | A | 1 | a0001c0003t0001g0042 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.43-5358C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100573297 | ||||||
chr14:100573387
|
C | T | 56 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(53): Show | 59 | HG00099.hp1 HG00408.hp1 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.43-5448G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100573387 | ||||||
chr14:100573672
|
A | G | 2 | a0001c0001t0001g0146a0001c0002t0001g0145 | 2 | HG00741.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.43-5733T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100573672 | ||||||
chr14:100573817
|
C | T | 3 | a0001c0003t0006g0303a0001c0003t0006g0304a0001c0004t0017g0305 | 3 | HG03209.hp1 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.43-5878G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100573817 | ||||||
chr14:100573933
|
C | G | 1 | a0001c0005t0001g0138 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.43-5994G>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100573933 | ||||||
chr14:100574061
|
C | T | 100 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(97): Show | 112 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.43-6122G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100574061 | ||||||
chr14:100574169
|
C | T | 1 | a0001c0001t0001g0063 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.43-6230G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100574169 | ||||||
chr14:100574370
|
T | C | 5 | a0001c0001t0001g0166a0001c0001t0001g0168a0001c0001t0001g0169others(2): Show | 5 | HG01099.hp2 HG02886.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.43-6431A>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100574370 | ||||||
chr14:100574432
|
C | T | 4 | a0001c0001t0001g0181a0001c0005t0002g0068a0001c0005t0002g0078others(1): Show | 4 | HG01891.hp2 HG02572.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.43-6493G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100574432 | ||||||
chr14:100574443
|
G | A | 11 | a0001c0001t0001g0017a0001c0001t0001g0072a0001c0001t0001g0073others(8): Show | 11 | HG02055.hp2 HG02622.hp1 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.43-6504C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100574443 | ||||||
chr14:100574518
|
G | GT | 17 | a0001c0001t0001g0036a0001c0001t0001g0149a0001c0001t0001g0227others(14): Show | 18 | HG00733.hp1 HG00741.hp1 HG01167.hp2 others(15): Show |
intron_variant | MODIFIER | c.43-6580dupA | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100574518 | ||||||
chr14:100574518
|
GT | G | 75 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(72): Show | 79 | HG00099.hp1 HG00408.hp1 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.43-6580delA | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100574518 | ||||||
chr14:100574518
|
GTT | G | 85 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(82): Show | 96 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.43-6581_43-6580del others(2): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100574518 | ||||||
chr14:100574518
|
GTTT | G | 17 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(14): Show | 19 | HG02055.hp1 HG02258.hp2 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.43-6582_43-6580del others(3): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100574518 | ||||||
chr14:100574539
|
T | A | 3 | a0001c0001t0001g0027a0001c0003t0001g0013a0001c0003t0001g0279 | 4 | HG02109.hp1 HG03098.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.43-6600A>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100574539 | ||||||
chr14:100574804
|
C | T | 3 | a0001c0004t0003g0028a0001c0004t0003g0031a0001c0004t0003g0032 | 3 | NA18979.hp2 NA18995.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.43-6865G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100574804 | ||||||
chr14:100574869
|
C | T | 3 | a0001c0001t0001g0027a0001c0003t0001g0013a0001c0003t0001g0279 | 4 | HG02109.hp1 HG03098.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.43-6930G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100574869 | ||||||
chr14:100574873
|
A | T | 21 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(18): Show | 23 | HG02055.hp1 HG02258.hp2 HG02280.hp2 others(20): Show |
intron_variant | MODIFIER | c.43-6934T>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100574873 | ||||||
chr14:100574887
|
C | A | 2 | a0001c0002t0001g0148a0001c0002t0001g0230 | 2 | NA19009.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.43-6948G>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100574887 | ||||||
chr14:100574889
|
C | G | 2 | a0001c0002t0001g0148a0001c0002t0001g0230 | 2 | NA19009.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.43-6950G>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100574889 | ||||||
chr14:100574995
|
C | T | 1 | a0001c0004t0003g0291 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.43-7056G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100574995 | ||||||
chr14:100574999
|
G | A | 1 | a0001c0005t0002g0139 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.43-7060C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100574999 | ||||||
chr14:100575172
|
A | G | 1 | a0001c0002t0005g0296 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.43-7233T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100575172 | ||||||
chr14:100575206
|
C | T | 5 | a0001c0002t0006g0302a0001c0002t0006g0307a0001c0005t0002g0076others(2): Show | 5 | HG02055.hp2 HG02723.hp2 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.43-7267G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100575206 | ||||||
chr14:100575209
|
G | A | 1 | a0001c0005t0001g0138 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.43-7270C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100575209 | ||||||
chr14:100575211
|
A | C | 3 | a0001c0001t0001g0027a0001c0003t0001g0013a0001c0003t0001g0279 | 4 | HG02109.hp1 HG03098.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.43-7272T>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100575211 | ||||||
chr14:100575328
|
A | C | 1 | a0001c0005t0010g0289 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.43-7389T>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100575328 | ||||||
chr14:100575407
|
T | A | 1 | a0001c0001t0001g0027 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.43-7468A>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100575407 | ||||||
chr14:100575631
|
T | C | 21 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(18): Show | 23 | HG02055.hp1 HG02258.hp2 HG02280.hp2 others(20): Show |
intron_variant | MODIFIER | c.43-7692A>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100575631 | ||||||
chr14:100575806
|
G | A | 1 | a0001c0001t0001g0059 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.43-7867C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100575806 | ||||||
chr14:100575808
|
C | A | 1 | a0001c0002t0001g0287 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.43-7869G>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100575808 | ||||||
chr14:100575861
|
G | T | 2 | a0001c0003t0001g0294a0001c0005t0010g0289 | 2 | HG02258.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.43-7922C>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100575861 | ||||||
chr14:100576002
|
G | A | 5 | a0001c0001t0001g0166a0001c0001t0001g0168a0001c0001t0001g0169others(2): Show | 5 | HG01099.hp2 HG02886.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.43-8063C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100576002 | ||||||
chr14:100576013
|
C | T | 1 | a0001c0005t0001g0138 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.43-8074G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100576013 | ||||||
chr14:100576047
|
T | A | 3 | a0001c0001t0001g0255a0001c0002t0001g0252a0006c0015t0001g0226 | 3 | HG01169.hp2 HG01261.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.43-8108A>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100576047 | ||||||
chr14:100576050
|
C | T | 93 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(90): Show | 105 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.43-8111G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100576050 | ||||||
chr14:100576132
|
G | A | 1 | a0001c0001t0001g0126 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.43-8193C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100576132 | ||||||
chr14:100576148
|
C | T | 2 | a0001c0001t0001g0146a0001c0002t0001g0145 | 2 | HG00741.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.43-8209G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100576148 | ||||||
chr14:100576378
|
A | C | 60 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(57): Show | 63 | HG00099.hp1 HG00408.hp1 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.43-8439T>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100576378 | ||||||
chr14:100576386
|
G | A | 11 | a0001c0001t0001g0036a0001c0002t0001g0135a0001c0004t0001g0004others(8): Show | 12 | HG02056.hp2 NA18964.hp1 NA18973.hp1 others(9): Show |
intron_variant | MODIFIER | c.43-8447C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100576386 | ||||||
chr14:100576462
|
G | A | 8 | a0001c0001t0001g0056a0001c0001t0001g0271a0001c0001t0001g0277others(5): Show | 8 | HG02615.hp2 HG02630.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.43-8523C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100576462 | ||||||
chr14:100576464
|
C | T | 4 | a0001c0001t0001g0181a0001c0005t0002g0068a0001c0005t0002g0078others(1): Show | 4 | HG01891.hp2 HG02572.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.43-8525G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100576464 | ||||||
chr14:100576637
|
C | T | 6 | a0001c0001t0008g0182a0001c0002t0001g0070a0001c0002t0001g0183others(3): Show | 6 | HG00558.hp2 HG01884.hp1 HG02015.hp2 others(3): Show |
intron_variant | MODIFIER | c.43-8698G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100576637 | ||||||
chr14:100576726
|
C | T | 5 | a0001c0001t0001g0166a0001c0001t0001g0168a0001c0001t0001g0169others(2): Show | 5 | HG01099.hp2 HG02886.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.43-8787G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100576726 | ||||||
chr14:100576735
|
C | T | 11 | a0001c0001t0001g0036a0001c0002t0001g0135a0001c0004t0001g0004others(8): Show | 12 | HG02056.hp2 NA18964.hp1 NA18973.hp1 others(9): Show |
intron_variant | MODIFIER | c.43-8796G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100576735 | ||||||
chr14:100576845
|
C | T | 11 | a0001c0001t0001g0036a0001c0002t0001g0135a0001c0004t0001g0004others(8): Show | 12 | HG02056.hp2 NA18964.hp1 NA18973.hp1 others(9): Show |
intron_variant | MODIFIER | c.43-8906G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100576845 | ||||||
chr14:100576890
|
C | T | 11 | a0001c0001t0001g0036a0001c0002t0001g0135a0001c0004t0001g0004others(8): Show | 12 | HG02056.hp2 NA18964.hp1 NA18973.hp1 others(9): Show |
intron_variant | MODIFIER | c.43-8951G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100576890 | ||||||
chr14:100577595
|
G | A | 1 | a0001c0001t0001g0050 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.42+9654C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100577595 | ||||||
chr14:100577766
|
G | T | 11 | a0001c0001t0001g0036a0001c0002t0001g0135a0001c0004t0001g0004others(8): Show | 12 | HG02056.hp2 NA18964.hp1 NA18973.hp1 others(9): Show |
intron_variant | MODIFIER | c.42+9483C>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100577766 | ||||||
chr14:100577849
|
T | C | 2 | a0001c0001t0001g0053a0001c0016t0001g0257 | 2 | HG00544.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.42+9400A>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100577849 | ||||||
chr14:100577935
|
G | A | 2 | a0001c0003t0001g0294a0001c0005t0010g0289 | 2 | HG02258.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.42+9314C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100577935 | ||||||
chr14:100577976
|
G | A | 1 | a0001c0005t0010g0289 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.42+9273C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100577976 | ||||||
chr14:100577993
|
C | A | 11 | a0001c0001t0001g0036a0001c0002t0001g0135a0001c0004t0001g0004others(8): Show | 12 | HG02056.hp2 NA18964.hp1 NA18973.hp1 others(9): Show |
intron_variant | MODIFIER | c.42+9256G>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100577993 | ||||||
chr14:100578082
|
C | A | 90 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(87): Show | 101 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.42+9167G>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100578082 | ||||||
chr14:100578091
|
C | T | 1 | a0001c0001t0001g0019 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.42+9158G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100578091 | ||||||
chr14:100578227
|
G | A | 11 | a0001c0001t0001g0036a0001c0002t0001g0135a0001c0004t0001g0004others(8): Show | 12 | HG02056.hp2 NA18964.hp1 NA18973.hp1 others(9): Show |
intron_variant | MODIFIER | c.42+9022C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100578227 | ||||||
chr14:100578353
|
A | G | 161 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(158): Show | 175 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.42+8896T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100578353 | ||||||
chr14:100578391
|
G | A | 2 | a0001c0002t0001g0026a0001c0002t0001g0253 | 2 | HG00140.hp1 HG00642.hp2 |
intron_variant | MODIFIER | c.42+8858C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100578391 | ||||||
chr14:100578455
|
C | T | 9 | a0001c0001t0001g0005a0001c0001t0001g0037a0001c0001t0001g0041others(6): Show | 10 | HG00544.hp1 HG00639.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.42+8794G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100578455 | ||||||
chr14:100578631
|
G | T | 1 | a0001c0001t0001g0227 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.42+8618C>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100578631 | ||||||
chr14:100578665
|
A | G | 11 | a0001c0001t0001g0036a0001c0002t0001g0135a0001c0004t0001g0004others(8): Show | 12 | HG02056.hp2 NA18964.hp1 NA18973.hp1 others(9): Show |
intron_variant | MODIFIER | c.42+8584T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100578665 | ||||||
chr14:100578794
|
T | G | 9 | a0001c0001t0001g0005a0001c0001t0001g0037a0001c0001t0001g0041others(6): Show | 10 | HG00544.hp1 HG00639.hp1 HG00733.hp2 others(7): Show |
intron_variant | MODIFIER | c.42+8455A>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100578794 | ||||||
chr14:100578856
|
C | CT | 21 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0037others(18): Show | 23 | HG00639.hp1 HG00733.hp2 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.42+8392dupA | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100578856 | ||||||
chr14:100578856
|
C | CTT | 87 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(84): Show | 99 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.42+8391_42+8392dup others(2): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100578856 | ||||||
chr14:100578856
|
C | CTTT | 25 | a0001c0001t0001g0009a0001c0001t0001g0021a0001c0001t0001g0022others(22): Show | 28 | HG02055.hp1 HG02109.hp2 HG02258.hp2 others(25): Show |
intron_variant | MODIFIER | c.42+8390_42+8392dup others(3): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100578856 | ||||||
chr14:100578856
|
CT | C | 11 | a0001c0001t0001g0061a0001c0001t0001g0063a0001c0001t0001g0165others(8): Show | 11 | HG01069.hp1 HG01169.hp2 HG01975.hp1 others(8): Show |
intron_variant | MODIFIER | c.42+8392delA | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100578856 | ||||||
chr14:100578876
|
T | C | 1 | a0001c0001t0001g0286 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.42+8373A>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100578876 | ||||||
chr14:100578891
|
C | T | 2 | a0001c0001t0001g0009a0006c0015t0001g0226 | 3 | HG01261.hp2 HG02109.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.42+8358G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100578891 | ||||||
chr14:100578892
|
G | A | 1 | a0001c0002t0001g0159 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.42+8357C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100578892 | ||||||
chr14:100578918
|
A | G | 2 | a0001c0001t0001g0080a0001c0001t0001g0081 | 2 | NA19068.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.42+8331T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100578918 | ||||||
chr14:100578930
|
C | T | 1 | a0001c0001t0001g0038 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.42+8319G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100578930 | ||||||
chr14:100578955
|
G | A | 1 | a0001c0002t0001g0197 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.42+8294C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100578955 | ||||||
chr14:100579034
|
T | C | 1 | a0001c0003t0001g0194 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.42+8215A>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100579034 | ||||||
chr14:100579062
|
T | C | 3 | a0001c0001t0001g0049a0001c0001t0001g0195a0001c0001t0014g0048 | 3 | HG01978.hp1 NA18977.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.42+8187A>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100579062 | ||||||
chr14:100579175
|
C | T | 4 | a0001c0004t0002g0045a0001c0004t0002g0170a0001c0004t0002g0268others(1): Show | 4 | HG02486.hp2 HG02809.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.42+8074G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100579175 | ||||||
chr14:100579471
|
G | T | 1 | a0001c0001t0001g0092 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.42+7778C>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100579471 | ||||||
chr14:100579551
|
G | C | 306 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(303): Show | 325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.42+7698C>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100579551 | ||||||
chr14:100579614
|
G | A | 1 | a0001c0002t0001g0256 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.42+7635C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100579614 | ||||||
chr14:100579677
|
T | C | 12 | a0001c0001t0001g0166a0001c0001t0001g0168a0001c0001t0001g0169others(9): Show | 12 | HG01099.hp2 HG02055.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.42+7572A>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100579677 | ||||||
chr14:100579706
|
G | A | 210 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(207): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.42+7543C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100579706 | ||||||
chr14:100579735
|
C | T | 1 | a0001c0002t0001g0225 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.42+7514G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100579735 | ||||||
chr14:100579747
|
A | G | 10 | a0001c0001t0001g0166a0001c0001t0001g0168a0001c0001t0001g0169others(7): Show | 10 | HG01099.hp2 HG02055.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.42+7502T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100579747 | ||||||
chr14:100579749
|
G | C | 4 | a0001c0001t0001g0181a0001c0005t0002g0068a0001c0005t0002g0078others(1): Show | 4 | HG01891.hp2 HG02572.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.42+7500C>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100579749 | ||||||
chr14:100579963
|
G | A | 8 | a0001c0001t0001g0005a0001c0001t0001g0041a0001c0001t0001g0053others(5): Show | 9 | HG00544.hp1 HG00733.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.42+7286C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100579963 | ||||||
chr14:100580028
|
G | GGT | 60 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(57): Show | 63 | HG00099.hp1 HG00408.hp1 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.42+7219_42+7220dup others(2): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100580028 | ||||||
chr14:100580032
|
C | T | 19 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(16): Show | 21 | HG02258.hp2 HG02280.hp2 HG02451.hp1 others(18): Show |
intron_variant | MODIFIER | c.42+7217G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100580032 | ||||||
chr14:100580079
|
C | T | 89 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(86): Show | 99 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.42+7170G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100580079 | ||||||
chr14:100580261
|
C | A | 1 | a0001c0002t0001g0160 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.42+6988G>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100580261 | ||||||
chr14:100580312
|
C | T | 108 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(105): Show | 115 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(112): Show |
intron_variant | MODIFIER | c.42+6937G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100580312 | ||||||
chr14:100580699
|
T | C | 1 | a0001c0003t0001g0174 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.42+6550A>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100580699 | ||||||
chr14:100580723
|
C | T | 1 | a0001c0001t0001g0091 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.42+6526G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100580723 | ||||||
chr14:100580975
|
G | A | 3 | a0001c0001t0001g0027a0001c0003t0001g0013a0001c0003t0001g0279 | 4 | HG02109.hp1 HG03098.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.42+6274C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100580975 | ||||||
chr14:100580979
|
C | T | 90 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(87): Show | 101 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.42+6270G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100580979 | ||||||
chr14:100580989
|
G | A | 2 | a0001c0001t0001g0196a0001c0002t0001g0197 | 2 | HG02080.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.42+6260C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100580989 | ||||||
chr14:100581118
|
T | A | 1 | a0001c0001t0001g0216 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.42+6131A>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100581118 | ||||||
chr14:100581163
|
T | C | 2 | a0001c0001t0001g0129a0001c0002t0001g0130 | 2 | HG00099.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.42+6086A>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100581163 | ||||||
chr14:100581198
|
C | G | 1 | a0001c0002t0001g0217 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.42+6051G>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100581198 | ||||||
chr14:100581208
|
T | A | 3 | a0001c0003t0001g0054a0001c0003t0001g0294a0001c0005t0010g0289 | 3 | HG02258.hp1 HG02895.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.42+6041A>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100581208 | ||||||
chr14:100581232
|
G | A | 13 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(10): Show | 15 | HG02258.hp2 HG02280.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.42+6017C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100581232 | ||||||
chr14:100581398
|
C | T | 4 | a0001c0001t0001g0181a0001c0005t0002g0068a0001c0005t0002g0078others(1): Show | 4 | HG01891.hp2 HG02572.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.42+5851G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100581398 | ||||||
chr14:100581467
|
C | T | 1 | a0001c0001t0001g0090 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.42+5782G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100581467 | ||||||
chr14:100581534
|
G | A | 3 | a0001c0005t0002g0051a0001c0005t0002g0052a0001c0005t0016g0301 | 3 | HG02280.hp1 HG03540.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.42+5715C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100581534 | ||||||
chr14:100581545
|
C | T | 1 | a0002c0007t0001g0029 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.42+5704G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100581545 | ||||||
chr14:100581557
|
G | A | 9 | a0001c0001t0001g0005a0001c0001t0001g0037a0001c0001t0001g0041others(6): Show | 10 | HG00544.hp1 HG00639.hp1 HG00733.hp2 others(7): Show |
intron_variant | MODIFIER | c.42+5692C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100581557 | ||||||
chr14:100581558
|
C | T | 3 | a0001c0005t0002g0051a0001c0005t0002g0052a0001c0005t0016g0301 | 3 | HG02280.hp1 HG03540.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.42+5691G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100581558 | ||||||
chr14:100581559
|
G | A | 1 | a0001c0002t0001g0135 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.42+5690C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100581559 | ||||||
chr14:100581669
|
C | T | 16 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0012others(13): Show | 19 | HG00597.hp2 HG00609.hp2 HG00673.hp2 others(16): Show |
intron_variant | MODIFIER | c.42+5580G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100581669 | ||||||
chr14:100581954
|
A | T | 1 | a0001c0003t0001g0172 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.42+5295T>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100581954 | ||||||
chr14:100581955
|
C | T | 1 | a0001c0003t0001g0172 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.42+5294G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100581955 | ||||||
chr14:100581956
|
A | T | 1 | a0001c0003t0001g0172 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.42+5293T>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100581956 | ||||||
chr14:100581957
|
G | A | 1 | a0001c0003t0001g0172 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.42+5292C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100581957 | ||||||
chr14:100581958
|
C | T | 1 | a0001c0003t0001g0172 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.42+5291G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100581958 | ||||||
chr14:100581959
|
A | T | 1 | a0001c0003t0001g0172 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.42+5290T>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100581959 | ||||||
chr14:100581960
|
G | T | 1 | a0001c0003t0001g0172 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.42+5289C>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100581960 | ||||||
chr14:100581961
|
G | C | 1 | a0001c0003t0001g0172 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.42+5288C>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100581961 | ||||||
chr14:100581963
|
C | T | 1 | a0001c0003t0001g0172 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.42+5286G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100581963 | ||||||
chr14:100581965
|
G | T | 1 | a0001c0003t0001g0172 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.42+5284C>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100581965 | ||||||
chr14:100581966
|
A | T | 1 | a0001c0003t0001g0172 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.42+5283T>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100581966 | ||||||
chr14:100581973
|
G | T | 1 | a0001c0003t0001g0172 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.42+5276C>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100581973 | ||||||
chr14:100581974
|
G | C | 1 | a0001c0003t0001g0172 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.42+5275C>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100581974 | ||||||
chr14:100581975
|
A | T | 1 | a0001c0003t0001g0172 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.42+5274T>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100581975 | ||||||
chr14:100581976
|
G | T | 1 | a0001c0003t0001g0172 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.42+5273C>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100581976 | ||||||
chr14:100581978
|
A | T | 1 | a0001c0003t0001g0172 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.42+5271T>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100581978 | ||||||
chr14:100581979
|
G | C | 1 | a0001c0003t0001g0172 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.42+5270C>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100581979 | ||||||
chr14:100581982
|
A | C | 1 | a0001c0003t0001g0172 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.42+5267T>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100581982 | ||||||
chr14:100581987
|
G | C | 1 | a0001c0003t0001g0172 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.42+5262C>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100581987 | ||||||
chr14:100581990
|
T | C | 1 | a0001c0003t0001g0172 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.42+5259A>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100581990 | ||||||
chr14:100581992
|
A | T | 1 | a0001c0003t0001g0172 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.42+5257T>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100581992 | ||||||
chr14:100581994
|
G | C | 1 | a0001c0003t0001g0172 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.42+5255C>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100581994 | ||||||
chr14:100581996
|
A | T | 1 | a0001c0003t0001g0172 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.42+5253T>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100581996 | ||||||
chr14:100581997
|
G | T | 1 | a0001c0003t0001g0172 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.42+5252C>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100581997 | ||||||
chr14:100581999
|
A | T | 1 | a0001c0003t0001g0172 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.42+5250T>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100581999 | ||||||
chr14:100582000
|
G | T | 1 | a0001c0003t0001g0172 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.42+5249C>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100582000 | ||||||
chr14:100582002
|
A | T | 1 | a0001c0003t0001g0172 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.42+5247T>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100582002 | ||||||
chr14:100582003
|
A | T | 1 | a0001c0003t0001g0172 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.42+5246T>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100582003 | ||||||
chr14:100582004
|
A | G | 1 | a0001c0003t0001g0172 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.42+5245T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100582004 | ||||||
chr14:100582005
|
C | T | 1 | a0001c0003t0001g0172 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.42+5244G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100582005 | ||||||
chr14:100582008
|
G | A | 1 | a0001c0003t0001g0172 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.42+5241C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100582008 | ||||||
chr14:100582009
|
G | T | 1 | a0001c0003t0001g0172 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.42+5240C>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100582009 | ||||||
chr14:100582017
|
G | T | 1 | a0001c0003t0001g0172 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.42+5232C>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100582017 | ||||||
chr14:100582019
|
G | A | 1 | a0001c0003t0001g0172 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.42+5230C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100582019 | ||||||
chr14:100582023
|
C | A | 1 | a0001c0003t0001g0172 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.42+5226G>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100582023 | ||||||
chr14:100582024
|
G | A | 9 | a0001c0001t0001g0005a0001c0001t0001g0037a0001c0001t0001g0041others(6): Show | 10 | HG00544.hp1 HG00639.hp1 HG00733.hp2 others(7): Show |
intron_variant | MODIFIER | c.42+5225C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100582024 | ||||||
chr14:100582025
|
G | T | 1 | a0001c0003t0001g0172 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.42+5224C>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100582025 | ||||||
chr14:100582026
|
G | A | 1 | a0001c0003t0001g0172 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.42+5223C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100582026 | ||||||
chr14:100582031
|
C | T | 1 | a0001c0003t0001g0174 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.42+5218G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100582031 | ||||||
chr14:100582051
|
G | A | 6 | a0001c0001t0001g0166a0001c0001t0001g0168a0001c0001t0001g0169others(3): Show | 6 | HG01099.hp2 HG02055.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.42+5198C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100582051 | ||||||
chr14:100582060
|
C | T | 216 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(213): Show | 224 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(221): Show |
intron_variant | MODIFIER | c.42+5189G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100582060 | ||||||
chr14:100582084
|
G | A | 5 | a0001c0002t0006g0302a0001c0002t0006g0307a0001c0005t0002g0076others(2): Show | 5 | HG02055.hp2 HG02723.hp2 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.42+5165C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100582084 | ||||||
chr14:100582127
|
A | AT | 6 | a0001c0001t0001g0166a0001c0001t0001g0168a0001c0001t0001g0169others(3): Show | 6 | HG01099.hp2 HG02055.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.42+5121dupA | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100582127 | ||||||
chr14:100582354
|
G | A | 215 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0011others(212): Show | 222 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(219): Show |
intron_variant | MODIFIER | c.42+4895C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100582354 | ||||||
chr14:100582394
|
C | T | 11 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(8): Show | 13 | HG02258.hp2 HG02280.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.42+4855G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100582394 | ||||||
chr14:100582397
|
C | T | 1 | a0001c0002t0004g0258 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.42+4852G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100582397 | ||||||
chr14:100582423
|
G | A | 2 | a0001c0003t0001g0013a0001c0003t0001g0279 | 3 | HG02109.hp1 HG03098.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.42+4826C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100582423 | ||||||
chr14:100582432
|
C | T | 1 | a0001c0002t0001g0223 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.42+4817G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100582432 | ||||||
chr14:100582439
|
A | G | 10 | a0001c0001t0001g0166a0001c0001t0001g0168a0001c0001t0001g0169others(7): Show | 10 | HG01099.hp2 HG02055.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.42+4810T>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100582439 | ||||||
chr14:100582563
|
T | C | 11 | a0001c0001t0001g0036a0001c0002t0001g0030a0001c0004t0001g0004others(8): Show | 12 | HG00423.hp1 HG02056.hp2 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.42+4686A>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100582563 | ||||||
chr14:100582717
|
C | T | 1 | a0001c0003t0001g0054 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.42+4532G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100582717 | ||||||
chr14:100582870
|
A | T | 6 | a0001c0001t0001g0062a0001c0003t0001g0140a0001c0003t0001g0141others(3): Show | 6 | HG02647.hp1 HG02809.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.42+4379T>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100582870 | ||||||
chr14:100583069
|
T | C | 60 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(57): Show | 63 | HG00099.hp1 HG00408.hp1 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.42+4180A>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100583069 | ||||||
chr14:100583335
|
T | C | 1 | a0001c0003t0001g0054 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.42+3914A>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100583335 | ||||||
chr14:100583569
|
C | T | 60 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(57): Show | 63 | HG00099.hp1 HG00408.hp1 HG00733.hp2 others(60): Show |
intron_variant | MODIFIER | c.42+3680G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100583569 | ||||||
chr14:100583632
|
CTCTT | C | 10 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0037others(7): Show | 11 | HG00621.hp1 HG00639.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.42+3613_42+3616del others(4): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100583632 | ||||||
chr14:100583692
|
C | CT | 7 | a0001c0001t0001g0055a0001c0001t0001g0080a0001c0001t0001g0081others(4): Show | 7 | HG02055.hp2 HG02071.hp1 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.42+3556dupA | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100583692 | ||||||
chr14:100583692
|
C | CTTTTTT | 12 | a0001c0001t0001g0023a0001c0001t0001g0036a0001c0002t0001g0030others(9): Show | 13 | HG00423.hp1 HG02056.hp2 HG02523.hp2 others(10): Show |
intron_variant | MODIFIER | c.42+3551_42+3556dup others(6): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100583692 | ||||||
chr14:100583692
|
C | CTTTTTTT | 13 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0046others(10): Show | 13 | HG02109.hp1 HG02258.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.42+3550_42+3556dup others(7): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100583692 | ||||||
chr14:100583692
|
C | CTTTTTTT others(1): Show |
30 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0037others(27): Show | 34 | HG00639.hp1 HG01884.hp2 HG02280.hp1 others(31): Show |
intron_variant | MODIFIER | c.42+3549_42+3556dup others(8): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100583692 | ||||||
chr14:100583692
|
C | CTTTTTTT others(2): Show |
74 | a0001c0001t0001g0063a0001c0001t0001g0149a0001c0001t0001g0151others(71): Show | 74 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.42+3548_42+3556dup others(9): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100583692 | ||||||
chr14:100583692
|
C | CTTTTTTT others(3): Show |
11 | a0001c0001t0001g0146a0001c0001t0001g0166a0001c0001t0001g0221others(8): Show | 11 | HG01106.hp2 HG01358.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.42+3547_42+3556dup others(10): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100583692 | ||||||
chr14:100583692
|
C | CTTTTTTT others(4): Show |
2 | a0001c0001t0001g0216a0001c0002t0001g0145 | 2 | HG00741.hp2 HG02071.hp2 |
intron_variant | MODIFIER | c.42+3546_42+3556dup others(11): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100583692 | ||||||
chr14:100583692
|
CTTTT | C | 60 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(57): Show | 63 | HG00099.hp1 HG00408.hp1 HG00733.hp2 others(60): Show |
intron_variant | MODIFIER | c.42+3553_42+3556del others(4): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100583692 | ||||||
chr14:100583887
|
C | T | 1 | a0001c0002t0001g0215 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.42+3362G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100583887 | ||||||
chr14:100584064
|
T | C | 1 | a0001c0005t0002g0078 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.42+3185A>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100584064 | ||||||
chr14:100584402
|
C | T | 4 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0164others(1): Show | 4 | HG03225.hp1 HG03471.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.42+2847G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100584402 | ||||||
chr14:100584641
|
T | G | 4 | a0001c0003t0006g0303a0001c0003t0006g0304a0001c0003t0006g0306others(1): Show | 4 | HG02717.hp2 HG03209.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.42+2608A>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100584641 | ||||||
chr14:100584833
|
C | T | 1 | a0001c0009t0001g0136 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.42+2416G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100584833 | ||||||
chr14:100584856
|
G | C | 1 | a0001c0003t0001g0294 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.42+2393C>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100584856 | ||||||
chr14:100584856
|
G | T | 90 | a0001c0001t0001g0063a0001c0001t0001g0146a0001c0001t0001g0149others(87): Show | 90 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.42+2393C>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100584856 | ||||||
chr14:100584885
|
C | A | 1 | a0001c0001t0001g0050 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.42+2364G>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100584885 | ||||||
chr14:100584935
|
C | T | 1 | a0001c0002t0001g0214 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.42+2314G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100584935 | ||||||
chr14:100585136
|
G | A | 4 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200others(1): Show | 4 | HG00408.hp1 HG01993.hp2 NA18612.hp2 others(1): Show |
intron_variant | MODIFIER | c.42+2113C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100585136 | ||||||
chr14:100585194
|
CCCAT | C | 29 | a0001c0001t0001g0005a0001c0001t0001g0037a0001c0001t0001g0041others(26): Show | 31 | HG00639.hp1 HG01884.hp2 HG01891.hp1 others(28): Show |
intron_variant | MODIFIER | c.42+2051_42+2054del others(4): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100585194 | ||||||
chr14:100585194
|
CCCATCCA others(1): Show |
C | 176 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(173): Show | 181 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.42+2047_42+2054del others(8): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100585194 | ||||||
chr14:100585194
|
CCCATCCA others(5): Show |
C | 1 | a0001c0003t0001g0202 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.42+2043_42+2054del others(12): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100585194 | ||||||
chr14:100585221
|
ATCCATCC others(5): Show |
A | 1 | a0001c0002t0001g0278 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.42+2016_42+2027del others(12): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100585221 | ||||||
chr14:100585225
|
ATCCATCC others(1): Show |
A | 11 | a0001c0001t0001g0036a0001c0002t0001g0030a0001c0004t0001g0004others(8): Show | 12 | HG00423.hp1 HG02056.hp2 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.42+2016_42+2023del others(8): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100585225 | ||||||
chr14:100585229
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A | C | 10 | a0001c0001t0001g0053a0001c0003t0001g0054a0001c0003t0006g0303others(7): Show | 10 | HG02258.hp1 HG02280.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.42+2020T>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100585229 | ||||||
chr14:100585233
|
C | A | 1 | a0001c0001t0001g0203 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.42+2016G>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100585233 | ||||||
chr14:100585259
|
TCCATCCA others(6): Show |
T | 1 | a0004c0014t0001g0079 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.42+1977_42+1989del others(13): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100585259 | ||||||
chr14:100585330
|
ATCCC | A | 11 | a0001c0001t0001g0036a0001c0002t0001g0030a0001c0004t0001g0004others(8): Show | 12 | HG00423.hp1 HG02056.hp2 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.42+1915_42+1918del others(4): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100585330 | ||||||
chr14:100585359
|
ATCCC | A | 5 | a0001c0001t0001g0053a0001c0005t0002g0051a0001c0005t0002g0052others(2): Show | 5 | HG02280.hp1 HG02886.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.42+1886_42+1889del others(4): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100585359 | ||||||
chr14:100585415
|
C | CCCAT | 35 | a0001c0001t0001g0005a0001c0001t0001g0021a0001c0001t0001g0022others(32): Show | 36 | HG01069.hp1 HG01070.hp2 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.42+1830_42+1833dup others(4): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100585415 | ||||||
chr14:100585415
|
C | CCCATCCA others(1): Show |
20 | a0001c0001t0001g0017a0001c0001t0001g0038a0001c0001t0001g0039others(17): Show | 20 | HG00609.hp2 HG01884.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.42+1826_42+1833dup others(8): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100585415 | ||||||
chr14:100585415
|
C | CCCATCCA others(5): Show |
1 | a0001c0001t0001g0037 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.42+1822_42+1833dup others(12): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100585415 | ||||||
chr14:100585415
|
CCCAT | C | 83 | a0001c0001t0001g0012a0001c0001t0001g0036a0001c0001t0001g0205others(80): Show | 84 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(81): Show |
intron_variant | MODIFIER | c.42+1830_42+1833del others(4): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100585415 | ||||||
chr14:100585415
|
CCCATCCA others(1): Show |
C | 12 | a0001c0001t0001g0281a0001c0001t0001g0286a0001c0002t0001g0280others(9): Show | 13 | HG00438.hp2 HG00609.hp1 HG02083.hp1 others(10): Show |
intron_variant | MODIFIER | c.42+1826_42+1833del others(8): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100585415 | ||||||
chr14:100585415
|
CCCATCCA others(17): Show |
C | 1 | a0001c0005t0010g0289 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.42+1810_42+1833del others(24): Show |
BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100585415 | ||||||
chr14:100585469
|
C | G | 11 | a0001c0001t0001g0036a0001c0002t0001g0030a0001c0004t0001g0004others(8): Show | 12 | HG00423.hp1 HG02056.hp2 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.42+1780G>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100585469 | ||||||
chr14:100585617
|
C | A | 1 | a0001c0001t0001g0290 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.42+1632G>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100585617 | ||||||
chr14:100585904
|
C | G | 1 | a0001c0001t0001g0027 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.42+1345G>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100585904 | ||||||
chr14:100585909
|
G | C | 1 | a0001c0004t0003g0291 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.42+1340C>G | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100585909 | ||||||
chr14:100586165
|
G | T | 1 | a0001c0002t0001g0026 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.42+1084C>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100586165 | ||||||
chr14:100586195
|
C | T | 1 | a0002c0007t0001g0025 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.42+1054G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100586195 | ||||||
chr14:100586251
|
G | A | 1 | a0001c0003t0001g0292 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.42+998C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100586251 | ||||||
chr14:100586326
|
G | T | 1 | a0001c0002t0001g0024 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.42+923C>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100586326 | ||||||
chr14:100586403
|
G | A | 1 | a0001c0002t0001g0293 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.42+846C>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100586403 | ||||||
chr14:100586785
|
C | T | 3 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023 | 3 | HG02895.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.42+464G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100586785 | ||||||
chr14:100586811
|
C | G | 1 | a0001c0002t0001g0020 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.42+438G>C | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100586811 | ||||||
chr14:100586898
|
C | A | 1 | a0001c0003t0001g0294 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.42+351G>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100586898 | ||||||
chr14:100587036
|
C | T | 1 | a0001c0001t0001g0019 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.42+213G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100587036 | ||||||
chr14:100587070
|
C | A | 1 | a0001c0002t0005g0300 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.42+179G>T | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100587070 | ||||||
chr14:100587108
|
C | CG | 5 | a0001c0001t0001g0017a0001c0001t0007g0015a0001c0002t0001g0018others(2): Show | 5 | HG02738.hp2 HG03516.hp1 NA18948.hp1 others(2): Show |
intron_variant | MODIFIER | c.42+140dupC | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100587108 | ||||||
chr14:100587176
|
C | T | 1 | a0005c0011t0009g0014 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.42+73G>A | BEGAIN | ENSG00000183092.18 | transcript | ENST00000554140.3 | protein_coding | 1/6 | chr14 | 100587176 |