geneid | 84140 |
---|---|
ensemblid | ENSG00000170264.13 |
hgncid | 25808 |
symbol | FAM161A |
name | FAM161 centrosomal protein A |
refseq_nuc | NM_001201543.2 |
refseq_prot | NP_001188472.1 |
ensembl_nuc | ENST00000404929.6 |
ensembl_prot | ENSP00000385158.1 |
mane_status | MANE Select |
chr | chr2 |
start | 61824848 |
end | 61854060 |
strand | - |
ver | v1.2 |
region | chr2:61824848-61854060 |
region5000 | chr2:61819848-61859060 |
regionname0 | FAM161A_chr2_61824848_61854060 |
regionname5000 | FAM161A_chr2_61819848_61859060 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 716 | 275 | 64 | 48 | 125 | 12 | 24 | 92 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
a0002 | 0/0 | 716 | 68 | 8 | 9 | 38 | 4 | 9 | 33 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
a0003 | 0/0 | 716 | 37 | 4 | 12 | 15 | 2 | 4 | 11 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
a0004 | 0/0 | 716 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
a0005 | 0/0 | 716 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
a0006 | 0/0 | 716 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
a0007 | 0/0 | 716 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
a0008 | 0/0 | 716 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
a0009 | 0/0 | 716 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
a0010 | 0/0 | 716 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
a0011 | 0/0 | 716 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
a0012 | 0/0 | 716 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
a0013 | 0/0 | 716 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
a0014 | 0/0 | 716 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
a0015 | 0/0 | 716 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 2151 | 215 | 61 | 30 | 93 | 9 | 21 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
c0002 | 0/0 | 2151 | 67 | 8 | 9 | 38 | 4 | 8 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
c0003 | 0/0 | 2151 | 54 | 1 | 16 | 32 | 2 | 3 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
c0004 | 0/0 | 2151 | 37 | 4 | 12 | 15 | 2 | 4 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
c0005 | 0/0 | 2151 | 6 | 6 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
c0006 | 1/0 | 2151 | 4 | 0 | 2 | 0 | 1 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
c0007 | 0/0 | 2151 | 2 | 2 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
c0008 | 0/0 | 2151 | 2 | 0 | 0 | 0 | 0 | 2 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
c0009 | 0/0 | 2151 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
c0010 | 0/0 | 2151 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
c0011 | 0/0 | 2151 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
c0012 | 0/0 | 2151 | 1 | 0 | 0 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
c0013 | 0/0 | 2151 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
c0014 | 0/0 | 2151 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
c0015 | 0/0 | 2151 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
c0016 | 0/0 | 2151 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
c0017 | 0/0 | 2151 | 1 | 0 | 0 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
c0018 | 0/0 | 2151 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
c0019 | 0/0 | 2151 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
c0020 | 0/0 | 2151 | 1 | 0 | 0 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
c0021 | 0/0 | 2151 | 1 | 0 | 0 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 1627 | 174 | 24 | 29 | 112 | 1 | 8 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
t0002 | 1/1 | 1627 | 138 | 40 | 19 | 49 | 6 | 22 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
t0003 | 0/0 | 1626 | 39 | 4 | 13 | 15 | 2 | 5 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
t0004 | 0/0 | 1624 | 20 | 0 | 9 | 0 | 4 | 7 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
t0005 | 0/0 | 1627 | 5 | 5 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
t0006 | 0/0 | 1627 | 2 | 2 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
t0007 | 0/0 | 1627 | 2 | 2 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
t0008 | 0/0 | 1627 | 2 | 0 | 0 | 0 | 2 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
t0009 | 0/0 | 1627 | 2 | 2 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
t0010 | 0/0 | 1627 | 2 | 2 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
t0011 | 0/0 | 1627 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
t0012 | 0/0 | 1627 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
t0013 | 0/0 | 1627 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
t0014 | 0/0 | 1627 | 1 | 0 | 0 | 0 | 1 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
t0015 | 0/0 | 1627 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
t0016 | 0/0 | 1627 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
t0017 | 0/0 | 1627 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
t0018 | 0/0 | 1627 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
t0019 | 0/0 | 1627 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
t0020 | 0/0 | 1627 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
t0021 | 0/0 | 1627 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
t0022 | 0/0 | 1627 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
t0023 | 0/0 | 1627 | 1 | 0 | 0 | 0 | 1 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
t0024 | 0/0 | 1624 | 1 | 0 | 0 | 0 | 1 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 16 | 0 | 8 | 8 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0002 | 0/0 | 15 | 0 | 0 | 12 | 0 | 3 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0003 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0004 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0005 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0006 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0007 | 0/1 | 5 | 0 | 1 | 0 | 0 | 3 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0008 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0009 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0010 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0013 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0015 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0016 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0017 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0019 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0027 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0033 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0037 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0039 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0040 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0041 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0044 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0288 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 2151 | 215 | 61 | 30 | 93 | 9 | 21 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
a0001c0003 | 0/0 | 2151 | 54 | 1 | 16 | 32 | 2 | 3 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
a0001c0006 | 1/0 | 2151 | 4 | 0 | 2 | 0 | 1 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
a0001c0013 | 0/0 | 2151 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
a0001c0019 | 0/0 | 2151 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
a0002c0002 | 0/0 | 2151 | 67 | 8 | 9 | 38 | 4 | 8 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
a0002c0020 | 0/0 | 2151 | 1 | 0 | 0 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
a0003c0004 | 0/0 | 2151 | 37 | 4 | 12 | 15 | 2 | 4 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
a0004c0005 | 0/0 | 2151 | 6 | 6 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
a0005c0007 | 0/0 | 2151 | 2 | 2 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
a0005c0010 | 0/0 | 2151 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
a0006c0008 | 0/0 | 2151 | 2 | 0 | 0 | 0 | 0 | 2 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
a0007c0021 | 0/0 | 2151 | 1 | 0 | 0 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
a0008c0018 | 0/0 | 2151 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
a0009c0009 | 0/0 | 2151 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
a0010c0011 | 0/0 | 2151 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
a0011c0012 | 0/0 | 2151 | 1 | 0 | 0 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
a0012c0014 | 0/0 | 2151 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
a0013c0015 | 0/0 | 2151 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
a0014c0016 | 0/0 | 2151 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
a0015c0017 | 0/0 | 2151 | 1 | 0 | 0 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 3777 | 119 | 22 | 13 | 79 | 0 | 5 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
a0001c0001t0002 | 0/1 | 3777 | 61 | 31 | 8 | 10 | 1 | 10 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
a0001c0001t0004 | 0/0 | 3774 | 19 | 0 | 9 | 0 | 4 | 6 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
a0001c0001t0006 | 0/0 | 3777 | 2 | 2 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
a0001c0001t0007 | 0/0 | 3777 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
a0001c0001t0008 | 0/0 | 3777 | 2 | 0 | 0 | 0 | 2 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
a0001c0001t0010 | 0/0 | 3777 | 2 | 2 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
a0001c0001t0011 | 0/0 | 3777 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
a0001c0001t0013 | 0/0 | 3777 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
a0001c0001t0016 | 0/0 | 3777 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
a0001c0001t0017 | 0/0 | 3777 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
a0001c0001t0020 | 0/0 | 3777 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
a0001c0001t0021 | 0/0 | 3777 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
a0001c0001t0022 | 0/0 | 3777 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
a0001c0001t0023 | 0/0 | 3777 | 1 | 0 | 0 | 0 | 1 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
a0001c0001t0024 | 0/0 | 3774 | 1 | 0 | 0 | 0 | 1 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
a0001c0003t0001 | 0/0 | 3777 | 53 | 1 | 16 | 32 | 1 | 3 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
a0001c0003t0014 | 0/0 | 3777 | 1 | 0 | 0 | 0 | 1 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
a0001c0006t0002 | 1/0 | 3777 | 4 | 0 | 2 | 0 | 1 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
a0001c0013t0001 | 0/0 | 3777 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
a0001c0019t0007 | 0/0 | 3777 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
a0002c0002t0002 | 0/0 | 3777 | 65 | 6 | 9 | 38 | 4 | 8 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
a0002c0002t0012 | 0/0 | 3777 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
a0002c0002t0019 | 0/0 | 3777 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
a0002c0020t0002 | 0/0 | 3777 | 1 | 0 | 0 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
a0003c0004t0003 | 0/0 | 3776 | 37 | 4 | 12 | 15 | 2 | 4 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
a0004c0005t0002 | 0/0 | 3777 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
a0004c0005t0005 | 0/0 | 3777 | 5 | 5 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
a0005c0007t0009 | 0/0 | 3777 | 2 | 2 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
a0005c0010t0018 | 0/0 | 3777 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
a0006c0008t0002 | 0/0 | 3777 | 2 | 0 | 0 | 0 | 0 | 2 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
a0007c0021t0004 | 0/0 | 3774 | 1 | 0 | 0 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
a0008c0018t0015 | 0/0 | 3777 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
a0009c0009t0002 | 0/0 | 3777 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
a0010c0011t0002 | 0/0 | 3777 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
a0011c0012t0002 | 0/0 | 3777 | 1 | 0 | 0 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
a0012c0014t0002 | 0/0 | 3777 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
a0013c0015t0001 | 0/0 | 3777 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
a0014c0016t0003 | 0/0 | 3776 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
a0015c0017t0003 | 0/0 | 3776 | 1 | 0 | 0 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | copy fasta | chr2 | 61819848 | 61859060 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 15 | 0 | 0 | 12 | 0 | 3 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0001g0004 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0001g0005 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0001g0008 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0001g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0001g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0002g0007 | 0/1 | 5 | 0 | 1 | 0 | 0 | 3 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0002g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0002g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0002g0015 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0002g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0002g0039 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0002g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0002g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0002g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0002g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0002g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0002g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0002g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0002g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0002g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0002g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0002g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0004g0009 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0004g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0004g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0004g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0004g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0004g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0004g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0004g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0004g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0004g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0004g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0004g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0004g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0004g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0004g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0006g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0006g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0007g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0008g0040 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0010g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0010g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0011g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0013g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0016g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0017g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0020g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0021g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0022g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0023g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0001t0024g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0003t0001g0001 | 0/0 | 16 | 0 | 8 | 8 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0003t0001g0006 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0003t0001g0013 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0003t0001g0027 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0003t0001g0033 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0003t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0003t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0003t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0003t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0003t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0003t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0003t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0003t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0003t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0003t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0003t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0003t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0003t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0003t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0003t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0003t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0003t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0003t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0003t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0003t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0003t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0003t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0003t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0003t0014g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0006t0002g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0006t0002g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0006t0002g0288 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0006t0002g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0013t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0001c0019t0007g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0002c0002t0002g0003 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0002c0002t0002g0016 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0002c0002t0002g0017 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0002c0002t0002g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0002c0002t0002g0019 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0002c0002t0002g0041 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0002c0002t0002g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0002c0002t0002g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0002c0002t0002g0044 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0002c0002t0002g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0002c0002t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0002c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0002c0002t0002g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0002c0002t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0002c0002t0002g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0002c0002t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0002c0002t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0002c0002t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0002c0002t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0002c0002t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0002c0002t0002g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0002c0002t0002g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0002c0002t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0002c0002t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0002c0002t0002g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0002c0002t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0002c0002t0002g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0002c0002t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0002c0002t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0002c0002t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0002c0002t0002g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0002c0002t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0002c0002t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0002c0002t0002g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0002c0002t0002g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0002c0002t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0002c0002t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0002c0002t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0002c0002t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0002c0002t0002g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0002c0002t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0002c0002t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0002c0002t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0002c0002t0002g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0002c0002t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0002c0002t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0002c0002t0012g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0002c0002t0019g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0002c0020t0002g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0003c0004t0003g0010 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0003c0004t0003g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0003c0004t0003g0037 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0003c0004t0003g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0003c0004t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0003c0004t0003g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0003c0004t0003g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0003c0004t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0003c0004t0003g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0003c0004t0003g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0003c0004t0003g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0003c0004t0003g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0003c0004t0003g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0003c0004t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0003c0004t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0003c0004t0003g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0003c0004t0003g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0003c0004t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0003c0004t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0003c0004t0003g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0003c0004t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0003c0004t0003g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0003c0004t0003g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0003c0004t0003g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0003c0004t0003g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0003c0004t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0003c0004t0003g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0003c0004t0003g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0003c0004t0003g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0003c0004t0003g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0003c0004t0003g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0004c0005t0002g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0004c0005t0005g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0004c0005t0005g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0004c0005t0005g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0004c0005t0005g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0005c0007t0009g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0005c0007t0009g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0005c0010t0018g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0006c0008t0002g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0006c0008t0002g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0007c0021t0004g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0008c0018t0015g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0009c0009t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0010c0011t0002g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0011c0012t0002g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0012c0014t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0013c0015t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0014c0016t0003g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
a0015c0017t0003g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0002 | t0002 | g0227 | EUR | GBR | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG00099 | hp2 | a0001 | c0001 | t0004 | g0009 | EUR | GBR | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG00140 | hp1 | a0003 | c0004 | t0003 | g0119 | EUR | GBR | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG00140 | hp2 | a0001 | c0001 | t0004 | g0058 | EUR | GBR | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG00280 | hp1 | a0003 | c0004 | t0003 | g0181 | EUR | FIN | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG00280 | hp2 | a0001 | c0006 | t0002 | g0286 | EUR | FIN | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG00323 | hp1 | a0001 | c0001 | t0024 | g0091 | EUR | FIN | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG00323 | hp2 | a0002 | c0002 | t0002 | g0242 | EUR | FIN | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG00408 | hp1 | a0002 | c0002 | t0002 | g0244 | EAS | CHS | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | CHS | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | CHS | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG00423 | hp2 | a0003 | c0004 | t0003 | g0176 | EAS | CHS | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG00438 | hp1 | a0001 | c0003 | t0001 | g0035 | EAS | CHS | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | CHS | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | CHS | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | CHS | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG00558 | hp1 | a0001 | c0003 | t0001 | g0155 | EAS | CHS | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG00597 | hp1 | a0001 | c0001 | t0022 | g0154 | EAS | CHS | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG00597 | hp2 | a0003 | c0004 | t0003 | g0174 | EAS | CHS | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG00621 | hp1 | a0001 | c0003 | t0001 | g0013 | EAS | CHS | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | CHS | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG00639 | hp1 | a0003 | c0004 | t0003 | g0010 | AMR | PUR | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0229 | AMR | PUR | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG00642 | hp1 | a0003 | c0004 | t0003 | g0183 | AMR | PUR | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG00673 | hp1 | a0003 | c0004 | t0003 | g0038 | EAS | CHS | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | CHS | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG00735 | hp2 | a0001 | c0001 | t0004 | g0093 | AMR | PUR | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG00738 | hp1 | a0001 | c0003 | t0001 | g0033 | AMR | PUR | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG00738 | hp2 | a0002 | c0002 | t0002 | g0219 | AMR | PUR | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG00741 | hp1 | a0003 | c0004 | t0003 | g0165 | AMR | PUR | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG00741 | hp2 | a0001 | c0001 | t0004 | g0061 | AMR | PUR | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG01070 | hp1 | a0001 | c0003 | t0001 | g0145 | AMR | PUR | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG01070 | hp2 | a0003 | c0004 | t0003 | g0180 | AMR | PUR | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG01071 | hp1 | a0001 | c0003 | t0001 | g0001 | AMR | PUR | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG01071 | hp2 | a0003 | c0004 | t0003 | g0172 | AMR | PUR | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG01074 | hp1 | a0001 | c0003 | t0001 | g0001 | AMR | PUR | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG01081 | hp1 | a0001 | c0001 | t0004 | g0056 | AMR | PUR | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG01081 | hp2 | a0003 | c0004 | t0003 | g0029 | AMR | PUR | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG01099 | hp1 | a0001 | c0003 | t0001 | g0158 | AMR | PUR | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG01099 | hp2 | a0003 | c0004 | t0003 | g0029 | AMR | PUR | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0015 | AMR | PUR | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG01109 | hp2 | a0003 | c0004 | t0003 | g0179 | AMR | PUR | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG01167 | hp2 | a0001 | c0001 | t0002 | g0212 | AMR | PUR | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG01169 | hp1 | a0002 | c0002 | t0002 | g0222 | AMR | PUR | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG01175 | hp1 | a0001 | c0003 | t0001 | g0027 | AMR | PUR | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG01175 | hp2 | a0001 | c0001 | t0002 | g0188 | AMR | PUR | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG01192 | hp1 | a0001 | c0003 | t0001 | g0160 | AMR | PUR | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG01192 | hp2 | a0002 | c0002 | t0002 | g0238 | AMR | PUR | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG01255 | hp1 | a0014 | c0016 | t0003 | g0182 | AMR | CLM | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0230 | AMR | CLM | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG01256 | hp1 | a0002 | c0002 | t0002 | g0016 | AMR | CLM | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG01256 | hp2 | a0002 | c0002 | t0002 | g0017 | AMR | CLM | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG01257 | hp1 | a0001 | c0001 | t0004 | g0009 | AMR | CLM | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0193 | AMR | CLM | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0199 | AMR | CLM | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG01258 | hp2 | a0002 | c0002 | t0002 | g0016 | AMR | CLM | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG01261 | hp1 | a0001 | c0003 | t0001 | g0001 | AMR | CLM | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG01261 | hp2 | a0001 | c0006 | t0002 | g0287 | AMR | CLM | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG01346 | hp1 | a0002 | c0002 | t0002 | g0254 | AMR | CLM | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG01346 | hp2 | a0003 | c0004 | t0003 | g0166 | AMR | CLM | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG01358 | hp1 | a0001 | c0003 | t0001 | g0001 | AMR | CLM | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG01358 | hp2 | a0001 | c0001 | t0004 | g0020 | AMR | CLM | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG01361 | hp1 | a0003 | c0004 | t0003 | g0110 | AMR | CLM | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG01361 | hp2 | a0001 | c0001 | t0004 | g0081 | AMR | CLM | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG01433 | hp1 | a0001 | c0001 | t0004 | g0059 | AMR | CLM | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG01433 | hp2 | a0001 | c0001 | t0004 | g0020 | AMR | CLM | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | CLM | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG01496 | hp2 | a0001 | c0001 | t0004 | g0009 | AMR | CLM | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG01515 | hp1 | a0001 | c0001 | t0008 | g0040 | EUR | IBS | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG01515 | hp2 | a0001 | c0003 | t0001 | g0259 | EUR | IBS | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG01516 | hp1 | a0001 | c0001 | t0004 | g0009 | EUR | IBS | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG01516 | hp2 | a0002 | c0002 | t0002 | g0017 | EUR | IBS | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG01517 | hp1 | a0001 | c0001 | t0008 | g0040 | EUR | IBS | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG01517 | hp2 | a0002 | c0002 | t0002 | g0017 | EUR | IBS | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | ACB | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG01884 | hp2 | a0001 | c0001 | t0002 | g0015 | AFR | ACB | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | ACB | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG01891 | hp2 | a0001 | c0001 | t0002 | g0192 | AFR | ACB | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG01928 | hp2 | a0001 | c0003 | t0001 | g0001 | AMR | PEL | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG01934 | hp1 | a0001 | c0003 | t0001 | g0148 | AMR | PEL | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG01943 | hp1 | a0002 | c0002 | t0002 | g0019 | AMR | PEL | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG01943 | hp2 | a0001 | c0006 | t0002 | g0289 | AMR | PEL | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG01978 | hp2 | a0001 | c0003 | t0001 | g0001 | AMR | PEL | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG01981 | hp1 | a0001 | c0003 | t0001 | g0013 | AMR | PEL | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG01981 | hp2 | a0003 | c0004 | t0003 | g0261 | AMR | PEL | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | PEL | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | PEL | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG02015 | hp1 | a0001 | c0003 | t0001 | g0143 | EAS | KHV | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG02015 | hp2 | a0001 | c0001 | t0013 | g0132 | EAS | KHV | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG02027 | hp2 | a0001 | c0003 | t0001 | g0006 | EAS | KHV | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | KHV | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG02040 | hp2 | a0001 | c0003 | t0001 | g0006 | EAS | KHV | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG02055 | hp2 | a0001 | c0001 | t0002 | g0189 | AFR | ACB | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG02056 | hp1 | a0002 | c0002 | t0002 | g0045 | EAS | KHV | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | KHV | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | KHV | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG02074 | hp1 | a0001 | c0003 | t0001 | g0157 | EAS | KHV | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG02074 | hp2 | a0002 | c0002 | t0002 | g0236 | EAS | KHV | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0151 | EAS | KHV | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG02129 | hp1 | a0001 | c0003 | t0001 | g0001 | EAS | KHV | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG02132 | hp1 | a0001 | c0003 | t0001 | g0163 | EAS | KHV | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG02132 | hp2 | a0003 | c0004 | t0003 | g0101 | EAS | KHV | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG02145 | hp1 | a0002 | c0002 | t0012 | g0116 | AFR | ACB | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | CDX | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | CDX | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG02258 | hp1 | a0003 | c0004 | t0003 | g0037 | AFR | ACB | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG02258 | hp2 | a0001 | c0001 | t0006 | g0128 | AFR | ACB | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG02273 | hp1 | a0001 | c0003 | t0001 | g0001 | AMR | PEL | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG02280 | hp1 | a0004 | c0005 | t0005 | g0268 | AFR | ACB | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0277 | AFR | ACB | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG02300 | hp1 | a0001 | c0003 | t0001 | g0001 | AMR | PEL | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG02300 | hp2 | a0002 | c0002 | t0002 | g0041 | AMR | PEL | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG02451 | hp1 | a0004 | c0005 | t0002 | g0266 | AFR | ACB | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG02451 | hp2 | a0001 | c0001 | t0002 | g0264 | AFR | ACB | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG02523 | hp1 | a0002 | c0002 | t0002 | g0255 | EAS | KHV | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | KHV | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG02572 | hp1 | a0005 | c0007 | t0009 | g0282 | AFR | GWD | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG02572 | hp2 | a0012 | c0014 | t0002 | g0201 | AFR | GWD | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG02602 | hp1 | a0003 | c0004 | t0003 | g0173 | SAS | PJL | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0205 | SAS | PJL | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG02615 | hp2 | a0001 | c0001 | t0002 | g0195 | AFR | GWD | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG02622 | hp1 | a0005 | c0010 | t0018 | g0280 | AFR | GWD | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG02622 | hp2 | a0001 | c0001 | t0002 | g0214 | AFR | GWD | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG02630 | hp1 | a0001 | c0001 | t0002 | g0283 | AFR | GWD | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG02647 | hp1 | a0002 | c0002 | t0002 | g0223 | AFR | GWD | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG02647 | hp2 | a0002 | c0002 | t0002 | g0042 | AFR | GWD | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG02683 | hp1 | a0002 | c0002 | t0002 | g0215 | SAS | PJL | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG02683 | hp2 | a0001 | c0001 | t0004 | g0062 | SAS | PJL | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG02698 | hp1 | a0001 | c0003 | t0001 | g0027 | SAS | PJL | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG02698 | hp2 | a0001 | c0001 | t0002 | g0007 | SAS | PJL | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG02723 | hp1 | a0002 | c0002 | t0002 | g0225 | AFR | GWD | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG02723 | hp2 | a0002 | c0002 | t0002 | g0042 | AFR | GWD | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0007 | SAS | PJL | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG02738 | hp1 | a0002 | c0002 | t0002 | g0247 | SAS | PJL | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0094 | SAS | PJL | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG02809 | hp1 | a0001 | c0003 | t0001 | g0144 | AFR | GWD | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0014 | AFR | GWD | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG02886 | hp1 | a0001 | c0001 | t0017 | g0118 | AFR | GWD | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG02886 | hp2 | a0001 | c0001 | t0020 | g0203 | AFR | GWD | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG02895 | hp2 | a0001 | c0001 | t0002 | g0234 | AFR | GWD | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG02896 | hp1 | a0002 | c0002 | t0002 | g0272 | AFR | GWD | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG02896 | hp2 | a0001 | c0001 | t0002 | g0269 | AFR | GWD | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG02897 | hp2 | a0001 | c0001 | t0002 | g0221 | AFR | GWD | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG02922 | hp1 | a0001 | c0001 | t0010 | g0291 | AFR | ESN | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG02922 | hp2 | a0001 | c0001 | t0002 | g0202 | AFR | ESN | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG02965 | hp1 | a0010 | c0011 | t0002 | g0263 | AFR | ESN | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG02965 | hp2 | a0003 | c0004 | t0003 | g0168 | AFR | ESN | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG02970 | hp1 | a0001 | c0001 | t0002 | g0197 | AFR | ESN | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG02970 | hp2 | a0001 | c0001 | t0010 | g0290 | AFR | ESN | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG02976 | hp1 | a0001 | c0001 | t0002 | g0220 | AFR | ESN | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | ESN | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG03017 | hp1 | a0007 | c0021 | t0004 | g0083 | SAS | PJL | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0007 | SAS | PJL | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG03041 | hp1 | a0004 | c0005 | t0005 | g0267 | AFR | GWD | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG03098 | hp1 | a0002 | c0002 | t0002 | g0233 | AFR | MSL | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG03098 | hp2 | a0001 | c0001 | t0002 | g0278 | AFR | MSL | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG03130 | hp1 | a0001 | c0001 | t0006 | g0126 | AFR | ESN | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG03130 | hp2 | a0005 | c0007 | t0009 | g0281 | AFR | ESN | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG03139 | hp1 | a0001 | c0001 | t0002 | g0014 | AFR | ESN | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG03195 | hp1 | a0008 | c0018 | t0015 | g0279 | AFR | ESN | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | ESN | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG03209 | hp1 | a0001 | c0001 | t0002 | g0011 | AFR | MSL | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | MSL | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG03225 | hp1 | a0001 | c0001 | t0002 | g0218 | AFR | MSL | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG03239 | hp1 | a0003 | c0004 | t0003 | g0169 | SAS | PJL | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG03239 | hp2 | a0001 | c0003 | t0001 | g0258 | SAS | PJL | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG03453 | hp1 | a0004 | c0005 | t0005 | g0265 | AFR | MSL | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG03453 | hp2 | a0001 | c0019 | t0007 | g0129 | AFR | MSL | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG03486 | hp1 | a0001 | c0013 | t0001 | g0105 | AFR | MSL | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG03486 | hp2 | a0002 | c0002 | t0019 | g0237 | AFR | MSL | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG03490 | hp1 | a0003 | c0004 | t0003 | g0185 | SAS | PJL | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG03490 | hp2 | a0001 | c0001 | t0004 | g0055 | SAS | PJL | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG03491 | hp2 | a0002 | c0002 | t0002 | g0044 | SAS | PJL | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG03492 | hp1 | a0002 | c0002 | t0002 | g0044 | SAS | PJL | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG03492 | hp2 | a0001 | c0001 | t0004 | g0060 | SAS | PJL | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG03540 | hp2 | a0004 | c0005 | t0005 | g0046 | AFR | GWD | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG03579 | hp1 | a0001 | c0001 | t0002 | g0276 | AFR | MSL | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG03579 | hp2 | a0001 | c0001 | t0002 | g0187 | AFR | MSL | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG03669 | hp1 | a0002 | c0002 | t0002 | g0235 | SAS | PJL | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG03669 | hp2 | a0002 | c0002 | t0002 | g0228 | SAS | PJL | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0213 | SAS | STU | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG03688 | hp2 | a0011 | c0012 | t0002 | g0200 | SAS | STU | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0039 | SAS | PJL | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG03704 | hp2 | a0006 | c0008 | t0002 | g0217 | SAS | PJL | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0039 | SAS | PJL | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG03710 | hp2 | a0015 | c0017 | t0003 | g0175 | SAS | PJL | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG03831 | hp1 | a0001 | c0001 | t0004 | g0052 | SAS | BEB | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0198 | SAS | BEB | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG03834 | hp1 | a0001 | c0001 | t0004 | g0080 | SAS | BEB | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG03834 | hp2 | a0002 | c0002 | t0002 | g0246 | SAS | BEB | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG03927 | hp1 | a0001 | c0003 | t0001 | g0147 | SAS | BEB | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG03927 | hp2 | a0001 | c0001 | t0002 | g0231 | SAS | BEB | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG04115 | hp2 | a0002 | c0002 | t0002 | g0016 | SAS | STU | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG04184 | hp1 | a0002 | c0020 | t0002 | g0245 | SAS | BEB | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0071 | SAS | BEB | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG04199 | hp1 | a0006 | c0008 | t0002 | g0251 | SAS | STU | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG04199 | hp2 | a0003 | c0004 | t0003 | g0260 | SAS | STU | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG04228 | hp1 | a0001 | c0001 | t0004 | g0051 | SAS | STU | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0207 | SAS | STU | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA18522 | hp1 | a0001 | c0001 | t0002 | g0194 | AFR | YRI | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA18522 | hp2 | a0001 | c0001 | t0002 | g0011 | AFR | YRI | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA18612 | hp1 | a0002 | c0002 | t0002 | g0239 | EAS | CHB | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | CHB | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA18747 | hp2 | a0001 | c0003 | t0001 | g0001 | EAS | CHB | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA18906 | hp1 | a0001 | c0001 | t0002 | g0186 | AFR | YRI | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | YRI | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA18939 | hp2 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA18940 | hp1 | a0001 | c0003 | t0001 | g0034 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA18940 | hp2 | a0003 | c0004 | t0003 | g0164 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA18944 | hp1 | a0001 | c0003 | t0001 | g0150 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA18946 | hp2 | a0002 | c0002 | t0002 | g0019 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA18948 | hp2 | a0001 | c0003 | t0001 | g0001 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA18949 | hp2 | a0002 | c0002 | t0002 | g0115 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA18954 | hp1 | a0001 | c0003 | t0001 | g0006 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA18957 | hp1 | a0001 | c0003 | t0001 | g0001 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA18960 | hp1 | a0001 | c0003 | t0001 | g0001 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA18961 | hp1 | a0002 | c0002 | t0002 | g0270 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA18962 | hp1 | a0002 | c0002 | t0002 | g0273 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA18966 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA18969 | hp1 | a0002 | c0002 | t0002 | g0240 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA18970 | hp2 | a0002 | c0002 | t0002 | g0043 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA18971 | hp1 | a0002 | c0002 | t0002 | g0019 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA18971 | hp2 | a0013 | c0015 | t0001 | g0082 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA18973 | hp1 | a0002 | c0002 | t0002 | g0226 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA18973 | hp2 | a0002 | c0002 | t0002 | g0241 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA18975 | hp1 | a0002 | c0002 | t0002 | g0243 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA18975 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA18977 | hp1 | a0002 | c0002 | t0002 | g0018 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA18979 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA18980 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA18980 | hp2 | a0002 | c0002 | t0002 | g0117 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA18982 | hp1 | a0001 | c0003 | t0001 | g0001 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA18985 | hp2 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA18988 | hp1 | a0003 | c0004 | t0003 | g0038 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA18988 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA18990 | hp1 | a0003 | c0004 | t0003 | g0010 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA18992 | hp2 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA18993 | hp2 | a0002 | c0002 | t0002 | g0250 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA18994 | hp1 | a0001 | c0003 | t0001 | g0092 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA18994 | hp2 | a0003 | c0004 | t0003 | g0170 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA18995 | hp2 | a0003 | c0004 | t0003 | g0171 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA18997 | hp1 | a0001 | c0001 | t0021 | g0152 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA18997 | hp2 | a0002 | c0002 | t0002 | g0232 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA18998 | hp1 | a0001 | c0003 | t0001 | g0099 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA18998 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA18999 | hp1 | a0002 | c0002 | t0002 | g0018 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA19002 | hp1 | a0001 | c0003 | t0001 | g0162 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA19004 | hp1 | a0001 | c0003 | t0001 | g0034 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA19004 | hp2 | a0002 | c0002 | t0002 | g0252 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA19005 | hp1 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA19005 | hp2 | a0001 | c0003 | t0001 | g0035 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA19007 | hp2 | a0003 | c0004 | t0003 | g0178 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA19009 | hp1 | a0002 | c0002 | t0002 | g0224 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA19011 | hp1 | a0003 | c0004 | t0003 | g0010 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA19012 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | LWK | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA19030 | hp2 | a0004 | c0005 | t0005 | g0046 | AFR | LWK | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | LWK | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | LWK | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA19054 | hp2 | a0002 | c0002 | t0002 | g0274 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA19055 | hp2 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA19056 | hp1 | a0001 | c0003 | t0001 | g0146 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA19059 | hp1 | a0003 | c0004 | t0003 | g0285 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA19059 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA19060 | hp1 | a0001 | c0003 | t0001 | g0033 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA19060 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA19062 | hp1 | a0001 | c0001 | t0011 | g0073 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA19062 | hp2 | a0001 | c0003 | t0001 | g0124 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA19065 | hp2 | a0002 | c0002 | t0002 | g0248 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA19066 | hp1 | a0002 | c0002 | t0002 | g0018 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA19068 | hp2 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA19075 | hp2 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA19080 | hp1 | a0002 | c0002 | t0002 | g0043 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA19080 | hp2 | a0003 | c0004 | t0003 | g0184 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA19081 | hp1 | a0001 | c0003 | t0001 | g0006 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA19083 | hp1 | a0002 | c0002 | t0002 | g0045 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA19083 | hp2 | a0001 | c0003 | t0001 | g0142 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA19084 | hp1 | a0001 | c0003 | t0001 | g0006 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA19084 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA19086 | hp1 | a0002 | c0002 | t0002 | g0041 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA19086 | hp2 | a0001 | c0003 | t0001 | g0001 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA19087 | hp1 | a0002 | c0002 | t0002 | g0216 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA19087 | hp2 | a0003 | c0004 | t0003 | g0010 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA19088 | hp2 | a0002 | c0002 | t0002 | g0249 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA19089 | hp1 | a0003 | c0004 | t0003 | g0262 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA19089 | hp2 | a0001 | c0003 | t0001 | g0159 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA19091 | hp1 | a0002 | c0002 | t0002 | g0271 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA19091 | hp2 | a0001 | c0003 | t0001 | g0001 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA19240 | hp1 | a0001 | c0001 | t0002 | g0253 | AFR | YRI | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | YRI | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0011 | AFR | ASW | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA20129 | hp2 | a0001 | c0001 | t0002 | g0014 | AFR | ASW | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0191 | EUR | TSI | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA20752 | hp2 | a0001 | c0003 | t0014 | g0156 | EUR | TSI | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA20805 | hp1 | a0001 | c0001 | t0023 | g0196 | EUR | TSI | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA20805 | hp2 | a0001 | c0001 | t0004 | g0090 | EUR | TSI | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG01123 | hp1 | a0001 | c0003 | t0001 | g0013 | AMR | CLM | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG01123 | hp2 | a0003 | c0004 | t0003 | g0037 | AMR | CLM | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG02109 | hp1 | a0001 | c0001 | t0007 | g0127 | AFR | ACB | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG02109 | hp2 | a0001 | c0001 | t0002 | g0113 | AFR | ACB | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG02559 | hp1 | a0001 | c0001 | t0002 | g0190 | AFR | ACB | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG02559 | hp2 | a0001 | c0001 | t0002 | g0015 | AFR | ACB | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG03471 | hp1 | a0001 | c0001 | t0002 | g0011 | AFR | MSL | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG03471 | hp2 | a0001 | c0001 | t0016 | g0103 | AFR | MSL | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG06807 | hp1 | a0003 | c0004 | t0003 | g0177 | AFR | USA | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | USA | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA18955 | hp1 | a0009 | c0009 | t0002 | g0204 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA18955 | hp2 | a0001 | c0003 | t0001 | g0149 | EAS | JPT | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA21309 | hp1 | a0003 | c0004 | t0003 | g0167 | AFR | LWK | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
NA21309 | hp2 | a0001 | c0001 | t0002 | g0284 | AFR | LWK | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0007 | REF | REF | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
homoSapiens_grch38 | hp1 | a0001 | c0006 | t0002 | g0288 | REF | REF | FAM161A_chr2_61819848_61859060 | FAM161A | chr2 | 61819848 | 61859060 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:61826484
|
C | T | 1 | a0010 | 1 | HG02965.hp1 | missense_variant | MODERATE | c.2122G>A | p.Glu708Lys | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 7/7 | 2141/3777 | 2122/2151 | 708/716 | chr2 | 61826484 | ||
chr2:61827107
|
T | A | 1 | a0011 | 1 | HG03688.hp2 | missense_variant | MODERATE | c.2003A>T | p.Glu668Val | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 6/7 | 2022/3777 | 2003/2151 | 668/716 | chr2 | 61827107 | ||
chr2:61827151
|
C | A | 1 | a0006 | 2 | HG03704.hp2 HG04199.hp1 |
missense_variant | MODERATE | c.1959G>T | p.Glu653Asp | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 6/7 | 1978/3777 | 1959/2151 | 653/716 | chr2 | 61827151 | ||
chr2:61838634
|
A | C | 2 | a0004a0005 | 9 | HG02280.hp1 HG02451.hp1 HG02572.hp1 others(6): Show |
missense_variant | MODERATE | c.1655T>G | p.Met552Arg | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 4/7 | 1674/3777 | 1655/2151 | 552/716 | chr2 | 61838634 | ||
chr2:61839520
|
C | T | 1 | a0009 | 1 | NA18955.hp1 | missense_variant | MODERATE | c.1484G>A | p.Arg495His | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 3/7 | 1503/3777 | 1484/2151 | 495/716 | chr2 | 61839520 | ||
chr2:61839871
|
A | C | 1 | a0014 | 1 | HG01255.hp1 | missense_variant | MODERATE | c.1133T>G | p.Leu378Arg | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 3/7 | 1152/3777 | 1133/2151 | 378/716 | chr2 | 61839871 | ||
chr2:61839895
|
T | C | 1 | a0015 | 1 | HG03710.hp2 | missense_variant | MODERATE | c.1109A>G | p.Asn370Ser | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 3/7 | 1128/3777 | 1109/2151 | 370/716 | chr2 | 61839895 | ||
chr2:61839991
|
C | T | 1 | a0004 | 6 | HG02280.hp1 HG02451.hp1 HG03041.hp1 others(3): Show |
missense_variant | MODERATE | c.1013G>A | p.Arg338Gln | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 3/7 | 1032/3777 | 1013/2151 | 338/716 | chr2 | 61839991 | ||
chr2:61840022
|
T | C | 1 | a0012 | 1 | HG02572.hp2 | missense_variant | MODERATE | c.982A>G | p.Ile328Val | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 3/7 | 1001/3777 | 982/2151 | 328/716 | chr2 | 61840022 | ||
chr2:61840088
|
G | A | 1 | a0013 | 1 | NA18971.hp2 | missense_variant | MODERATE | c.916C>T | p.Arg306Trp | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 3/7 | 935/3777 | 916/2151 | 306/716 | chr2 | 61840088 | ||
chr2:61840298
|
T | C | 3 | a0003a0014a0015 | 39 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(36): Show |
missense_variant | MODERATE | c.706A>G | p.Ile236Val | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 3/7 | 725/3777 | 706/2151 | 236/716 | chr2 | 61840298 | ||
chr2:61840406
|
T | C | 1 | a0008 | 1 | HG03195.hp1 | missense_variant | MODERATE | c.598A>G | p.Asn200Asp | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 3/7 | 617/3777 | 598/2151 | 200/716 | chr2 | 61840406 | ||
chr2:61842223
|
T | C | 2 | a0002a0006 | 70 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(67): Show |
missense_variant | MODERATE | c.321A>G | p.Ile107Met | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 2/7 | 340/3777 | 321/2151 | 107/716 | chr2 | 61842223 | ||
chr2:61842347
|
G | A | 1 | a0007 | 1 | HG03017.hp1 | missense_variant | MODERATE | c.197C>T | p.Thr66Ile | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 2/7 | 216/3777 | 197/2151 | 66/716 | chr2 | 61842347 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:61838624
|
C | T | 2 | a0001c0003a0007c0021 | 55 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(52): Show |
synonymous_variant | LOW | c.1665G>A | p.Leu555Leu | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 4/7 | 1684/3777 | 1665/2151 | 555/716 | chr2 | 61838624 | ||
chr2:61839453
|
C | T | 1 | a0005c0007 | 2 | HG02572.hp1 HG03130.hp2 |
synonymous_variant | LOW | c.1551G>A | p.Thr517Thr | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 3/7 | 1570/3777 | 1551/2151 | 517/716 | chr2 | 61839453 | ||
chr2:61839462
|
G | C | 1 | a0001c0013 | 1 | HG03486.hp1 | synonymous_variant | LOW | c.1542C>G | p.Pro514Pro | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 3/7 | 1561/3777 | 1542/2151 | 514/716 | chr2 | 61839462 | ||
chr2:61839792
|
A | G | 20 | a0001c0001a0001c0003a0001c0013others(17): Show | 396 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(393): Show |
synonymous_variant | LOW | c.1212T>C | p.Cys404Cys | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 3/7 | 1231/3777 | 1212/2151 | 404/716 | chr2 | 61839792 | ||
chr2:61840098
|
T | C | 1 | a0008c0018 | 1 | HG03195.hp1 | synonymous_variant | LOW | c.906A>G | p.Gln302Gln | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 3/7 | 925/3777 | 906/2151 | 302/716 | chr2 | 61840098 | ||
chr2:61840452
|
C | T | 1 | a0002c0020 | 1 | HG04184.hp1 | synonymous_variant | LOW | c.552G>A | p.Glu184Glu | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 3/7 | 571/3777 | 552/2151 | 184/716 | chr2 | 61840452 | ||
chr2:61840533
|
T | C | 1 | a0001c0019 | 1 | HG03453.hp2 | synonymous_variant | LOW | c.471A>G | p.Ser157Ser | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 3/7 | 490/3777 | 471/2151 | 157/716 | chr2 | 61840533 | ||
chr2:61853877
|
A | C | 20 | a0001c0001a0001c0003a0001c0013others(17): Show | 396 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(393): Show |
synonymous_variant | LOW | c.165T>G | p.Ala55Ala | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/7 | 184/3777 | 165/2151 | 55/716 | chr2 | 61853877 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:61824904
|
T | G | 1 | a0001c0001t0008 | 2 | HG01515.hp1 HG01517.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1551A>C | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 7/7 | 1551 | chr2 | 61824904 | |||||
chr2:61824906
|
C | A | 3 | a0004c0005t0005a0005c0007t0009a0005c0010t0018 | 8 | HG02280.hp1 HG02572.hp1 HG02622.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1549G>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 7/7 | 1549 | chr2 | 61824906 | |||||
chr2:61824974
|
T | C | 1 | a0002c0002t0019 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1481A>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 7/7 | 1481 | chr2 | 61824974 | |||||
chr2:61824997
|
C | T | 2 | a0001c0001t0007a0001c0019t0007 | 2 | HG02109.hp1 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1458G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 7/7 | 1458 | chr2 | 61824997 | |||||
chr2:61825023
|
A | G | 1 | a0001c0001t0013 | 1 | HG02015.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1432T>C | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 7/7 | 1432 | chr2 | 61825023 | |||||
chr2:61825087
|
T | G | 1 | a0001c0003t0014 | 1 | NA20752.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1368A>C | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 7/7 | 1368 | chr2 | 61825087 | |||||
chr2:61825174
|
A | G | 1 | a0001c0001t0016 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1281T>C | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 7/7 | 1281 | chr2 | 61825174 | |||||
chr2:61825245
|
A | G | 16 | a0001c0001t0001a0001c0001t0004a0001c0001t0006others(13): Show | 206 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(203): Show |
3_prime_UTR_variant | MODIFIER | c.*1210T>C | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 7/7 | 1210 | chr2 | 61825245 | |||||
chr2:61825311
|
A | C | 1 | a0002c0002t0012 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1144T>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 7/7 | 1144 | chr2 | 61825311 | |||||
chr2:61825485
|
T | C | 1 | a0001c0001t0020 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*970A>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 7/7 | 970 | chr2 | 61825485 | |||||
chr2:61825564
|
T | C | 1 | a0001c0001t0021 | 1 | NA18997.hp1 | 3_prime_UTR_variant | MODIFIER | c.*891A>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 7/7 | 891 | chr2 | 61825564 | |||||
chr2:61825626
|
A | G | 1 | a0001c0001t0016 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*829T>C | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 7/7 | 829 | chr2 | 61825626 | |||||
chr2:61825679
|
C | T | 1 | a0008c0018t0015 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*776G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 7/7 | 776 | chr2 | 61825679 | |||||
chr2:61825782
|
C | T | 1 | a0001c0001t0011 | 1 | NA19062.hp1 | 3_prime_UTR_variant | MODIFIER | c.*673G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 7/7 | 673 | chr2 | 61825782 | |||||
chr2:61825838
|
C | T | 1 | a0001c0001t0006 | 2 | HG02258.hp2 HG03130.hp1 |
3_prime_UTR_variant | MODIFIER | c.*617G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 7/7 | 617 | chr2 | 61825838 | |||||
chr2:61825915
|
G | C | 1 | a0005c0007t0009 | 2 | HG02572.hp1 HG03130.hp2 |
3_prime_UTR_variant | MODIFIER | c.*540C>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 7/7 | 540 | chr2 | 61825915 | |||||
chr2:61825946
|
T | G | 1 | a0001c0001t0022 | 1 | HG00597.hp1 | 3_prime_UTR_variant | MODIFIER | c.*509A>C | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 7/7 | 509 | chr2 | 61825946 | |||||
chr2:61826144
|
T | G | 3 | a0003c0004t0003a0014c0016t0003a0015c0017t0003 | 39 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*311A>C | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 7/7 | 311 | chr2 | 61826144 | |||||
chr2:61826155
|
A | G | 15 | a0001c0001t0001a0001c0001t0004a0001c0001t0006others(12): Show | 205 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(202): Show |
3_prime_UTR_variant | MODIFIER | c.*300T>C | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 7/7 | 300 | chr2 | 61826155 | |||||
chr2:61826206
|
TA | T | 3 | a0003c0004t0003a0014c0016t0003a0015c0017t0003 | 39 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*248delT | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 7/7 | 248 | chr2 | 61826206 | |||||
chr2:61826247
|
G | C | 1 | a0001c0001t0024 | 1 | HG00323.hp1 | 3_prime_UTR_variant | MODIFIER | c.*208C>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 7/7 | 208 | chr2 | 61826247 | |||||
chr2:61826395
|
G | A | 1 | a0001c0001t0023 | 1 | NA20805.hp1 | 3_prime_UTR_variant | MODIFIER | c.*60C>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 7/7 | 60 | chr2 | 61826395 | |||||
chr2:61826411
|
CGCT | C | 3 | a0001c0001t0004a0001c0001t0024a0007c0021t0004 | 21 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*41_*43delAGC | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 7/7 | 41 | chr2 | 61826411 | |||||
chr2:61826429
|
G | A | 1 | a0004c0005t0005 | 5 | HG02280.hp1 HG03041.hp1 HG03453.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*26C>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 7/7 | 26 | chr2 | 61826429 | |||||
chr2:61854057
|
G | C | 1 | a0001c0001t0010 | 2 | HG02922.hp1 HG02970.hp2 |
5_prime_UTR_variant | MODIFIER | c.-16C>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/7 | 16 | chr2 | 61854057 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:61826743
|
G | GA | 287 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(284): Show | 396 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(393): Show |
intron_variant | MODIFIER | c.2007-145dupT | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 6/6 | chr2 | 61826743 | ||||||
chr2:61826847
|
G | A | 2 | a0001c0001t0001g0108a0001c0001t0001g0109 | 2 | HG01243.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2007-248C>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 6/6 | chr2 | 61826847 | ||||||
chr2:61826934
|
C | T | 39 | a0001c0001t0002g0007a0001c0001t0002g0014a0001c0001t0002g0015others(36): Show | 50 | HG00597.hp1 HG01109.hp1 HG01167.hp2 others(47): Show |
intron_variant | MODIFIER | c.2006+170G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 6/6 | chr2 | 61826934 | ||||||
chr2:61827444
|
A | T | 1 | a0001c0001t0001g0109 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1852-186T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61827444 | ||||||
chr2:61827500
|
C | T | 1 | a0010c0011t0002g0263 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1852-242G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61827500 | ||||||
chr2:61827526
|
C | T | 1 | a0001c0001t0002g0276 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1852-268G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61827526 | ||||||
chr2:61827541
|
C | T | 1 | a0002c0002t0002g0252 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1852-283G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61827541 | ||||||
chr2:61827609
|
C | CA | 210 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0012others(207): Show | 285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.1852-352dupT | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61827609 | ||||||
chr2:61827609
|
C | CAA | 27 | a0001c0001t0001g0005a0001c0001t0001g0028a0001c0001t0001g0076others(24): Show | 34 | HG00323.hp2 HG00558.hp2 HG01175.hp2 others(31): Show |
intron_variant | MODIFIER | c.1852-353_1852-352d others(4): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61827609 | ||||||
chr2:61827630
|
T | A | 34 | a0001c0001t0001g0004a0001c0001t0001g0121a0001c0001t0001g0125others(31): Show | 64 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.1852-372A>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61827630 | ||||||
chr2:61827813
|
G | A | 1 | a0001c0006t0002g0287 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1852-555C>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61827813 | ||||||
chr2:61828002
|
T | C | 40 | a0001c0001t0002g0007a0001c0001t0002g0014a0001c0001t0002g0015others(37): Show | 53 | HG00597.hp1 HG01109.hp1 HG01167.hp2 others(50): Show |
intron_variant | MODIFIER | c.1852-744A>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61828002 | ||||||
chr2:61828253
|
T | C | 2 | a0001c0001t0002g0186a0001c0001t0002g0187 | 2 | HG03579.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1852-995A>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61828253 | ||||||
chr2:61828284
|
GA | G | 271 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(268): Show | 377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.1852-1027delT | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61828284 | ||||||
chr2:61828323
|
A | AG | 5 | a0001c0001t0002g0014a0001c0001t0002g0189a0001c0001t0002g0194others(2): Show | 7 | HG02055.hp2 HG02615.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1852-1066dupC | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61828323 | ||||||
chr2:61828336
|
C | CT | 45 | a0001c0001t0001g0100a0001c0001t0001g0123a0001c0001t0001g0130others(42): Show | 58 | HG00597.hp1 HG00735.hp1 HG01109.hp1 others(55): Show |
intron_variant | MODIFIER | c.1852-1079dupA | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61828336 | ||||||
chr2:61828552
|
T | G | 5 | a0001c0001t0002g0036a0001c0001t0002g0151a0001c0001t0002g0153others(2): Show | 6 | HG00597.hp1 HG02080.hp1 NA18980.hp1 others(3): Show |
intron_variant | MODIFIER | c.1852-1294A>C | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61828552 | ||||||
chr2:61828732
|
T | C | 1 | a0001c0001t0001g0109 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1852-1474A>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61828732 | ||||||
chr2:61828843
|
T | A | 1 | a0003c0004t0003g0177 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1852-1585A>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61828843 | ||||||
chr2:61828912
|
T | C | 3 | a0002c0002t0002g0223a0002c0002t0002g0225a0002c0002t0019g0237 | 3 | HG02647.hp1 HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1852-1654A>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61828912 | ||||||
chr2:61829010
|
G | A | 2 | a0001c0001t0001g0047a0001c0001t0001g0277 | 3 | HG02280.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1852-1752C>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61829010 | ||||||
chr2:61829131
|
C | T | 4 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0070others(1): Show | 4 | HG00673.hp2 HG04184.hp2 NA19068.hp1 others(1): Show |
intron_variant | MODIFIER | c.1852-1873G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61829131 | ||||||
chr2:61829212
|
T | C | 1 | a0001c0006t0002g0287 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1852-1954A>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61829212 | ||||||
chr2:61829294
|
G | C | 1 | a0006c0008t0002g0251 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1852-2036C>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61829294 | ||||||
chr2:61829347
|
T | A | 1 | a0007c0021t0004g0083 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1852-2089A>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61829347 | ||||||
chr2:61829378
|
C | G | 1 | a0001c0003t0001g0147 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1852-2120G>C | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61829378 | ||||||
chr2:61829685
|
TA | T | 6 | a0001c0001t0001g0031a0001c0001t0001g0054a0001c0001t0001g0069others(3): Show | 7 | NA18945.hp1 NA18945.hp2 NA19055.hp1 others(4): Show |
intron_variant | MODIFIER | c.1852-2428delT | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61829685 | ||||||
chr2:61829978
|
T | TA | 66 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0002g0011others(63): Show | 84 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.1852-2721dupT | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61829978 | ||||||
chr2:61829997
|
C | T | 287 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(284): Show | 396 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(393): Show |
intron_variant | MODIFIER | c.1852-2739G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61829997 | ||||||
chr2:61830116
|
T | A | 1 | a0010c0011t0002g0263 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1852-2858A>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61830116 | ||||||
chr2:61830182
|
G | A | 61 | a0001c0001t0002g0011a0001c0001t0002g0113a0001c0001t0002g0218others(58): Show | 81 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.1852-2924C>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61830182 | ||||||
chr2:61830245
|
A | C | 3 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0017g0118 | 3 | HG01243.hp1 HG02886.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1852-2987T>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61830245 | ||||||
chr2:61830413
|
G | A | 41 | a0001c0001t0002g0007a0001c0001t0002g0014a0001c0001t0002g0015others(38): Show | 54 | HG00597.hp1 HG01109.hp1 HG01167.hp2 others(51): Show |
intron_variant | MODIFIER | c.1852-3155C>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61830413 | ||||||
chr2:61830510
|
G | A | 1 | a0001c0001t0001g0109 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1852-3252C>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61830510 | ||||||
chr2:61830633
|
G | A | 40 | a0001c0001t0002g0007a0001c0001t0002g0014a0001c0001t0002g0015others(37): Show | 51 | HG00597.hp1 HG01109.hp1 HG01167.hp2 others(48): Show |
intron_variant | MODIFIER | c.1852-3375C>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61830633 | ||||||
chr2:61830678
|
T | A | 4 | a0001c0001t0001g0021a0001c0001t0001g0095a0001c0001t0001g0096others(1): Show | 5 | HG01167.hp1 HG01169.hp2 HG01243.hp2 others(2): Show |
intron_variant | MODIFIER | c.1852-3420A>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61830678 | ||||||
chr2:61830683
|
C | CA | 63 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0002g0007others(60): Show | 84 | HG00408.hp1 HG00597.hp1 HG00639.hp2 others(81): Show |
intron_variant | MODIFIER | c.1852-3426dupT | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61830683 | ||||||
chr2:61830683
|
C | CAA | 144 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(141): Show | 212 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.1852-3427_1852-342 others(6): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61830683 | ||||||
chr2:61830683
|
C | CAAA | 26 | a0001c0001t0001g0028a0001c0001t0001g0050a0001c0001t0001g0068others(23): Show | 31 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(28): Show |
intron_variant | MODIFIER | c.1852-3428_1852-342 others(7): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61830683 | ||||||
chr2:61830833
|
G | A | 40 | a0001c0001t0002g0007a0001c0001t0002g0014a0001c0001t0002g0015others(37): Show | 53 | HG00597.hp1 HG01109.hp1 HG01167.hp2 others(50): Show |
intron_variant | MODIFIER | c.1852-3575C>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61830833 | ||||||
chr2:61830955
|
A | G | 1 | a0001c0001t0016g0103 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1852-3697T>C | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61830955 | ||||||
chr2:61831067
|
G | A | 3 | a0001c0001t0002g0192a0001c0001t0002g0264a0001c0001t0017g0118 | 3 | HG01891.hp2 HG02451.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1852-3809C>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61831067 | ||||||
chr2:61831111
|
C | CA | 30 | a0003c0004t0003g0010a0003c0004t0003g0029a0003c0004t0003g0037others(27): Show | 36 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(33): Show |
intron_variant | MODIFIER | c.1852-3854dupT | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61831111 | ||||||
chr2:61831111
|
CA | C | 218 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(215): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(312): Show |
intron_variant | MODIFIER | c.1852-3854delT | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61831111 | ||||||
chr2:61831216
|
T | C | 1 | a0001c0001t0002g0283 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1852-3958A>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61831216 | ||||||
chr2:61831261
|
G | C | 1 | a0001c0001t0002g0283 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1852-4003C>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61831261 | ||||||
chr2:61831343
|
G | C | 1 | a0010c0011t0002g0263 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1852-4085C>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61831343 | ||||||
chr2:61831407
|
C | T | 3 | a0001c0001t0001g0012a0001c0001t0001g0104a0001c0001t0001g0112 | 5 | HG01891.hp1 HG02145.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1852-4149G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61831407 | ||||||
chr2:61831506
|
T | C | 1 | a0003c0004t0003g0168 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1852-4248A>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61831506 | ||||||
chr2:61831970
|
G | A | 1 | a0001c0001t0002g0276 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1851+4040C>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61831970 | ||||||
chr2:61832023
|
T | A | 3 | a0001c0003t0001g0034a0001c0003t0001g0099a0001c0003t0014g0156 | 4 | NA18940.hp1 NA18998.hp1 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.1851+3987A>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61832023 | ||||||
chr2:61832151
|
G | A | 1 | a0003c0004t0003g0168 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1851+3859C>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61832151 | ||||||
chr2:61832242
|
C | CA | 92 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(89): Show | 154 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.1851+3767dupT | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61832242 | ||||||
chr2:61832242
|
C | CAA | 37 | a0001c0001t0001g0024a0001c0001t0001g0028a0001c0001t0001g0050others(34): Show | 42 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(39): Show |
intron_variant | MODIFIER | c.1851+3767_1851+376 others(6): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61832242 | ||||||
chr2:61832244
|
C | A | 135 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(132): Show | 202 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(199): Show |
intron_variant | MODIFIER | c.1851+3766G>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61832244 | ||||||
chr2:61832246
|
C | A | 135 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(132): Show | 202 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(199): Show |
intron_variant | MODIFIER | c.1851+3764G>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61832246 | ||||||
chr2:61832248
|
C | A | 135 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(132): Show | 202 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(199): Show |
intron_variant | MODIFIER | c.1851+3762G>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61832248 | ||||||
chr2:61832250
|
C | A | 168 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(165): Show | 241 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(238): Show |
intron_variant | MODIFIER | c.1851+3760G>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61832250 | ||||||
chr2:61832252
|
A | C | 44 | a0001c0001t0001g0012a0001c0001t0001g0104a0001c0001t0002g0007others(41): Show | 57 | HG00597.hp1 HG01109.hp1 HG01167.hp2 others(54): Show |
intron_variant | MODIFIER | c.1851+3758T>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61832252 | ||||||
chr2:61832263
|
A | C | 62 | a0001c0001t0002g0011a0001c0001t0002g0113a0001c0001t0002g0218others(59): Show | 84 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.1851+3747T>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61832263 | ||||||
chr2:61832266
|
A | C | 25 | a0002c0002t0002g0018a0002c0002t0002g0019a0002c0002t0002g0042others(22): Show | 31 | HG00323.hp2 HG00408.hp1 HG01943.hp1 others(28): Show |
intron_variant | MODIFIER | c.1851+3744T>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61832266 | ||||||
chr2:61832296
|
A | C | 2 | a0001c0001t0001g0137a0001c0001t0016g0103 | 2 | HG02165.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1851+3714T>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61832296 | ||||||
chr2:61832808
|
T | C | 287 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(284): Show | 396 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(393): Show |
intron_variant | MODIFIER | c.1851+3202A>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61832808 | ||||||
chr2:61832832
|
C | T | 1 | a0001c0006t0002g0289 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1851+3178G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61832832 | ||||||
chr2:61832849
|
G | A | 1 | a0001c0001t0002g0276 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1851+3161C>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61832849 | ||||||
chr2:61832866
|
A | G | 1 | a0010c0011t0002g0263 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1851+3144T>C | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61832866 | ||||||
chr2:61833121
|
T | A | 104 | a0001c0001t0002g0007a0001c0001t0002g0011a0001c0001t0002g0014others(101): Show | 137 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.1851+2889A>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61833121 | ||||||
chr2:61833289
|
G | A | 1 | a0002c0002t0002g0274 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.1851+2721C>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61833289 | ||||||
chr2:61833295
|
G | A | 2 | a0001c0001t0004g0056a0001c0001t0004g0093 | 2 | HG00735.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.1851+2715C>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61833295 | ||||||
chr2:61833425
|
C | CA | 41 | a0001c0001t0002g0221a0001c0001t0002g0269a0001c0001t0002g0278others(38): Show | 47 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(44): Show |
intron_variant | MODIFIER | c.1851+2584dupT | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61833425 | ||||||
chr2:61833425
|
CA | C | 6 | a0001c0001t0001g0012a0001c0001t0001g0104a0001c0001t0001g0112others(3): Show | 8 | HG01891.hp1 HG02145.hp2 HG02165.hp2 others(5): Show |
intron_variant | MODIFIER | c.1851+2584delT | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61833425 | ||||||
chr2:61833425
|
CAA | C | 128 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(125): Show | 195 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.1851+2583_1851+258 others(6): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61833425 | ||||||
chr2:61833457
|
A | G | 5 | a0001c0001t0002g0036a0001c0001t0002g0151a0001c0001t0002g0153others(2): Show | 6 | HG00597.hp1 HG02080.hp1 NA18980.hp1 others(3): Show |
intron_variant | MODIFIER | c.1851+2553T>C | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61833457 | ||||||
chr2:61833510
|
C | G | 128 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(125): Show | 194 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.1851+2500G>C | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61833510 | ||||||
chr2:61833511
|
C | T | 272 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(269): Show | 378 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(375): Show |
intron_variant | MODIFIER | c.1851+2499G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61833511 | ||||||
chr2:61833593
|
C | T | 4 | a0002c0002t0002g0003a0002c0002t0002g0224a0002c0002t0002g0270others(1): Show | 10 | NA18961.hp1 NA18966.hp1 NA18975.hp2 others(7): Show |
intron_variant | MODIFIER | c.1851+2417G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61833593 | ||||||
chr2:61833622
|
C | T | 2 | a0001c0001t0004g0055a0001c0001t0004g0060 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1851+2388G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61833622 | ||||||
chr2:61833671
|
C | G | 33 | a0003c0004t0003g0010a0003c0004t0003g0029a0003c0004t0003g0037others(30): Show | 39 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(36): Show |
intron_variant | MODIFIER | c.1851+2339G>C | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61833671 | ||||||
chr2:61833714
|
C | T | 1 | a0010c0011t0002g0263 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1851+2296G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61833714 | ||||||
chr2:61833736
|
AAGAC | A | 130 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(127): Show | 197 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.1851+2270_1851+227 others(8): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61833736 | ||||||
chr2:61833757
|
C | G | 1 | a0001c0001t0002g0212 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1851+2253G>C | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61833757 | ||||||
chr2:61833820
|
A | T | 2 | a0001c0001t0010g0290a0001c0001t0010g0291 | 2 | HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1851+2190T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61833820 | ||||||
chr2:61834226
|
T | C | 130 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(127): Show | 197 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.1851+1784A>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61834226 | ||||||
chr2:61834269
|
T | C | 130 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(127): Show | 197 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.1851+1741A>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61834269 | ||||||
chr2:61834410
|
A | C | 3 | a0001c0001t0002g0278a0001c0001t0002g0283a0001c0001t0002g0284 | 3 | HG02630.hp1 HG03098.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1851+1600T>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61834410 | ||||||
chr2:61834624
|
G | A | 1 | a0001c0001t0002g0283 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1851+1386C>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61834624 | ||||||
chr2:61834689
|
C | T | 1 | a0008c0018t0015g0279 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1851+1321G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61834689 | ||||||
chr2:61834786
|
C | T | 3 | a0001c0001t0001g0012a0001c0001t0001g0104a0001c0001t0001g0112 | 5 | HG01891.hp1 HG02145.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1851+1224G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61834786 | ||||||
chr2:61834791
|
A | C | 1 | a0002c0002t0002g0239 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1851+1219T>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61834791 | ||||||
chr2:61834808
|
A | T | 64 | a0001c0001t0002g0011a0001c0001t0002g0113a0001c0001t0002g0218others(61): Show | 86 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.1851+1202T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61834808 | ||||||
chr2:61834821
|
A | AAAAT | 4 | a0001c0001t0001g0108a0001c0001t0002g0186a0001c0001t0002g0187others(1): Show | 4 | HG02886.hp1 HG03579.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1851+1185_1851+118 others(8): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61834821 | ||||||
chr2:61835066
|
C | T | 133 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(130): Show | 200 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.1851+944G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61835066 | ||||||
chr2:61835080
|
A | G | 1 | a0008c0018t0015g0279 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1851+930T>C | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61835080 | ||||||
chr2:61835468
|
TA | T | 39 | a0001c0001t0002g0007a0001c0001t0002g0014a0001c0001t0002g0015others(36): Show | 50 | HG00597.hp1 HG01109.hp1 HG01167.hp2 others(47): Show |
intron_variant | MODIFIER | c.1851+541delT | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61835468 | ||||||
chr2:61835883
|
C | T | 1 | a0001c0001t0002g0283 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1851+127G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61835883 | ||||||
chr2:61835884
|
A | C | 1 | a0001c0001t0002g0283 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1851+126T>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61835884 | ||||||
chr2:61835958
|
TA | T | 252 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(249): Show | 356 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(353): Show |
intron_variant | MODIFIER | c.1851+51delT | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61835958 | ||||||
chr2:61835958
|
TAA | T | 7 | a0001c0001t0001g0022a0001c0001t0001g0064a0001c0001t0001g0069others(4): Show | 8 | HG00423.hp1 HG01070.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1851+50_1851+51del others(2): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61835958 | ||||||
chr2:61835972
|
A | C | 1 | a0001c0001t0001g0109 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1851+38T>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 5/6 | chr2 | 61835972 | ||||||
chr2:61836206
|
TG | T | 40 | a0001c0001t0002g0007a0001c0001t0002g0014a0001c0001t0002g0015others(37): Show | 51 | HG00597.hp1 HG01109.hp1 HG01167.hp2 others(48): Show |
intron_variant | MODIFIER | c.1752-98delC | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 4/6 | chr2 | 61836206 | ||||||
chr2:61836290
|
T | C | 1 | a0001c0003t0001g0150 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1752-181A>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 4/6 | chr2 | 61836290 | ||||||
chr2:61836452
|
G | T | 1 | a0010c0011t0002g0263 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1752-343C>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 4/6 | chr2 | 61836452 | ||||||
chr2:61836512
|
T | C | 8 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(5): Show | 12 | HG00408.hp2 HG00544.hp1 HG02071.hp1 others(9): Show |
intron_variant | MODIFIER | c.1752-403A>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 4/6 | chr2 | 61836512 | ||||||
chr2:61836761
|
T | A | 41 | a0001c0001t0001g0004a0001c0001t0001g0121a0001c0001t0001g0125others(38): Show | 71 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(68): Show |
intron_variant | MODIFIER | c.1752-652A>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 4/6 | chr2 | 61836761 | ||||||
chr2:61836898
|
C | T | 3 | a0004c0005t0002g0266a0004c0005t0005g0046a0004c0005t0005g0267 | 4 | HG02451.hp1 HG03041.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1752-789G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 4/6 | chr2 | 61836898 | ||||||
chr2:61836935
|
G | A | 1 | a0001c0001t0001g0104 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1752-826C>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 4/6 | chr2 | 61836935 | ||||||
chr2:61836952
|
A | C | 1 | a0001c0001t0001g0069 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1752-843T>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 4/6 | chr2 | 61836952 | ||||||
chr2:61837038
|
T | A | 5 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0140others(2): Show | 5 | HG01243.hp1 HG03579.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.1752-929A>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 4/6 | chr2 | 61837038 | ||||||
chr2:61837150
|
G | A | 1 | a0007c0021t0004g0083 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1752-1041C>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 4/6 | chr2 | 61837150 | ||||||
chr2:61837269
|
C | T | 272 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(269): Show | 378 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(375): Show |
intron_variant | MODIFIER | c.1752-1160G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 4/6 | chr2 | 61837269 | ||||||
chr2:61837530
|
A | G | 1 | a0005c0010t0018g0280 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1751+1008T>C | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 4/6 | chr2 | 61837530 | ||||||
chr2:61837535
|
A | G | 272 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(269): Show | 378 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(375): Show |
intron_variant | MODIFIER | c.1751+1003T>C | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 4/6 | chr2 | 61837535 | ||||||
chr2:61837629
|
C | T | 1 | a0001c0001t0002g0186 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1751+909G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 4/6 | chr2 | 61837629 | ||||||
chr2:61837662
|
T | C | 39 | a0001c0001t0002g0007a0001c0001t0002g0014a0001c0001t0002g0015others(36): Show | 50 | HG00597.hp1 HG01109.hp1 HG01167.hp2 others(47): Show |
intron_variant | MODIFIER | c.1751+876A>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 4/6 | chr2 | 61837662 | ||||||
chr2:61837667
|
G | A | 1 | a0001c0001t0002g0283 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1751+871C>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 4/6 | chr2 | 61837667 | ||||||
chr2:61837674
|
C | A | 130 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(127): Show | 197 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.1751+864G>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 4/6 | chr2 | 61837674 | ||||||
chr2:61837818
|
C | T | 9 | a0001c0001t0001g0008a0001c0001t0001g0021a0001c0001t0001g0048others(6): Show | 13 | HG00642.hp2 HG01074.hp2 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.1751+720G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 4/6 | chr2 | 61837818 | ||||||
chr2:61837914
|
A | G | 1 | a0001c0003t0001g0092 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1751+624T>C | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 4/6 | chr2 | 61837914 | ||||||
chr2:61838033
|
A | G | 272 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(269): Show | 378 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(375): Show |
intron_variant | MODIFIER | c.1751+505T>C | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 4/6 | chr2 | 61838033 | ||||||
chr2:61838390
|
A | G | 287 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(284): Show | 396 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(393): Show |
intron_variant | MODIFIER | c.1751+148T>C | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 4/6 | chr2 | 61838390 | ||||||
chr2:61838419
|
A | T | 1 | a0002c0002t0002g0228 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1751+119T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 4/6 | chr2 | 61838419 | ||||||
chr2:61838716
|
C | T | 35 | a0001c0001t0001g0108a0001c0001t0001g0109a0003c0004t0003g0010others(32): Show | 41 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(38): Show |
intron_variant | MODIFIER | c.1584-11G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 3/6 | chr2 | 61838716 | ||||||
chr2:61838854
|
A | ATATT | 113 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0028others(110): Show | 168 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.1584-153_1584-150d others(6): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 3/6 | chr2 | 61838854 | ||||||
chr2:61838854
|
A | ATATTTAT others(1): Show |
57 | a0001c0001t0001g0063a0001c0001t0001g0133a0001c0001t0001g0139others(54): Show | 69 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.1584-157_1584-150d others(10): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 3/6 | chr2 | 61838854 | ||||||
chr2:61838854
|
A | ATATTTAT others(5): Show |
2 | a0001c0001t0001g0108a0003c0004t0003g0101 | 2 | HG02132.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1584-161_1584-150d others(14): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 3/6 | chr2 | 61838854 | ||||||
chr2:61838854
|
ATATTTAT others(1): Show |
A | 55 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0021others(52): Show | 82 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.1584-157_1584-150d others(10): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 3/6 | chr2 | 61838854 | ||||||
chr2:61838888
|
A | ATTTT | 5 | a0001c0001t0002g0151a0001c0001t0002g0192a0001c0001t0002g0205others(2): Show | 5 | HG01891.hp2 HG02080.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1584-184_1584-183i others(6): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 3/6 | chr2 | 61838888 | ||||||
chr2:61838888
|
A | T | 6 | a0001c0001t0001g0057a0001c0001t0001g0064a0001c0001t0001g0065others(3): Show | 6 | HG00423.hp1 HG01243.hp1 NA18948.hp1 others(3): Show |
intron_variant | MODIFIER | c.1584-183T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 3/6 | chr2 | 61838888 | ||||||
chr2:61838892
|
A | ATTTATTT others(5): Show |
2 | a0005c0007t0009g0282a0005c0010t0018g0280 | 2 | HG02572.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.1584-188_1584-187i others(14): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 3/6 | chr2 | 61838892 | ||||||
chr2:61838892
|
A | ATTTATTT others(1): Show |
5 | a0001c0001t0002g0039a0001c0001t0002g0188a0001c0001t0002g0191others(2): Show | 6 | HG01175.hp2 HG03579.hp1 HG03688.hp1 others(3): Show |
intron_variant | MODIFIER | c.1584-188_1584-187i others(10): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 3/6 | chr2 | 61838892 | ||||||
chr2:61838892
|
A | ATTTATTT others(5): Show |
1 | a0005c0007t0009g0281 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1584-188_1584-187i others(14): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 3/6 | chr2 | 61838892 | ||||||
chr2:61838892
|
A | ATTTT | 25 | a0001c0001t0002g0007a0001c0001t0002g0014a0001c0001t0002g0015others(22): Show | 35 | HG00597.hp1 HG01109.hp1 HG01167.hp2 others(32): Show |
intron_variant | MODIFIER | c.1584-191_1584-188d others(6): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 3/6 | chr2 | 61838892 | ||||||
chr2:61838892
|
A | T | 49 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0021others(46): Show | 72 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.1584-187T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 3/6 | chr2 | 61838892 | ||||||
chr2:61838896
|
T | A | 60 | a0001c0001t0002g0011a0001c0001t0002g0113a0001c0001t0002g0218others(57): Show | 81 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.1584-191A>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 3/6 | chr2 | 61838896 | ||||||
chr2:61838943
|
C | T | 2 | a0001c0001t0002g0186a0001c0001t0002g0187 | 2 | HG03579.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1584-238G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 3/6 | chr2 | 61838943 | ||||||
chr2:61838974
|
C | T | 26 | a0001c0001t0001g0005a0001c0001t0001g0028a0001c0001t0001g0030others(23): Show | 35 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(32): Show |
intron_variant | MODIFIER | c.1584-269G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 3/6 | chr2 | 61838974 | ||||||
chr2:61839010
|
G | A | 1 | a0001c0001t0002g0195 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1584-305C>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 3/6 | chr2 | 61839010 | ||||||
chr2:61839029
|
C | T | 1 | a0001c0001t0017g0118 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1584-324G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 3/6 | chr2 | 61839029 | ||||||
chr2:61839031
|
C | T | 2 | a0001c0001t0001g0047a0001c0001t0001g0277 | 3 | HG02280.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1584-326G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 3/6 | chr2 | 61839031 | ||||||
chr2:61839089
|
C | A | 1 | a0008c0018t0015g0279 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1583+332G>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 3/6 | chr2 | 61839089 | ||||||
chr2:61839280
|
T | C | 1 | a0010c0011t0002g0263 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1583+141A>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 3/6 | chr2 | 61839280 | ||||||
chr2:61839282
|
ATATAT | A | 138 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(135): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(203): Show |
intron_variant | MODIFIER | c.1583+134_1583+138d others(7): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 3/6 | chr2 | 61839282 | ||||||
chr2:61839417
|
T | C | 1 | a0001c0001t0001g0108 | 1 | NA19030.hp1 | splice_region_variant&intron_variant | LOW | c.1583+4A>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 3/6 | chr2 | 61839417 | ||||||
chr2:61840588
|
G | A | 2 | a0001c0001t0002g0276a0010c0011t0002g0263 | 2 | HG02965.hp1 HG03579.hp1 |
splice_region_variant&intron_variant | LOW | c.423-7C>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 2/6 | chr2 | 61840588 | ||||||
chr2:61840619
|
T | C | 4 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0002g0186others(1): Show | 4 | HG01243.hp1 HG03579.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.423-38A>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 2/6 | chr2 | 61840619 | ||||||
chr2:61840621
|
T | A | 1 | a0003c0004t0003g0176 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.423-40A>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 2/6 | chr2 | 61840621 | ||||||
chr2:61840745
|
G | C | 133 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(130): Show | 200 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.423-164C>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 2/6 | chr2 | 61840745 | ||||||
chr2:61840794
|
G | A | 1 | a0002c0002t0002g0044 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.423-213C>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 2/6 | chr2 | 61840794 | ||||||
chr2:61841036
|
T | G | 4 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0002g0186others(1): Show | 4 | HG01243.hp1 HG03579.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.423-455A>C | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 2/6 | chr2 | 61841036 | ||||||
chr2:61841041
|
C | A | 1 | a0003c0004t0003g0176 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.423-460G>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 2/6 | chr2 | 61841041 | ||||||
chr2:61841169
|
G | A | 5 | a0001c0001t0002g0036a0001c0001t0002g0151a0001c0001t0002g0153others(2): Show | 6 | HG00597.hp1 HG02080.hp1 NA18980.hp1 others(3): Show |
intron_variant | MODIFIER | c.423-588C>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 2/6 | chr2 | 61841169 | ||||||
chr2:61841517
|
T | C | 1 | a0008c0018t0015g0279 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.422+605A>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 2/6 | chr2 | 61841517 | ||||||
chr2:61841580
|
T | C | 1 | a0001c0001t0002g0212 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.422+542A>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 2/6 | chr2 | 61841580 | ||||||
chr2:61842008
|
G | A | 1 | a0001c0001t0002g0283 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.422+114C>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 2/6 | chr2 | 61842008 | ||||||
chr2:61842377
|
A | C | 1 | a0001c0001t0017g0118 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.184-17T>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61842377 | ||||||
chr2:61842391
|
G | T | 1 | a0002c0002t0002g0233 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.184-31C>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61842391 | ||||||
chr2:61842393
|
C | T | 61 | a0001c0001t0002g0011a0001c0001t0002g0113a0001c0001t0002g0218others(58): Show | 81 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.184-33G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61842393 | ||||||
chr2:61842564
|
G | C | 1 | a0001c0001t0001g0084 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.184-204C>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61842564 | ||||||
chr2:61842678
|
T | C | 1 | a0003c0004t0003g0172 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.184-318A>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61842678 | ||||||
chr2:61842728
|
G | A | 1 | a0001c0001t0017g0118 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.184-368C>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61842728 | ||||||
chr2:61842887
|
C | T | 1 | a0003c0004t0003g0172 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.184-527G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61842887 | ||||||
chr2:61842929
|
G | A | 1 | a0001c0003t0001g0155 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.184-569C>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61842929 | ||||||
chr2:61843075
|
G | A | 2 | a0001c0001t0001g0108a0001c0001t0001g0109 | 2 | HG01243.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.184-715C>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61843075 | ||||||
chr2:61843138
|
TTTTG | T | 137 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(134): Show | 207 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.184-782_184-779del others(4): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61843138 | ||||||
chr2:61843235
|
C | G | 4 | a0001c0001t0002g0278a0001c0001t0002g0283a0001c0001t0002g0284others(1): Show | 4 | HG02630.hp1 HG03098.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.184-875G>C | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61843235 | ||||||
chr2:61843373
|
C | T | 34 | a0001c0001t0002g0007a0001c0001t0002g0014a0001c0001t0002g0015others(31): Show | 44 | HG01109.hp1 HG01167.hp2 HG01175.hp2 others(41): Show |
intron_variant | MODIFIER | c.184-1013G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61843373 | ||||||
chr2:61843417
|
G | A | 2 | a0001c0001t0001g0030a0001c0001t0001g0120 | 3 | HG00544.hp2 HG02040.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.184-1057C>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61843417 | ||||||
chr2:61843425
|
C | T | 6 | a0001c0001t0002g0014a0001c0001t0002g0189a0001c0001t0002g0190others(3): Show | 8 | HG02055.hp2 HG02559.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.184-1065G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61843425 | ||||||
chr2:61843426
|
C | A | 1 | a0005c0010t0018g0280 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.184-1066G>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61843426 | ||||||
chr2:61843460
|
A | C | 1 | a0001c0001t0017g0118 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.184-1100T>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61843460 | ||||||
chr2:61843470
|
A | C | 1 | a0002c0002t0002g0228 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.184-1110T>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61843470 | ||||||
chr2:61843541
|
T | C | 2 | a0002c0002t0002g0016a0002c0002t0002g0238 | 4 | HG01192.hp2 HG01256.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.184-1181A>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61843541 | ||||||
chr2:61843679
|
A | C | 1 | a0001c0001t0002g0276 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.184-1319T>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61843679 | ||||||
chr2:61843776
|
T | G | 2 | a0001c0001t0002g0202a0001c0001t0020g0203 | 2 | HG02886.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.184-1416A>C | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61843776 | ||||||
chr2:61843898
|
C | A | 2 | a0001c0001t0002g0186a0001c0001t0002g0187 | 2 | HG03579.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.184-1538G>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61843898 | ||||||
chr2:61843922
|
T | A | 1 | a0001c0001t0016g0103 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.184-1562A>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61843922 | ||||||
chr2:61844047
|
G | A | 1 | a0010c0011t0002g0263 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.184-1687C>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61844047 | ||||||
chr2:61844137
|
T | C | 1 | a0001c0001t0017g0118 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.184-1777A>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61844137 | ||||||
chr2:61844203
|
T | C | 35 | a0001c0001t0002g0007a0001c0001t0002g0014a0001c0001t0002g0015others(32): Show | 45 | HG01109.hp1 HG01167.hp2 HG01175.hp2 others(42): Show |
intron_variant | MODIFIER | c.184-1843A>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61844203 | ||||||
chr2:61844349
|
T | C | 133 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(130): Show | 200 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.184-1989A>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61844349 | ||||||
chr2:61844376
|
G | C | 2 | a0002c0002t0002g0215a0002c0002t0002g0228 | 2 | HG02683.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.184-2016C>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61844376 | ||||||
chr2:61844383
|
T | G | 287 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(284): Show | 396 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(393): Show |
intron_variant | MODIFIER | c.184-2023A>C | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61844383 | ||||||
chr2:61844407
|
C | T | 63 | a0001c0001t0002g0011a0001c0001t0002g0113a0001c0001t0002g0218others(60): Show | 85 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.184-2047G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61844407 | ||||||
chr2:61844427
|
A | T | 66 | a0001c0001t0002g0011a0001c0001t0002g0113a0001c0001t0002g0186others(63): Show | 88 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.184-2067T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61844427 | ||||||
chr2:61844658
|
C | T | 1 | a0001c0001t0004g0062 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.184-2298G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61844658 | ||||||
chr2:61844923
|
C | T | 1 | a0008c0018t0015g0279 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.184-2563G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61844923 | ||||||
chr2:61844972
|
G | C | 133 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(130): Show | 200 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.184-2612C>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61844972 | ||||||
chr2:61845039
|
G | C | 1 | a0001c0001t0016g0103 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.184-2679C>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61845039 | ||||||
chr2:61845148
|
A | G | 287 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(284): Show | 396 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(393): Show |
intron_variant | MODIFIER | c.184-2788T>C | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61845148 | ||||||
chr2:61845338
|
G | A | 2 | a0001c0001t0001g0047a0001c0001t0001g0277 | 3 | HG02280.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.184-2978C>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61845338 | ||||||
chr2:61845341
|
C | T | 1 | a0002c0002t0002g0232 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.184-2981G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61845341 | ||||||
chr2:61845342
|
A | T | 138 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(135): Show | 208 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.184-2982T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61845342 | ||||||
chr2:61845371
|
C | T | 1 | a0001c0001t0004g0059 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.184-3011G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61845371 | ||||||
chr2:61845670
|
T | A | 90 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0008others(87): Show | 126 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.184-3310A>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61845670 | ||||||
chr2:61845744
|
G | A | 12 | a0001c0001t0002g0278a0001c0001t0002g0283a0001c0001t0002g0284others(9): Show | 13 | HG02280.hp1 HG02451.hp1 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.184-3384C>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61845744 | ||||||
chr2:61845787
|
C | T | 8 | a0001c0001t0004g0020a0001c0001t0004g0055a0001c0001t0004g0056others(5): Show | 9 | HG00735.hp2 HG00741.hp2 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.184-3427G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61845787 | ||||||
chr2:61845816
|
C | T | 1 | a0002c0002t0002g0223 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.184-3456G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61845816 | ||||||
chr2:61845925
|
C | T | 14 | a0002c0002t0002g0018a0002c0002t0002g0019a0002c0002t0002g0045others(11): Show | 19 | HG00323.hp2 HG00408.hp1 HG01943.hp1 others(16): Show |
intron_variant | MODIFIER | c.184-3565G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61845925 | ||||||
chr2:61846043
|
C | T | 3 | a0001c0001t0002g0229a0001c0001t0002g0230a0001c0001t0002g0231 | 3 | HG00639.hp2 HG01255.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.184-3683G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61846043 | ||||||
chr2:61846064
|
C | T | 1 | a0001c0001t0013g0132 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.184-3704G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61846064 | ||||||
chr2:61846088
|
CA | C | 107 | a0001c0001t0001g0012a0001c0001t0001g0085a0001c0001t0001g0086others(104): Show | 142 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.184-3729delT | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61846088 | ||||||
chr2:61846088
|
CAA | C | 129 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(126): Show | 175 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.184-3730_184-3729d others(4): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61846088 | ||||||
chr2:61846088
|
CAAA | C | 38 | a0001c0001t0001g0057a0001c0001t0002g0036a0001c0001t0002g0151others(35): Show | 65 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.184-3731_184-3729d others(5): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61846088 | ||||||
chr2:61846161
|
A | T | 1 | a0001c0001t0002g0229 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.184-3801T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61846161 | ||||||
chr2:61846199
|
G | A | 1 | a0001c0001t0001g0087 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.184-3839C>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61846199 | ||||||
chr2:61846333
|
G | A | 1 | a0001c0001t0024g0091 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.184-3973C>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61846333 | ||||||
chr2:61846621
|
C | G | 2 | a0001c0001t0010g0290a0001c0001t0010g0291 | 2 | HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.184-4261G>C | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61846621 | ||||||
chr2:61846627
|
C | T | 1 | a0002c0002t0002g0239 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.184-4267G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61846627 | ||||||
chr2:61846688
|
C | T | 4 | a0001c0001t0001g0030a0001c0001t0001g0106a0001c0001t0001g0114others(1): Show | 5 | HG00544.hp2 HG02040.hp1 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.184-4328G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61846688 | ||||||
chr2:61846783
|
C | T | 148 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0002g0007others(145): Show | 187 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.184-4423G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61846783 | ||||||
chr2:61846882
|
G | C | 24 | a0001c0001t0001g0005a0001c0001t0001g0028a0001c0001t0001g0030others(21): Show | 33 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(30): Show |
intron_variant | MODIFIER | c.184-4522C>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61846882 | ||||||
chr2:61846962
|
G | A | 59 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0021others(56): Show | 86 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.184-4602C>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61846962 | ||||||
chr2:61847005
|
A | AAC | 287 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(284): Show | 396 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(393): Show |
intron_variant | MODIFIER | c.184-4647_184-4646d others(4): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61847005 | ||||||
chr2:61847019
|
G | A | 33 | a0003c0004t0003g0010a0003c0004t0003g0029a0003c0004t0003g0037others(30): Show | 39 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(36): Show |
intron_variant | MODIFIER | c.184-4659C>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61847019 | ||||||
chr2:61847054
|
C | T | 2 | a0001c0001t0001g0088a0001c0001t0001g0089 | 2 | NA19064.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.184-4694G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61847054 | ||||||
chr2:61847424
|
C | G | 1 | a0001c0001t0001g0114 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.184-5064G>C | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61847424 | ||||||
chr2:61847424
|
C | T | 132 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(129): Show | 199 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.184-5064G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61847424 | ||||||
chr2:61847589
|
G | T | 1 | a0001c0001t0002g0278 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.184-5229C>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61847589 | ||||||
chr2:61847702
|
G | A | 132 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(129): Show | 199 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.184-5342C>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61847702 | ||||||
chr2:61847716
|
G | A | 2 | a0001c0001t0001g0088a0001c0001t0001g0089 | 2 | NA19064.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.184-5356C>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61847716 | ||||||
chr2:61847797
|
G | A | 132 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(129): Show | 199 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.184-5437C>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61847797 | ||||||
chr2:61847983
|
T | C | 1 | a0003c0004t0003g0170 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.184-5623A>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61847983 | ||||||
chr2:61847988
|
T | G | 33 | a0003c0004t0003g0010a0003c0004t0003g0029a0003c0004t0003g0037others(30): Show | 39 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(36): Show |
intron_variant | MODIFIER | c.184-5628A>C | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61847988 | ||||||
chr2:61848241
|
G | C | 1 | a0001c0001t0001g0109 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.183+5618C>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848241 | ||||||
chr2:61848320
|
A | G | 2 | a0002c0002t0002g0042a0002c0002t0002g0272 | 3 | HG02647.hp2 HG02723.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.183+5539T>C | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848320 | ||||||
chr2:61848597
|
T | C | 287 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(284): Show | 396 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(393): Show |
intron_variant | MODIFIER | c.183+5262A>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848597 | ||||||
chr2:61848814
|
T | G | 1 | a0001c0001t0017g0118 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.183+5045A>C | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848814 | ||||||
chr2:61848814
|
TTA | T | 61 | a0001c0001t0001g0114a0001c0001t0002g0011a0001c0001t0002g0113others(58): Show | 83 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.183+5043_183+5044d others(4): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848814 | ||||||
chr2:61848816
|
ATATATAT others(5): Show |
A | 1 | a0002c0002t0019g0237 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.183+5031_183+5042d others(14): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848816 | ||||||
chr2:61848816
|
ATATATAT others(15): Show |
A | 3 | a0004c0005t0002g0266a0004c0005t0005g0046a0004c0005t0005g0267 | 4 | HG02451.hp1 HG03041.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.183+5021_183+5042d others(24): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848816 | ||||||
chr2:61848818
|
ATATATAT others(3): Show |
A | 5 | a0001c0001t0002g0278a0001c0001t0002g0284a0005c0010t0018g0280others(2): Show | 5 | HG02622.hp1 HG02965.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.183+5031_183+5040d others(12): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848818 | ||||||
chr2:61848818
|
ATATATAT others(115): Show |
A | 2 | a0005c0007t0009g0281a0005c0007t0009g0282 | 2 | HG02572.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.183+4919_183+5040d others(2): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848818 | ||||||
chr2:61848824
|
A | ATATTTAT others(9): Show |
1 | a0003c0004t0003g0177 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.183+5034_183+5035i others(18): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848824 | ||||||
chr2:61848824
|
A | T | 135 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(132): Show | 205 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(202): Show |
intron_variant | MODIFIER | c.183+5035T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848824 | ||||||
chr2:61848824
|
ATATCTAT others(19): Show |
A | 1 | a0002c0002t0002g0238 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.183+5009_183+5034d others(28): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848824 | ||||||
chr2:61848826
|
A | T | 2 | a0004c0005t0005g0265a0004c0005t0005g0268 | 2 | HG02280.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.183+5033T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848826 | ||||||
chr2:61848826
|
ATC | A | 130 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(127): Show | 197 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.183+5031_183+5032d others(4): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848826 | ||||||
chr2:61848828
|
C | A | 9 | a0001c0001t0001g0012a0001c0001t0001g0047a0001c0001t0001g0098others(6): Show | 12 | HG01891.hp1 HG02145.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.183+5031G>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848828 | ||||||
chr2:61848828
|
C | T | 136 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0114others(133): Show | 174 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.183+5031G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848828 | ||||||
chr2:61848828
|
CTATATAT others(17): Show |
C | 3 | a0001c0006t0002g0286a0001c0006t0002g0287a0001c0006t0002g0289 | 3 | HG00280.hp2 HG01261.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.183+5007_183+5030d others(26): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848828 | ||||||
chr2:61848830
|
A | G | 1 | a0001c0001t0001g0054 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.183+5029T>C | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848830 | ||||||
chr2:61848833
|
T | A | 1 | a0001c0001t0002g0284 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.183+5026A>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848833 | ||||||
chr2:61848834
|
ATATTTAT others(137): Show |
A | 1 | a0001c0001t0002g0283 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.183+4881_183+5024d others(2): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848834 | ||||||
chr2:61848836
|
A | ATATT | 32 | a0003c0004t0003g0010a0003c0004t0003g0029a0003c0004t0003g0037others(29): Show | 38 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(35): Show |
intron_variant | MODIFIER | c.183+5022_183+5023i others(6): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848836 | ||||||
chr2:61848836
|
A | T | 5 | a0001c0001t0001g0012a0001c0001t0001g0047a0001c0001t0001g0104others(2): Show | 8 | HG01891.hp1 HG02145.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.183+5023T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848836 | ||||||
chr2:61848838
|
T | A | 39 | a0001c0001t0001g0012a0001c0001t0001g0047a0001c0001t0001g0104others(36): Show | 48 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(45): Show |
intron_variant | MODIFIER | c.183+5021A>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848838 | ||||||
chr2:61848840
|
A | T | 2 | a0001c0001t0001g0108a0001c0001t0001g0109 | 2 | HG01243.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.183+5019T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848840 | ||||||
chr2:61848850
|
T | A | 1 | a0001c0001t0001g0109 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.183+5009A>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848850 | ||||||
chr2:61848850
|
TTA | T | 18 | a0001c0001t0001g0121a0002c0002t0002g0003a0002c0002t0002g0017others(15): Show | 27 | HG00099.hp1 HG01169.hp1 HG01256.hp2 others(24): Show |
intron_variant | MODIFIER | c.183+5007_183+5008d others(4): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848850 | ||||||
chr2:61848850
|
TTATATAT others(131): Show |
T | 1 | a0001c0001t0001g0053 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.183+4871_183+5008d others(2): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848850 | ||||||
chr2:61848852
|
A | ATATATAT others(3): Show |
7 | a0001c0001t0002g0039a0001c0001t0002g0189a0001c0001t0002g0192others(4): Show | 8 | HG01070.hp2 HG01891.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.183+4997_183+5006d others(12): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848852 | ||||||
chr2:61848852
|
A | T | 3 | a0001c0001t0001g0109a0002c0002t0002g0238a0003c0004t0003g0171 | 3 | HG01192.hp2 HG01243.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.183+5007T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848852 | ||||||
chr2:61848852
|
ATATATAT others(3): Show |
A | 1 | a0001c0001t0017g0118 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.183+4997_183+5006d others(12): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848852 | ||||||
chr2:61848862
|
T | TTA | 3 | a0003c0004t0003g0119a0003c0004t0003g0170a0003c0004t0003g0181 | 3 | HG00140.hp1 HG00280.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.183+4995_183+4996d others(4): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848862 | ||||||
chr2:61848862
|
TTA | T | 55 | a0001c0001t0001g0114a0001c0001t0002g0011a0001c0001t0002g0113others(52): Show | 68 | HG00323.hp2 HG00408.hp1 HG00639.hp2 others(65): Show |
intron_variant | MODIFIER | c.183+4995_183+4996d others(4): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848862 | ||||||
chr2:61848862
|
TTATA | T | 124 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(121): Show | 193 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.183+4993_183+4996d others(6): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848862 | ||||||
chr2:61848862
|
TTATATAT others(119): Show |
T | 1 | a0001c0001t0001g0141 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.183+4871_183+4996d others(2): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848862 | ||||||
chr2:61848864
|
A | ATATATAT others(95): Show |
1 | a0003c0004t0003g0184 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.183+4994_183+4995i others(104): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848864 | ||||||
chr2:61848864
|
A | ATATATAT others(117): Show |
1 | a0003c0004t0003g0169 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.183+4994_183+4995i others(126): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848864 | ||||||
chr2:61848864
|
A | ATATATAT others(71): Show |
1 | a0003c0004t0003g0178 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.183+4994_183+4995i others(80): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848864 | ||||||
chr2:61848864
|
A | ATATATAT others(95): Show |
1 | a0003c0004t0003g0168 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.183+4994_183+4995i others(104): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848864 | ||||||
chr2:61848864
|
A | ATATATAT others(47): Show |
2 | a0003c0004t0003g0179a0003c0004t0003g0183 | 2 | HG00642.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.183+4994_183+4995i others(56): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848864 | ||||||
chr2:61848864
|
A | ATATATAT others(69): Show |
16 | a0003c0004t0003g0010a0003c0004t0003g0029a0003c0004t0003g0038others(13): Show | 21 | HG00423.hp2 HG00597.hp2 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.183+4994_183+4995i others(78): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848864 | ||||||
chr2:61848864
|
A | ATATATAT others(91): Show |
5 | a0003c0004t0003g0037a0003c0004t0003g0110a0003c0004t0003g0185others(2): Show | 6 | HG01123.hp2 HG01361.hp1 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.183+4994_183+4995i others(100): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848864 | ||||||
chr2:61848866
|
A | ATATATAA others(17): Show |
1 | a0001c0001t0002g0015 | 3 | HG01109.hp1 HG01884.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.183+4992_183+4993i others(26): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848866 | ||||||
chr2:61848866
|
A | ATATATTT others(15): Show |
17 | a0001c0001t0002g0007a0001c0001t0002g0014a0001c0001t0002g0190others(14): Show | 24 | HG01257.hp2 HG01258.hp1 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.183+4992_183+4993i others(24): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848866 | ||||||
chr2:61848866
|
A | T | 5 | a0001c0001t0002g0111a0001c0001t0002g0208a0001c0001t0002g0209others(2): Show | 5 | NA18939.hp2 NA18985.hp2 NA18992.hp2 others(2): Show |
intron_variant | MODIFIER | c.183+4993T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848866 | ||||||
chr2:61848870
|
A | T | 6 | a0001c0001t0001g0028a0001c0001t0001g0102a0001c0001t0001g0139others(3): Show | 7 | HG01192.hp1 NA18946.hp1 NA18947.hp2 others(4): Show |
intron_variant | MODIFIER | c.183+4989T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848870 | ||||||
chr2:61848872
|
ATT | A | 3 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0257 | 3 | NA18946.hp1 NA18985.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.183+4985_183+4986d others(4): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848872 | ||||||
chr2:61848872
|
ATTTATAT others(137): Show |
A | 2 | a0001c0001t0001g0028a0001c0001t0001g0102 | 3 | NA18947.hp2 NA19064.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.183+4843_183+4986d others(2): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848872 | ||||||
chr2:61848874
|
T | A | 1 | a0001c0003t0001g0160 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.183+4985A>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848874 | ||||||
chr2:61848874
|
TTATA | T | 5 | a0001c0001t0002g0278a0001c0001t0002g0284a0004c0005t0005g0265others(2): Show | 5 | HG02280.hp1 HG03098.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.183+4981_183+4984d others(6): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848874 | ||||||
chr2:61848876
|
ATATATAT others(3): Show |
A | 1 | a0001c0001t0016g0103 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.183+4973_183+4982d others(12): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848876 | ||||||
chr2:61848876
|
ATATATAT others(133): Show |
A | 2 | a0001c0001t0001g0121a0005c0010t0018g0280 | 2 | HG02622.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.183+4843_183+4982d others(2): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848876 | ||||||
chr2:61848878
|
A | T | 7 | a0001c0001t0002g0039a0001c0001t0002g0189a0001c0001t0002g0192others(4): Show | 8 | HG01167.hp2 HG01891.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.183+4981T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848878 | ||||||
chr2:61848881
|
TATATTTA others(181): Show |
T | 1 | a0001c0001t0004g0090 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.183+4790_183+4977d others(2): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848881 | ||||||
chr2:61848882
|
A | T | 2 | a0001c0003t0001g0124a0001c0003t0001g0160 | 2 | HG01192.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.183+4977T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848882 | ||||||
chr2:61848883
|
TATTTATA others(179): Show |
T | 1 | a0001c0003t0001g0124 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.183+4790_183+4975d others(2): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848883 | ||||||
chr2:61848884
|
A | T | 27 | a0001c0001t0001g0108a0001c0001t0002g0007a0001c0001t0002g0014others(24): Show | 37 | HG01109.hp1 HG01257.hp2 HG01258.hp1 others(34): Show |
intron_variant | MODIFIER | c.183+4975T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848884 | ||||||
chr2:61848886
|
T | A | 28 | a0001c0001t0001g0108a0001c0001t0002g0007a0001c0001t0002g0014others(25): Show | 38 | HG01109.hp1 HG01192.hp1 HG01257.hp2 others(35): Show |
intron_variant | MODIFIER | c.183+4973A>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848886 | ||||||
chr2:61848886
|
T | TTATATAT others(5): Show |
1 | a0001c0001t0002g0212 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.183+4961_183+4972d others(14): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848886 | ||||||
chr2:61848886
|
TTA | T | 6 | a0001c0001t0001g0012a0001c0001t0001g0047a0001c0001t0001g0104others(3): Show | 9 | HG01891.hp1 HG02132.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.183+4971_183+4972d others(4): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848886 | ||||||
chr2:61848886
|
TTATATAT others(35): Show |
T | 17 | a0001c0001t0001g0114a0001c0001t0002g0011a0001c0001t0002g0229others(14): Show | 23 | HG00639.hp2 HG01255.hp2 HG02074.hp2 others(20): Show |
intron_variant | MODIFIER | c.183+4931_183+4972d others(44): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848886 | ||||||
chr2:61848886
|
TTATATAT others(75): Show |
T | 3 | a0001c0001t0002g0186a0001c0001t0002g0187a0001c0001t0002g0276 | 3 | HG03579.hp1 HG03579.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.183+4891_183+4972d others(84): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848886 | ||||||
chr2:61848888
|
ATATATAT others(185): Show |
A | 1 | a0001c0003t0001g0162 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.183+4779_183+4970d others(2): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848888 | ||||||
chr2:61848889
|
TATATATT others(173): Show |
T | 30 | a0001c0001t0002g0036a0001c0001t0002g0151a0001c0001t0002g0153others(27): Show | 56 | HG00438.hp1 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.183+4790_183+4969d others(2): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848889 | ||||||
chr2:61848890
|
A | T | 4 | a0001c0001t0002g0188a0001c0001t0002g0205a0001c0001t0002g0206others(1): Show | 4 | HG01175.hp2 HG02602.hp2 NA18955.hp1 others(1): Show |
intron_variant | MODIFIER | c.183+4969T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848890 | ||||||
chr2:61848890
|
ATATATTT others(11): Show |
A | 2 | a0002c0002t0002g0016a0002c0002t0002g0219 | 4 | HG00738.hp2 HG01256.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.183+4951_183+4968d others(20): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848890 | ||||||
chr2:61848890
|
ATATATTT others(81): Show |
A | 1 | a0002c0002t0002g0216 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.183+4881_183+4968d others(90): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848890 | ||||||
chr2:61848893
|
TATTTATA others(169): Show |
T | 90 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(87): Show | 130 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.183+4790_183+4965d others(2): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848893 | ||||||
chr2:61848896
|
T | A | 25 | a0001c0001t0002g0188a0001c0001t0002g0205a0001c0001t0002g0206others(22): Show | 32 | HG00323.hp2 HG00408.hp1 HG01175.hp2 others(29): Show |
intron_variant | MODIFIER | c.183+4963A>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848896 | ||||||
chr2:61848898
|
A | T | 25 | a0001c0001t0002g0188a0001c0001t0002g0205a0001c0001t0002g0206others(22): Show | 32 | HG00323.hp2 HG00408.hp1 HG01175.hp2 others(29): Show |
intron_variant | MODIFIER | c.183+4961T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848898 | ||||||
chr2:61848898
|
ATATATAT others(111): Show |
A | 1 | a0004c0005t0005g0268 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.183+4843_183+4960d others(2): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848898 | ||||||
chr2:61848902
|
ATATATTT others(170): Show |
A | 1 | a0001c0001t0001g0098 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.183+4780_183+4956d others(2): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848902 | ||||||
chr2:61848904
|
A | T | 1 | a0001c0001t0001g0108 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.183+4955T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848904 | ||||||
chr2:61848908
|
T | A | 1 | a0001c0001t0002g0207 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.183+4951A>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848908 | ||||||
chr2:61848908
|
T | TTA | 27 | a0003c0004t0003g0010a0003c0004t0003g0029a0003c0004t0003g0037others(24): Show | 33 | HG00423.hp2 HG00597.hp2 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.183+4949_183+4950d others(4): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848908 | ||||||
chr2:61848908
|
T | TTATATAT others(107): Show |
1 | a0003c0004t0003g0181 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.183+4950_183+4951i others(116): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848908 | ||||||
chr2:61848908
|
T | TTATATAT others(93): Show |
1 | a0003c0004t0003g0170 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.183+4950_183+4951i others(102): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848908 | ||||||
chr2:61848908
|
T | TTATATAT others(61): Show |
1 | a0003c0004t0003g0177 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.183+4950_183+4951i others(70): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848908 | ||||||
chr2:61848908
|
T | TTATATAT others(95): Show |
1 | a0003c0004t0003g0167 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.183+4950_183+4951i others(104): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848908 | ||||||
chr2:61848908
|
T | TTATATAT others(117): Show |
1 | a0003c0004t0003g0180 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.183+4950_183+4951i others(126): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848908 | ||||||
chr2:61848910
|
ATATATT | A | 3 | a0002c0002t0002g0238a0002c0002t0002g0249a0002c0002t0002g0252 | 3 | HG01192.hp2 NA19004.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.183+4943_183+4948d others(8): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848910 | ||||||
chr2:61848911
|
TATATTTA others(151): Show |
T | 2 | a0001c0003t0001g0160a0001c0003t0001g0163 | 2 | HG01192.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.183+4790_183+4947d others(2): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848911 | ||||||
chr2:61848911
|
TATATTTA others(177): Show |
T | 1 | a0001c0001t0024g0091 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.183+4764_183+4947d others(2): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848911 | ||||||
chr2:61848912
|
ATATTTAT others(59): Show |
A | 17 | a0002c0002t0002g0018a0002c0002t0002g0019a0002c0002t0002g0045others(14): Show | 22 | HG00323.hp2 HG00408.hp1 HG01943.hp1 others(19): Show |
intron_variant | MODIFIER | c.183+4881_183+4946d others(68): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848912 | ||||||
chr2:61848912
|
ATATTTAT others(137): Show |
A | 1 | a0004c0005t0005g0265 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.183+4803_183+4946d others(2): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848912 | ||||||
chr2:61848916
|
T | A | 28 | a0001c0001t0002g0039a0001c0001t0002g0113a0001c0001t0002g0188others(25): Show | 36 | HG00099.hp1 HG00140.hp1 HG01169.hp1 others(33): Show |
intron_variant | MODIFIER | c.183+4943A>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848916 | ||||||
chr2:61848918
|
A | ATT | 3 | a0001c0001t0002g0039a0001c0001t0002g0213a0003c0004t0003g0119 | 4 | HG00140.hp1 HG03688.hp1 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.183+4940_183+4941i others(4): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848918 | ||||||
chr2:61848918
|
A | T | 20 | a0001c0001t0002g0113a0001c0001t0002g0220a0001c0001t0002g0221others(17): Show | 27 | HG00099.hp1 HG01169.hp1 HG01346.hp1 others(24): Show |
intron_variant | MODIFIER | c.183+4941T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848918 | ||||||
chr2:61848918
|
ATATATAT others(83): Show |
A | 1 | a0001c0001t0001g0109 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.183+4851_183+4940d others(92): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848918 | ||||||
chr2:61848920
|
A | T | 5 | a0001c0001t0002g0188a0001c0001t0002g0205a0001c0001t0002g0206others(2): Show | 5 | HG01175.hp2 HG02602.hp2 NA18955.hp1 others(2): Show |
intron_variant | MODIFIER | c.183+4939T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848920 | ||||||
chr2:61848925
|
TTTATATA others(137): Show |
T | 1 | a0001c0001t0002g0278 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.183+4790_183+4933d others(2): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848925 | ||||||
chr2:61848926
|
T | A | 38 | a0001c0001t0002g0188a0001c0001t0002g0205a0001c0001t0002g0206others(35): Show | 44 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(41): Show |
intron_variant | MODIFIER | c.183+4933A>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848926 | ||||||
chr2:61848926
|
TTA | T | 4 | a0001c0001t0002g0218a0002c0002t0002g0016a0002c0002t0002g0219others(1): Show | 6 | HG00738.hp2 HG01256.hp1 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.183+4931_183+4932d others(4): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848926 | ||||||
chr2:61848926
|
TTATATAT others(33): Show |
T | 1 | a0001c0001t0017g0118 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.183+4893_183+4932d others(42): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848926 | ||||||
chr2:61848926
|
TTATATAT others(149): Show |
T | 2 | a0001c0001t0001g0104a0001c0001t0001g0112 | 2 | HG01891.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.183+4777_183+4932d others(2): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848926 | ||||||
chr2:61848927
|
TATATATA others(161): Show |
T | 1 | a0010c0011t0002g0263 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.183+4764_183+4931d others(2): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848927 | ||||||
chr2:61848928
|
A | T | 33 | a0003c0004t0003g0010a0003c0004t0003g0029a0003c0004t0003g0037others(30): Show | 39 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(36): Show |
intron_variant | MODIFIER | c.183+4931T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848928 | ||||||
chr2:61848928
|
ATATATAT others(5): Show |
A | 1 | a0002c0002t0002g0017 | 3 | HG01256.hp2 HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.183+4919_183+4930d others(14): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848928 | ||||||
chr2:61848928
|
ATATATAT others(81): Show |
A | 3 | a0004c0005t0002g0266a0004c0005t0005g0046a0004c0005t0005g0267 | 4 | HG02451.hp1 HG03041.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.183+4843_183+4930d others(90): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848928 | ||||||
chr2:61848929
|
TATATATA others(159): Show |
T | 1 | a0001c0001t0001g0012 | 3 | HG02145.hp2 HG02630.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.183+4764_183+4929d others(2): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848929 | ||||||
chr2:61848930
|
A | T | 1 | a0002c0002t0002g0250 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.183+4929T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848930 | ||||||
chr2:61848932
|
A | T | 6 | a0001c0001t0001g0108a0001c0001t0002g0188a0001c0001t0002g0205others(3): Show | 6 | HG01175.hp2 HG02602.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.183+4927T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848932 | ||||||
chr2:61848934
|
ATATATTT others(151): Show |
A | 1 | a0001c0001t0002g0284 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.183+4767_183+4924d others(2): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848934 | ||||||
chr2:61848936
|
A | T | 24 | a0001c0001t0002g0039a0001c0001t0002g0113a0001c0001t0002g0213others(21): Show | 32 | HG00099.hp1 HG01169.hp1 HG01192.hp2 others(29): Show |
intron_variant | MODIFIER | c.183+4923T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848936 | ||||||
chr2:61848938
|
A | T | 31 | a0001c0001t0001g0047a0001c0001t0001g0277a0001c0001t0002g0007others(28): Show | 41 | HG01109.hp1 HG01167.hp2 HG01257.hp2 others(38): Show |
intron_variant | MODIFIER | c.183+4921T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848938 | ||||||
chr2:61848938
|
ATT | A | 21 | a0001c0001t0002g0113a0001c0001t0002g0220a0001c0001t0002g0221others(18): Show | 28 | HG00099.hp1 HG01169.hp1 HG01192.hp2 others(25): Show |
intron_variant | MODIFIER | c.183+4919_183+4920d others(4): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848938 | ||||||
chr2:61848939
|
TTTATATA others(149): Show |
T | 2 | a0001c0001t0001g0047a0001c0001t0001g0277 | 3 | HG02280.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.183+4764_183+4919d others(2): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848939 | ||||||
chr2:61848940
|
T | A | 32 | a0001c0001t0002g0007a0001c0001t0002g0014a0001c0001t0002g0015others(29): Show | 42 | HG01109.hp1 HG01167.hp2 HG01257.hp2 others(39): Show |
intron_variant | MODIFIER | c.183+4919A>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848940 | ||||||
chr2:61848942
|
A | T | 2 | a0001c0001t0016g0103a0003c0004t0003g0165 | 2 | HG00741.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.183+4917T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848942 | ||||||
chr2:61848948
|
A | T | 3 | a0001c0001t0002g0039a0001c0001t0002g0213a0002c0002t0002g0249 | 4 | HG03688.hp1 HG03704.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.183+4911T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848948 | ||||||
chr2:61848950
|
T | A | 3 | a0001c0001t0002g0039a0001c0001t0002g0213a0002c0002t0002g0249 | 4 | HG03688.hp1 HG03704.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.183+4909A>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848950 | ||||||
chr2:61848954
|
A | ATATATT | 5 | a0001c0001t0002g0111a0001c0001t0002g0208a0001c0001t0002g0209others(2): Show | 5 | NA18939.hp2 NA18985.hp2 NA18992.hp2 others(2): Show |
intron_variant | MODIFIER | c.183+4904_183+4905i others(8): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848954 | ||||||
chr2:61848956
|
A | ATT | 22 | a0001c0001t0002g0007a0001c0001t0002g0014a0001c0001t0002g0015others(19): Show | 31 | HG01109.hp1 HG01167.hp2 HG01257.hp2 others(28): Show |
intron_variant | MODIFIER | c.183+4902_183+4903i others(4): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848956 | ||||||
chr2:61848956
|
A | T | 2 | a0001c0001t0002g0039a0001c0001t0002g0213 | 3 | HG03688.hp1 HG03704.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.183+4903T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848956 | ||||||
chr2:61848957
|
TATATTTA others(105): Show |
T | 1 | a0002c0002t0002g0250 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.183+4790_183+4901d others(2): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848957 | ||||||
chr2:61848958
|
A | T | 23 | a0001c0001t0002g0113a0001c0001t0002g0191a0001c0001t0002g0220others(20): Show | 32 | HG00099.hp1 HG01169.hp1 HG01256.hp2 others(29): Show |
intron_variant | MODIFIER | c.183+4901T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848958 | ||||||
chr2:61848958
|
ATATTTAT others(127): Show |
A | 1 | a0008c0018t0015g0279 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.183+4767_183+4900d others(2): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848958 | ||||||
chr2:61848962
|
T | A | 52 | a0001c0001t0002g0007a0001c0001t0002g0014a0001c0001t0002g0015others(49): Show | 71 | HG00099.hp1 HG01109.hp1 HG01167.hp2 others(68): Show |
intron_variant | MODIFIER | c.183+4897A>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848962 | ||||||
chr2:61848962
|
TTATATA | T | 19 | a0001c0001t0001g0114a0001c0001t0002g0011a0001c0001t0002g0218others(16): Show | 27 | HG00639.hp2 HG00738.hp2 HG01192.hp2 others(24): Show |
intron_variant | MODIFIER | c.183+4891_183+4896d others(8): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848962 | ||||||
chr2:61848966
|
A | ATATATTT others(89): Show |
1 | a0003c0004t0003g0119 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.183+4892_183+4893i others(98): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848966 | ||||||
chr2:61848966
|
A | T | 30 | a0001c0001t0002g0007a0001c0001t0002g0014a0001c0001t0002g0015others(27): Show | 40 | HG01109.hp1 HG01167.hp2 HG01257.hp2 others(37): Show |
intron_variant | MODIFIER | c.183+4893T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848966 | ||||||
chr2:61848968
|
A | ATATATT | 30 | a0003c0004t0003g0010a0003c0004t0003g0029a0003c0004t0003g0037others(27): Show | 36 | HG00280.hp1 HG00423.hp2 HG00597.hp2 others(33): Show |
intron_variant | MODIFIER | c.183+4890_183+4891i others(8): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848968 | ||||||
chr2:61848968
|
A | T | 23 | a0001c0001t0002g0113a0001c0001t0002g0191a0001c0001t0002g0220others(20): Show | 32 | HG00099.hp1 HG01169.hp1 HG01256.hp2 others(29): Show |
intron_variant | MODIFIER | c.183+4891T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848968 | ||||||
chr2:61848972
|
A | T | 1 | a0003c0004t0003g0168 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.183+4887T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848972 | ||||||
chr2:61848974
|
A | T | 7 | a0001c0001t0002g0205a0001c0001t0002g0206a0005c0007t0009g0281others(4): Show | 7 | HG02572.hp1 HG02602.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.183+4885T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848974 | ||||||
chr2:61848976
|
ATT | A | 3 | a0003c0004t0003g0168a0006c0008t0002g0217a0006c0008t0002g0251 | 3 | HG02965.hp2 HG03704.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.183+4881_183+4882d others(4): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848976 | ||||||
chr2:61848978
|
T | A | 5 | a0001c0001t0002g0205a0001c0001t0002g0206a0005c0007t0009g0281others(2): Show | 5 | HG02572.hp1 HG02602.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.183+4881A>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848978 | ||||||
chr2:61848984
|
A | T | 6 | a0001c0001t0002g0205a0001c0001t0002g0206a0001c0001t0002g0283others(3): Show | 6 | HG02572.hp1 HG02602.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.183+4875T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848984 | ||||||
chr2:61848986
|
T | A | 39 | a0001c0001t0002g0188a0001c0001t0002g0205a0001c0001t0002g0206others(36): Show | 45 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(42): Show |
intron_variant | MODIFIER | c.183+4873A>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848986 | ||||||
chr2:61848988
|
A | T | 32 | a0003c0004t0003g0010a0003c0004t0003g0029a0003c0004t0003g0037others(29): Show | 38 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(35): Show |
intron_variant | MODIFIER | c.183+4871T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848988 | ||||||
chr2:61848990
|
A | T | 1 | a0001c0001t0002g0188 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.183+4869T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848990 | ||||||
chr2:61848996
|
T | A | 4 | a0001c0001t0002g0188a0003c0004t0003g0168a0006c0008t0002g0217others(1): Show | 4 | HG01175.hp2 HG02965.hp2 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.183+4863A>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848996 | ||||||
chr2:61848996
|
TTA | T | 27 | a0001c0001t0002g0007a0001c0001t0002g0014a0001c0001t0002g0015others(24): Show | 37 | HG01109.hp1 HG01167.hp2 HG01257.hp2 others(34): Show |
intron_variant | MODIFIER | c.183+4861_183+4862d others(4): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848996 | ||||||
chr2:61848998
|
A | T | 4 | a0001c0001t0002g0188a0003c0004t0003g0168a0006c0008t0002g0217others(1): Show | 4 | HG01175.hp2 HG02965.hp2 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.183+4861T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61848998 | ||||||
chr2:61849006
|
A | T | 3 | a0001c0001t0001g0108a0001c0001t0002g0189a0001c0001t0002g0190 | 3 | HG02055.hp2 HG02559.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.183+4853T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849006 | ||||||
chr2:61849008
|
T | A | 1 | a0001c0001t0001g0108 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.183+4851A>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849008 | ||||||
chr2:61849008
|
TTATATAT others(83): Show |
T | 23 | a0001c0001t0002g0113a0001c0001t0002g0220a0001c0001t0002g0221others(20): Show | 32 | HG00099.hp1 HG01169.hp1 HG01256.hp2 others(29): Show |
intron_variant | MODIFIER | c.183+4761_183+4850d others(92): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849008 | ||||||
chr2:61849010
|
A | ATATATTT others(21): Show |
1 | a0001c0001t0002g0111 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.183+4848_183+4849i others(30): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849010 | ||||||
chr2:61849010
|
A | T | 27 | a0001c0001t0002g0007a0001c0001t0002g0014a0001c0001t0002g0015others(24): Show | 37 | HG01109.hp1 HG01167.hp2 HG01175.hp2 others(34): Show |
intron_variant | MODIFIER | c.183+4849T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849010 | ||||||
chr2:61849016
|
T | A | 2 | a0002c0002t0002g0216a0003c0004t0003g0168 | 2 | HG02965.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.183+4843A>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849016 | ||||||
chr2:61849018
|
A | T | 2 | a0002c0002t0002g0216a0003c0004t0003g0168 | 2 | HG02965.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.183+4841T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849018 | ||||||
chr2:61849026
|
T | A | 2 | a0001c0001t0001g0108a0002c0002t0002g0216 | 2 | NA19030.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.183+4833A>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849026 | ||||||
chr2:61849026
|
TTA | T | 42 | a0001c0001t0001g0114a0001c0001t0002g0011a0001c0001t0002g0208others(39): Show | 55 | HG00323.hp2 HG00408.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.183+4831_183+4832d others(4): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849026 | ||||||
chr2:61849028
|
A | T | 1 | a0001c0001t0002g0276 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.183+4831T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849028 | ||||||
chr2:61849030
|
A | T | 1 | a0002c0002t0002g0216 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.183+4829T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849030 | ||||||
chr2:61849036
|
A | T | 27 | a0001c0001t0002g0007a0001c0001t0002g0014a0001c0001t0002g0015others(24): Show | 37 | HG01109.hp1 HG01167.hp2 HG01175.hp2 others(34): Show |
intron_variant | MODIFIER | c.183+4823T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849036 | ||||||
chr2:61849040
|
A | T | 4 | a0001c0001t0002g0208a0001c0001t0002g0209a0001c0001t0002g0210others(1): Show | 4 | NA18939.hp2 NA18985.hp2 NA18992.hp2 others(1): Show |
intron_variant | MODIFIER | c.183+4819T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849040 | ||||||
chr2:61849041
|
T | G | 1 | a0006c0008t0002g0251 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.183+4818A>C | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849041 | ||||||
chr2:61849046
|
T | A | 1 | a0001c0001t0001g0108 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.183+4813A>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849046 | ||||||
chr2:61849052
|
A | ATT | 4 | a0001c0001t0002g0039a0001c0001t0002g0188a0001c0001t0002g0213others(1): Show | 5 | HG01175.hp2 HG02965.hp2 HG03688.hp1 others(2): Show |
intron_variant | MODIFIER | c.183+4806_183+4807i others(4): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849052 | ||||||
chr2:61849052
|
ATATT | A | 7 | a0001c0001t0001g0028a0001c0001t0001g0102a0001c0001t0001g0121others(4): Show | 9 | HG02280.hp1 HG02451.hp1 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.183+4803_183+4806d others(6): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849052 | ||||||
chr2:61849056
|
T | A | 4 | a0001c0001t0002g0039a0001c0001t0002g0188a0001c0001t0002g0213others(1): Show | 5 | HG01175.hp2 HG02965.hp2 HG03688.hp1 others(2): Show |
intron_variant | MODIFIER | c.183+4803A>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849056 | ||||||
chr2:61849056
|
TTATATAT others(7): Show |
T | 1 | a0001c0001t0001g0141 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.183+4789_183+4802d others(16): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849056 | ||||||
chr2:61849056
|
TTATATAT others(45): Show |
T | 1 | a0001c0001t0017g0118 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.183+4751_183+4802d others(54): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849056 | ||||||
chr2:61849058
|
A | T | 4 | a0004c0005t0002g0266a0004c0005t0005g0046a0004c0005t0005g0267others(1): Show | 5 | HG02280.hp1 HG02451.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.183+4801T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849058 | ||||||
chr2:61849059
|
T | A | 1 | a0001c0001t0001g0108 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.183+4800A>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849059 | ||||||
chr2:61849062
|
A | ATATATTT others(17): Show |
1 | a0003c0004t0003g0183 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.183+4796_183+4797i others(26): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849062 | ||||||
chr2:61849062
|
A | ATATT | 25 | a0001c0001t0002g0007a0001c0001t0002g0014a0001c0001t0002g0015others(22): Show | 34 | HG01109.hp1 HG01167.hp2 HG01257.hp2 others(31): Show |
intron_variant | MODIFIER | c.183+4796_183+4797i others(6): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849062 | ||||||
chr2:61849062
|
A | ATATTTTT others(67): Show |
4 | a0001c0001t0002g0208a0001c0001t0002g0209a0001c0001t0002g0210others(1): Show | 4 | NA18939.hp2 NA18985.hp2 NA18992.hp2 others(1): Show |
intron_variant | MODIFIER | c.183+4796_183+4797i others(76): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849062 | ||||||
chr2:61849062
|
A | ATATTTTT others(55): Show |
3 | a0001c0001t0002g0205a0001c0001t0002g0206a0009c0009t0002g0204 | 3 | HG02602.hp2 NA18955.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.183+4796_183+4797i others(64): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849062 | ||||||
chr2:61849062
|
A | T | 7 | a0001c0001t0001g0028a0001c0001t0001g0102a0001c0001t0001g0121others(4): Show | 9 | HG01175.hp2 HG02965.hp2 HG03688.hp1 others(6): Show |
intron_variant | MODIFIER | c.183+4797T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849062 | ||||||
chr2:61849063
|
TATATAA | T | 35 | a0001c0001t0001g0053a0002c0002t0002g0216a0003c0004t0003g0010others(32): Show | 41 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(38): Show |
intron_variant | MODIFIER | c.183+4790_183+4795d others(8): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849063 | ||||||
chr2:61849063
|
TATATAAA others(25): Show |
T | 1 | a0001c0001t0002g0253 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.183+4764_183+4795d others(34): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849063 | ||||||
chr2:61849064
|
A | T | 1 | a0004c0005t0005g0265 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.183+4795T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849064 | ||||||
chr2:61849065
|
TATAAATA others(23): Show |
T | 37 | a0001c0001t0001g0114a0001c0001t0002g0011a0001c0001t0002g0186others(34): Show | 50 | HG00323.hp2 HG00408.hp1 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.183+4764_183+4793d others(32): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849065 | ||||||
chr2:61849066
|
A | T | 2 | a0001c0001t0002g0276a0005c0010t0018g0280 | 2 | HG02622.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.183+4793T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849066 | ||||||
chr2:61849068
|
A | T | 1 | a0001c0001t0002g0283 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.183+4791T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849068 | ||||||
chr2:61849069
|
A | T | 43 | a0001c0001t0001g0028a0001c0001t0001g0102a0001c0001t0001g0108others(40): Show | 54 | HG00642.hp1 HG01109.hp1 HG01167.hp2 others(51): Show |
intron_variant | MODIFIER | c.183+4790T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849069 | ||||||
chr2:61849070
|
A | T | 169 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(166): Show | 226 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(223): Show |
intron_variant | MODIFIER | c.183+4789T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849070 | ||||||
chr2:61849072
|
A | T | 4 | a0001c0001t0002g0278a0004c0005t0005g0265a0005c0007t0009g0281others(1): Show | 4 | HG02572.hp1 HG03098.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.183+4787T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849072 | ||||||
chr2:61849076
|
A | T | 3 | a0001c0001t0002g0276a0001c0001t0002g0283a0005c0010t0018g0280 | 3 | HG02622.hp1 HG02630.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.183+4783T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849076 | ||||||
chr2:61849080
|
T | A | 3 | a0001c0001t0002g0276a0001c0001t0002g0283a0005c0010t0018g0280 | 3 | HG02622.hp1 HG02630.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.183+4779A>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849080 | ||||||
chr2:61849082
|
A | T | 1 | a0001c0001t0001g0098 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.183+4777T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849082 | ||||||
chr2:61849084
|
A | T | 2 | a0001c0001t0002g0283a0005c0010t0018g0280 | 2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.183+4775T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849084 | ||||||
chr2:61849086
|
A | T | 1 | a0001c0001t0002g0276 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.183+4773T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849086 | ||||||
chr2:61849088
|
ATATT | A | 8 | a0001c0001t0002g0278a0004c0005t0002g0266a0004c0005t0005g0046others(5): Show | 9 | HG02280.hp1 HG02451.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.183+4767_183+4770d others(6): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849088 | ||||||
chr2:61849092
|
T | A | 4 | a0001c0001t0002g0276a0001c0001t0002g0283a0001c0003t0001g0124others(1): Show | 4 | HG02622.hp1 HG02630.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.183+4767A>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849092 | ||||||
chr2:61849092
|
TTAAATA | T | 4 | a0002c0002t0002g0216a0002c0002t0002g0250a0006c0008t0002g0217others(1): Show | 4 | HG03704.hp2 HG04199.hp1 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.183+4761_183+4766d others(8): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849092 | ||||||
chr2:61849094
|
A | T | 1 | a0001c0003t0001g0124 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.183+4765T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849094 | ||||||
chr2:61849095
|
A | T | 132 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(129): Show | 199 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(196): Show |
intron_variant | MODIFIER | c.183+4764T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849095 | ||||||
chr2:61849098
|
A | T | 39 | a0001c0001t0001g0114a0001c0001t0002g0011a0001c0001t0002g0186others(36): Show | 52 | HG00323.hp2 HG00408.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.183+4761T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849098 | ||||||
chr2:61849106
|
TTA | T | 37 | a0001c0001t0001g0123a0001c0001t0002g0007a0001c0001t0002g0014others(34): Show | 47 | HG00741.hp1 HG01109.hp1 HG01175.hp2 others(44): Show |
intron_variant | MODIFIER | c.183+4751_183+4752d others(4): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849106 | ||||||
chr2:61849121
|
A | T | 1 | a0001c0001t0001g0122 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.183+4738T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849121 | ||||||
chr2:61849136
|
ATATATAT others(13): Show |
A | 1 | a0001c0001t0002g0213 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.183+4703_183+4722d others(22): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849136 | ||||||
chr2:61849140
|
ATATTTAT others(5): Show |
A | 4 | a0001c0001t0002g0278a0001c0001t0002g0283a0001c0001t0002g0284others(1): Show | 4 | HG02630.hp1 HG03098.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.183+4707_183+4718d others(14): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849140 | ||||||
chr2:61849293
|
G | A | 1 | a0001c0001t0004g0093 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.183+4566C>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849293 | ||||||
chr2:61849415
|
G | A | 1 | a0001c0003t0001g0163 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.183+4444C>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849415 | ||||||
chr2:61849443
|
C | A | 1 | a0001c0001t0002g0253 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.183+4416G>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849443 | ||||||
chr2:61849676
|
TCAGGAGG others(6): Show |
T | 2 | a0001c0001t0001g0028a0001c0001t0001g0102 | 3 | NA18947.hp2 NA19064.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.183+4170_183+4182d others(15): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849676 | ||||||
chr2:61849775
|
C | T | 1 | a0008c0018t0015g0279 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.183+4084G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849775 | ||||||
chr2:61849783
|
C | CA | 8 | a0001c0001t0001g0094a0001c0001t0001g0108a0001c0001t0001g0109others(5): Show | 9 | HG01081.hp2 HG01099.hp2 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.183+4075dupT | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849783 | ||||||
chr2:61849857
|
A | G | 1 | a0001c0001t0004g0052 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.183+4002T>C | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849857 | ||||||
chr2:61849865
|
T | TAACACAG others(1): Show |
287 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(284): Show | 396 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(393): Show |
intron_variant | MODIFIER | c.183+3993_183+3994i others(10): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849865 | ||||||
chr2:61849884
|
A | C | 1 | a0003c0004t0003g0164 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.183+3975T>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849884 | ||||||
chr2:61849885
|
C | T | 1 | a0003c0004t0003g0164 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.183+3974G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849885 | ||||||
chr2:61849892
|
T | A | 1 | a0003c0004t0003g0164 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.183+3967A>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849892 | ||||||
chr2:61849901
|
G | T | 1 | a0003c0004t0003g0164 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.183+3958C>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61849901 | ||||||
chr2:61850004
|
T | G | 1 | a0001c0001t0001g0109 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.183+3855A>C | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61850004 | ||||||
chr2:61850128
|
A | T | 1 | a0010c0011t0002g0263 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.183+3731T>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61850128 | ||||||
chr2:61850159
|
G | A | 1 | a0002c0002t0002g0254 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.183+3700C>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61850159 | ||||||
chr2:61850171
|
C | T | 1 | a0002c0002t0002g0215 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.183+3688G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61850171 | ||||||
chr2:61850256
|
C | T | 2 | a0001c0001t0001g0108a0001c0001t0001g0109 | 2 | HG01243.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.183+3603G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61850256 | ||||||
chr2:61850258
|
T | C | 1 | a0003c0004t0003g0185 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.183+3601A>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61850258 | ||||||
chr2:61850454
|
T | C | 33 | a0003c0004t0003g0010a0003c0004t0003g0029a0003c0004t0003g0037others(30): Show | 39 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(36): Show |
intron_variant | MODIFIER | c.183+3405A>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61850454 | ||||||
chr2:61850489
|
C | T | 1 | a0001c0001t0001g0121 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.183+3370G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61850489 | ||||||
chr2:61850525
|
G | A | 2 | a0001c0001t0001g0047a0001c0001t0001g0277 | 3 | HG02280.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.183+3334C>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61850525 | ||||||
chr2:61850614
|
G | A | 2 | a0001c0001t0002g0283a0001c0001t0002g0284 | 2 | HG02630.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.183+3245C>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61850614 | ||||||
chr2:61850790
|
C | A | 287 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(284): Show | 396 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(393): Show |
intron_variant | MODIFIER | c.183+3069G>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61850790 | ||||||
chr2:61850929
|
C | G | 1 | a0001c0001t0004g0051 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.183+2930G>C | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61850929 | ||||||
chr2:61851036
|
G | T | 1 | a0001c0001t0001g0120 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.183+2823C>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61851036 | ||||||
chr2:61851104
|
C | A | 1 | a0001c0001t0001g0095 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.183+2755G>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61851104 | ||||||
chr2:61851166
|
G | A | 67 | a0001c0001t0001g0114a0001c0001t0002g0011a0001c0001t0002g0113others(64): Show | 89 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.183+2693C>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61851166 | ||||||
chr2:61851194
|
G | A | 149 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0114others(146): Show | 188 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.183+2665C>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61851194 | ||||||
chr2:61851360
|
A | G | 287 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(284): Show | 396 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(393): Show |
intron_variant | MODIFIER | c.183+2499T>C | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61851360 | ||||||
chr2:61851455
|
C | T | 137 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(134): Show | 207 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.183+2404G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61851455 | ||||||
chr2:61851514
|
T | C | 5 | a0004c0005t0002g0266a0004c0005t0005g0046a0004c0005t0005g0265others(2): Show | 6 | HG02280.hp1 HG02451.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.183+2345A>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61851514 | ||||||
chr2:61851642
|
C | T | 7 | a0001c0001t0002g0278a0001c0001t0002g0283a0001c0001t0002g0284others(4): Show | 7 | HG02572.hp1 HG02622.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.183+2217G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61851642 | ||||||
chr2:61851730
|
C | T | 2 | a0003c0004t0003g0029a0003c0004t0003g0119 | 3 | HG00140.hp1 HG01081.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.183+2129G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61851730 | ||||||
chr2:61851810
|
T | G | 2 | a0002c0002t0002g0117a0002c0002t0002g0255 | 2 | HG02523.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.183+2049A>C | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61851810 | ||||||
chr2:61851814
|
G | C | 2 | a0001c0001t0001g0096a0001c0001t0001g0097 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.183+2045C>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61851814 | ||||||
chr2:61851943
|
A | G | 1 | a0001c0001t0017g0118 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.183+1916T>C | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61851943 | ||||||
chr2:61852132
|
T | G | 39 | a0001c0001t0002g0007a0001c0001t0002g0014a0001c0001t0002g0015others(36): Show | 50 | HG01109.hp1 HG01167.hp2 HG01175.hp2 others(47): Show |
intron_variant | MODIFIER | c.183+1727A>C | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61852132 | ||||||
chr2:61852319
|
C | G | 1 | a0001c0001t0016g0103 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.183+1540G>C | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61852319 | ||||||
chr2:61852408
|
C | G | 2 | a0001c0001t0001g0049a0001c0001t0001g0050 | 2 | HG00642.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.183+1451G>C | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61852408 | ||||||
chr2:61852515
|
G | C | 1 | a0001c0001t0001g0112 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.183+1344C>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61852515 | ||||||
chr2:61852582
|
C | G | 2 | a0001c0001t0001g0047a0001c0001t0001g0277 | 3 | HG02280.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.183+1277G>C | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61852582 | ||||||
chr2:61852760
|
T | C | 63 | a0001c0001t0001g0114a0001c0001t0002g0011a0001c0001t0002g0113others(60): Show | 85 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.183+1099A>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61852760 | ||||||
chr2:61852846
|
A | G | 2 | a0001c0001t0001g0028a0001c0001t0001g0102 | 3 | NA18947.hp2 NA19064.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.183+1013T>C | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61852846 | ||||||
chr2:61852938
|
CT | C | 243 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(240): Show | 345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.183+920delA | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61852938 | ||||||
chr2:61852938
|
CTT | C | 24 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0047others(21): Show | 28 | HG01515.hp2 HG01981.hp2 HG02280.hp1 others(25): Show |
intron_variant | MODIFIER | c.183+919_183+920del others(2): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61852938 | ||||||
chr2:61853045
|
A | G | 287 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(284): Show | 396 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(393): Show |
intron_variant | MODIFIER | c.183+814T>C | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61853045 | ||||||
chr2:61853056
|
G | T | 287 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(284): Show | 396 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(393): Show |
intron_variant | MODIFIER | c.183+803C>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61853056 | ||||||
chr2:61853109
|
A | G | 1 | a0003c0004t0003g0101 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.183+750T>C | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61853109 | ||||||
chr2:61853184
|
A | G | 1 | a0001c0001t0001g0100 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.183+675T>C | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61853184 | ||||||
chr2:61853200
|
G | A | 1 | a0001c0001t0001g0275 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.183+659C>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61853200 | ||||||
chr2:61853201
|
C | A | 1 | a0001c0001t0001g0275 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.183+658G>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61853201 | ||||||
chr2:61853214
|
T | C | 1 | a0001c0001t0002g0276 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.183+645A>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61853214 | ||||||
chr2:61853250
|
C | T | 1 | a0001c0003t0001g0099 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.183+609G>A | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61853250 | ||||||
chr2:61853288
|
T | A | 2 | a0001c0001t0001g0047a0001c0001t0001g0277 | 3 | HG02280.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.183+571A>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61853288 | ||||||
chr2:61853338
|
A | G | 61 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0021others(58): Show | 88 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.183+521T>C | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61853338 | ||||||
chr2:61853347
|
G | A | 7 | a0001c0001t0002g0278a0001c0001t0002g0283a0001c0001t0002g0284others(4): Show | 7 | HG02572.hp1 HG02622.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.183+512C>T | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61853347 | ||||||
chr2:61853786
|
C | G | 1 | a0003c0004t0003g0285 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.183+73G>C | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61853786 | ||||||
chr2:61853787
|
G | C | 1 | a0003c0004t0003g0285 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.183+72C>G | FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | 61853787 |