geneid | 220108 |
---|---|
ensemblid | ENSG00000150510.17 |
hgncid | 26413 |
symbol | FAM124A |
name | family with sequence similarity 124 member A |
refseq_nuc | NM_001242312.2 |
refseq_prot | NP_001229241.1 |
ensembl_nuc | ENST00000322475.13 |
ensembl_prot | ENSP00000324625.8 |
mane_status | MANE Select |
chr | chr13 |
start | 51222398 |
end | 51284239 |
strand | + |
ver | v1.2 |
region | chr13:51222398-51284239 |
region5000 | chr13:51217398-51289239 |
regionname0 | FAM124A_chr13_51222398_51284239 |
regionname5000 | FAM124A_chr13_51217398_51289239 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 546 | 336 | 61 | 56 | 167 | 12 | 38 | 122 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
a0002 | 0/0 | 546 | 43 | 15 | 7 | 16 | 3 | 2 | 15 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
a0003 | 0/0 | 546 | 12 | 11 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
a0004 | 0/0 | 546 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
a0005 | 0/0 | 546 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
a0006 | 0/0 | 546 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
a0007 | 0/0 | 546 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
a0008 | 0/0 | 546 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
a0009 | 0/0 | 546 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
a0010 | 0/0 | 546 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
a0011 | 0/0 | 546 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1641 | 325 | 54 | 56 | 163 | 12 | 38 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
c0002 | 0/0 | 1641 | 36 | 13 | 7 | 11 | 3 | 2 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
c0003 | 0/0 | 1641 | 12 | 11 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
c0004 | 0/0 | 1641 | 7 | 2 | 0 | 5 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
c0005 | 0/0 | 1641 | 6 | 6 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
c0006 | 0/0 | 1641 | 4 | 1 | 0 | 3 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
c0007 | 0/0 | 1641 | 3 | 3 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
c0008 | 0/0 | 1641 | 2 | 0 | 0 | 2 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
c0009 | 0/0 | 1641 | 2 | 2 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
c0010 | 0/0 | 1641 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
c0011 | 0/0 | 1641 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
c0012 | 0/0 | 1641 | 1 | 0 | 0 | 0 | 1 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
c0013 | 0/0 | 1641 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
c0014 | 0/0 | 1641 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
c0015 | 0/0 | 1641 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
c0016 | 0/0 | 1641 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
c0017 | 0/0 | 1641 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
c0018 | 0/0 | 1641 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 3089 | 94 | 11 | 23 | 44 | 5 | 11 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
t0002 | 1/1 | 3088 | 92 | 12 | 15 | 49 | 7 | 7 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
t0003 | 0/0 | 3090 | 36 | 1 | 1 | 33 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
t0004 | 0/0 | 3090 | 31 | 5 | 8 | 11 | 0 | 7 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
t0005 | 0/0 | 3091 | 20 | 1 | 1 | 17 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
t0006 | 0/0 | 3093 | 17 | 1 | 2 | 6 | 2 | 6 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
t0007 | 0/0 | 3087 | 16 | 10 | 4 | 2 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
t0008 | 0/0 | 3081 | 10 | 8 | 2 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
t0009 | 0/0 | 3088 | 9 | 2 | 4 | 0 | 1 | 2 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
t0010 | 0/0 | 3091 | 8 | 2 | 0 | 6 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
t0011 | 0/0 | 3094 | 7 | 0 | 2 | 2 | 0 | 3 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
t0012 | 0/0 | 3090 | 7 | 7 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
t0013 | 0/0 | 3092 | 6 | 6 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
t0014 | 0/0 | 3091 | 4 | 4 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
t0015 | 0/0 | 3089 | 4 | 0 | 0 | 4 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
t0016 | 0/0 | 3092 | 3 | 1 | 0 | 2 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
t0017 | 0/0 | 3091 | 3 | 3 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
t0018 | 0/0 | 3091 | 3 | 3 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
t0019 | 0/0 | 3090 | 3 | 2 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
t0020 | 0/0 | 3100 | 2 | 2 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
t0021 | 0/0 | 3089 | 2 | 0 | 2 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
t0022 | 0/0 | 3093 | 2 | 2 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
t0023 | 0/0 | 3090 | 2 | 1 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
t0024 | 0/0 | 3081 | 2 | 2 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
t0025 | 0/0 | 3090 | 2 | 0 | 0 | 2 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
t0026 | 0/0 | 3092 | 2 | 1 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
t0027 | 0/0 | 3093 | 2 | 2 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
t0028 | 0/0 | 3091 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
t0029 | 0/0 | 3091 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
t0030 | 0/0 | 3087 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
t0031 | 0/0 | 3086 | 1 | 0 | 0 | 0 | 1 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
t0032 | 0/0 | 3087 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
t0033 | 0/0 | 3080 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
t0034 | 0/0 | 3090 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
t0035 | 0/0 | 3090 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
t0036 | 0/0 | 3088 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
t0037 | 0/0 | 3089 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
t0038 | 0/0 | 3093 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
t0039 | 0/0 | 3090 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
t0040 | 0/0 | 3088 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
t0041 | 0/0 | 3090 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
t0042 | 0/0 | 3091 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
t0043 | 0/0 | 3088 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
t0044 | 0/0 | 3092 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 8 | 0 | 0 | 6 | 1 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0003 | 0/0 | 4 | 1 | 1 | 1 | 1 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0004 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0005 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0006 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0008 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0012 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0015 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0024 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0026 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0027 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0041 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0042 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0174 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0248 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0297 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0327 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0332 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1641 | 325 | 54 | 56 | 163 | 12 | 38 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
a0001c0006 | 0/0 | 1641 | 4 | 1 | 0 | 3 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
a0001c0007 | 0/0 | 1641 | 3 | 3 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
a0001c0009 | 0/0 | 1641 | 2 | 2 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
a0001c0016 | 0/0 | 1641 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
a0001c0017 | 0/0 | 1641 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
a0002c0002 | 0/0 | 1641 | 36 | 13 | 7 | 11 | 3 | 2 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
a0002c0004 | 0/0 | 1641 | 7 | 2 | 0 | 5 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
a0003c0003 | 0/0 | 1641 | 12 | 11 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
a0004c0005 | 0/0 | 1641 | 6 | 6 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
a0004c0011 | 0/0 | 1641 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
a0005c0008 | 0/0 | 1641 | 2 | 0 | 0 | 2 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
a0006c0014 | 0/0 | 1641 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
a0007c0018 | 0/0 | 1641 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
a0008c0015 | 0/0 | 1641 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
a0009c0013 | 0/0 | 1641 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
a0010c0012 | 0/0 | 1641 | 1 | 0 | 0 | 0 | 1 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
a0011c0010 | 0/0 | 1641 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 4729 | 86 | 7 | 22 | 41 | 5 | 11 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
a0001c0001t0002 | 1/1 | 4728 | 83 | 10 | 15 | 43 | 6 | 7 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
a0001c0001t0003 | 0/0 | 4730 | 35 | 1 | 1 | 32 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
a0001c0001t0004 | 0/0 | 4730 | 29 | 4 | 7 | 11 | 0 | 7 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
a0001c0001t0005 | 0/0 | 4731 | 19 | 1 | 1 | 16 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
a0001c0001t0006 | 0/0 | 4733 | 16 | 1 | 2 | 6 | 1 | 6 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
a0001c0001t0007 | 0/0 | 4727 | 7 | 4 | 3 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
a0001c0001t0009 | 0/0 | 4728 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
a0001c0001t0011 | 0/0 | 4734 | 6 | 0 | 2 | 1 | 0 | 3 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
a0001c0001t0012 | 0/0 | 4730 | 7 | 7 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
a0001c0001t0013 | 0/0 | 4732 | 2 | 2 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
a0001c0001t0014 | 0/0 | 4731 | 4 | 4 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
a0001c0001t0015 | 0/0 | 4729 | 4 | 0 | 0 | 4 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
a0001c0001t0017 | 0/0 | 4731 | 3 | 3 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
a0001c0001t0018 | 0/0 | 4731 | 2 | 2 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
a0001c0001t0019 | 0/0 | 4730 | 2 | 2 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
a0001c0001t0021 | 0/0 | 4729 | 2 | 0 | 2 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
a0001c0001t0022 | 0/0 | 4733 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
a0001c0001t0023 | 0/0 | 4730 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
a0001c0001t0025 | 0/0 | 4730 | 2 | 0 | 0 | 2 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
a0001c0001t0026 | 0/0 | 4732 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
a0001c0001t0028 | 0/0 | 4731 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
a0001c0001t0029 | 0/0 | 4731 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
a0001c0001t0030 | 0/0 | 4727 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
a0001c0001t0034 | 0/0 | 4730 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
a0001c0001t0035 | 0/0 | 4730 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
a0001c0001t0036 | 0/0 | 4728 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
a0001c0001t0037 | 0/0 | 4729 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
a0001c0001t0038 | 0/0 | 4733 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
a0001c0001t0041 | 0/0 | 4730 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
a0001c0001t0042 | 0/0 | 4731 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
a0001c0001t0043 | 0/0 | 4728 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
a0001c0001t0044 | 0/0 | 4732 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
a0001c0006t0010 | 0/0 | 4731 | 3 | 0 | 0 | 3 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
a0001c0006t0016 | 0/0 | 4732 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
a0001c0007t0001 | 0/0 | 4729 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
a0001c0007t0013 | 0/0 | 4732 | 2 | 2 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
a0001c0009t0020 | 0/0 | 4740 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
a0001c0009t0033 | 0/0 | 4720 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
a0001c0016t0002 | 0/0 | 4728 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
a0001c0017t0001 | 0/0 | 4729 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
a0002c0002t0001 | 0/0 | 4729 | 6 | 2 | 1 | 3 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
a0002c0002t0002 | 0/0 | 4728 | 6 | 1 | 0 | 4 | 1 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
a0002c0002t0004 | 0/0 | 4730 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
a0002c0002t0007 | 0/0 | 4727 | 9 | 6 | 1 | 2 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
a0002c0002t0009 | 0/0 | 4728 | 8 | 1 | 4 | 0 | 1 | 2 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
a0002c0002t0011 | 0/0 | 4734 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
a0002c0002t0018 | 0/0 | 4731 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
a0002c0002t0019 | 0/0 | 4730 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
a0002c0002t0031 | 0/0 | 4726 | 1 | 0 | 0 | 0 | 1 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
a0002c0002t0032 | 0/0 | 4727 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
a0002c0002t0040 | 0/0 | 4728 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
a0002c0004t0010 | 0/0 | 4731 | 5 | 2 | 0 | 3 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
a0002c0004t0016 | 0/0 | 4732 | 2 | 0 | 0 | 2 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
a0003c0003t0008 | 0/0 | 4721 | 9 | 8 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
a0003c0003t0024 | 0/0 | 4721 | 2 | 2 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
a0003c0003t0039 | 0/0 | 4730 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
a0004c0005t0013 | 0/0 | 4732 | 2 | 2 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
a0004c0005t0022 | 0/0 | 4733 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
a0004c0005t0023 | 0/0 | 4730 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
a0004c0005t0027 | 0/0 | 4733 | 2 | 2 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
a0004c0011t0002 | 0/0 | 4728 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
a0005c0008t0003 | 0/0 | 4730 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
a0005c0008t0005 | 0/0 | 4731 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
a0006c0014t0026 | 0/0 | 4732 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
a0007c0018t0002 | 0/0 | 4728 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
a0008c0015t0004 | 0/0 | 4730 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
a0009c0013t0008 | 0/0 | 4721 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
a0010c0012t0006 | 0/0 | 4733 | 1 | 0 | 0 | 0 | 1 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
a0011c0010t0020 | 0/0 | 4740 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | copy fasta | chr13 | 51217398 | 51289239 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0001g0003 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0001g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0001g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0002g0001 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0002g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0002g0006 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0002g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0002g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0002g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0002g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0002g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0002g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0002g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0002g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0002g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0002g0174 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0002g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0002g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0002g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0002g0248 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0002g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0002g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0002g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0002g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0002g0327 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0002g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0002g0332 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0002g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0002g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0003g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0003g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0003g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0003g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0003g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0003g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0003g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0003g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0003g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0003g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0004g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0004g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0004g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0004g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0004g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0004g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0004g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0004g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0004g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0004g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0004g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0004g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0004g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0004g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0004g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0004g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0004g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0004g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0004g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0004g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0004g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0004g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0004g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0004g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0004g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0004g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0005g0008 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0005g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0005g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0005g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0005g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0005g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0005g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0005g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0005g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0005g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0005g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0005g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0005g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0005g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0005g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0005g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0005g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0006g0027 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0006g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0006g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0006g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0006g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0006g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0006g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0006g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0006g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0006g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0006g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0006g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0006g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0006g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0006g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0007g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0007g0015 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0007g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0007g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0007g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0009g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0011g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0011g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0011g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0011g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0011g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0011g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0012g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0012g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0012g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0012g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0012g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0012g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0013g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0013g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0014g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0014g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0014g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0014g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0015g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0015g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0015g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0015g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0017g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0017g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0017g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0018g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0018g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0019g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0019g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0021g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0021g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0022g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0023g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0025g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0025g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0026g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0028g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0029g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0030g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0034g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0035g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0036g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0037g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0038g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0041g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0042g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0043g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0001t0044g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0006t0010g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0006t0010g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0006t0010g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0006t0016g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0007t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0007t0013g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0007t0013g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0009t0020g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0009t0033g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0016t0002g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0001c0017t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0002c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0002c0002t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0002c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0002c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0002c0002t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0002c0002t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0002c0002t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0002c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0002c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0002c0002t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0002c0002t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0002c0002t0002g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0002c0002t0004g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0002c0002t0007g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0002c0002t0007g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0002c0002t0007g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0002c0002t0007g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0002c0002t0007g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0002c0002t0007g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0002c0002t0007g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0002c0002t0007g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0002c0002t0007g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0002c0002t0009g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0002c0002t0009g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0002c0002t0009g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0002c0002t0009g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0002c0002t0009g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0002c0002t0009g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0002c0002t0009g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0002c0002t0009g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0002c0002t0011g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0002c0002t0018g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0002c0002t0019g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0002c0002t0031g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0002c0002t0032g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0002c0002t0040g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0002c0004t0010g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0002c0004t0010g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0002c0004t0010g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0002c0004t0010g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0002c0004t0010g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0002c0004t0016g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0002c0004t0016g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0003c0003t0008g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0003c0003t0008g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0003c0003t0008g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0003c0003t0008g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0003c0003t0008g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0003c0003t0008g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0003c0003t0008g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0003c0003t0008g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0003c0003t0024g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0003c0003t0024g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0003c0003t0039g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0004c0005t0013g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0004c0005t0013g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0004c0005t0022g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0004c0005t0023g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0004c0005t0027g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0004c0005t0027g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0004c0011t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0005c0008t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0005c0008t0005g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0006c0014t0026g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0007c0018t0002g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0008c0015t0004g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0009c0013t0008g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0010c0012t0006g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
a0011c0010t0020g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0332 | EUR | GBR | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0172 | EUR | GBR | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG00140 | hp1 | a0002 | c0002 | t0002 | g0041 | EUR | GBR | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG00140 | hp2 | a0010 | c0012 | t0006 | g0125 | EUR | GBR | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG00280 | hp1 | a0001 | c0001 | t0002 | g0213 | EUR | FIN | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG00280 | hp2 | a0001 | c0001 | t0002 | g0001 | EUR | FIN | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0327 | EUR | FIN | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG00323 | hp2 | a0002 | c0002 | t0031 | g0222 | EUR | FIN | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG00408 | hp1 | a0001 | c0001 | t0003 | g0075 | EAS | CHS | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG00408 | hp2 | a0001 | c0016 | t0002 | g0001 | EAS | CHS | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG00423 | hp1 | a0001 | c0006 | t0010 | g0271 | EAS | CHS | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | CHS | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0057 | EAS | CHS | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0028 | EAS | CHS | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG00544 | hp1 | a0001 | c0001 | t0006 | g0236 | EAS | CHS | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | CHS | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | CHS | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG00558 | hp2 | a0001 | c0001 | t0036 | g0303 | EAS | CHS | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG00597 | hp1 | a0001 | c0001 | t0005 | g0070 | EAS | CHS | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0126 | EAS | CHS | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0259 | EAS | CHS | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG00621 | hp1 | a0001 | c0001 | t0004 | g0076 | EAS | CHS | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG00621 | hp2 | a0001 | c0001 | t0003 | g0254 | EAS | CHS | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0272 | AMR | PUR | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0185 | AMR | PUR | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | CHS | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG00673 | hp2 | a0001 | c0001 | t0002 | g0099 | EAS | CHS | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0243 | AMR | PUR | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0217 | AMR | PUR | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG00735 | hp2 | a0001 | c0001 | t0004 | g0221 | AMR | PUR | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG00738 | hp1 | a0001 | c0001 | t0004 | g0218 | AMR | PUR | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG00738 | hp2 | a0001 | c0001 | t0007 | g0014 | AMR | PUR | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG01069 | hp2 | a0001 | c0001 | t0011 | g0320 | AMR | PUR | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG01070 | hp1 | a0001 | c0001 | t0007 | g0015 | AMR | PUR | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0223 | AMR | PUR | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG01074 | hp2 | a0002 | c0002 | t0007 | g0042 | AMR | PUR | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0334 | AMR | PUR | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG01106 | hp1 | a0002 | c0002 | t0001 | g0229 | AMR | PUR | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG01106 | hp2 | a0001 | c0001 | t0004 | g0134 | AMR | PUR | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG01109 | hp1 | a0001 | c0001 | t0004 | g0012 | AMR | PUR | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG01109 | hp2 | a0001 | c0001 | t0023 | g0313 | AMR | PUR | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0287 | AMR | PUR | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG01167 | hp2 | a0002 | c0002 | t0009 | g0295 | AMR | PUR | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG01168 | hp1 | a0001 | c0001 | t0021 | g0247 | AMR | PUR | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG01168 | hp2 | a0001 | c0001 | t0007 | g0014 | AMR | PUR | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG01169 | hp1 | a0002 | c0002 | t0009 | g0326 | AMR | PUR | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG01169 | hp2 | a0001 | c0001 | t0021 | g0286 | AMR | PUR | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG01175 | hp1 | a0002 | c0002 | t0009 | g0250 | AMR | PUR | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG01175 | hp2 | a0008 | c0015 | t0004 | g0004 | AMR | PUR | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0306 | AMR | PUR | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG01192 | hp2 | a0003 | c0003 | t0008 | g0199 | AMR | PUR | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG01243 | hp1 | a0002 | c0002 | t0019 | g0324 | AMR | PUR | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0341 | AMR | PUR | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG01255 | hp1 | a0001 | c0001 | t0005 | g0024 | AMR | CLM | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG01255 | hp2 | a0002 | c0002 | t0009 | g0280 | AMR | CLM | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0219 | AMR | CLM | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | CLM | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG01346 | hp1 | a0001 | c0001 | t0011 | g0215 | AMR | CLM | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG01346 | hp2 | a0001 | c0001 | t0003 | g0023 | AMR | CLM | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG01358 | hp1 | a0001 | c0001 | t0004 | g0164 | AMR | CLM | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG01358 | hp2 | a0001 | c0001 | t0002 | g0212 | AMR | CLM | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | CLM | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG01516 | hp1 | a0001 | c0001 | t0002 | g0297 | EUR | IBS | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0207 | EUR | IBS | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0146 | EUR | IBS | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG01884 | hp1 | a0003 | c0003 | t0008 | g0205 | AFR | ACB | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG01884 | hp2 | a0011 | c0010 | t0020 | g0067 | AFR | ACB | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG01891 | hp1 | a0004 | c0005 | t0022 | g0315 | AFR | ACB | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG01891 | hp2 | a0001 | c0007 | t0013 | g0089 | AFR | ACB | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0023 | AMR | PEL | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | PEL | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG01934 | hp1 | a0001 | c0001 | t0006 | g0177 | AMR | PEL | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG01934 | hp2 | a0001 | c0001 | t0004 | g0012 | AMR | PEL | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG01943 | hp1 | a0001 | c0001 | t0006 | g0153 | AMR | PEL | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | PEL | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PEL | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | PEL | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG01975 | hp1 | a0009 | c0013 | t0008 | g0230 | AMR | PEL | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG01975 | hp2 | a0001 | c0001 | t0002 | g0072 | AMR | PEL | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PEL | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0029 | AMR | PEL | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG01981 | hp1 | a0001 | c0001 | t0004 | g0004 | AMR | PEL | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | PEL | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | PEL | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG01993 | hp2 | a0001 | c0001 | t0002 | g0273 | AMR | PEL | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG02027 | hp1 | a0001 | c0001 | t0011 | g0081 | EAS | KHV | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG02027 | hp2 | a0001 | c0001 | t0003 | g0253 | EAS | KHV | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG02055 | hp1 | a0001 | c0001 | t0004 | g0227 | AFR | ACB | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG02055 | hp2 | a0001 | c0001 | t0004 | g0003 | AFR | ACB | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG02056 | hp1 | a0001 | c0001 | t0002 | g0307 | EAS | KHV | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG02056 | hp2 | a0001 | c0001 | t0004 | g0291 | EAS | KHV | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | KHV | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG02071 | hp2 | a0001 | c0001 | t0003 | g0101 | EAS | KHV | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG02074 | hp1 | a0001 | c0001 | t0005 | g0097 | EAS | KHV | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG02074 | hp2 | a0001 | c0001 | t0015 | g0284 | EAS | KHV | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG02080 | hp1 | a0001 | c0001 | t0005 | g0082 | EAS | KHV | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG02080 | hp2 | a0001 | c0001 | t0004 | g0038 | EAS | KHV | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG02083 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | KHV | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG02083 | hp2 | a0001 | c0001 | t0006 | g0155 | EAS | KHV | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG02129 | hp1 | a0001 | c0001 | t0004 | g0046 | EAS | KHV | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG02129 | hp2 | a0001 | c0001 | t0003 | g0180 | EAS | KHV | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | KHV | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG02132 | hp2 | a0002 | c0004 | t0016 | g0325 | EAS | KHV | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG02135 | hp1 | a0001 | c0001 | t0005 | g0102 | EAS | KHV | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG02135 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | KHV | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG02145 | hp1 | a0001 | c0001 | t0014 | g0005 | AFR | ACB | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG02145 | hp2 | a0001 | c0001 | t0018 | g0127 | AFR | ACB | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | CDX | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | CDX | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | CDX | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG02257 | hp1 | a0001 | c0001 | t0012 | g0005 | AFR | ACB | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | ACB | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG02258 | hp1 | a0001 | c0001 | t0030 | g0112 | AFR | ACB | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG02258 | hp2 | a0002 | c0002 | t0007 | g0277 | AFR | ACB | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG02273 | hp1 | a0001 | c0001 | t0002 | g0018 | AMR | PEL | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PEL | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG02280 | hp1 | a0001 | c0006 | t0016 | g0343 | AFR | ACB | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0202 | AFR | ACB | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | PEL | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG02293 | hp2 | a0001 | c0001 | t0002 | g0029 | AMR | PEL | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PEL | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0018 | AMR | PEL | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG02451 | hp1 | a0001 | c0001 | t0019 | g0337 | AFR | ACB | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG02451 | hp2 | a0001 | c0001 | t0002 | g0239 | AFR | ACB | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | KHV | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG02523 | hp2 | a0001 | c0001 | t0002 | g0135 | EAS | KHV | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG02572 | hp1 | a0001 | c0001 | t0002 | g0193 | AFR | GWD | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG02572 | hp2 | a0004 | c0005 | t0023 | g0322 | AFR | GWD | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0333 | SAS | PJL | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG02602 | hp2 | a0001 | c0001 | t0006 | g0300 | SAS | PJL | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG02615 | hp1 | a0001 | c0001 | t0003 | g0342 | AFR | GWD | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG02615 | hp2 | a0001 | c0001 | t0002 | g0228 | AFR | GWD | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG02622 | hp1 | a0001 | c0001 | t0017 | g0032 | AFR | GWD | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG02622 | hp2 | a0002 | c0002 | t0007 | g0296 | AFR | GWD | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG02630 | hp1 | a0001 | c0001 | t0013 | g0032 | AFR | GWD | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG02630 | hp2 | a0002 | c0002 | t0002 | g0330 | AFR | GWD | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG02647 | hp1 | a0001 | c0017 | t0001 | g0173 | AFR | GWD | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG02647 | hp2 | a0001 | c0007 | t0001 | g0020 | AFR | GWD | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0220 | SAS | PJL | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG02683 | hp2 | a0001 | c0001 | t0006 | g0148 | SAS | PJL | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG02717 | hp1 | a0001 | c0001 | t0012 | g0241 | AFR | GWD | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG02717 | hp2 | a0002 | c0002 | t0007 | g0310 | AFR | GWD | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG02723 | hp1 | a0001 | c0001 | t0017 | g0200 | AFR | GWD | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG02723 | hp2 | a0001 | c0001 | t0043 | g0005 | AFR | GWD | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0214 | SAS | PJL | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG02735 | hp2 | a0001 | c0001 | t0004 | g0244 | SAS | PJL | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG02738 | hp1 | a0001 | c0001 | t0004 | g0088 | SAS | PJL | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0181 | SAS | PJL | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG02818 | hp1 | a0001 | c0007 | t0013 | g0020 | AFR | GWD | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG02818 | hp2 | a0001 | c0001 | t0002 | g0194 | AFR | GWD | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG02886 | hp1 | a0001 | c0001 | t0009 | g0035 | AFR | GWD | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG02886 | hp2 | a0003 | c0003 | t0008 | g0204 | AFR | GWD | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG02895 | hp1 | a0002 | c0002 | t0009 | g0257 | AFR | GWD | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG02895 | hp2 | a0001 | c0001 | t0012 | g0336 | AFR | GWD | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG02896 | hp1 | a0003 | c0003 | t0039 | g0031 | AFR | GWD | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | GWD | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG02897 | hp1 | a0001 | c0001 | t0012 | g0338 | AFR | GWD | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG02897 | hp2 | a0003 | c0003 | t0024 | g0031 | AFR | GWD | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG02922 | hp1 | a0002 | c0002 | t0001 | g0321 | AFR | ESN | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG02922 | hp2 | a0003 | c0003 | t0008 | g0211 | AFR | ESN | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG02965 | hp1 | a0004 | c0005 | t0013 | g0276 | AFR | ESN | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG02965 | hp2 | a0003 | c0003 | t0008 | g0128 | AFR | ESN | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG02970 | hp1 | a0001 | c0001 | t0013 | g0195 | AFR | ESN | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | ESN | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG02976 | hp1 | a0001 | c0001 | t0012 | g0340 | AFR | ESN | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | ESN | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0144 | SAS | PJL | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG03041 | hp1 | a0001 | c0001 | t0007 | g0035 | AFR | GWD | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG03041 | hp2 | a0001 | c0001 | t0012 | g0005 | AFR | GWD | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG03098 | hp1 | a0001 | c0001 | t0038 | g0245 | AFR | MSL | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG03098 | hp2 | a0001 | c0001 | t0002 | g0339 | AFR | MSL | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG03130 | hp1 | a0001 | c0001 | t0002 | g0192 | AFR | ESN | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG03130 | hp2 | a0002 | c0002 | t0007 | g0279 | AFR | ESN | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG03139 | hp1 | a0004 | c0005 | t0013 | g0316 | AFR | ESN | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG03139 | hp2 | a0002 | c0002 | t0007 | g0312 | AFR | ESN | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG03195 | hp1 | a0001 | c0001 | t0017 | g0196 | AFR | ESN | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG03195 | hp2 | a0002 | c0002 | t0001 | g0311 | AFR | ESN | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG03209 | hp1 | a0004 | c0005 | t0027 | g0317 | AFR | MSL | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG03209 | hp2 | a0001 | c0009 | t0033 | g0210 | AFR | MSL | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG03453 | hp1 | a0002 | c0002 | t0004 | g0323 | AFR | MSL | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG03453 | hp2 | a0003 | c0003 | t0008 | g0198 | AFR | MSL | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG03486 | hp1 | a0003 | c0003 | t0008 | g0201 | AFR | MSL | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG03486 | hp2 | a0001 | c0001 | t0002 | g0130 | AFR | MSL | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG03490 | hp1 | a0001 | c0001 | t0002 | g0139 | SAS | PJL | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG03490 | hp2 | a0001 | c0001 | t0006 | g0138 | SAS | PJL | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0283 | SAS | PJL | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG03492 | hp1 | a0001 | c0001 | t0006 | g0027 | SAS | PJL | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG03516 | hp1 | a0001 | c0001 | t0004 | g0034 | AFR | ESN | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG03516 | hp2 | a0002 | c0002 | t0018 | g0290 | AFR | ESN | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG03540 | hp1 | a0003 | c0003 | t0008 | g0033 | AFR | GWD | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG03540 | hp2 | a0001 | c0001 | t0014 | g0246 | AFR | GWD | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG03579 | hp1 | a0001 | c0001 | t0014 | g0255 | AFR | MSL | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG03579 | hp2 | a0006 | c0014 | t0026 | g0261 | AFR | MSL | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG03669 | hp2 | a0001 | c0001 | t0006 | g0027 | SAS | PJL | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG03704 | hp1 | a0001 | c0001 | t0004 | g0292 | SAS | PJL | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG03704 | hp2 | a0001 | c0001 | t0004 | g0274 | SAS | PJL | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0186 | SAS | PJL | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG03710 | hp2 | a0001 | c0001 | t0006 | g0159 | SAS | PJL | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG03831 | hp1 | a0001 | c0001 | t0034 | g0001 | SAS | BEB | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG03831 | hp2 | a0002 | c0002 | t0009 | g0256 | SAS | BEB | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0189 | SAS | BEB | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG03834 | hp2 | a0001 | c0001 | t0003 | g0105 | SAS | BEB | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0269 | SAS | BEB | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0178 | SAS | BEB | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG03942 | hp1 | a0002 | c0002 | t0009 | g0231 | SAS | BEB | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG03942 | hp2 | a0001 | c0001 | t0005 | g0084 | SAS | BEB | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG04115 | hp1 | a0001 | c0001 | t0011 | g0160 | SAS | STU | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG04115 | hp2 | a0001 | c0001 | t0004 | g0191 | SAS | STU | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0282 | SAS | BEB | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0056 | SAS | BEB | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0026 | SAS | STU | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG04199 | hp2 | a0001 | c0001 | t0011 | g0238 | SAS | STU | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG04204 | hp1 | a0001 | c0001 | t0004 | g0158 | SAS | STU | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG04204 | hp2 | a0001 | c0001 | t0004 | g0265 | SAS | STU | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA18522 | hp1 | a0001 | c0001 | t0012 | g0090 | AFR | YRI | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA18522 | hp2 | a0003 | c0003 | t0008 | g0033 | AFR | YRI | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0061 | EAS | CHB | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA18612 | hp2 | a0001 | c0001 | t0044 | g0140 | EAS | CHB | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0117 | EAS | CHB | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0030 | EAS | CHB | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA18906 | hp1 | a0002 | c0004 | t0010 | g0331 | AFR | YRI | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA18906 | hp2 | a0004 | c0005 | t0027 | g0281 | AFR | YRI | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA18939 | hp1 | a0002 | c0002 | t0002 | g0288 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA18939 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA18940 | hp2 | a0001 | c0001 | t0003 | g0124 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA18941 | hp1 | a0001 | c0001 | t0005 | g0071 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA18941 | hp2 | a0001 | c0001 | t0003 | g0096 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA18942 | hp1 | a0001 | c0001 | t0003 | g0120 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA18942 | hp2 | a0001 | c0001 | t0006 | g0137 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA18945 | hp1 | a0001 | c0001 | t0005 | g0021 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA18945 | hp2 | a0001 | c0001 | t0002 | g0293 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA18947 | hp2 | a0001 | c0001 | t0003 | g0103 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA18949 | hp2 | a0002 | c0002 | t0001 | g0240 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA18950 | hp1 | a0001 | c0001 | t0004 | g0039 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA18950 | hp2 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA18951 | hp1 | a0002 | c0002 | t0040 | g0319 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA18952 | hp1 | a0001 | c0006 | t0010 | g0001 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA18952 | hp2 | a0002 | c0004 | t0010 | g0329 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA18954 | hp1 | a0001 | c0001 | t0003 | g0106 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA18954 | hp2 | a0001 | c0001 | t0025 | g0013 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA18956 | hp1 | a0002 | c0002 | t0001 | g0258 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA18956 | hp2 | a0001 | c0001 | t0025 | g0285 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA18959 | hp1 | a0001 | c0001 | t0004 | g0036 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA18959 | hp2 | a0001 | c0001 | t0006 | g0150 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA18960 | hp2 | a0002 | c0004 | t0010 | g0298 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA18961 | hp2 | a0005 | c0008 | t0003 | g0051 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA18963 | hp1 | a0001 | c0001 | t0003 | g0122 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA18963 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA18965 | hp2 | a0001 | c0001 | t0005 | g0008 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA18966 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA18966 | hp2 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA18967 | hp1 | a0001 | c0001 | t0041 | g0040 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA18967 | hp2 | a0001 | c0001 | t0005 | g0078 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA18969 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA18969 | hp2 | a0005 | c0008 | t0005 | g0052 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA18970 | hp2 | a0001 | c0001 | t0003 | g0111 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA18971 | hp2 | a0002 | c0004 | t0010 | g0275 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA18973 | hp1 | a0001 | c0001 | t0003 | g0109 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA18973 | hp2 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA18978 | hp2 | a0001 | c0001 | t0005 | g0093 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA18980 | hp1 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA18980 | hp2 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA18982 | hp2 | a0001 | c0001 | t0003 | g0068 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA18983 | hp1 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA18983 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA18986 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA18986 | hp2 | a0002 | c0002 | t0002 | g0037 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA18988 | hp1 | a0001 | c0001 | t0028 | g0308 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA18990 | hp1 | a0001 | c0001 | t0003 | g0091 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA18990 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA18993 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA18993 | hp2 | a0001 | c0001 | t0006 | g0301 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA18995 | hp1 | a0001 | c0001 | t0004 | g0039 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA18997 | hp1 | a0001 | c0001 | t0029 | g0149 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA18997 | hp2 | a0001 | c0001 | t0004 | g0118 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA18999 | hp1 | a0002 | c0002 | t0011 | g0114 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA18999 | hp2 | a0001 | c0001 | t0003 | g0104 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA19000 | hp1 | a0001 | c0001 | t0004 | g0233 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA19002 | hp2 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA19003 | hp1 | a0001 | c0001 | t0005 | g0021 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA19003 | hp2 | a0001 | c0006 | t0010 | g0270 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA19004 | hp1 | a0002 | c0002 | t0002 | g0294 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA19004 | hp2 | a0001 | c0001 | t0026 | g0079 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA19007 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA19007 | hp2 | a0001 | c0001 | t0003 | g0086 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA19010 | hp1 | a0001 | c0001 | t0015 | g0040 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA19011 | hp1 | a0001 | c0001 | t0005 | g0080 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA19011 | hp2 | a0001 | c0001 | t0003 | g0095 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA19012 | hp1 | a0001 | c0001 | t0003 | g0121 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA19012 | hp2 | a0002 | c0002 | t0001 | g0037 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA19030 | hp1 | a0001 | c0001 | t0019 | g0165 | AFR | LWK | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | LWK | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA19043 | hp1 | a0001 | c0001 | t0002 | g0335 | AFR | LWK | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA19043 | hp2 | a0001 | c0001 | t0007 | g0209 | AFR | LWK | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA19054 | hp1 | a0001 | c0001 | t0002 | g0328 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA19054 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA19056 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA19056 | hp2 | a0001 | c0001 | t0003 | g0110 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA19057 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA19057 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA19058 | hp2 | a0001 | c0001 | t0003 | g0073 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA19060 | hp1 | a0001 | c0001 | t0003 | g0094 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA19060 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA19063 | hp2 | a0001 | c0001 | t0003 | g0024 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA19064 | hp1 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA19065 | hp2 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA19066 | hp2 | a0001 | c0001 | t0004 | g0017 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA19068 | hp1 | a0001 | c0001 | t0002 | g0162 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA19068 | hp2 | a0001 | c0001 | t0005 | g0151 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA19072 | hp1 | a0002 | c0004 | t0016 | g0263 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA19072 | hp2 | a0002 | c0002 | t0002 | g0074 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA19074 | hp1 | a0001 | c0001 | t0005 | g0232 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA19074 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA19077 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA19077 | hp2 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA19078 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA19078 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA19081 | hp1 | a0002 | c0002 | t0007 | g0234 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA19081 | hp2 | a0001 | c0001 | t0015 | g0157 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA19082 | hp1 | a0002 | c0002 | t0007 | g0318 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA19082 | hp2 | a0001 | c0001 | t0004 | g0108 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA19083 | hp1 | a0001 | c0001 | t0005 | g0179 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA19083 | hp2 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA19084 | hp1 | a0001 | c0001 | t0003 | g0092 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA19084 | hp2 | a0001 | c0001 | t0006 | g0152 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA19085 | hp1 | a0001 | c0001 | t0015 | g0003 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA19086 | hp1 | a0001 | c0001 | t0003 | g0289 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA19088 | hp1 | a0007 | c0018 | t0002 | g0001 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA19088 | hp2 | a0001 | c0001 | t0003 | g0087 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA19089 | hp1 | a0001 | c0001 | t0005 | g0064 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA19089 | hp2 | a0001 | c0001 | t0042 | g0085 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA19090 | hp1 | a0001 | c0001 | t0005 | g0069 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA19091 | hp1 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA19240 | hp1 | a0001 | c0001 | t0022 | g0314 | AFR | YRI | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA19240 | hp2 | a0003 | c0003 | t0024 | g0203 | AFR | YRI | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA20129 | hp1 | a0001 | c0001 | t0005 | g0008 | AFR | ASW | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA20129 | hp2 | a0001 | c0001 | t0035 | g0167 | AFR | ASW | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0175 | EUR | TSI | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA20752 | hp2 | a0001 | c0001 | t0006 | g0224 | EUR | TSI | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA20805 | hp1 | a0002 | c0002 | t0009 | g0041 | EUR | TSI | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0145 | EUR | TSI | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA20905 | hp1 | a0001 | c0001 | t0037 | g0147 | SAS | GIH | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA20905 | hp2 | a0001 | c0001 | t0011 | g0264 | SAS | GIH | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG02109 | hp1 | a0001 | c0001 | t0014 | g0260 | AFR | ACB | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG02109 | hp2 | a0001 | c0001 | t0007 | g0197 | AFR | ACB | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG02486 | hp1 | a0001 | c0001 | t0002 | g0249 | AFR | ACB | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | ACB | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG02559 | hp1 | a0004 | c0011 | t0002 | g0116 | AFR | ACB | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG02559 | hp2 | a0001 | c0001 | t0004 | g0034 | AFR | ACB | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG03471 | hp1 | a0002 | c0002 | t0032 | g0042 | AFR | MSL | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG03471 | hp2 | a0002 | c0002 | t0007 | g0133 | AFR | MSL | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG06807 | hp1 | a0002 | c0004 | t0010 | g0278 | AFR | USA | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | USA | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA20300 | hp1 | a0001 | c0001 | t0018 | g0129 | AFR | USA | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA20300 | hp2 | a0001 | c0009 | t0020 | g0107 | AFR | USA | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA21309 | hp1 | a0001 | c0001 | t0007 | g0015 | AFR | LWK | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
NA21309 | hp2 | a0001 | c0001 | t0006 | g0184 | AFR | LWK | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0174 | REF | REF | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0248 | REF | REF | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:51251545
|
C | A | 1 | a0011 | 1 | HG01884.hp2 | missense_variant | MODERATE | c.178C>A | p.Pro60Thr | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/4 | 282/4728 | 178/1641 | 60/546 | chr13 | 51251545 | ||
chr13:51251614
|
G | A | 1 | a0010 | 1 | HG00140.hp2 | missense_variant | MODERATE | c.247G>A | p.Glu83Lys | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/4 | 351/4728 | 247/1641 | 83/546 | chr13 | 51251614 | ||
chr13:51251656
|
G | A | 1 | a0005 | 2 | NA18961.hp2 NA18969.hp2 |
missense_variant | MODERATE | c.289G>A | p.Ala97Thr | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/4 | 393/4728 | 289/1641 | 97/546 | chr13 | 51251656 | ||
chr13:51251903
|
G | T | 1 | a0011 | 1 | HG01884.hp2 | missense_variant | MODERATE | c.536G>T | p.Arg179Leu | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/4 | 640/4728 | 536/1641 | 179/546 | chr13 | 51251903 | ||
chr13:51251908
|
G | C | 2 | a0002a0009 | 44 | HG00140.hp1 HG00323.hp2 HG01074.hp2 others(41): Show |
missense_variant | MODERATE | c.541G>C | p.Asp181His | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/4 | 645/4728 | 541/1641 | 181/546 | chr13 | 51251908 | ||
chr13:51280514
|
G | A | 1 | a0006 | 1 | HG03579.hp2 | missense_variant | MODERATE | c.899G>A | p.Arg300His | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 4/4 | 1003/4728 | 899/1641 | 300/546 | chr13 | 51280514 | ||
chr13:51280532
|
C | T | 1 | a0007 | 1 | NA19088.hp1 | missense_variant | MODERATE | c.917C>T | p.Pro306Leu | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 4/4 | 1021/4728 | 917/1641 | 306/546 | chr13 | 51280532 | ||
chr13:51280648
|
G | A | 1 | a0008 | 1 | HG01175.hp2 | missense_variant | MODERATE | c.1033G>A | p.Gly345Arg | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 4/4 | 1137/4728 | 1033/1641 | 345/546 | chr13 | 51280648 | ||
chr13:51280907
|
A | G | 2 | a0003a0009 | 13 | HG01192.hp2 HG01884.hp1 HG01975.hp1 others(10): Show |
missense_variant | MODERATE | c.1292A>G | p.Tyr431Cys | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 4/4 | 1396/4728 | 1292/1641 | 431/546 | chr13 | 51280907 | ||
chr13:51280978
|
G | T | 1 | a0004 | 7 | HG01891.hp1 HG02559.hp1 HG02572.hp2 others(4): Show |
missense_variant | MODERATE | c.1363G>T | p.Ala455Ser | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 4/4 | 1467/4728 | 1363/1641 | 455/546 | chr13 | 51280978 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:51251598
|
G | A | 3 | a0001c0007a0004c0011a0011c0010 | 5 | HG01884.hp2 HG01891.hp2 HG02559.hp1 others(2): Show |
synonymous_variant | LOW | c.231G>A | p.Pro77Pro | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/4 | 335/4728 | 231/1641 | 77/546 | chr13 | 51251598 | ||
chr13:51280503
|
C | T | 2 | a0001c0009a0011c0010 | 3 | HG01884.hp2 HG03209.hp2 NA20300.hp2 |
synonymous_variant | LOW | c.888C>T | p.Ser296Ser | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 4/4 | 992/4728 | 888/1641 | 296/546 | chr13 | 51280503 | ||
chr13:51280815
|
C | T | 1 | a0001c0017 | 1 | HG02647.hp1 | synonymous_variant | LOW | c.1200C>T | p.Leu400Leu | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 4/4 | 1304/4728 | 1200/1641 | 400/546 | chr13 | 51280815 | ||
chr13:51280824
|
C | T | 1 | a0006c0014 | 1 | HG03579.hp2 | synonymous_variant | LOW | c.1209C>T | p.Ile403Ile | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 4/4 | 1313/4728 | 1209/1641 | 403/546 | chr13 | 51280824 | ||
chr13:51280950
|
C | T | 1 | a0001c0016 | 1 | HG00408.hp2 | synonymous_variant | LOW | c.1335C>T | p.Leu445Leu | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 4/4 | 1439/4728 | 1335/1641 | 445/546 | chr13 | 51280950 | ||
chr13:51280956
|
C | T | 2 | a0001c0006a0002c0004 | 11 | HG00423.hp1 HG02132.hp2 HG02280.hp1 others(8): Show |
synonymous_variant | LOW | c.1341C>T | p.Ser447Ser | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 4/4 | 1445/4728 | 1341/1641 | 447/546 | chr13 | 51280956 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:51222416
|
C | T | 1 | a0001c0001t0044 | 1 | NA18612.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-86C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/4 | chr13 | 51222416 | ||||||
chr13:51281343
|
A | G | 1 | a0001c0001t0043 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*87A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 4/4 | 87 | chr13 | 51281343 | |||||
chr13:51281403
|
T | TG | 6 | a0001c0001t0006a0001c0001t0011a0001c0001t0028others(3): Show | 26 | HG00140.hp2 HG00544.hp1 HG01069.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*153dupG | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 4/4 | 154 | INFO_REALIGN_3_PRIME | chr13 | 51281403 | ||||
chr13:51281570
|
AAAG | A | 7 | a0001c0001t0007a0001c0001t0009a0001c0001t0030others(4): Show | 28 | HG00323.hp2 HG00738.hp2 HG01070.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*317_*319delGAA | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 4/4 | 317 | INFO_REALIGN_3_PRIME | chr13 | 51281570 | ||||
chr13:51281812
|
G | T | 1 | a0004c0005t0027 | 2 | HG03209.hp1 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*556G>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 4/4 | 556 | chr13 | 51281812 | |||||
chr13:51281871
|
T | G | 3 | a0001c0009t0020a0001c0009t0033a0011c0010t0020 | 3 | HG01884.hp2 HG03209.hp2 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*615T>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 4/4 | 615 | chr13 | 51281871 | |||||
chr13:51281874
|
A | C | 11 | a0001c0001t0003a0001c0001t0005a0001c0001t0015others(8): Show | 67 | HG00408.hp1 HG00597.hp1 HG00621.hp2 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*618A>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 4/4 | 618 | chr13 | 51281874 | |||||
chr13:51282167
|
C | T | 1 | a0002c0002t0032 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*911C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 4/4 | 911 | chr13 | 51282167 | |||||
chr13:51282197
|
G | A | 1 | a0001c0001t0025 | 2 | NA18954.hp2 NA18956.hp2 |
3_prime_UTR_variant | MODIFIER | c.*941G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 4/4 | 941 | chr13 | 51282197 | |||||
chr13:51282263
|
A | T | 1 | a0001c0001t0042 | 1 | NA19089.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1007A>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 4/4 | 1007 | chr13 | 51282263 | |||||
chr13:51282303
|
C | T | 1 | a0002c0002t0040 | 1 | NA18951.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1047C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 4/4 | 1047 | chr13 | 51282303 | |||||
chr13:51282304
|
G | A | 1 | a0001c0009t0033 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1048G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 4/4 | 1048 | chr13 | 51282304 | |||||
chr13:51282323
|
G | A | 3 | a0001c0009t0020a0001c0009t0033a0011c0010t0020 | 3 | HG01884.hp2 HG03209.hp2 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1067G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 4/4 | 1067 | chr13 | 51282323 | |||||
chr13:51282349
|
T | G | 1 | a0001c0001t0021 | 2 | HG01168.hp1 HG01169.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1093T>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 4/4 | 1093 | chr13 | 51282349 | |||||
chr13:51282711
|
C | G | 2 | a0001c0001t0012a0001c0001t0014 | 11 | HG02109.hp1 HG02145.hp1 HG02257.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1455C>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 4/4 | 1455 | chr13 | 51282711 | |||||
chr13:51282954
|
C | CTT | 40 | a0001c0001t0003a0001c0001t0005a0001c0001t0006others(37): Show | 145 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(142): Show |
3_prime_UTR_variant | MODIFIER | c.*1699_*1700dupTT | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 4/4 | 1701 | INFO_REALIGN_3_PRIME | chr13 | 51282954 | ||||
chr13:51283045
|
A | C | 2 | a0003c0003t0024a0003c0003t0039 | 3 | HG02896.hp1 HG02897.hp2 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1789A>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 4/4 | 1789 | chr13 | 51283045 | |||||
chr13:51283065
|
G | A | 1 | a0001c0001t0034 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1809G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 4/4 | 1809 | chr13 | 51283065 | |||||
chr13:51283098
|
A | G | 6 | a0001c0001t0012a0001c0001t0014a0001c0001t0018others(3): Show | 17 | HG01243.hp1 HG02109.hp1 HG02145.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1842A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 4/4 | 1842 | chr13 | 51283098 | |||||
chr13:51283336
|
C | T | 1 | a0001c0001t0037 | 1 | NA20905.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2080C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 4/4 | 2080 | chr13 | 51283336 | |||||
chr13:51283446
|
C | T | 1 | a0001c0001t0038 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2190C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 4/4 | 2190 | chr13 | 51283446 | |||||
chr13:51283511
|
A | G | 15 | a0001c0001t0003a0001c0001t0005a0001c0001t0026others(12): Show | 76 | HG00408.hp1 HG00597.hp1 HG00621.hp2 others(73): Show |
3_prime_UTR_variant | MODIFIER | c.*2255A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 4/4 | 2255 | chr13 | 51283511 | |||||
chr13:51283589
|
C | G | 4 | a0003c0003t0008a0003c0003t0024a0003c0003t0039others(1): Show | 13 | HG01192.hp2 HG01884.hp1 HG01975.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2333C>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 4/4 | 2333 | chr13 | 51283589 | |||||
chr13:51283705
|
G | T | 3 | a0001c0009t0020a0001c0009t0033a0011c0010t0020 | 3 | HG01884.hp2 HG03209.hp2 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2449G>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 4/4 | 2449 | chr13 | 51283705 | |||||
chr13:51283767
|
C | CA | 17 | a0001c0001t0001a0001c0001t0005a0001c0001t0014others(14): Show | 141 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(138): Show |
3_prime_UTR_variant | MODIFIER | c.*2539dupA | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 4/4 | 2540 | INFO_REALIGN_3_PRIME | chr13 | 51283767 | ||||
chr13:51283767
|
C | CAA | 22 | a0001c0001t0004a0001c0001t0006a0001c0001t0007others(19): Show | 84 | HG00140.hp2 HG00544.hp1 HG00621.hp1 others(81): Show |
3_prime_UTR_variant | MODIFIER | c.*2538_*2539dupAA | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 4/4 | 2540 | INFO_REALIGN_3_PRIME | chr13 | 51283767 | ||||
chr13:51283767
|
C | CAAA | 8 | a0001c0001t0009a0001c0001t0011a0001c0001t0022others(5): Show | 21 | HG01069.hp2 HG01167.hp2 HG01169.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*2537_*2539dupAAA | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 4/4 | 2540 | INFO_REALIGN_3_PRIME | chr13 | 51283767 | ||||
chr13:51283767
|
C | CAAAAAAA others(3): Show |
2 | a0001c0009t0020a0011c0010t0020 | 2 | HG01884.hp2 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2530_*2539dupAAAA others(6): Show |
FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 4/4 | 2540 | INFO_REALIGN_3_PRIME | chr13 | 51283767 | ||||
chr13:51283767
|
CAAAAAAA others(2): Show |
C | 3 | a0003c0003t0008a0003c0003t0024a0009c0013t0008 | 12 | HG01192.hp2 HG01884.hp1 HG01975.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2531_*2539delAAAA others(5): Show |
FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 4/4 | 2531 | INFO_REALIGN_3_PRIME | chr13 | 51283767 | ||||
chr13:51283767
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0009t0033 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2530_*2539delAAAA others(6): Show |
FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 4/4 | 2530 | INFO_REALIGN_3_PRIME | chr13 | 51283767 | ||||
chr13:51283887
|
A | G | 1 | a0001c0001t0036 | 1 | HG00558.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2631A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 4/4 | 2631 | chr13 | 51283887 | |||||
chr13:51284030
|
A | C | 1 | a0001c0001t0028 | 1 | NA18988.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2774A>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 4/4 | 2774 | chr13 | 51284030 | |||||
chr13:51284171
|
T | C | 2 | a0001c0001t0030a0001c0001t0035 | 2 | HG02258.hp1 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2915T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 4/4 | 2915 | chr13 | 51284171 | |||||
chr13:51284208
|
T | C | 4 | a0001c0006t0010a0001c0006t0016a0002c0004t0010others(1): Show | 11 | HG00423.hp1 HG02132.hp2 HG02280.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2952T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 4/4 | 2952 | chr13 | 51284208 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:51222707
|
T | C | 216 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(213): Show | 241 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(238): Show |
intron_variant | MODIFIER | c.68+138T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51222707 | ||||||
chr13:51222838
|
C | G | 216 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(213): Show | 241 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(238): Show |
intron_variant | MODIFIER | c.68+269C>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51222838 | ||||||
chr13:51222958
|
A | G | 218 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(215): Show | 243 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(240): Show |
intron_variant | MODIFIER | c.68+389A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51222958 | ||||||
chr13:51223018
|
C | T | 1 | a0001c0001t0001g0208 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.68+449C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51223018 | ||||||
chr13:51223195
|
CT | C | 203 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(200): Show | 227 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(224): Show |
intron_variant | MODIFIER | c.68+639delT | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 51223195 | |||||
chr13:51223257
|
G | C | 37 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0016others(34): Show | 44 | HG00438.hp1 HG00738.hp2 HG01070.hp1 others(41): Show |
intron_variant | MODIFIER | c.68+688G>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51223257 | ||||||
chr13:51223296
|
C | A | 1 | a0011c0010t0020g0067 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.68+727C>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51223296 | ||||||
chr13:51223301
|
G | C | 233 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(230): Show | 258 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(255): Show |
intron_variant | MODIFIER | c.68+732G>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51223301 | ||||||
chr13:51223344
|
G | C | 1 | a0001c0001t0003g0068 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.68+775G>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51223344 | ||||||
chr13:51223414
|
C | G | 7 | a0001c0001t0001g0341a0001c0001t0002g0335a0001c0001t0002g0339others(4): Show | 7 | HG01243.hp2 HG02451.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.68+845C>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51223414 | ||||||
chr13:51223597
|
C | G | 1 | a0001c0001t0001g0226 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.68+1028C>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51223597 | ||||||
chr13:51223684
|
C | T | 2 | a0001c0001t0003g0342a0001c0006t0016g0343 | 2 | HG02280.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.68+1115C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51223684 | ||||||
chr13:51223829
|
C | CTG | 205 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(202): Show | 229 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(226): Show |
intron_variant | MODIFIER | c.68+1260_68+1261ins others(2): Show |
FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51223829 | ||||||
chr13:51223979
|
T | C | 3 | a0001c0001t0005g0069a0001c0001t0005g0070a0001c0001t0005g0071 | 3 | HG00597.hp1 NA18941.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.68+1410T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51223979 | ||||||
chr13:51224079
|
G | C | 3 | a0001c0001t0002g0228a0001c0001t0004g0034a0001c0001t0004g0227 | 4 | HG02055.hp1 HG02559.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.68+1510G>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51224079 | ||||||
chr13:51224194
|
T | C | 218 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(215): Show | 243 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(240): Show |
intron_variant | MODIFIER | c.68+1625T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51224194 | ||||||
chr13:51224230
|
T | A | 205 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(202): Show | 229 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(226): Show |
intron_variant | MODIFIER | c.68+1661T>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51224230 | ||||||
chr13:51224331
|
T | C | 205 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(202): Show | 229 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(226): Show |
intron_variant | MODIFIER | c.68+1762T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51224331 | ||||||
chr13:51224339
|
C | T | 1 | a0001c0001t0001g0225 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.68+1770C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51224339 | ||||||
chr13:51224433
|
T | G | 71 | a0001c0001t0001g0010a0001c0001t0001g0077a0001c0001t0001g0083others(68): Show | 80 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.68+1864T>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51224433 | ||||||
chr13:51224459
|
A | G | 204 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(201): Show | 228 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(225): Show |
intron_variant | MODIFIER | c.68+1890A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51224459 | ||||||
chr13:51224464
|
T | A | 119 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0010others(116): Show | 135 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.68+1895T>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51224464 | ||||||
chr13:51224465
|
C | A | 119 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0010others(116): Show | 135 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.68+1896C>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51224465 | ||||||
chr13:51224472
|
C | CA | 94 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(91): Show | 102 | HG00099.hp2 HG00438.hp2 HG00597.hp1 others(99): Show |
intron_variant | MODIFIER | c.68+1912dupA | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 51224472 | |||||
chr13:51224802
|
C | T | 1 | a0001c0001t0002g0126 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.68+2233C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51224802 | ||||||
chr13:51224884
|
C | T | 1 | a0010c0012t0006g0125 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.68+2315C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51224884 | ||||||
chr13:51224893
|
T | C | 1 | a0003c0003t0008g0128 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.68+2324T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51224893 | ||||||
chr13:51225056
|
A | C | 90 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(87): Show | 98 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.68+2487A>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51225056 | ||||||
chr13:51225131
|
T | C | 2 | a0002c0002t0001g0229a0009c0013t0008g0230 | 2 | HG01106.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.68+2562T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51225131 | ||||||
chr13:51225138
|
T | C | 3 | a0001c0001t0007g0035a0001c0001t0007g0209a0001c0001t0009g0035 | 3 | HG02886.hp1 HG03041.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.68+2569T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51225138 | ||||||
chr13:51225311
|
C | T | 13 | a0001c0001t0002g0202a0001c0001t0013g0032a0001c0001t0017g0032others(10): Show | 14 | HG01192.hp2 HG01884.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.68+2742C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51225311 | ||||||
chr13:51225361
|
T | C | 88 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(85): Show | 96 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.68+2792T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51225361 | ||||||
chr13:51225444
|
A | G | 3 | a0001c0001t0002g0192a0001c0001t0002g0193a0001c0001t0002g0194 | 3 | HG02572.hp1 HG02818.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.68+2875A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51225444 | ||||||
chr13:51225466
|
T | C | 206 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(203): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.68+2897T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51225466 | ||||||
chr13:51225499
|
C | T | 87 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(84): Show | 95 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.68+2930C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51225499 | ||||||
chr13:51225666
|
A | G | 4 | a0001c0001t0001g0223a0001c0001t0004g0134a0001c0001t0006g0224others(1): Show | 4 | HG00323.hp2 HG01070.hp2 HG01106.hp2 others(1): Show |
intron_variant | MODIFIER | c.68+3097A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51225666 | ||||||
chr13:51225770
|
G | A | 1 | a0002c0002t0009g0231 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.68+3201G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51225770 | ||||||
chr13:51225968
|
CTTGCTTT others(6): Show |
C | 1 | a0001c0001t0004g0191 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.68+3402_68+3414del others(13): Show |
FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 51225968 | |||||
chr13:51225968
|
CTTGCTTT others(7): Show |
C | 15 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0186others(12): Show | 17 | HG00099.hp1 HG00642.hp2 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.68+3402_68+3415del others(14): Show |
FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 51225968 | |||||
chr13:51225968
|
CTTGCTTT others(8): Show |
C | 2 | a0001c0001t0001g0182a0001c0001t0001g0183 | 2 | HG00639.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.68+3402_68+3416del others(15): Show |
FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 51225968 | |||||
chr13:51225975
|
T | G | 3 | a0001c0001t0007g0035a0001c0001t0009g0035a0003c0003t0008g0198 | 3 | HG02886.hp1 HG03041.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.68+3406T>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51225975 | ||||||
chr13:51225976
|
C | CT | 37 | a0001c0001t0001g0299a0001c0001t0001g0302a0001c0001t0001g0304others(34): Show | 38 | HG00558.hp2 HG01106.hp1 HG01109.hp2 others(35): Show |
intron_variant | MODIFIER | c.68+3442dupT | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 51225976 | |||||
chr13:51225976
|
C | CTT | 17 | a0001c0001t0001g0341a0001c0001t0002g0327a0001c0001t0002g0328others(14): Show | 17 | HG00140.hp1 HG00323.hp1 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.68+3441_68+3442dup others(2): Show |
FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 51225976 | |||||
chr13:51225976
|
C | CTTTTTTT others(4): Show |
1 | a0001c0006t0016g0343 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.68+3432_68+3442dup others(11): Show |
FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 51225976 | |||||
chr13:51225976
|
CT | C | 17 | a0001c0001t0001g0036a0001c0001t0001g0123a0001c0001t0001g0242others(14): Show | 18 | HG00733.hp1 HG01168.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.68+3442delT | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 51225976 | |||||
chr13:51225976
|
CTTTTTT | C | 7 | a0001c0001t0001g0063a0001c0001t0002g0065a0001c0001t0003g0120others(4): Show | 7 | HG00140.hp2 NA18942.hp1 NA18950.hp2 others(4): Show |
intron_variant | MODIFIER | c.68+3437_68+3442del others(6): Show |
FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 51225976 | |||||
chr13:51225976
|
CTTTTTTT | C | 90 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0010others(87): Show | 106 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.68+3436_68+3442del others(7): Show |
FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 51225976 | |||||
chr13:51225976
|
CTTTTTTT others(1): Show |
C | 8 | a0001c0001t0001g0043a0001c0001t0002g0013a0001c0001t0002g0044others(5): Show | 8 | HG01975.hp2 HG02165.hp2 NA18954.hp2 others(5): Show |
intron_variant | MODIFIER | c.68+3435_68+3442del others(8): Show |
FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 51225976 | |||||
chr13:51225976
|
CTTTTTTT others(3): Show |
C | 63 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0026others(60): Show | 69 | HG00099.hp2 HG00438.hp2 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.68+3433_68+3442del others(10): Show |
FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 51225976 | |||||
chr13:51225976
|
CTTTTTTT others(4): Show |
C | 11 | a0001c0001t0001g0131a0001c0001t0001g0136a0001c0001t0001g0206others(8): Show | 11 | HG02109.hp2 HG02970.hp1 HG02976.hp2 others(8): Show |
intron_variant | MODIFIER | c.68+3432_68+3442del others(11): Show |
FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 51225976 | |||||
chr13:51225976
|
CTTTTTTT others(5): Show |
C | 13 | a0001c0001t0002g0135a0001c0001t0002g0202a0001c0001t0013g0032others(10): Show | 14 | HG01192.hp2 HG01884.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.68+3431_68+3442del others(12): Show |
FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 51225976 | |||||
chr13:51225976
|
CTTTTTTT others(6): Show |
C | 16 | a0001c0001t0001g0214a0001c0001t0001g0216a0001c0001t0001g0217others(13): Show | 16 | HG00280.hp1 HG00733.hp2 HG00735.hp1 others(13): Show |
intron_variant | MODIFIER | c.68+3430_68+3442del others(13): Show |
FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 51225976 | |||||
chr13:51225976
|
CTTTTTTT others(7): Show |
C | 3 | a0001c0001t0001g0223a0002c0002t0031g0222a0003c0003t0008g0211 | 3 | HG00323.hp2 HG01070.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.68+3429_68+3442del others(14): Show |
FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 51225976 | |||||
chr13:51225976
|
CTTTTTTT others(9): Show |
C | 7 | a0001c0001t0001g0237a0001c0001t0002g0235a0001c0001t0004g0233others(4): Show | 7 | HG00544.hp1 HG00558.hp1 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.68+3427_68+3442del others(16): Show |
FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 51225976 | |||||
chr13:51225976
|
CTTTTTTT others(10): Show |
C | 1 | a0001c0001t0005g0232 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.68+3426_68+3442del others(17): Show |
FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 51225976 | |||||
chr13:51225985
|
T | C | 1 | a0001c0001t0004g0191 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.68+3416T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51225985 | ||||||
chr13:51225986
|
T | C | 15 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0186others(12): Show | 17 | HG00099.hp1 HG00642.hp2 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.68+3417T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51225986 | ||||||
chr13:51225987
|
T | C | 2 | a0001c0001t0001g0182a0001c0001t0001g0183 | 2 | HG00639.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.68+3418T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51225987 | ||||||
chr13:51226061
|
T | C | 2 | a0001c0001t0007g0209a0003c0003t0008g0128 | 2 | HG02965.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.68+3492T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51226061 | ||||||
chr13:51226198
|
A | G | 1 | a0001c0001t0001g0131 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.68+3629A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51226198 | ||||||
chr13:51226318
|
A | G | 2 | a0001c0001t0001g0132a0002c0002t0007g0133 | 2 | HG02257.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.68+3749A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51226318 | ||||||
chr13:51226419
|
G | T | 1 | a0002c0002t0040g0319 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.68+3850G>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51226419 | ||||||
chr13:51226912
|
A | G | 126 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0010others(123): Show | 143 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(140): Show |
intron_variant | MODIFIER | c.68+4343A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51226912 | ||||||
chr13:51226921
|
G | T | 109 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0010others(106): Show | 125 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.68+4352G>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51226921 | ||||||
chr13:51226980
|
G | A | 1 | a0001c0001t0007g0209 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.69-4368G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51226980 | ||||||
chr13:51227222
|
C | G | 237 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(234): Show | 262 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.69-4126C>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51227222 | ||||||
chr13:51227280
|
C | T | 1 | a0001c0001t0001g0225 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.69-4068C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51227280 | ||||||
chr13:51227569
|
G | A | 1 | a0001c0001t0004g0291 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.69-3779G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51227569 | ||||||
chr13:51227885
|
T | G | 7 | a0001c0001t0001g0011a0001c0001t0001g0136a0001c0001t0001g0142others(4): Show | 9 | HG02523.hp2 NA18951.hp2 NA18966.hp1 others(6): Show |
intron_variant | MODIFIER | c.69-3463T>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51227885 | ||||||
chr13:51227965
|
A | G | 201 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0010others(198): Show | 214 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.69-3383A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51227965 | ||||||
chr13:51228222
|
GTAT | G | 3 | a0001c0001t0001g0287a0001c0001t0021g0247a0001c0001t0021g0286 | 3 | HG01167.hp1 HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.69-3124_69-3122del others(3): Show |
FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 51228222 | |||||
chr13:51228271
|
A | T | 1 | a0003c0003t0008g0128 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.69-3077A>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51228271 | ||||||
chr13:51228311
|
C | G | 73 | a0001c0001t0001g0077a0001c0001t0001g0083a0001c0001t0001g0098others(70): Show | 80 | HG00140.hp2 HG00597.hp1 HG00621.hp1 others(77): Show |
intron_variant | MODIFIER | c.69-3037C>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51228311 | ||||||
chr13:51228425
|
G | A | 1 | a0002c0002t0001g0321 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.69-2923G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51228425 | ||||||
chr13:51228461
|
C | T | 1 | a0001c0001t0001g0220 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.69-2887C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51228461 | ||||||
chr13:51228668
|
G | T | 1 | a0004c0011t0002g0116 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.69-2680G>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51228668 | ||||||
chr13:51228769
|
AG | A | 4 | a0001c0001t0015g0040a0001c0001t0015g0284a0001c0001t0025g0285others(1): Show | 4 | HG02074.hp2 NA18956.hp2 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.69-2577delG | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 51228769 | |||||
chr13:51229390
|
G | A | 5 | a0001c0001t0003g0289a0001c0001t0007g0035a0001c0001t0007g0209others(2): Show | 5 | HG01884.hp2 HG02886.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.69-1958G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51229390 | ||||||
chr13:51229477
|
T | C | 2 | a0001c0001t0003g0342a0001c0006t0016g0343 | 2 | HG02280.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.69-1871T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51229477 | ||||||
chr13:51229504
|
T | G | 1 | a0001c0001t0004g0292 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.69-1844T>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51229504 | ||||||
chr13:51229657
|
A | C | 1 | a0002c0002t0007g0318 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.69-1691A>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51229657 | ||||||
chr13:51229929
|
T | C | 15 | a0001c0001t0001g0077a0001c0001t0001g0083a0001c0001t0002g0018others(12): Show | 17 | HG00597.hp1 HG00621.hp1 HG00673.hp1 others(14): Show |
intron_variant | MODIFIER | c.69-1419T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51229929 | ||||||
chr13:51229948
|
C | G | 375 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(372): Show | 405 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(402): Show |
intron_variant | MODIFIER | c.69-1400C>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51229948 | ||||||
chr13:51230075
|
T | TTA | 73 | a0001c0001t0001g0077a0001c0001t0001g0083a0001c0001t0001g0098others(70): Show | 80 | HG00140.hp2 HG00597.hp1 HG00621.hp1 others(77): Show |
intron_variant | MODIFIER | c.69-1259_69-1258dup others(2): Show |
FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 51230075 | |||||
chr13:51230075
|
T | TTATATAT others(1): Show |
3 | a0001c0001t0001g0132a0001c0001t0004g0292a0002c0002t0007g0133 | 3 | HG02257.hp2 HG03471.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.69-1265_69-1258dup others(8): Show |
FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 51230075 | |||||
chr13:51230075
|
T | TTATATAT others(3): Show |
1 | a0004c0005t0023g0322 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.69-1267_69-1258dup others(10): Show |
FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 51230075 | |||||
chr13:51230075
|
T | TTATATAT others(5): Show |
1 | a0003c0003t0008g0211 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.69-1269_69-1258dup others(12): Show |
FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 51230075 | |||||
chr13:51230077
|
A | T | 13 | a0001c0001t0002g0202a0001c0001t0013g0032a0001c0001t0017g0032others(10): Show | 14 | HG01192.hp2 HG01884.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.69-1271A>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51230077 | ||||||
chr13:51230083
|
A | T | 1 | a0001c0001t0014g0246 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.69-1265A>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51230083 | ||||||
chr13:51230108
|
T | G | 1 | a0001c0001t0001g0132 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.69-1240T>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51230108 | ||||||
chr13:51230131
|
G | C | 1 | a0001c0001t0042g0085 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.69-1217G>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51230131 | ||||||
chr13:51230138
|
T | C | 3 | a0001c0001t0001g0333a0001c0001t0001g0334a0001c0001t0002g0332 | 3 | HG00099.hp1 HG01081.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.69-1210T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51230138 | ||||||
chr13:51230315
|
T | A | 3 | a0001c0001t0001g0132a0002c0002t0001g0321a0002c0002t0004g0323 | 3 | HG02257.hp2 HG02922.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.69-1033T>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51230315 | ||||||
chr13:51230460
|
A | T | 1 | a0001c0001t0038g0245 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.69-888A>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51230460 | ||||||
chr13:51230496
|
C | G | 2 | a0001c0001t0001g0283a0001c0001t0002g0282 | 2 | HG03491.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.69-852C>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51230496 | ||||||
chr13:51230529
|
G | A | 73 | a0001c0001t0001g0077a0001c0001t0001g0083a0001c0001t0001g0098others(70): Show | 80 | HG00140.hp2 HG00597.hp1 HG00621.hp1 others(77): Show |
intron_variant | MODIFIER | c.69-819G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51230529 | ||||||
chr13:51230569
|
C | T | 1 | a0001c0001t0002g0181 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.69-779C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51230569 | ||||||
chr13:51230707
|
A | G | 6 | a0001c0001t0001g0132a0001c0001t0004g0292a0001c0009t0033g0210others(3): Show | 6 | HG02257.hp2 HG02572.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.69-641A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51230707 | ||||||
chr13:51230855
|
G | C | 5 | a0001c0001t0001g0132a0001c0001t0004g0292a0002c0002t0007g0133others(2): Show | 5 | HG02257.hp2 HG02572.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.69-493G>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51230855 | ||||||
chr13:51230889
|
G | A | 71 | a0001c0001t0001g0077a0001c0001t0001g0083a0001c0001t0001g0098others(68): Show | 78 | HG00140.hp2 HG00597.hp1 HG00621.hp1 others(75): Show |
intron_variant | MODIFIER | c.69-459G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51230889 | ||||||
chr13:51231192
|
C | G | 2 | a0002c0002t0001g0229a0009c0013t0008g0230 | 2 | HG01106.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.69-156C>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51231192 | ||||||
chr13:51231196
|
A | G | 5 | a0001c0001t0001g0030a0001c0001t0001g0178a0001c0001t0002g0030others(2): Show | 5 | HG02129.hp2 HG03927.hp2 NA18747.hp2 others(2): Show |
intron_variant | MODIFIER | c.69-152A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51231196 | ||||||
chr13:51231234
|
T | C | 1 | a0001c0001t0001g0341 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.69-114T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51231234 | ||||||
chr13:51231666
|
C | T | 18 | a0001c0001t0022g0314a0001c0001t0023g0313a0002c0002t0001g0311others(15): Show | 18 | HG01074.hp2 HG01109.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.100+287C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51231666 | ||||||
chr13:51231945
|
T | C | 1 | a0001c0001t0004g0191 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.100+566T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51231945 | ||||||
chr13:51232173
|
A | G | 1 | a0002c0002t0002g0288 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.100+794A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51232173 | ||||||
chr13:51232254
|
T | C | 1 | a0001c0001t0003g0086 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.100+875T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51232254 | ||||||
chr13:51232304
|
C | CTTAT | 167 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(164): Show | 187 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(184): Show |
intron_variant | MODIFIER | c.100+928_100+931dup others(4): Show |
FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 51232304 | |||||
chr13:51232328
|
T | C | 1 | a0001c0001t0001g0132 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.100+949T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51232328 | ||||||
chr13:51232378
|
T | C | 1 | a0001c0001t0001g0182 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.100+999T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51232378 | ||||||
chr13:51232458
|
A | G | 1 | a0001c0001t0001g0190 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.100+1079A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51232458 | ||||||
chr13:51232562
|
A | G | 1 | a0001c0001t0001g0182 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.100+1183A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51232562 | ||||||
chr13:51232744
|
C | T | 1 | a0001c0001t0003g0342 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.100+1365C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51232744 | ||||||
chr13:51232795
|
A | G | 1 | a0002c0002t0009g0250 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.100+1416A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51232795 | ||||||
chr13:51232830
|
A | G | 1 | a0001c0001t0001g0283 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.100+1451A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51232830 | ||||||
chr13:51232861
|
C | T | 2 | a0001c0001t0001g0119a0001c0001t0001g0176 | 2 | HG00544.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.100+1482C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51232861 | ||||||
chr13:51232957
|
T | C | 91 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0077others(88): Show | 100 | HG00140.hp2 HG00597.hp1 HG00621.hp1 others(97): Show |
intron_variant | MODIFIER | c.100+1578T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51232957 | ||||||
chr13:51233052
|
G | A | 160 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(157): Show | 180 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(177): Show |
intron_variant | MODIFIER | c.100+1673G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51233052 | ||||||
chr13:51233109
|
G | A | 1 | a0001c0001t0002g0060 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.100+1730G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51233109 | ||||||
chr13:51233163
|
G | A | 164 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(161): Show | 184 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(181): Show |
intron_variant | MODIFIER | c.100+1784G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51233163 | ||||||
chr13:51233262
|
G | A | 8 | a0001c0001t0001g0017a0001c0001t0001g0066a0001c0001t0002g0062others(5): Show | 8 | HG00597.hp2 NA18945.hp2 NA18961.hp1 others(5): Show |
intron_variant | MODIFIER | c.100+1883G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51233262 | ||||||
chr13:51233389
|
T | C | 5 | a0001c0001t0001g0132a0001c0001t0004g0292a0002c0002t0007g0133others(2): Show | 5 | HG02257.hp2 HG02572.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.100+2010T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51233389 | ||||||
chr13:51233493
|
A | T | 1 | a0001c0001t0005g0084 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.100+2114A>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51233493 | ||||||
chr13:51233652
|
C | T | 68 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0011others(65): Show | 79 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.100+2273C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51233652 | ||||||
chr13:51233912
|
A | G | 161 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(158): Show | 181 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(178): Show |
intron_variant | MODIFIER | c.100+2533A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51233912 | ||||||
chr13:51233935
|
T | C | 373 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(370): Show | 403 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(400): Show |
intron_variant | MODIFIER | c.100+2556T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51233935 | ||||||
chr13:51234008
|
G | A | 2 | a0001c0001t0007g0035a0001c0001t0009g0035 | 2 | HG02886.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.100+2629G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51234008 | ||||||
chr13:51234076
|
C | G | 1 | a0002c0004t0010g0275 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.100+2697C>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51234076 | ||||||
chr13:51234106
|
G | A | 162 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(159): Show | 182 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(179): Show |
intron_variant | MODIFIER | c.100+2727G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51234106 | ||||||
chr13:51234224
|
T | C | 96 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0077others(93): Show | 105 | HG00140.hp2 HG00408.hp1 HG00597.hp1 others(102): Show |
intron_variant | MODIFIER | c.100+2845T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51234224 | ||||||
chr13:51234488
|
T | C | 107 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0077others(104): Show | 117 | HG00140.hp2 HG00597.hp1 HG00621.hp1 others(114): Show |
intron_variant | MODIFIER | c.100+3109T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51234488 | ||||||
chr13:51234501
|
G | A | 107 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0077others(104): Show | 117 | HG00140.hp2 HG00597.hp1 HG00621.hp1 others(114): Show |
intron_variant | MODIFIER | c.100+3122G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51234501 | ||||||
chr13:51234674
|
A | T | 1 | a0002c0002t0011g0114 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.100+3295A>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51234674 | ||||||
chr13:51234751
|
G | C | 1 | a0002c0002t0011g0114 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.100+3372G>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51234751 | ||||||
chr13:51234780
|
T | C | 38 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0016others(35): Show | 46 | HG00438.hp1 HG00438.hp2 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.100+3401T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51234780 | ||||||
chr13:51234846
|
A | G | 302 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(299): Show | 328 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(325): Show |
intron_variant | MODIFIER | c.100+3467A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51234846 | ||||||
chr13:51235065
|
G | A | 1 | a0001c0001t0003g0087 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.100+3686G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51235065 | ||||||
chr13:51235090
|
A | AT | 71 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0083others(68): Show | 75 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.100+3717dupT | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 51235090 | |||||
chr13:51235110
|
G | T | 1 | a0001c0001t0003g0111 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.100+3731G>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51235110 | ||||||
chr13:51235131
|
C | T | 1 | a0001c0001t0006g0152 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.100+3752C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51235131 | ||||||
chr13:51235303
|
T | C | 4 | a0001c0001t0001g0115a0001c0001t0002g0130a0001c0001t0003g0342others(1): Show | 4 | HG02258.hp1 HG02615.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.100+3924T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51235303 | ||||||
chr13:51235322
|
T | C | 1 | a0001c0001t0004g0088 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.100+3943T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51235322 | ||||||
chr13:51235346
|
ATTAT | A | 6 | a0001c0001t0001g0341a0001c0001t0002g0239a0001c0001t0002g0335others(3): Show | 6 | HG01243.hp2 HG02451.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.100+3972_100+3975d others(6): Show |
FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 51235346 | |||||
chr13:51235389
|
G | GA | 7 | a0001c0001t0012g0090a0001c0001t0030g0112a0001c0006t0016g0343others(4): Show | 7 | HG01891.hp2 HG02258.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.100+4017dupA | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 51235389 | |||||
chr13:51235420
|
C | T | 33 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0016others(30): Show | 41 | HG00438.hp1 HG00438.hp2 HG00738.hp2 others(38): Show |
intron_variant | MODIFIER | c.100+4041C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51235420 | ||||||
chr13:51235441
|
TTGAA | T | 4 | a0001c0001t0001g0115a0001c0001t0002g0130a0001c0001t0003g0342others(1): Show | 4 | HG02258.hp1 HG02615.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.100+4064_100+4067d others(6): Show |
FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 51235441 | |||||
chr13:51235516
|
A | G | 2 | a0001c0001t0001g0131a0001c0001t0018g0129 | 2 | HG02976.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.100+4137A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51235516 | ||||||
chr13:51235598
|
TA | T | 75 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0098others(72): Show | 81 | HG00140.hp2 HG00408.hp1 HG00597.hp1 others(78): Show |
intron_variant | MODIFIER | c.100+4220delA | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51235598 | ||||||
chr13:51235788
|
A | T | 1 | a0001c0001t0004g0292 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.100+4409A>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51235788 | ||||||
chr13:51235821
|
G | T | 1 | a0001c0001t0001g0175 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.100+4442G>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51235821 | ||||||
chr13:51235929
|
A | T | 1 | a0001c0001t0001g0309 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.100+4550A>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51235929 | ||||||
chr13:51236201
|
G | A | 2 | a0002c0002t0001g0311a0004c0005t0013g0276 | 2 | HG02965.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.100+4822G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51236201 | ||||||
chr13:51236376
|
T | G | 37 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0016others(34): Show | 45 | HG00438.hp1 HG00438.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.100+4997T>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51236376 | ||||||
chr13:51236526
|
A | C | 80 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0098others(77): Show | 87 | HG00140.hp2 HG00408.hp1 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.100+5147A>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51236526 | ||||||
chr13:51236580
|
C | T | 74 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0011others(71): Show | 85 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.100+5201C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51236580 | ||||||
chr13:51236671
|
G | T | 1 | a0001c0001t0007g0209 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.100+5292G>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51236671 | ||||||
chr13:51236817
|
A | G | 34 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0016others(31): Show | 42 | HG00438.hp1 HG00438.hp2 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.100+5438A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51236817 | ||||||
chr13:51236839
|
TAG | T | 38 | a0001c0001t0001g0011a0001c0001t0001g0026a0001c0001t0001g0131others(35): Show | 41 | HG00099.hp2 HG00639.hp2 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.100+5463_100+5464d others(4): Show |
FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 51236839 | |||||
chr13:51237015
|
C | A | 13 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0022others(10): Show | 17 | HG02074.hp1 NA18941.hp2 NA18965.hp2 others(14): Show |
intron_variant | MODIFIER | c.100+5636C>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51237015 | ||||||
chr13:51237115
|
A | C | 1 | a0011c0010t0020g0067 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.100+5736A>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51237115 | ||||||
chr13:51237235
|
A | C | 68 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0083others(65): Show | 71 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.100+5856A>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51237235 | ||||||
chr13:51237307
|
T | C | 1 | a0001c0001t0004g0292 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.100+5928T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51237307 | ||||||
chr13:51237348
|
G | C | 7 | a0001c0001t0001g0208a0001c0001t0002g0062a0001c0001t0002g0126others(4): Show | 7 | HG00423.hp2 HG00597.hp2 NA18945.hp2 others(4): Show |
intron_variant | MODIFIER | c.100+5969G>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51237348 | ||||||
chr13:51237364
|
A | G | 65 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0083others(62): Show | 68 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.100+5985A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51237364 | ||||||
chr13:51237573
|
G | A | 1 | a0003c0003t0008g0211 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.100+6194G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51237573 | ||||||
chr13:51237669
|
T | G | 227 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(224): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.100+6290T>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51237669 | ||||||
chr13:51237765
|
T | C | 1 | a0001c0009t0033g0210 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.100+6386T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51237765 | ||||||
chr13:51237789
|
TG | T | 45 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0083others(42): Show | 47 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.100+6411delG | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51237789 | ||||||
chr13:51238219
|
G | A | 3 | a0001c0001t0001g0098a0001c0001t0004g0088a0001c0001t0004g0292 | 3 | HG02738.hp1 HG03017.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.100+6840G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51238219 | ||||||
chr13:51238285
|
CA | C | 3 | a0001c0001t0002g0130a0001c0001t0003g0342a0001c0001t0030g0112 | 3 | HG02258.hp1 HG02615.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.100+6907delA | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51238285 | ||||||
chr13:51238286
|
A | T | 1 | a0011c0010t0020g0067 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.100+6907A>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51238286 | ||||||
chr13:51238396
|
C | T | 1 | a0003c0003t0008g0205 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.100+7017C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51238396 | ||||||
chr13:51238397
|
G | A | 1 | a0001c0001t0001g0047 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.100+7018G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51238397 | ||||||
chr13:51238489
|
A | C | 1 | a0001c0001t0002g0162 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.100+7110A>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51238489 | ||||||
chr13:51239000
|
A | T | 13 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0022others(10): Show | 17 | HG02074.hp1 NA18941.hp2 NA18965.hp2 others(14): Show |
intron_variant | MODIFIER | c.100+7621A>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51239000 | ||||||
chr13:51239019
|
G | A | 1 | a0004c0011t0002g0116 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.100+7640G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51239019 | ||||||
chr13:51239059
|
C | T | 1 | a0001c0001t0003g0110 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.100+7680C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51239059 | ||||||
chr13:51239253
|
A | G | 1 | a0001c0001t0005g0082 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.100+7874A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51239253 | ||||||
chr13:51239305
|
G | A | 1 | a0001c0009t0033g0210 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.100+7926G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51239305 | ||||||
chr13:51239642
|
A | G | 2 | a0004c0005t0027g0281a0004c0005t0027g0317 | 2 | HG03209.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.100+8263A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51239642 | ||||||
chr13:51239774
|
G | A | 3 | a0001c0001t0001g0049a0001c0001t0002g0044a0001c0001t0002g0048 | 3 | NA18940.hp1 NA18969.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.100+8395G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51239774 | ||||||
chr13:51239778
|
G | T | 1 | a0001c0001t0007g0209 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.100+8399G>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51239778 | ||||||
chr13:51239832
|
GTAGA | G | 35 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0016others(32): Show | 43 | HG00438.hp1 HG00438.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.100+8461_100+8464d others(6): Show |
FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 51239832 | |||||
chr13:51239867
|
G | A | 1 | a0001c0001t0002g0006 | 3 | HG01433.hp1 HG01952.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.100+8488G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51239867 | ||||||
chr13:51239895
|
T | C | 16 | a0001c0001t0002g0202a0001c0001t0004g0292a0001c0001t0013g0032others(13): Show | 17 | HG01192.hp2 HG01884.hp1 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.100+8516T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51239895 | ||||||
chr13:51240022
|
T | C | 1 | a0001c0001t0001g0123 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.100+8643T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51240022 | ||||||
chr13:51240198
|
G | A | 3 | a0001c0001t0001g0299a0002c0004t0010g0298a0002c0004t0010g0329 | 3 | NA18952.hp2 NA18960.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.100+8819G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51240198 | ||||||
chr13:51240228
|
C | T | 16 | a0001c0001t0002g0202a0001c0001t0004g0292a0001c0001t0013g0032others(13): Show | 17 | HG01192.hp2 HG01884.hp1 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.100+8849C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51240228 | ||||||
chr13:51240295
|
C | T | 5 | a0001c0001t0005g0151a0001c0001t0006g0137a0001c0001t0006g0150others(2): Show | 5 | NA18942.hp2 NA18959.hp2 NA18988.hp1 others(2): Show |
intron_variant | MODIFIER | c.100+8916C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51240295 | ||||||
chr13:51240391
|
T | G | 163 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(160): Show | 175 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.100+9012T>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51240391 | ||||||
chr13:51240596
|
G | T | 1 | a0004c0011t0002g0116 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.100+9217G>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51240596 | ||||||
chr13:51240605
|
A | G | 15 | a0001c0001t0001g0237a0001c0001t0001g0333a0001c0001t0001g0334others(12): Show | 15 | HG00544.hp1 HG00558.hp1 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.100+9226A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51240605 | ||||||
chr13:51240629
|
G | A | 1 | a0001c0001t0002g0332 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.100+9250G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51240629 | ||||||
chr13:51240650
|
C | T | 2 | a0002c0002t0001g0229a0009c0013t0008g0230 | 2 | HG01106.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.100+9271C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51240650 | ||||||
chr13:51240845
|
C | T | 1 | a0001c0001t0007g0209 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.100+9466C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51240845 | ||||||
chr13:51240917
|
A | G | 5 | a0001c0001t0012g0090a0001c0006t0016g0343a0001c0007t0001g0020others(2): Show | 5 | HG01891.hp2 HG02280.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.100+9538A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51240917 | ||||||
chr13:51241143
|
TA | T | 3 | a0001c0001t0001g0132a0004c0005t0027g0281a0004c0005t0027g0317 | 3 | HG02257.hp2 HG03209.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.100+9768delA | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 51241143 | |||||
chr13:51241217
|
A | G | 1 | a0001c0001t0030g0112 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.100+9838A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51241217 | ||||||
chr13:51241287
|
C | A | 1 | a0001c0001t0002g0185 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.100+9908C>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51241287 | ||||||
chr13:51241303
|
T | TC | 5 | a0001c0001t0012g0090a0001c0006t0016g0343a0001c0007t0001g0020others(2): Show | 5 | HG01891.hp2 HG02280.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.100+9925dupC | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 51241303 | |||||
chr13:51241305
|
A | G | 109 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0017others(106): Show | 118 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.100+9926A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51241305 | ||||||
chr13:51241416
|
C | T | 3 | a0001c0001t0003g0073a0001c0001t0003g0109a0001c0001t0003g0111 | 3 | NA18970.hp2 NA18973.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.100+10037C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51241416 | ||||||
chr13:51241702
|
A | C | 1 | a0001c0001t0004g0108 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.101-9766A>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51241702 | ||||||
chr13:51241741
|
CA | C | 225 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0010others(222): Show | 244 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.101-9714delA | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 51241741 | |||||
chr13:51241741
|
CAA | C | 45 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0083others(42): Show | 47 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.101-9715_101-9714d others(4): Show |
FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 51241741 | |||||
chr13:51241787
|
G | T | 1 | a0001c0001t0007g0209 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.101-9681G>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51241787 | ||||||
chr13:51241986
|
G | T | 35 | a0001c0001t0001g0011a0001c0001t0001g0026a0001c0001t0001g0136others(32): Show | 38 | HG00099.hp2 HG00639.hp2 HG01069.hp1 others(35): Show |
intron_variant | MODIFIER | c.101-9482G>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51241986 | ||||||
chr13:51241997
|
C | T | 2 | a0001c0001t0004g0244a0001c0001t0006g0177 | 2 | HG01934.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.101-9471C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51241997 | ||||||
chr13:51242098
|
T | C | 1 | a0001c0001t0001g0050 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.101-9370T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51242098 | ||||||
chr13:51242183
|
G | A | 1 | a0001c0001t0002g0130 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.101-9285G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51242183 | ||||||
chr13:51242209
|
G | A | 1 | a0002c0002t0007g0277 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.101-9259G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51242209 | ||||||
chr13:51242259
|
TG | T | 16 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0038others(13): Show | 18 | HG00280.hp1 HG00323.hp1 HG00544.hp2 others(15): Show |
intron_variant | MODIFIER | c.101-9207delG | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 51242259 | |||||
chr13:51242268
|
G | C | 1 | a0001c0006t0016g0343 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.101-9200G>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51242268 | ||||||
chr13:51242315
|
A | G | 1 | a0001c0001t0006g0155 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.101-9153A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51242315 | ||||||
chr13:51242322
|
C | A | 1 | a0010c0012t0006g0125 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.101-9146C>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51242322 | ||||||
chr13:51242361
|
A | G | 17 | a0001c0001t0002g0202a0001c0001t0004g0292a0001c0001t0013g0032others(14): Show | 18 | HG01192.hp2 HG01884.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.101-9107A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51242361 | ||||||
chr13:51242478
|
A | C | 5 | a0001c0001t0012g0090a0001c0006t0016g0343a0001c0007t0001g0020others(2): Show | 5 | HG01891.hp2 HG02280.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.101-8990A>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51242478 | ||||||
chr13:51242509
|
A | G | 1 | a0001c0001t0002g0339 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.101-8959A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51242509 | ||||||
chr13:51242529
|
T | C | 327 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(324): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(354): Show |
intron_variant | MODIFIER | c.101-8939T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51242529 | ||||||
chr13:51242724
|
C | T | 1 | a0001c0001t0005g0097 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.101-8744C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51242724 | ||||||
chr13:51242752
|
C | T | 1 | a0002c0002t0009g0280 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.101-8716C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51242752 | ||||||
chr13:51242826
|
C | T | 1 | a0001c0001t0030g0112 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.101-8642C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51242826 | ||||||
chr13:51242835
|
T | A | 2 | a0002c0002t0002g0330a0002c0002t0007g0310 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.101-8633T>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51242835 | ||||||
chr13:51242899
|
C | G | 1 | a0001c0001t0030g0112 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.101-8569C>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51242899 | ||||||
chr13:51243007
|
G | A | 84 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(81): Show | 89 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.101-8461G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51243007 | ||||||
chr13:51243081
|
T | G | 1 | a0001c0001t0042g0085 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.101-8387T>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51243081 | ||||||
chr13:51243208
|
C | G | 1 | a0001c0001t0002g0045 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.101-8260C>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51243208 | ||||||
chr13:51243359
|
C | T | 60 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0043others(57): Show | 65 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.101-8109C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51243359 | ||||||
chr13:51243456
|
C | G | 1 | a0001c0001t0005g0071 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.101-8012C>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51243456 | ||||||
chr13:51243514
|
C | T | 194 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0010others(191): Show | 208 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.101-7954C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51243514 | ||||||
chr13:51243534
|
G | T | 1 | a0001c0001t0002g0174 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.101-7934G>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51243534 | ||||||
chr13:51243584
|
G | A | 194 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0010others(191): Show | 208 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.101-7884G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51243584 | ||||||
chr13:51243698
|
T | G | 1 | a0001c0001t0007g0209 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.101-7770T>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51243698 | ||||||
chr13:51243723
|
A | G | 2 | a0001c0001t0003g0009a0001c0001t0003g0096 | 4 | NA18941.hp2 NA19007.hp1 NA19054.hp2 others(1): Show |
intron_variant | MODIFIER | c.101-7745A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51243723 | ||||||
chr13:51243787
|
C | T | 31 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0016others(28): Show | 39 | HG00438.hp1 HG00438.hp2 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.101-7681C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51243787 | ||||||
chr13:51243952
|
G | T | 1 | a0001c0001t0014g0255 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.101-7516G>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51243952 | ||||||
chr13:51243986
|
G | T | 1 | a0001c0001t0002g0307 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.101-7482G>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51243986 | ||||||
chr13:51244348
|
G | A | 114 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0011others(111): Show | 125 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.101-7120G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51244348 | ||||||
chr13:51244392
|
A | G | 1 | a0001c0009t0033g0210 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.101-7076A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51244392 | ||||||
chr13:51244642
|
C | G | 1 | a0001c0001t0001g0161 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.101-6826C>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51244642 | ||||||
chr13:51244805
|
C | T | 299 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(296): Show | 323 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(320): Show |
intron_variant | MODIFIER | c.101-6663C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51244805 | ||||||
chr13:51244836
|
C | T | 1 | a0001c0001t0011g0160 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.101-6632C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51244836 | ||||||
chr13:51244950
|
A | G | 3 | a0001c0001t0002g0130a0001c0001t0003g0342a0001c0001t0007g0209 | 3 | HG02615.hp1 HG03486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.101-6518A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51244950 | ||||||
chr13:51244965
|
G | A | 1 | a0001c0001t0004g0164 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.101-6503G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51244965 | ||||||
chr13:51245099
|
G | A | 2 | a0001c0001t0002g0130a0001c0001t0003g0342 | 2 | HG02615.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.101-6369G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51245099 | ||||||
chr13:51245131
|
A | G | 15 | a0001c0001t0002g0202a0001c0001t0013g0032a0001c0001t0017g0032others(12): Show | 16 | HG01192.hp2 HG01884.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.101-6337A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51245131 | ||||||
chr13:51245211
|
G | A | 2 | a0001c0001t0013g0032a0001c0001t0017g0032 | 2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.101-6257G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51245211 | ||||||
chr13:51245303
|
A | G | 2 | a0001c0001t0001g0049a0001c0001t0002g0044 | 2 | NA18940.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.101-6165A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51245303 | ||||||
chr13:51245330
|
G | A | 6 | a0001c0001t0001g0049a0001c0001t0002g0044a0001c0001t0002g0048others(3): Show | 6 | HG03209.hp2 NA18940.hp1 NA18969.hp1 others(3): Show |
intron_variant | MODIFIER | c.101-6138G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51245330 | ||||||
chr13:51245398
|
G | A | 1 | a0002c0002t0002g0330 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.101-6070G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51245398 | ||||||
chr13:51245830
|
G | A | 1 | a0001c0001t0004g0292 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.101-5638G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51245830 | ||||||
chr13:51246026
|
T | C | 1 | a0001c0001t0001g0163 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.101-5442T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51246026 | ||||||
chr13:51246208
|
C | T | 108 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(105): Show | 114 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(111): Show |
intron_variant | MODIFIER | c.101-5260C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51246208 | ||||||
chr13:51246382
|
C | T | 1 | a0001c0001t0001g0163 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.101-5086C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51246382 | ||||||
chr13:51246399
|
T | TG | 28 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0026others(25): Show | 30 | HG01069.hp1 HG01070.hp2 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.101-5065dupG | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 51246399 | |||||
chr13:51246399
|
T | TGG | 7 | a0001c0001t0001g0216a0001c0001t0001g0217a0001c0001t0001g0226others(4): Show | 7 | HG00099.hp1 HG00733.hp2 HG00735.hp1 others(4): Show |
intron_variant | MODIFIER | c.101-5066_101-5065d others(4): Show |
FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 51246399 | |||||
chr13:51246399
|
T | TGGG | 13 | a0001c0001t0001g0214a0001c0001t0001g0237a0001c0001t0004g0134others(10): Show | 13 | HG00140.hp2 HG00544.hp1 HG00558.hp1 others(10): Show |
intron_variant | MODIFIER | c.101-5067_101-5065d others(5): Show |
FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 51246399 | |||||
chr13:51246399
|
T | TGGGC | 33 | a0001c0001t0001g0066a0001c0001t0001g0156a0001c0001t0001g0161others(30): Show | 34 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(31): Show |
intron_variant | MODIFIER | c.101-5066_101-5065i others(6): Show |
FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 51246399 | |||||
chr13:51246399
|
T | TGGGCG | 9 | a0001c0001t0001g0003a0001c0001t0001g0098a0001c0001t0002g0023others(6): Show | 10 | HG01346.hp2 HG01433.hp2 HG01517.hp1 others(7): Show |
intron_variant | MODIFIER | c.101-5066_101-5065i others(7): Show |
FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 51246399 | |||||
chr13:51246400
|
G | GGGC | 35 | a0001c0001t0001g0030a0001c0001t0001g0123a0001c0001t0002g0030others(32): Show | 40 | HG00621.hp2 HG00735.hp2 HG02165.hp1 others(37): Show |
intron_variant | MODIFIER | c.101-5066_101-5065i others(5): Show |
FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 51246400 | |||||
chr13:51246401
|
GGGT | G | 68 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0036others(65): Show | 76 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.101-5064_101-5062d others(5): Show |
FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 51246401 | |||||
chr13:51246402
|
G | C | 1 | a0011c0010t0020g0067 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.101-5066G>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51246402 | ||||||
chr13:51246402
|
GGT | G | 25 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0077others(22): Show | 28 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(25): Show |
intron_variant | MODIFIER | c.101-5064_101-5063d others(4): Show |
FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 51246402 | |||||
chr13:51246403
|
GT | G | 41 | a0001c0001t0001g0038a0001c0001t0001g0131a0001c0001t0001g0172others(38): Show | 43 | HG00099.hp2 HG01168.hp1 HG01358.hp2 others(40): Show |
intron_variant | MODIFIER | c.101-5064delT | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51246403 | ||||||
chr13:51246404
|
T | C | 5 | a0001c0001t0001g0166a0001c0001t0007g0197a0001c0001t0013g0195others(2): Show | 5 | HG02109.hp2 HG02970.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.101-5064T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51246404 | ||||||
chr13:51246404
|
T | G | 163 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(160): Show | 174 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.101-5064T>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51246404 | ||||||
chr13:51246405
|
G | C | 2 | a0001c0001t0001g0176a0001c0001t0035g0167 | 2 | HG02486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.101-5063G>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51246405 | ||||||
chr13:51246406
|
G | T | 1 | a0001c0017t0001g0173 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.101-5062G>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51246406 | ||||||
chr13:51246407
|
G | C | 1 | a0001c0001t0007g0209 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.101-5061G>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51246407 | ||||||
chr13:51246410
|
G | A | 1 | a0001c0001t0004g0292 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.101-5058G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51246410 | ||||||
chr13:51246758
|
C | T | 1 | a0001c0001t0004g0158 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.101-4710C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51246758 | ||||||
chr13:51246766
|
C | T | 17 | a0001c0001t0004g0244a0001c0001t0005g0151a0001c0001t0006g0137others(14): Show | 17 | HG00140.hp2 HG01069.hp2 HG01934.hp1 others(14): Show |
intron_variant | MODIFIER | c.101-4702C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51246766 | ||||||
chr13:51246780
|
G | A | 1 | a0001c0001t0001g0186 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.101-4688G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51246780 | ||||||
chr13:51246913
|
G | A | 2 | a0001c0001t0002g0130a0001c0001t0003g0342 | 2 | HG02615.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.101-4555G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51246913 | ||||||
chr13:51246917
|
T | C | 2 | a0004c0011t0002g0116a0011c0010t0020g0067 | 2 | HG01884.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.101-4551T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51246917 | ||||||
chr13:51247106
|
G | A | 1 | a0002c0002t0009g0231 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.101-4362G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51247106 | ||||||
chr13:51247176
|
G | T | 1 | a0001c0001t0004g0292 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.101-4292G>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51247176 | ||||||
chr13:51247315
|
C | T | 1 | a0001c0001t0006g0300 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.101-4153C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51247315 | ||||||
chr13:51247343
|
G | C | 2 | a0001c0001t0001g0146a0001c0001t0001g0207 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.101-4125G>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51247343 | ||||||
chr13:51247589
|
G | A | 1 | a0001c0001t0042g0085 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.101-3879G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51247589 | ||||||
chr13:51247672
|
G | A | 1 | a0001c0001t0001g0156 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.101-3796G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51247672 | ||||||
chr13:51247733
|
G | A | 2 | a0001c0001t0001g0136a0001c0001t0002g0025 | 3 | NA18970.hp1 NA18990.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.101-3735G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51247733 | ||||||
chr13:51247746
|
G | C | 1 | a0001c0001t0001g0131 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.101-3722G>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51247746 | ||||||
chr13:51247781
|
C | T | 103 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(100): Show | 108 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(105): Show |
intron_variant | MODIFIER | c.101-3687C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51247781 | ||||||
chr13:51247826
|
C | G | 307 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(304): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(328): Show |
intron_variant | MODIFIER | c.101-3642C>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51247826 | ||||||
chr13:51247865
|
G | A | 1 | a0001c0001t0002g0130 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.101-3603G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51247865 | ||||||
chr13:51247872
|
G | C | 2 | a0004c0011t0002g0116a0011c0010t0020g0067 | 2 | HG01884.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.101-3596G>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51247872 | ||||||
chr13:51248034
|
C | T | 2 | a0001c0001t0001g0283a0001c0001t0002g0282 | 2 | HG03491.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.101-3434C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51248034 | ||||||
chr13:51248053
|
C | A | 297 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(294): Show | 321 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(318): Show |
intron_variant | MODIFIER | c.101-3415C>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51248053 | ||||||
chr13:51248210
|
A | G | 303 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(300): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(324): Show |
intron_variant | MODIFIER | c.101-3258A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51248210 | ||||||
chr13:51248222
|
C | T | 3 | a0004c0005t0023g0322a0004c0005t0027g0281a0004c0005t0027g0317 | 3 | HG02572.hp2 HG03209.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.101-3246C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51248222 | ||||||
chr13:51248337
|
G | A | 1 | a0001c0001t0007g0209 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.101-3131G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51248337 | ||||||
chr13:51248382
|
G | A | 2 | a0001c0001t0001g0115a0001c0001t0002g0130 | 2 | HG03486.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.101-3086G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51248382 | ||||||
chr13:51248430
|
T | C | 111 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(108): Show | 117 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(114): Show |
intron_variant | MODIFIER | c.101-3038T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51248430 | ||||||
chr13:51248634
|
C | T | 1 | a0001c0006t0016g0343 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.101-2834C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51248634 | ||||||
chr13:51249049
|
T | C | 81 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0098others(78): Show | 88 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(85): Show |
intron_variant | MODIFIER | c.101-2419T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51249049 | ||||||
chr13:51249073
|
C | T | 302 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(299): Show | 326 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(323): Show |
intron_variant | MODIFIER | c.101-2395C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51249073 | ||||||
chr13:51249086
|
C | T | 1 | a0001c0001t0002g0130 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.101-2382C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51249086 | ||||||
chr13:51249125
|
A | G | 28 | a0001c0001t0001g0007a0001c0001t0001g0016a0001c0001t0001g0047others(25): Show | 34 | HG00438.hp2 HG00642.hp2 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.101-2343A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51249125 | ||||||
chr13:51249239
|
C | G | 1 | a0001c0001t0002g0130 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.101-2229C>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51249239 | ||||||
chr13:51249270
|
T | C | 1 | a0001c0001t0022g0314 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.101-2198T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51249270 | ||||||
chr13:51249310
|
T | C | 1 | a0011c0010t0020g0067 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.101-2158T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51249310 | ||||||
chr13:51249561
|
C | T | 1 | a0001c0001t0005g0084 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.101-1907C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51249561 | ||||||
chr13:51249842
|
G | T | 73 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0098others(70): Show | 80 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(77): Show |
intron_variant | MODIFIER | c.101-1626G>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51249842 | ||||||
chr13:51250096
|
C | T | 3 | a0001c0001t0003g0342a0001c0001t0014g0255a0001c0001t0018g0129 | 3 | HG02615.hp1 HG03579.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.101-1372C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51250096 | ||||||
chr13:51250192
|
A | G | 38 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0083others(35): Show | 40 | HG00099.hp1 HG00639.hp1 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.101-1276A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51250192 | ||||||
chr13:51250200
|
AT | A | 3 | a0001c0001t0001g0168a0001c0001t0001g0170a0001c0001t0004g0164 | 3 | HG01069.hp1 HG01074.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.101-1267delT | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51250200 | ||||||
chr13:51250565
|
C | T | 330 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(327): Show | 360 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(357): Show |
intron_variant | MODIFIER | c.101-903C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51250565 | ||||||
chr13:51250600
|
G | A | 1 | a0001c0001t0001g0166 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.101-868G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51250600 | ||||||
chr13:51250647
|
A | C | 1 | a0006c0014t0026g0261 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.101-821A>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51250647 | ||||||
chr13:51250655
|
A | G | 195 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(192): Show | 208 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(205): Show |
intron_variant | MODIFIER | c.101-813A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51250655 | ||||||
chr13:51250657
|
A | T | 1 | a0001c0001t0001g0154 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.101-811A>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51250657 | ||||||
chr13:51250811
|
A | G | 11 | a0001c0001t0001g0166a0001c0001t0007g0035a0001c0001t0007g0209others(8): Show | 11 | HG01884.hp2 HG01891.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.101-657A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51250811 | ||||||
chr13:51250943
|
G | A | 1 | a0002c0002t0004g0323 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.101-525G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51250943 | ||||||
chr13:51250950
|
G | A | 2 | a0002c0004t0010g0298a0002c0004t0010g0329 | 2 | NA18952.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.101-518G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51250950 | ||||||
chr13:51251016
|
C | T | 1 | a0004c0011t0002g0116 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.101-452C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51251016 | ||||||
chr13:51251163
|
G | A | 1 | a0001c0001t0001g0115 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.101-305G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51251163 | ||||||
chr13:51251279
|
T | C | 2 | a0001c0001t0001g0098a0001c0001t0004g0088 | 2 | HG02738.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.101-189T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51251279 | ||||||
chr13:51251290
|
G | C | 5 | a0001c0001t0001g0166a0001c0001t0007g0035a0001c0001t0009g0035others(2): Show | 5 | HG02145.hp2 HG02886.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.101-178G>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51251290 | ||||||
chr13:51251386
|
C | G | 1 | a0001c0001t0004g0274 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.101-82C>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51251386 | ||||||
chr13:51251412
|
T | C | 85 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0098others(82): Show | 92 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(89): Show |
intron_variant | MODIFIER | c.101-56T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51251412 | ||||||
chr13:51252258
|
G | C | 1 | a0001c0001t0003g0342 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.834+57G>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51252258 | ||||||
chr13:51252402
|
C | T | 1 | a0004c0011t0002g0116 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.834+201C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51252402 | ||||||
chr13:51252507
|
A | G | 67 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(64): Show | 75 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.834+306A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51252507 | ||||||
chr13:51253190
|
G | A | 2 | a0001c0001t0001g0176a0001c0001t0035g0167 | 2 | HG02486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.834+989G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51253190 | ||||||
chr13:51253470
|
G | A | 250 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(247): Show | 274 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(271): Show |
intron_variant | MODIFIER | c.834+1269G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51253470 | ||||||
chr13:51253774
|
T | G | 1 | a0001c0001t0002g0130 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.834+1573T>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51253774 | ||||||
chr13:51253783
|
G | T | 1 | a0001c0001t0005g0084 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.834+1582G>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51253783 | ||||||
chr13:51253804
|
G | A | 1 | a0002c0002t0040g0319 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.834+1603G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51253804 | ||||||
chr13:51253945
|
C | G | 76 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0098others(73): Show | 83 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(80): Show |
intron_variant | MODIFIER | c.834+1744C>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51253945 | ||||||
chr13:51253946
|
T | C | 266 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(263): Show | 290 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(287): Show |
intron_variant | MODIFIER | c.834+1745T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51253946 | ||||||
chr13:51253948
|
C | A | 1 | a0001c0001t0030g0112 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.834+1747C>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51253948 | ||||||
chr13:51254104
|
G | T | 39 | a0002c0002t0001g0037a0002c0002t0001g0240a0002c0002t0001g0258others(36): Show | 39 | HG00140.hp1 HG00323.hp2 HG01074.hp2 others(36): Show |
intron_variant | MODIFIER | c.834+1903G>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51254104 | ||||||
chr13:51254396
|
C | CT | 12 | a0001c0001t0001g0166a0001c0001t0002g0219a0001c0001t0007g0209others(9): Show | 12 | HG01261.hp1 HG01884.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.834+2204dupT | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 51254396 | |||||
chr13:51254563
|
C | T | 1 | a0001c0001t0001g0188 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.834+2362C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51254563 | ||||||
chr13:51254824
|
T | C | 267 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(264): Show | 291 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(288): Show |
intron_variant | MODIFIER | c.834+2623T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51254824 | ||||||
chr13:51254863
|
T | C | 153 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(150): Show | 165 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.834+2662T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51254863 | ||||||
chr13:51254900
|
G | A | 1 | a0001c0009t0033g0210 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.834+2699G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51254900 | ||||||
chr13:51254920
|
T | C | 8 | a0001c0001t0001g0049a0001c0001t0001g0055a0001c0001t0001g0063others(5): Show | 8 | HG02083.hp1 NA18940.hp1 NA18969.hp1 others(5): Show |
intron_variant | MODIFIER | c.834+2719T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51254920 | ||||||
chr13:51255062
|
G | A | 1 | a0002c0002t0001g0311 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.834+2861G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51255062 | ||||||
chr13:51255202
|
G | A | 261 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(258): Show | 285 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(282): Show |
intron_variant | MODIFIER | c.834+3001G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51255202 | ||||||
chr13:51255305
|
A | G | 1 | a0003c0003t0008g0199 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.834+3104A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51255305 | ||||||
chr13:51255343
|
G | A | 1 | a0001c0001t0005g0082 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.834+3142G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51255343 | ||||||
chr13:51255349
|
A | T | 1 | a0001c0001t0003g0095 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.834+3148A>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51255349 | ||||||
chr13:51255355
|
T | A | 4 | a0001c0001t0002g0130a0001c0001t0014g0255a0001c0001t0018g0127others(1): Show | 4 | HG02145.hp2 HG03486.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.834+3154T>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51255355 | ||||||
chr13:51255357
|
A | G | 153 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(150): Show | 165 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.834+3156A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51255357 | ||||||
chr13:51255444
|
G | A | 3 | a0001c0001t0002g0192a0001c0001t0002g0193a0001c0001t0002g0194 | 3 | HG02572.hp1 HG02818.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.834+3243G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51255444 | ||||||
chr13:51255524
|
A | C | 1 | a0001c0001t0019g0165 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.834+3323A>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51255524 | ||||||
chr13:51255575
|
A | G | 2 | a0001c0001t0001g0243a0001c0001t0002g0306 | 2 | HG00733.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.834+3374A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51255575 | ||||||
chr13:51255682
|
C | G | 251 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(248): Show | 275 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.834+3481C>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51255682 | ||||||
chr13:51255738
|
AG | A | 40 | a0001c0001t0007g0197a0002c0002t0001g0037a0002c0002t0001g0240others(37): Show | 40 | HG00140.hp1 HG00323.hp2 HG01074.hp2 others(37): Show |
intron_variant | MODIFIER | c.834+3539delG | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 51255738 | |||||
chr13:51255749
|
G | GT | 115 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(112): Show | 127 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.834+3548_834+3549i others(3): Show |
FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51255749 | ||||||
chr13:51255978
|
G | A | 1 | a0001c0001t0002g0099 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.834+3777G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51255978 | ||||||
chr13:51256337
|
C | T | 104 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0049others(101): Show | 116 | HG00408.hp1 HG00438.hp2 HG00597.hp1 others(113): Show |
intron_variant | MODIFIER | c.834+4136C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51256337 | ||||||
chr13:51256395
|
C | A | 1 | a0001c0001t0019g0165 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.834+4194C>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51256395 | ||||||
chr13:51256434
|
T | C | 3 | a0001c0001t0003g0022a0001c0001t0003g0087a0001c0001t0003g0091 | 4 | NA18983.hp1 NA18990.hp1 NA19064.hp1 others(1): Show |
intron_variant | MODIFIER | c.834+4233T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51256434 | ||||||
chr13:51256509
|
A | T | 2 | a0001c0001t0001g0131a0002c0002t0007g0279 | 2 | HG02976.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.834+4308A>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51256509 | ||||||
chr13:51256531
|
T | C | 1 | a0001c0001t0002g0249 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.834+4330T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51256531 | ||||||
chr13:51256577
|
G | C | 111 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0049others(108): Show | 123 | HG00408.hp1 HG00438.hp2 HG00597.hp1 others(120): Show |
intron_variant | MODIFIER | c.834+4376G>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51256577 | ||||||
chr13:51256675
|
A | G | 5 | a0001c0007t0001g0020a0001c0007t0013g0020a0001c0007t0013g0089others(2): Show | 5 | HG01884.hp2 HG01891.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.834+4474A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51256675 | ||||||
chr13:51256770
|
C | A | 75 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0098others(72): Show | 82 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(79): Show |
intron_variant | MODIFIER | c.834+4569C>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51256770 | ||||||
chr13:51256856
|
G | A | 4 | a0001c0001t0014g0255a0001c0001t0018g0127a0001c0001t0018g0129others(1): Show | 4 | HG01243.hp1 HG02145.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.834+4655G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51256856 | ||||||
chr13:51256884
|
C | G | 1 | a0001c0001t0005g0151 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.834+4683C>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51256884 | ||||||
chr13:51256992
|
A | G | 2 | a0001c0001t0004g0292a0001c0009t0033g0210 | 2 | HG03209.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.834+4791A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51256992 | ||||||
chr13:51256997
|
T | C | 14 | a0001c0001t0001g0166a0001c0001t0007g0035a0001c0001t0007g0209others(11): Show | 14 | HG01243.hp1 HG01884.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.834+4796T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51256997 | ||||||
chr13:51257017
|
C | T | 2 | a0001c0001t0001g0176a0001c0001t0035g0167 | 2 | HG02486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.834+4816C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51257017 | ||||||
chr13:51257150
|
G | A | 237 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(234): Show | 256 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(253): Show |
intron_variant | MODIFIER | c.834+4949G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51257150 | ||||||
chr13:51257161
|
T | C | 1 | a0002c0002t0019g0324 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.834+4960T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51257161 | ||||||
chr13:51257256
|
C | G | 2 | a0004c0005t0027g0281a0004c0005t0027g0317 | 2 | HG03209.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.834+5055C>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51257256 | ||||||
chr13:51257383
|
C | T | 22 | a0001c0001t0001g0049a0001c0001t0001g0055a0001c0001t0001g0056others(19): Show | 27 | HG00438.hp2 HG00642.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.834+5182C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51257383 | ||||||
chr13:51257703
|
A | G | 269 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(266): Show | 293 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(290): Show |
intron_variant | MODIFIER | c.834+5502A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51257703 | ||||||
chr13:51257868
|
C | T | 1 | a0001c0001t0002g0130 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.834+5667C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51257868 | ||||||
chr13:51257919
|
A | C | 6 | a0002c0002t0002g0041a0002c0002t0007g0296a0002c0002t0009g0041others(3): Show | 6 | HG00140.hp1 HG00323.hp2 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.834+5718A>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51257919 | ||||||
chr13:51257924
|
C | T | 1 | a0001c0001t0006g0300 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.834+5723C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51257924 | ||||||
chr13:51258026
|
A | G | 4 | a0001c0001t0001g0166a0001c0001t0007g0035a0001c0001t0009g0035others(1): Show | 4 | HG02886.hp1 HG02970.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.834+5825A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51258026 | ||||||
chr13:51258041
|
T | G | 134 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0017others(131): Show | 148 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(145): Show |
intron_variant | MODIFIER | c.834+5840T>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51258041 | ||||||
chr13:51258074
|
T | C | 78 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0098others(75): Show | 85 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(82): Show |
intron_variant | MODIFIER | c.834+5873T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51258074 | ||||||
chr13:51258132
|
C | T | 22 | a0001c0001t0001g0049a0001c0001t0001g0055a0001c0001t0001g0056others(19): Show | 27 | HG00438.hp2 HG00642.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.834+5931C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51258132 | ||||||
chr13:51258169
|
T | C | 1 | a0001c0001t0001g0131 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.834+5968T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51258169 | ||||||
chr13:51258184
|
G | C | 1 | a0001c0001t0001g0190 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.834+5983G>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51258184 | ||||||
chr13:51258194
|
A | G | 6 | a0001c0001t0002g0272a0001c0001t0002g0273a0001c0001t0004g0274others(3): Show | 6 | HG00642.hp1 HG01346.hp1 HG01943.hp1 others(3): Show |
intron_variant | MODIFIER | c.834+5993A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51258194 | ||||||
chr13:51258214
|
C | T | 1 | a0004c0011t0002g0116 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.834+6013C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51258214 | ||||||
chr13:51258218
|
A | G | 1 | a0001c0001t0015g0157 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.834+6017A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51258218 | ||||||
chr13:51258543
|
G | A | 9 | a0001c0001t0014g0255a0001c0001t0018g0127a0001c0001t0018g0129others(6): Show | 9 | HG01243.hp1 HG01884.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.834+6342G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51258543 | ||||||
chr13:51258544
|
C | A | 9 | a0001c0001t0014g0255a0001c0001t0018g0127a0001c0001t0018g0129others(6): Show | 9 | HG01243.hp1 HG01884.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.834+6343C>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51258544 | ||||||
chr13:51258763
|
C | G | 1 | a0001c0001t0002g0145 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.834+6562C>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51258763 | ||||||
chr13:51258783
|
G | A | 1 | a0004c0011t0002g0116 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.834+6582G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51258783 | ||||||
chr13:51258928
|
T | G | 1 | a0001c0001t0002g0272 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.834+6727T>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51258928 | ||||||
chr13:51258963
|
G | C | 1 | a0001c0001t0013g0195 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.834+6762G>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51258963 | ||||||
chr13:51258990
|
G | A | 16 | a0001c0001t0002g0202a0001c0001t0003g0092a0001c0001t0013g0032others(13): Show | 17 | HG01192.hp2 HG01884.hp1 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.834+6789G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51258990 | ||||||
chr13:51258999
|
G | A | 1 | a0001c0001t0007g0209 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.834+6798G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51258999 | ||||||
chr13:51259054
|
C | G | 17 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0038others(14): Show | 19 | HG00280.hp1 HG00323.hp1 HG00544.hp2 others(16): Show |
intron_variant | MODIFIER | c.834+6853C>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51259054 | ||||||
chr13:51259111
|
C | T | 39 | a0001c0001t0007g0197a0002c0002t0001g0037a0002c0002t0001g0240others(36): Show | 39 | HG00140.hp1 HG00323.hp2 HG01074.hp2 others(36): Show |
intron_variant | MODIFIER | c.834+6910C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51259111 | ||||||
chr13:51259146
|
C | T | 15 | a0001c0001t0002g0202a0001c0001t0013g0032a0001c0001t0017g0032others(12): Show | 16 | HG01192.hp2 HG01884.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.834+6945C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51259146 | ||||||
chr13:51259396
|
C | T | 15 | a0001c0001t0002g0202a0001c0001t0013g0032a0001c0001t0017g0032others(12): Show | 16 | HG01192.hp2 HG01884.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.834+7195C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51259396 | ||||||
chr13:51259402
|
C | CCT | 22 | a0001c0001t0001g0049a0001c0001t0001g0055a0001c0001t0001g0056others(19): Show | 27 | HG00438.hp2 HG00642.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.834+7205_834+7206d others(4): Show |
FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 51259402 | |||||
chr13:51259452
|
C | T | 1 | a0001c0001t0011g0215 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.834+7251C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51259452 | ||||||
chr13:51259465
|
C | T | 72 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0083others(69): Show | 75 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.834+7264C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51259465 | ||||||
chr13:51259521
|
C | G | 1 | a0002c0002t0001g0258 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.834+7320C>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51259521 | ||||||
chr13:51259521
|
C | T | 1 | a0001c0001t0002g0339 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.834+7320C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51259521 | ||||||
chr13:51259523
|
G | C | 1 | a0002c0002t0001g0258 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.834+7322G>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51259523 | ||||||
chr13:51259582
|
G | A | 55 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0083others(52): Show | 57 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.834+7381G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51259582 | ||||||
chr13:51259601
|
G | A | 1 | a0001c0001t0030g0112 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.834+7400G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51259601 | ||||||
chr13:51259740
|
C | A | 1 | a0002c0002t0001g0258 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.834+7539C>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51259740 | ||||||
chr13:51259808
|
A | C | 87 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0098others(84): Show | 94 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.834+7607A>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51259808 | ||||||
chr13:51259893
|
G | A | 4 | a0001c0001t0001g0166a0001c0001t0007g0035a0001c0001t0009g0035others(1): Show | 4 | HG02258.hp1 HG02886.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.834+7692G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51259893 | ||||||
chr13:51259919
|
T | G | 1 | a0001c0001t0002g0192 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.834+7718T>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51259919 | ||||||
chr13:51259937
|
G | T | 23 | a0001c0001t0001g0049a0001c0001t0001g0055a0001c0001t0001g0056others(20): Show | 27 | HG00438.hp2 HG00642.hp2 HG01070.hp1 others(24): Show |
intron_variant | MODIFIER | c.834+7736G>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51259937 | ||||||
chr13:51259994
|
G | C | 11 | a0001c0001t0005g0021a0001c0001t0005g0069a0001c0001t0005g0070others(8): Show | 12 | HG00597.hp1 HG02080.hp1 HG03942.hp2 others(9): Show |
intron_variant | MODIFIER | c.834+7793G>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51259994 | ||||||
chr13:51260192
|
C | T | 1 | a0001c0006t0010g0271 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.834+7991C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51260192 | ||||||
chr13:51260227
|
C | T | 73 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0012others(70): Show | 79 | HG00099.hp1 HG00544.hp2 HG00621.hp1 others(76): Show |
intron_variant | MODIFIER | c.834+8026C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51260227 | ||||||
chr13:51260292
|
T | C | 7 | a0001c0001t0001g0166a0001c0001t0007g0035a0001c0001t0009g0035others(4): Show | 7 | HG02258.hp1 HG02572.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.834+8091T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51260292 | ||||||
chr13:51260565
|
C | T | 1 | a0001c0001t0002g0130 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.834+8364C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51260565 | ||||||
chr13:51260581
|
G | T | 7 | a0001c0001t0001g0166a0001c0001t0007g0035a0001c0001t0009g0035others(4): Show | 7 | HG02258.hp1 HG02572.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.834+8380G>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51260581 | ||||||
chr13:51260634
|
C | T | 1 | a0001c0001t0004g0292 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.834+8433C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51260634 | ||||||
chr13:51260748
|
G | T | 70 | a0001c0001t0001g0003a0001c0001t0001g0098a0001c0001t0001g0123others(67): Show | 77 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.834+8547G>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51260748 | ||||||
chr13:51260790
|
G | C | 24 | a0001c0001t0001g0214a0001c0001t0003g0342a0001c0001t0004g0244others(21): Show | 24 | HG00140.hp2 HG00544.hp1 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.834+8589G>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51260790 | ||||||
chr13:51260919
|
G | A | 1 | a0001c0001t0018g0129 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.834+8718G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51260919 | ||||||
chr13:51261011
|
T | C | 1 | a0004c0011t0002g0116 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.834+8810T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51261011 | ||||||
chr13:51261013
|
A | T | 61 | a0001c0001t0002g0202a0001c0001t0002g0212a0001c0001t0002g0213others(58): Show | 64 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.834+8812A>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51261013 | ||||||
chr13:51261098
|
C | A | 1 | a0001c0001t0002g0053 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.834+8897C>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51261098 | ||||||
chr13:51261163
|
C | T | 19 | a0001c0001t0001g0214a0001c0001t0004g0244a0001c0001t0005g0151others(16): Show | 19 | HG00140.hp2 HG00544.hp1 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.834+8962C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51261163 | ||||||
chr13:51261312
|
T | A | 1 | a0002c0002t0001g0258 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.834+9111T>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51261312 | ||||||
chr13:51261349
|
G | A | 148 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(145): Show | 162 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(159): Show |
intron_variant | MODIFIER | c.834+9148G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51261349 | ||||||
chr13:51261471
|
A | G | 13 | a0001c0001t0014g0255a0001c0001t0018g0127a0001c0001t0018g0129others(10): Show | 13 | HG01243.hp1 HG01884.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.834+9270A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51261471 | ||||||
chr13:51261506
|
C | T | 8 | a0001c0001t0001g0007a0001c0001t0001g0016a0001c0001t0001g0047others(5): Show | 9 | NA18747.hp1 NA18939.hp2 NA18957.hp1 others(6): Show |
intron_variant | MODIFIER | c.834+9305C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51261506 | ||||||
chr13:51261518
|
G | A | 3 | a0001c0001t0013g0032a0001c0001t0017g0032a0001c0001t0017g0200 | 3 | HG02622.hp1 HG02630.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.834+9317G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51261518 | ||||||
chr13:51261565
|
T | TCCATAGT others(13): Show |
65 | a0001c0001t0001g0166a0001c0001t0002g0202a0001c0001t0002g0212others(62): Show | 68 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.834+9364_834+9365i others(22): Show |
FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51261565 | ||||||
chr13:51261918
|
G | T | 1 | a0001c0001t0007g0209 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.834+9717G>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51261918 | ||||||
chr13:51261984
|
C | T | 1 | a0001c0001t0004g0292 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.834+9783C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51261984 | ||||||
chr13:51262177
|
C | T | 2 | a0004c0011t0002g0116a0011c0010t0020g0067 | 2 | HG01884.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.834+9976C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51262177 | ||||||
chr13:51262266
|
G | C | 266 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(263): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(287): Show |
intron_variant | MODIFIER | c.834+10065G>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51262266 | ||||||
chr13:51262365
|
C | CA | 375 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(372): Show | 405 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(402): Show |
intron_variant | MODIFIER | c.834+10170dupA | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 51262365 | |||||
chr13:51262483
|
G | A | 277 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(274): Show | 301 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(298): Show |
intron_variant | MODIFIER | c.834+10282G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51262483 | ||||||
chr13:51262484
|
T | A | 2 | a0001c0001t0001g0333a0001c0001t0001g0334 | 2 | HG01081.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.834+10283T>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51262484 | ||||||
chr13:51262710
|
T | C | 343 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(340): Show | 370 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(367): Show |
intron_variant | MODIFIER | c.834+10509T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51262710 | ||||||
chr13:51262713
|
C | G | 1 | a0001c0001t0019g0165 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.834+10512C>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51262713 | ||||||
chr13:51262766
|
T | C | 1 | a0001c0001t0001g0309 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.834+10565T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51262766 | ||||||
chr13:51262797
|
C | T | 13 | a0001c0001t0012g0005a0001c0001t0012g0090a0001c0001t0012g0241others(10): Show | 14 | HG01891.hp1 HG02109.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.834+10596C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51262797 | ||||||
chr13:51262854
|
C | T | 2 | a0001c0001t0003g0009a0001c0001t0003g0096 | 4 | NA18941.hp2 NA19007.hp1 NA19054.hp2 others(1): Show |
intron_variant | MODIFIER | c.834+10653C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51262854 | ||||||
chr13:51262998
|
C | A | 1 | a0009c0013t0008g0230 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.834+10797C>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51262998 | ||||||
chr13:51263016
|
C | T | 20 | a0001c0001t0001g0049a0001c0001t0001g0055a0001c0001t0001g0056others(17): Show | 23 | HG00438.hp2 HG00642.hp2 HG01433.hp1 others(20): Show |
intron_variant | MODIFIER | c.834+10815C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51263016 | ||||||
chr13:51263163
|
A | G | 64 | a0001c0001t0002g0202a0001c0001t0002g0212a0001c0001t0002g0213others(61): Show | 67 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.834+10962A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51263163 | ||||||
chr13:51263170
|
C | T | 1 | a0001c0001t0004g0292 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.834+10969C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51263170 | ||||||
chr13:51263217
|
C | T | 1 | a0001c0001t0002g0065 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.834+11016C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51263217 | ||||||
chr13:51263318
|
A | G | 6 | a0001c0001t0002g0023a0001c0001t0003g0023a0001c0001t0003g0024others(3): Show | 6 | HG01255.hp1 HG01346.hp2 HG01928.hp1 others(3): Show |
intron_variant | MODIFIER | c.834+11117A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51263318 | ||||||
chr13:51263706
|
T | C | 1 | a0001c0001t0004g0292 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.834+11505T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51263706 | ||||||
chr13:51264009
|
A | G | 2 | a0001c0001t0002g0269a0001c0001t0002g0307 | 2 | HG02056.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.834+11808A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51264009 | ||||||
chr13:51264473
|
C | T | 2 | a0001c0001t0004g0292a0001c0001t0007g0209 | 2 | HG03704.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.834+12272C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51264473 | ||||||
chr13:51264475
|
C | A | 1 | a0001c0001t0001g0115 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.834+12274C>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51264475 | ||||||
chr13:51264501
|
G | C | 97 | a0001c0001t0001g0003a0001c0001t0001g0098a0001c0001t0001g0131others(94): Show | 104 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.834+12300G>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51264501 | ||||||
chr13:51264544
|
C | G | 6 | a0001c0007t0001g0020a0001c0007t0013g0020a0001c0007t0013g0089others(3): Show | 6 | HG01884.hp2 HG01891.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.834+12343C>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51264544 | ||||||
chr13:51264545
|
G | A | 144 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(141): Show | 158 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.834+12344G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51264545 | ||||||
chr13:51264650
|
A | T | 1 | a0001c0001t0004g0292 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.834+12449A>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51264650 | ||||||
chr13:51264774
|
C | T | 2 | a0001c0001t0015g0040a0001c0001t0041g0040 | 2 | NA18967.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.834+12573C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51264774 | ||||||
chr13:51264861
|
G | A | 374 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(371): Show | 404 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(401): Show |
intron_variant | MODIFIER | c.834+12660G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51264861 | ||||||
chr13:51264922
|
C | T | 1 | a0001c0001t0001g0299 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.834+12721C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51264922 | ||||||
chr13:51265074
|
C | T | 341 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(338): Show | 368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.834+12873C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51265074 | ||||||
chr13:51265200
|
G | A | 69 | a0001c0001t0001g0003a0001c0001t0001g0098a0001c0001t0001g0156others(66): Show | 76 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(73): Show |
intron_variant | MODIFIER | c.834+12999G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51265200 | ||||||
chr13:51265280
|
C | T | 14 | a0001c0001t0007g0197a0002c0002t0001g0311a0002c0002t0001g0321others(11): Show | 14 | HG01074.hp2 HG01167.hp2 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.834+13079C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51265280 | ||||||
chr13:51265414
|
T | C | 1 | a0002c0002t0007g0277 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.834+13213T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51265414 | ||||||
chr13:51265426
|
C | T | 1 | a0001c0009t0020g0107 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.834+13225C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51265426 | ||||||
chr13:51265545
|
C | T | 1 | a0001c0001t0002g0139 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.834+13344C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51265545 | ||||||
chr13:51265829
|
C | A | 1 | a0001c0001t0002g0029 | 2 | HG01978.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.834+13628C>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51265829 | ||||||
chr13:51265970
|
T | C | 61 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0038others(58): Show | 67 | HG00438.hp2 HG00544.hp2 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.834+13769T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51265970 | ||||||
chr13:51266054
|
T | A | 2 | a0001c0001t0007g0014a0001c0001t0007g0015 | 4 | HG00738.hp2 HG01070.hp1 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.834+13853T>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51266054 | ||||||
chr13:51266077
|
GTGT | G | 25 | a0001c0001t0001g0214a0001c0001t0003g0342a0001c0001t0004g0244others(22): Show | 26 | HG00140.hp2 HG00544.hp1 HG01069.hp2 others(23): Show |
intron_variant | MODIFIER | c.834+13881_834+1388 others(7): Show |
FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 51266077 | |||||
chr13:51266113
|
T | G | 2 | a0001c0001t0007g0035a0001c0001t0009g0035 | 2 | HG02886.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.834+13912T>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51266113 | ||||||
chr13:51266357
|
T | C | 1 | a0001c0001t0011g0238 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.835-14093T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51266357 | ||||||
chr13:51266434
|
G | T | 20 | a0001c0001t0001g0049a0001c0001t0001g0055a0001c0001t0001g0056others(17): Show | 23 | HG00438.hp2 HG00642.hp2 HG01433.hp1 others(20): Show |
intron_variant | MODIFIER | c.835-14016G>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51266434 | ||||||
chr13:51266594
|
T | G | 1 | a0001c0001t0005g0082 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.835-13856T>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51266594 | ||||||
chr13:51267021
|
C | T | 49 | a0001c0001t0001g0049a0001c0001t0001g0055a0001c0001t0001g0056others(46): Show | 53 | HG00438.hp2 HG00642.hp2 HG01243.hp1 others(50): Show |
intron_variant | MODIFIER | c.835-13429C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51267021 | ||||||
chr13:51267155
|
G | A | 14 | a0001c0001t0002g0029a0001c0001t0002g0130a0001c0001t0002g0174others(11): Show | 15 | HG00280.hp1 HG00323.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.835-13295G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51267155 | ||||||
chr13:51267678
|
T | G | 1 | a0001c0001t0001g0131 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.835-12772T>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51267678 | ||||||
chr13:51267713
|
C | T | 1 | a0001c0001t0002g0135 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.835-12737C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51267713 | ||||||
chr13:51267852
|
G | A | 4 | a0001c0001t0001g0216a0001c0001t0001g0217a0001c0001t0001g0226others(1): Show | 4 | HG00733.hp2 HG00735.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.835-12598G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51267852 | ||||||
chr13:51267911
|
G | T | 2 | a0001c0001t0006g0224a0001c0001t0011g0215 | 2 | HG01346.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.835-12539G>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51267911 | ||||||
chr13:51267943
|
A | G | 1 | a0001c0001t0007g0209 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.835-12507A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51267943 | ||||||
chr13:51268101
|
T | A | 1 | a0001c0001t0018g0129 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.835-12349T>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51268101 | ||||||
chr13:51268330
|
G | A | 14 | a0001c0001t0001g0131a0001c0001t0002g0202a0003c0003t0008g0033others(11): Show | 15 | HG01192.hp2 HG01884.hp1 HG01975.hp1 others(12): Show |
intron_variant | MODIFIER | c.835-12120G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51268330 | ||||||
chr13:51268377
|
A | G | 104 | a0001c0001t0001g0003a0001c0001t0001g0098a0001c0001t0001g0161others(101): Show | 112 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.835-12073A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51268377 | ||||||
chr13:51268399
|
A | T | 1 | a0001c0001t0019g0165 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.835-12051A>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51268399 | ||||||
chr13:51268414
|
A | G | 1 | a0001c0001t0001g0268 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.835-12036A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51268414 | ||||||
chr13:51268814
|
G | A | 193 | a0001c0001t0001g0003a0001c0001t0001g0049a0001c0001t0001g0055others(190): Show | 207 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.835-11636G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51268814 | ||||||
chr13:51269566
|
T | A | 1 | a0001c0001t0004g0265 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.835-10884T>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51269566 | ||||||
chr13:51269635
|
A | C | 1 | a0001c0001t0003g0094 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.835-10815A>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51269635 | ||||||
chr13:51269636
|
G | C | 1 | a0001c0017t0001g0173 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.835-10814G>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51269636 | ||||||
chr13:51269642
|
A | G | 1 | a0001c0001t0011g0081 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.835-10808A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51269642 | ||||||
chr13:51269742
|
A | G | 9 | a0001c0001t0001g0049a0001c0001t0001g0055a0001c0001t0001g0058others(6): Show | 9 | HG02083.hp1 NA18940.hp1 NA18969.hp1 others(6): Show |
intron_variant | MODIFIER | c.835-10708A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51269742 | ||||||
chr13:51269999
|
A | G | 42 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0038others(39): Show | 45 | HG00544.hp2 HG00621.hp1 HG01243.hp1 others(42): Show |
intron_variant | MODIFIER | c.835-10451A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51269999 | ||||||
chr13:51270040
|
A | C | 4 | a0001c0009t0020g0107a0001c0009t0033g0210a0004c0011t0002g0116others(1): Show | 4 | HG01884.hp2 HG02559.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.835-10410A>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51270040 | ||||||
chr13:51270057
|
T | C | 1 | a0001c0001t0003g0073 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.835-10393T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51270057 | ||||||
chr13:51270115
|
G | A | 14 | a0001c0001t0002g0029a0001c0001t0002g0130a0001c0001t0002g0174others(11): Show | 15 | HG00280.hp1 HG00323.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.835-10335G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51270115 | ||||||
chr13:51270158
|
C | G | 20 | a0001c0001t0001g0049a0001c0001t0001g0055a0001c0001t0001g0056others(17): Show | 23 | HG00438.hp2 HG00642.hp2 HG01433.hp1 others(20): Show |
intron_variant | MODIFIER | c.835-10292C>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51270158 | ||||||
chr13:51270169
|
G | A | 101 | a0001c0001t0001g0003a0001c0001t0001g0098a0001c0001t0001g0161others(98): Show | 109 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.835-10281G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51270169 | ||||||
chr13:51270230
|
G | C | 6 | a0001c0001t0004g0244a0001c0001t0006g0177a0001c0001t0006g0184others(3): Show | 6 | HG01069.hp2 HG01934.hp1 HG02602.hp2 others(3): Show |
intron_variant | MODIFIER | c.835-10220G>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51270230 | ||||||
chr13:51270293
|
C | T | 8 | a0001c0001t0002g0029a0001c0001t0002g0174a0001c0001t0002g0212others(5): Show | 9 | HG00280.hp1 HG00323.hp1 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.835-10157C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51270293 | ||||||
chr13:51270472
|
C | T | 1 | a0001c0001t0002g0181 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.835-9978C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51270472 | ||||||
chr13:51270593
|
G | A | 2 | a0001c0001t0001g0016a0001c0001t0002g0016 | 2 | NA18939.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.835-9857G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51270593 | ||||||
chr13:51270734
|
C | T | 1 | a0002c0002t0009g0256 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.835-9716C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51270734 | ||||||
chr13:51270798
|
C | T | 1 | a0001c0001t0004g0292 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.835-9652C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51270798 | ||||||
chr13:51270933
|
G | A | 1 | a0001c0001t0004g0292 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.835-9517G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51270933 | ||||||
chr13:51271027
|
ATGTGGCA others(18): Show |
A | 1 | a0001c0001t0001g0142 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.835-9422_835-9398d others(27): Show |
FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51271027 | ||||||
chr13:51271104
|
A | G | 20 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0038others(17): Show | 22 | HG00544.hp2 HG00621.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.835-9346A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51271104 | ||||||
chr13:51271112
|
A | G | 1 | a0001c0001t0019g0165 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.835-9338A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51271112 | ||||||
chr13:51271188
|
C | T | 25 | a0001c0001t0001g0214a0001c0001t0004g0244a0001c0001t0005g0151others(22): Show | 26 | HG00140.hp2 HG00544.hp1 HG01069.hp2 others(23): Show |
intron_variant | MODIFIER | c.835-9262C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51271188 | ||||||
chr13:51271206
|
C | A | 1 | a0001c0001t0001g0175 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.835-9244C>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51271206 | ||||||
chr13:51271261
|
C | T | 1 | a0001c0001t0001g0208 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.835-9189C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51271261 | ||||||
chr13:51271515
|
G | A | 4 | a0001c0001t0002g0130a0001c0001t0013g0032a0001c0001t0017g0032others(1): Show | 4 | HG02622.hp1 HG02630.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.835-8935G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51271515 | ||||||
chr13:51271884
|
G | A | 2 | a0001c0001t0012g0336a0001c0001t0012g0338 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.835-8566G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51271884 | ||||||
chr13:51271930
|
T | C | 30 | a0001c0001t0007g0014a0001c0001t0007g0015a0001c0001t0007g0197others(27): Show | 32 | HG00140.hp1 HG00323.hp2 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.835-8520T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51271930 | ||||||
chr13:51272126
|
G | A | 28 | a0001c0001t0001g0214a0001c0001t0001g0333a0001c0001t0001g0334others(25): Show | 29 | HG00140.hp2 HG00544.hp1 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.835-8324G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51272126 | ||||||
chr13:51272191
|
C | G | 1 | a0002c0002t0018g0290 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.835-8259C>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51272191 | ||||||
chr13:51272233
|
G | A | 1 | a0001c0007t0013g0089 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.835-8217G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51272233 | ||||||
chr13:51272249
|
T | C | 1 | a0001c0001t0007g0014 | 2 | HG00738.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.835-8201T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51272249 | ||||||
chr13:51272443
|
C | A | 1 | a0001c0001t0002g0130 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.835-8007C>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51272443 | ||||||
chr13:51272469
|
T | C | 220 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0017others(217): Show | 236 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.835-7981T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51272469 | ||||||
chr13:51272566
|
T | TAC | 18 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0038others(15): Show | 20 | HG00544.hp2 HG00621.hp1 HG00733.hp1 others(17): Show |
intron_variant | MODIFIER | c.835-7857_835-7856d others(4): Show |
FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 51272566 | |||||
chr13:51272566
|
T | TACAC | 170 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0049others(167): Show | 183 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.835-7859_835-7856d others(6): Show |
FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 51272566 | |||||
chr13:51272566
|
T | TACACAC | 13 | a0001c0001t0003g0289a0001c0001t0005g0082a0001c0001t0006g0236others(10): Show | 13 | HG00544.hp1 HG01884.hp2 HG02080.hp1 others(10): Show |
intron_variant | MODIFIER | c.835-7861_835-7856d others(8): Show |
FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 51272566 | |||||
chr13:51272566
|
T | TACACACA others(1): Show |
16 | a0001c0001t0001g0131a0001c0001t0002g0099a0001c0001t0002g0202others(13): Show | 17 | HG00673.hp2 HG01109.hp2 HG01192.hp2 others(14): Show |
intron_variant | MODIFIER | c.835-7863_835-7856d others(10): Show |
FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 51272566 | |||||
chr13:51272566
|
T | TACACACA others(3): Show |
4 | a0001c0001t0013g0032a0001c0001t0017g0032a0001c0001t0017g0200others(1): Show | 4 | HG02622.hp1 HG02630.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.835-7865_835-7856d others(12): Show |
FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 51272566 | |||||
chr13:51272566
|
T | TACACACA others(5): Show |
1 | a0001c0001t0002g0130 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.835-7867_835-7856d others(14): Show |
FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 51272566 | |||||
chr13:51272566
|
T | TACACACA others(15): Show |
1 | a0001c0001t0004g0292 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.835-7877_835-7856d others(24): Show |
FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 51272566 | |||||
chr13:51272566
|
TAC | T | 36 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0083others(33): Show | 38 | HG00639.hp1 HG00639.hp2 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.835-7857_835-7856d others(4): Show |
FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 51272566 | |||||
chr13:51272593
|
A | C | 1 | a0001c0001t0002g0332 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.835-7857A>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51272593 | ||||||
chr13:51272709
|
A | AGGAGTGC others(32): Show |
2 | a0002c0004t0010g0278a0002c0004t0010g0331 | 2 | HG06807.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.835-7733_835-7695d others(41): Show |
FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 51272709 | |||||
chr13:51272972
|
G | A | 13 | a0001c0001t0007g0014a0001c0001t0007g0015a0001c0001t0030g0112others(10): Show | 15 | HG00140.hp1 HG00323.hp2 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.835-7478G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51272972 | ||||||
chr13:51272990
|
C | A | 2 | a0001c0001t0022g0314a0001c0001t0023g0313 | 2 | HG01109.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.835-7460C>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51272990 | ||||||
chr13:51273300
|
C | T | 1 | a0001c0001t0001g0115 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.835-7150C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51273300 | ||||||
chr13:51273486
|
C | T | 75 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0098others(72): Show | 81 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(78): Show |
intron_variant | MODIFIER | c.835-6964C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51273486 | ||||||
chr13:51273494
|
A | G | 2 | a0004c0005t0027g0281a0004c0005t0027g0317 | 2 | HG03209.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.835-6956A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51273494 | ||||||
chr13:51273574
|
A | AT | 34 | a0001c0001t0001g0214a0001c0001t0003g0342a0001c0001t0004g0244others(31): Show | 35 | HG00140.hp2 HG00544.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.835-6867dupT | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 51273574 | |||||
chr13:51273574
|
A | T | 17 | a0001c0001t0002g0251a0001c0001t0003g0068a0001c0001t0003g0073others(14): Show | 17 | HG00597.hp1 HG02071.hp2 HG02129.hp2 others(14): Show |
intron_variant | MODIFIER | c.835-6876A>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51273574 | ||||||
chr13:51273583
|
T | A | 2 | a0001c0001t0003g0104a0001c0001t0005g0179 | 2 | NA18999.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.835-6867T>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51273583 | ||||||
chr13:51274015
|
A | G | 4 | a0001c0001t0001g0036a0001c0001t0001g0267a0001c0001t0004g0036others(1): Show | 5 | NA18949.hp1 NA18950.hp1 NA18959.hp1 others(2): Show |
intron_variant | MODIFIER | c.835-6435A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51274015 | ||||||
chr13:51274029
|
A | G | 1 | a0001c0001t0002g0332 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.835-6421A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51274029 | ||||||
chr13:51274030
|
G | T | 1 | a0001c0001t0002g0332 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.835-6420G>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51274030 | ||||||
chr13:51274034
|
T | A | 1 | a0001c0001t0002g0332 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.835-6416T>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51274034 | ||||||
chr13:51274168
|
C | A | 1 | a0001c0001t0002g0099 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.835-6282C>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51274168 | ||||||
chr13:51274241
|
A | G | 219 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0017others(216): Show | 235 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.835-6209A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51274241 | ||||||
chr13:51274261
|
A | G | 39 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0038others(36): Show | 42 | HG00544.hp2 HG00621.hp1 HG01243.hp1 others(39): Show |
intron_variant | MODIFIER | c.835-6189A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51274261 | ||||||
chr13:51274367
|
A | G | 17 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0038others(14): Show | 19 | HG00544.hp2 HG00621.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.835-6083A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51274367 | ||||||
chr13:51274398
|
G | T | 1 | a0001c0001t0001g0142 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.835-6052G>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51274398 | ||||||
chr13:51274530
|
A | T | 1 | a0001c0001t0001g0142 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.835-5920A>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51274530 | ||||||
chr13:51274542
|
A | C | 1 | a0001c0001t0001g0142 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.835-5908A>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51274542 | ||||||
chr13:51274624
|
G | T | 35 | a0001c0001t0001g0049a0001c0001t0001g0055a0001c0001t0001g0056others(32): Show | 39 | HG00438.hp2 HG00642.hp2 HG01192.hp2 others(36): Show |
intron_variant | MODIFIER | c.835-5826G>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51274624 | ||||||
chr13:51274745
|
A | T | 8 | a0001c0001t0001g0183a0001c0001t0001g0186a0001c0001t0001g0188others(5): Show | 8 | HG00639.hp1 HG01167.hp1 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.835-5705A>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51274745 | ||||||
chr13:51274852
|
C | T | 2 | a0001c0001t0002g0117a0001c0001t0002g0235 | 2 | NA18747.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.835-5598C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51274852 | ||||||
chr13:51274860
|
AGTGAAGA others(9): Show |
A | 1 | a0001c0001t0004g0118 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.835-5589_835-5574d others(18): Show |
FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51274860 | ||||||
chr13:51274928
|
G | A | 14 | a0001c0001t0001g0131a0001c0001t0002g0202a0003c0003t0008g0033others(11): Show | 15 | HG01192.hp2 HG01884.hp1 HG01975.hp1 others(12): Show |
intron_variant | MODIFIER | c.835-5522G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51274928 | ||||||
chr13:51274944
|
C | T | 1 | a0001c0001t0002g0139 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.835-5506C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51274944 | ||||||
chr13:51275205
|
T | A | 7 | a0001c0001t0001g0011a0001c0001t0001g0136a0001c0001t0001g0142others(4): Show | 9 | HG02523.hp2 NA18951.hp2 NA18966.hp1 others(6): Show |
intron_variant | MODIFIER | c.835-5245T>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51275205 | ||||||
chr13:51275209
|
C | CA | 102 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(99): Show | 110 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.835-5222dupA | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 51275209 | |||||
chr13:51275209
|
CA | C | 59 | a0001c0001t0001g0214a0001c0001t0001g0217a0001c0001t0001g0223others(56): Show | 61 | HG00140.hp2 HG00544.hp1 HG00733.hp2 others(58): Show |
intron_variant | MODIFIER | c.835-5222delA | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 51275209 | |||||
chr13:51275345
|
G | A | 26 | a0001c0001t0012g0005a0001c0001t0012g0090a0001c0001t0012g0241others(23): Show | 27 | HG01243.hp1 HG01884.hp2 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.835-5105G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51275345 | ||||||
chr13:51275606
|
GC | G | 31 | a0001c0001t0001g0214a0001c0001t0003g0342a0001c0001t0004g0244others(28): Show | 32 | HG00140.hp2 HG00544.hp1 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.835-4841delC | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 51275606 | |||||
chr13:51275612
|
A | T | 31 | a0001c0001t0001g0214a0001c0001t0003g0342a0001c0001t0004g0244others(28): Show | 32 | HG00140.hp2 HG00544.hp1 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.835-4838A>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51275612 | ||||||
chr13:51275774
|
A | G | 65 | a0001c0001t0001g0049a0001c0001t0001g0055a0001c0001t0001g0056others(62): Show | 71 | HG00140.hp1 HG00323.hp2 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.835-4676A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51275774 | ||||||
chr13:51275976
|
T | A | 1 | a0003c0003t0008g0204 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.835-4474T>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51275976 | ||||||
chr13:51276059
|
G | A | 139 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0098others(136): Show | 147 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.835-4391G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51276059 | ||||||
chr13:51276071
|
C | T | 74 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0098others(71): Show | 80 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(77): Show |
intron_variant | MODIFIER | c.835-4379C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51276071 | ||||||
chr13:51276072
|
G | A | 1 | a0001c0001t0004g0292 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.835-4378G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51276072 | ||||||
chr13:51276209
|
G | A | 2 | a0002c0002t0007g0234a0002c0002t0007g0318 | 2 | NA19081.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.835-4241G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51276209 | ||||||
chr13:51276373
|
G | A | 1 | a0005c0008t0003g0051 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.835-4077G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51276373 | ||||||
chr13:51276422
|
T | G | 1 | a0001c0001t0001g0302 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.835-4028T>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51276422 | ||||||
chr13:51276607
|
CA | C | 4 | a0001c0001t0001g0242a0001c0001t0001g0266a0001c0001t0001g0304others(1): Show | 4 | NA18960.hp1 NA18978.hp1 NA18988.hp2 others(1): Show |
intron_variant | MODIFIER | c.835-3842delA | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51276607 | ||||||
chr13:51276744
|
T | C | 26 | a0001c0001t0001g0214a0001c0001t0004g0244a0001c0001t0005g0151others(23): Show | 27 | HG00140.hp2 HG00544.hp1 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.835-3706T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51276744 | ||||||
chr13:51276752
|
T | C | 24 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0083others(21): Show | 26 | HG00099.hp1 HG00639.hp1 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.835-3698T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51276752 | ||||||
chr13:51276786
|
CT | C | 14 | a0001c0001t0001g0030a0001c0001t0001g0178a0001c0001t0002g0030others(11): Show | 14 | HG00609.hp2 HG02080.hp1 HG03927.hp2 others(11): Show |
intron_variant | MODIFIER | c.835-3663delT | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51276786 | ||||||
chr13:51276789
|
TG | T | 13 | a0001c0001t0001g0030a0001c0001t0001g0178a0001c0001t0002g0030others(10): Show | 13 | HG00609.hp2 HG02080.hp1 HG03927.hp2 others(10): Show |
intron_variant | MODIFIER | c.835-3660delG | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51276789 | ||||||
chr13:51276975
|
C | T | 2 | a0002c0002t0007g0279a0002c0002t0009g0280 | 2 | HG01255.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.835-3475C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51276975 | ||||||
chr13:51276986
|
G | A | 82 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0098others(79): Show | 88 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.835-3464G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51276986 | ||||||
chr13:51277042
|
A | G | 3 | a0001c0009t0020g0107a0001c0009t0033g0210a0011c0010t0020g0067 | 3 | HG01884.hp2 HG03209.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.835-3408A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51277042 | ||||||
chr13:51277048
|
G | A | 204 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0049others(201): Show | 218 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.835-3402G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51277048 | ||||||
chr13:51277051
|
C | T | 75 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0098others(72): Show | 81 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(78): Show |
intron_variant | MODIFIER | c.835-3399C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51277051 | ||||||
chr13:51277094
|
G | A | 1 | a0001c0001t0025g0285 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.835-3356G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51277094 | ||||||
chr13:51277103
|
G | GA | 27 | a0001c0001t0011g0215a0001c0001t0012g0005a0001c0001t0012g0090others(24): Show | 28 | HG01243.hp1 HG01346.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.835-3338dupA | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 51277103 | |||||
chr13:51277116
|
G | A | 2 | a0001c0001t0019g0337a0002c0002t0019g0324 | 2 | HG01243.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.835-3334G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51277116 | ||||||
chr13:51277154
|
G | A | 1 | a0004c0005t0022g0315 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.835-3296G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51277154 | ||||||
chr13:51277261
|
G | A | 3 | a0001c0007t0001g0020a0001c0007t0013g0020a0001c0007t0013g0089 | 3 | HG01891.hp2 HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.835-3189G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51277261 | ||||||
chr13:51277337
|
G | A | 37 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0083others(34): Show | 39 | HG00099.hp1 HG00639.hp1 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.835-3113G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51277337 | ||||||
chr13:51277414
|
A | G | 2 | a0001c0001t0007g0035a0001c0001t0009g0035 | 2 | HG02886.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.835-3036A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51277414 | ||||||
chr13:51277650
|
C | T | 50 | a0001c0001t0001g0049a0001c0001t0001g0055a0001c0001t0001g0056others(47): Show | 55 | HG00140.hp1 HG00323.hp2 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.835-2800C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51277650 | ||||||
chr13:51277665
|
G | A | 4 | a0001c0001t0013g0195a0001c0001t0017g0196a0003c0003t0008g0199others(1): Show | 4 | HG01192.hp2 HG01975.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.835-2785G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51277665 | ||||||
chr13:51277771
|
CGACAGAG others(79): Show |
C | 65 | a0001c0001t0001g0049a0001c0001t0001g0055a0001c0001t0001g0056others(62): Show | 71 | HG00140.hp1 HG00323.hp2 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.835-2678_835-2593d others(88): Show |
FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51277771 | ||||||
chr13:51277780
|
G | A | 1 | a0004c0011t0002g0116 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.835-2670G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51277780 | ||||||
chr13:51277884
|
G | A | 26 | a0001c0001t0012g0005a0001c0001t0012g0090a0001c0001t0012g0241others(23): Show | 27 | HG01243.hp1 HG01884.hp2 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.835-2566G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51277884 | ||||||
chr13:51277899
|
G | A | 82 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0098others(79): Show | 88 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.835-2551G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51277899 | ||||||
chr13:51278119
|
T | C | 1 | a0001c0001t0003g0342 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.835-2331T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51278119 | ||||||
chr13:51278140
|
G | A | 2 | a0002c0002t0007g0279a0002c0002t0009g0280 | 2 | HG01255.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.835-2310G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51278140 | ||||||
chr13:51278149
|
G | A | 1 | a0001c0001t0001g0304 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.835-2301G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51278149 | ||||||
chr13:51278318
|
G | A | 22 | a0001c0001t0012g0005a0001c0001t0012g0090a0001c0001t0012g0241others(19): Show | 23 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.835-2132G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51278318 | ||||||
chr13:51278404
|
C | T | 1 | a0004c0011t0002g0116 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.835-2046C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51278404 | ||||||
chr13:51278601
|
A | G | 1 | a0003c0003t0024g0203 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.835-1849A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51278601 | ||||||
chr13:51278619
|
A | T | 1 | a0001c0001t0001g0055 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.835-1831A>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51278619 | ||||||
chr13:51278981
|
C | T | 200 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0049others(197): Show | 214 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(211): Show |
intron_variant | MODIFIER | c.835-1469C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51278981 | ||||||
chr13:51279180
|
T | C | 1 | a0001c0001t0002g0202 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.835-1270T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51279180 | ||||||
chr13:51279609
|
A | T | 23 | a0001c0001t0001g0049a0001c0001t0001g0055a0001c0001t0001g0056others(20): Show | 26 | HG00438.hp2 HG00642.hp2 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.835-841A>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51279609 | ||||||
chr13:51279760
|
C | T | 4 | a0001c0001t0002g0126a0001c0001t0002g0251a0001c0001t0002g0252others(1): Show | 4 | HG00597.hp2 NA18945.hp2 NA18961.hp1 others(1): Show |
intron_variant | MODIFIER | c.835-690C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51279760 | ||||||
chr13:51280168
|
G | A | 1 | a0001c0001t0005g0071 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.835-282G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51280168 |