geneid | 283742 |
---|---|
ensemblid | ENSG00000171262.11 |
hgncid | 26773 |
symbol | FAM98B |
name | family with sequence similarity 98 member B |
refseq_nuc | NM_173611.4 |
refseq_prot | NP_775882.2 |
ensembl_nuc | ENST00000397609.6 |
ensembl_prot | ENSP00000380734.2 |
mane_status | MANE Select |
chr | chr15 |
start | 38454127 |
end | 38487710 |
strand | + |
ver | v1.2 |
region | chr15:38454127-38487710 |
region5000 | chr15:38449127-38492710 |
regionname0 | FAM98B_chr15_38454127_38487710 |
regionname5000 | FAM98B_chr15_38449127_38492710 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 433 | 357 | 86 | 59 | 159 | 18 | 33 | 123 | FAM98B_chr15_38449127_38492710 | FAM98B | copy fasta | chr15 | 38449127 | 38492710 |
a0002 | 0/0 | 430 | 30 | 3 | 9 | 15 | 0 | 3 | 12 | FAM98B_chr15_38449127_38492710 | FAM98B | copy fasta | chr15 | 38449127 | 38492710 |
a0003 | 0/0 | 427 | 4 | 0 | 0 | 1 | 0 | 3 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | copy fasta | chr15 | 38449127 | 38492710 |
a0004 | 0/0 | 433 | 3 | 0 | 2 | 0 | 0 | 1 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | copy fasta | chr15 | 38449127 | 38492710 |
a0005 | 0/0 | 433 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | copy fasta | chr15 | 38449127 | 38492710 |
a0006 | 0/0 | 433 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | copy fasta | chr15 | 38449127 | 38492710 |
a0007 | 0/0 | 433 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | copy fasta | chr15 | 38449127 | 38492710 |
a0008 | 0/0 | 424 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | copy fasta | chr15 | 38449127 | 38492710 |
a0009 | 0/0 | 433 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | copy fasta | chr15 | 38449127 | 38492710 |
a0010 | 0/0 | 433 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | copy fasta | chr15 | 38449127 | 38492710 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1302 | 337 | 71 | 56 | 158 | 18 | 32 | FAM98B_chr15_38449127_38492710 | FAM98B | copy fasta | chr15 | 38449127 | 38492710 |
c0002 | 0/0 | 1293 | 29 | 3 | 9 | 15 | 0 | 2 | FAM98B_chr15_38449127_38492710 | FAM98B | copy fasta | chr15 | 38449127 | 38492710 |
c0003 | 0/0 | 1302 | 12 | 8 | 3 | 0 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | copy fasta | chr15 | 38449127 | 38492710 |
c0004 | 0/0 | 1302 | 7 | 7 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | copy fasta | chr15 | 38449127 | 38492710 |
c0005 | 0/0 | 1284 | 4 | 0 | 0 | 1 | 0 | 3 | FAM98B_chr15_38449127_38492710 | FAM98B | copy fasta | chr15 | 38449127 | 38492710 |
c0006 | 0/0 | 1302 | 3 | 0 | 2 | 0 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | copy fasta | chr15 | 38449127 | 38492710 |
c0007 | 0/0 | 1293 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | copy fasta | chr15 | 38449127 | 38492710 |
c0008 | 0/0 | 1302 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | copy fasta | chr15 | 38449127 | 38492710 |
c0009 | 0/0 | 1302 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | copy fasta | chr15 | 38449127 | 38492710 |
c0010 | 0/0 | 1302 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | copy fasta | chr15 | 38449127 | 38492710 |
c0011 | 0/0 | 1275 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | copy fasta | chr15 | 38449127 | 38492710 |
c0012 | 0/0 | 1302 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | copy fasta | chr15 | 38449127 | 38492710 |
c0013 | 0/0 | 1302 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | copy fasta | chr15 | 38449127 | 38492710 |
c0014 | 0/0 | 1302 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | copy fasta | chr15 | 38449127 | 38492710 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 3087 | 143 | 10 | 25 | 84 | 7 | 16 | FAM98B_chr15_38449127_38492710 | FAM98B | copy fasta | chr15 | 38449127 | 38492710 |
t0002 | 1/0 | 3087 | 118 | 30 | 24 | 50 | 5 | 8 | FAM98B_chr15_38449127_38492710 | FAM98B | copy fasta | chr15 | 38449127 | 38492710 |
t0003 | 0/0 | 3087 | 48 | 0 | 9 | 36 | 0 | 3 | FAM98B_chr15_38449127_38492710 | FAM98B | copy fasta | chr15 | 38449127 | 38492710 |
t0004 | 0/0 | 3087 | 34 | 9 | 10 | 1 | 4 | 10 | FAM98B_chr15_38449127_38492710 | FAM98B | copy fasta | chr15 | 38449127 | 38492710 |
t0005 | 0/0 | 3087 | 22 | 18 | 3 | 0 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | copy fasta | chr15 | 38449127 | 38492710 |
t0006 | 0/0 | 3087 | 6 | 6 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | copy fasta | chr15 | 38449127 | 38492710 |
t0007 | 0/0 | 3086 | 4 | 4 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | copy fasta | chr15 | 38449127 | 38492710 |
t0008 | 0/0 | 3087 | 3 | 0 | 0 | 0 | 1 | 2 | FAM98B_chr15_38449127_38492710 | FAM98B | copy fasta | chr15 | 38449127 | 38492710 |
t0009 | 0/0 | 3087 | 3 | 3 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | copy fasta | chr15 | 38449127 | 38492710 |
t0010 | 0/0 | 3087 | 3 | 3 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | copy fasta | chr15 | 38449127 | 38492710 |
t0011 | 0/0 | 3087 | 2 | 2 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | copy fasta | chr15 | 38449127 | 38492710 |
t0012 | 0/0 | 3087 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | copy fasta | chr15 | 38449127 | 38492710 |
t0013 | 0/0 | 3087 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | copy fasta | chr15 | 38449127 | 38492710 |
t0014 | 0/0 | 3087 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | copy fasta | chr15 | 38449127 | 38492710 |
t0015 | 0/0 | 3087 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | copy fasta | chr15 | 38449127 | 38492710 |
t0016 | 0/0 | 3087 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | copy fasta | chr15 | 38449127 | 38492710 |
t0017 | 0/0 | 3087 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | copy fasta | chr15 | 38449127 | 38492710 |
t0018 | 0/0 | 3087 | 1 | 0 | 0 | 0 | 1 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | copy fasta | chr15 | 38449127 | 38492710 |
t0019 | 0/0 | 3087 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | copy fasta | chr15 | 38449127 | 38492710 |
t0020 | 0/0 | 3087 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | copy fasta | chr15 | 38449127 | 38492710 |
t0021 | 0/0 | 3087 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | copy fasta | chr15 | 38449127 | 38492710 |
t0022 | 0/0 | 3086 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | copy fasta | chr15 | 38449127 | 38492710 |
t0023 | 0/0 | 3087 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | copy fasta | chr15 | 38449127 | 38492710 |
t0024 | 0/0 | 3087 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | copy fasta | chr15 | 38449127 | 38492710 |
t0025 | 0/0 | 3087 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | copy fasta | chr15 | 38449127 | 38492710 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 23 | 2 | 3 | 17 | 1 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0002 | 0/0 | 16 | 0 | 4 | 11 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0003 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0004 | 0/0 | 7 | 0 | 2 | 0 | 2 | 3 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0005 | 0/0 | 7 | 0 | 1 | 6 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0006 | 0/0 | 6 | 0 | 4 | 2 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0007 | 0/0 | 6 | 0 | 1 | 1 | 1 | 3 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0008 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0009 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0010 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0012 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0013 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0014 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0015 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0016 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0017 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0019 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0020 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0021 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0023 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0028 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0029 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0033 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0044 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0045 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0048 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0052 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0053 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0054 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0055 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0116 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0137 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1302 | 337 | 71 | 56 | 158 | 18 | 32 | FAM98B_chr15_38449127_38492710 | FAM98B | copy fasta | chr15 | 38449127 | 38492710 |
a0001c0003 | 0/0 | 1302 | 12 | 8 | 3 | 0 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | copy fasta | chr15 | 38449127 | 38492710 |
a0001c0004 | 0/0 | 1302 | 7 | 7 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | copy fasta | chr15 | 38449127 | 38492710 |
a0001c0014 | 0/0 | 1302 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | copy fasta | chr15 | 38449127 | 38492710 |
a0002c0002 | 0/0 | 1293 | 29 | 3 | 9 | 15 | 0 | 2 | FAM98B_chr15_38449127_38492710 | FAM98B | copy fasta | chr15 | 38449127 | 38492710 |
a0002c0007 | 0/0 | 1293 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | copy fasta | chr15 | 38449127 | 38492710 |
a0003c0005 | 0/0 | 1284 | 4 | 0 | 0 | 1 | 0 | 3 | FAM98B_chr15_38449127_38492710 | FAM98B | copy fasta | chr15 | 38449127 | 38492710 |
a0004c0006 | 0/0 | 1302 | 3 | 0 | 2 | 0 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | copy fasta | chr15 | 38449127 | 38492710 |
a0005c0012 | 0/0 | 1302 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | copy fasta | chr15 | 38449127 | 38492710 |
a0006c0008 | 0/0 | 1302 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | copy fasta | chr15 | 38449127 | 38492710 |
a0007c0009 | 0/0 | 1302 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | copy fasta | chr15 | 38449127 | 38492710 |
a0008c0011 | 0/0 | 1275 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | copy fasta | chr15 | 38449127 | 38492710 |
a0009c0010 | 0/0 | 1302 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | copy fasta | chr15 | 38449127 | 38492710 |
a0010c0013 | 0/0 | 1302 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | copy fasta | chr15 | 38449127 | 38492710 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 4388 | 136 | 10 | 24 | 82 | 7 | 12 | FAM98B_chr15_38449127_38492710 | FAM98B | copy fasta | chr15 | 38449127 | 38492710 |
a0001c0001t0002 | 1/0 | 4388 | 110 | 26 | 21 | 50 | 5 | 7 | FAM98B_chr15_38449127_38492710 | FAM98B | copy fasta | chr15 | 38449127 | 38492710 |
a0001c0001t0003 | 0/0 | 4388 | 24 | 0 | 3 | 21 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | copy fasta | chr15 | 38449127 | 38492710 |
a0001c0001t0004 | 0/0 | 4388 | 30 | 9 | 7 | 1 | 4 | 9 | FAM98B_chr15_38449127_38492710 | FAM98B | copy fasta | chr15 | 38449127 | 38492710 |
a0001c0001t0005 | 0/0 | 4388 | 12 | 12 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | copy fasta | chr15 | 38449127 | 38492710 |
a0001c0001t0007 | 0/0 | 4387 | 4 | 4 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | copy fasta | chr15 | 38449127 | 38492710 |
a0001c0001t0008 | 0/0 | 4388 | 3 | 0 | 0 | 0 | 1 | 2 | FAM98B_chr15_38449127_38492710 | FAM98B | copy fasta | chr15 | 38449127 | 38492710 |
a0001c0001t0009 | 0/0 | 4388 | 3 | 3 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | copy fasta | chr15 | 38449127 | 38492710 |
a0001c0001t0010 | 0/0 | 4388 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | copy fasta | chr15 | 38449127 | 38492710 |
a0001c0001t0011 | 0/0 | 4388 | 2 | 2 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | copy fasta | chr15 | 38449127 | 38492710 |
a0001c0001t0012 | 0/0 | 4388 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | copy fasta | chr15 | 38449127 | 38492710 |
a0001c0001t0013 | 0/0 | 4388 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | copy fasta | chr15 | 38449127 | 38492710 |
a0001c0001t0015 | 0/0 | 4388 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | copy fasta | chr15 | 38449127 | 38492710 |
a0001c0001t0016 | 0/0 | 4388 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | copy fasta | chr15 | 38449127 | 38492710 |
a0001c0001t0017 | 0/0 | 4388 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | copy fasta | chr15 | 38449127 | 38492710 |
a0001c0001t0018 | 0/0 | 4388 | 1 | 0 | 0 | 0 | 1 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | copy fasta | chr15 | 38449127 | 38492710 |
a0001c0001t0019 | 0/0 | 4388 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | copy fasta | chr15 | 38449127 | 38492710 |
a0001c0001t0020 | 0/0 | 4388 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | copy fasta | chr15 | 38449127 | 38492710 |
a0001c0001t0021 | 0/0 | 4388 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | copy fasta | chr15 | 38449127 | 38492710 |
a0001c0001t0022 | 0/0 | 4387 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | copy fasta | chr15 | 38449127 | 38492710 |
a0001c0001t0023 | 0/0 | 4388 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | copy fasta | chr15 | 38449127 | 38492710 |
a0001c0001t0024 | 0/0 | 4388 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | copy fasta | chr15 | 38449127 | 38492710 |
a0001c0003t0002 | 0/0 | 4388 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | copy fasta | chr15 | 38449127 | 38492710 |
a0001c0003t0005 | 0/0 | 4388 | 10 | 6 | 3 | 0 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | copy fasta | chr15 | 38449127 | 38492710 |
a0001c0003t0014 | 0/0 | 4388 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | copy fasta | chr15 | 38449127 | 38492710 |
a0001c0004t0006 | 0/0 | 4388 | 5 | 5 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | copy fasta | chr15 | 38449127 | 38492710 |
a0001c0004t0010 | 0/0 | 4388 | 2 | 2 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | copy fasta | chr15 | 38449127 | 38492710 |
a0001c0014t0001 | 0/0 | 4388 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | copy fasta | chr15 | 38449127 | 38492710 |
a0002c0002t0002 | 0/0 | 4379 | 6 | 3 | 3 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | copy fasta | chr15 | 38449127 | 38492710 |
a0002c0002t0003 | 0/0 | 4379 | 21 | 0 | 5 | 14 | 0 | 2 | FAM98B_chr15_38449127_38492710 | FAM98B | copy fasta | chr15 | 38449127 | 38492710 |
a0002c0002t0004 | 0/0 | 4379 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | copy fasta | chr15 | 38449127 | 38492710 |
a0002c0002t0025 | 0/0 | 4379 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | copy fasta | chr15 | 38449127 | 38492710 |
a0002c0007t0003 | 0/0 | 4379 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | copy fasta | chr15 | 38449127 | 38492710 |
a0003c0005t0001 | 0/0 | 4370 | 4 | 0 | 0 | 1 | 0 | 3 | FAM98B_chr15_38449127_38492710 | FAM98B | copy fasta | chr15 | 38449127 | 38492710 |
a0004c0006t0004 | 0/0 | 4388 | 3 | 0 | 2 | 0 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | copy fasta | chr15 | 38449127 | 38492710 |
a0005c0012t0006 | 0/0 | 4388 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | copy fasta | chr15 | 38449127 | 38492710 |
a0006c0008t0001 | 0/0 | 4388 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | copy fasta | chr15 | 38449127 | 38492710 |
a0007c0009t0002 | 0/0 | 4388 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | copy fasta | chr15 | 38449127 | 38492710 |
a0008c0011t0003 | 0/0 | 4361 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | copy fasta | chr15 | 38449127 | 38492710 |
a0009c0010t0001 | 0/0 | 4388 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | copy fasta | chr15 | 38449127 | 38492710 |
a0010c0013t0003 | 0/0 | 4388 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | copy fasta | chr15 | 38449127 | 38492710 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 23 | 2 | 3 | 17 | 1 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0001g0005 | 0/0 | 7 | 0 | 1 | 6 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0001g0007 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0001g0009 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0001g0010 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0001g0020 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0001g0021 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0001g0023 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0001g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0001g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0001g0048 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0001g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0001g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0001g0052 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0001g0054 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0001g0116 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0002g0004 | 0/0 | 7 | 0 | 2 | 0 | 2 | 3 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0002g0006 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0002g0008 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0002g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0002g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0002g0017 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0002g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0002g0019 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0002g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0002g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0002g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0002g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0002g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0002g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0002g0045 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0002g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0002g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0002g0137 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0002g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0002g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0002g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0003g0002 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0003g0003 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0003g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0004g0012 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0004g0029 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0004g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0004g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0004g0033 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0004g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0004g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0004g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0004g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0004g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0004g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0004g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0004g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0004g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0004g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0004g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0004g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0004g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0004g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0004g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0004g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0004g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0005g0014 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0005g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0005g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0005g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0005g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0005g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0005g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0005g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0005g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0007g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0007g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0007g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0008g0007 | 0/0 | 3 | 0 | 0 | 0 | 1 | 2 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0009g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0009g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0009g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0010g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0011g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0011g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0012g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0013g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0015g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0016g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0017g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0018g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0019g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0020g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0021g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0022g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0023g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0001t0024g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0003t0002g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0003t0005g0013 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0003t0005g0055 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0003t0005g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0003t0005g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0003t0005g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0003t0005g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0003t0014g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0004t0006g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0004t0006g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0004t0006g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0004t0010g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0004t0010g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0001c0014t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0002c0002t0002g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0002c0002t0002g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0002c0002t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0002c0002t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0002c0002t0002g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0002c0002t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0002c0002t0003g0002 | 0/0 | 11 | 0 | 1 | 10 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0002c0002t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0002c0002t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0002c0002t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0002c0002t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0002c0002t0003g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0002c0002t0003g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0002c0002t0003g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0002c0002t0003g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0002c0002t0003g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0002c0002t0003g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0002c0002t0004g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0002c0002t0025g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0002c0007t0003g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0003c0005t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0003c0005t0001g0053 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0003c0005t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0004c0006t0004g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0004c0006t0004g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0004c0006t0004g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0005c0012t0006g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0006c0008t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0007c0009t0002g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0008c0011t0003g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0009c0010t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
a0010c0013t0003g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0219 | EUR | GBR | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0004 | EUR | GBR | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG00140 | hp1 | a0001 | c0001 | t0008 | g0007 | EUR | GBR | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0190 | EUR | GBR | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG00280 | hp1 | a0001 | c0001 | t0002 | g0016 | EUR | FIN | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG00280 | hp2 | a0001 | c0001 | t0004 | g0089 | EUR | FIN | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0217 | EUR | FIN | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG00323 | hp2 | a0001 | c0001 | t0004 | g0101 | EUR | FIN | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG00423 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | CHS | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0114 | EAS | CHS | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG00438 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | CHS | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG00544 | hp1 | a0001 | c0001 | t0002 | g0120 | EAS | CHS | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG00544 | hp2 | a0001 | c0001 | t0003 | g0067 | EAS | CHS | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG00558 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | CHS | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0131 | EAS | CHS | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0165 | EAS | CHS | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG00597 | hp2 | a0001 | c0001 | t0003 | g0069 | EAS | CHS | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0136 | EAS | CHS | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | CHS | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | CHS | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0123 | EAS | CHS | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0085 | AMR | PUR | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG00639 | hp2 | a0001 | c0001 | t0004 | g0033 | AMR | PUR | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG00642 | hp1 | a0002 | c0002 | t0003 | g0184 | AMR | PUR | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0155 | AMR | PUR | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0162 | EAS | CHS | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | CHS | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG00733 | hp1 | a0001 | c0001 | t0002 | g0142 | AMR | PUR | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG00733 | hp2 | a0001 | c0001 | t0004 | g0077 | AMR | PUR | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG00735 | hp2 | a0001 | c0001 | t0004 | g0029 | AMR | PUR | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG00738 | hp2 | a0002 | c0002 | t0003 | g0185 | AMR | PUR | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG01069 | hp1 | a0001 | c0003 | t0005 | g0055 | AMR | PUR | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0249 | AMR | PUR | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0084 | AMR | PUR | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG01071 | hp1 | a0001 | c0003 | t0005 | g0055 | AMR | PUR | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0153 | AMR | PUR | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0083 | AMR | PUR | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | PUR | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG01099 | hp2 | a0001 | c0001 | t0004 | g0236 | AMR | PUR | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG01106 | hp1 | a0001 | c0001 | t0022 | g0180 | AMR | PUR | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0133 | AMR | PUR | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG01109 | hp2 | a0001 | c0003 | t0005 | g0013 | AMR | PUR | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | PUR | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0240 | AMR | PUR | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG01169 | hp1 | a0002 | c0002 | t0004 | g0096 | AMR | PUR | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG01243 | hp1 | a0002 | c0002 | t0002 | g0140 | AMR | PUR | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG01243 | hp2 | a0001 | c0001 | t0002 | g0045 | AMR | PUR | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG01255 | hp1 | a0001 | c0001 | t0004 | g0099 | AMR | CLM | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0043 | AMR | CLM | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG01256 | hp1 | a0001 | c0001 | t0004 | g0078 | AMR | CLM | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG01256 | hp2 | a0001 | c0001 | t0002 | g0168 | AMR | CLM | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG01257 | hp1 | a0002 | c0002 | t0002 | g0115 | AMR | CLM | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | CLM | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG01258 | hp1 | a0001 | c0001 | t0004 | g0032 | AMR | CLM | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | CLM | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG01346 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | CLM | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG01358 | hp1 | a0001 | c0001 | t0002 | g0143 | AMR | CLM | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG01361 | hp2 | a0001 | c0001 | t0002 | g0172 | AMR | CLM | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG01433 | hp1 | a0002 | c0002 | t0003 | g0151 | AMR | CLM | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | CLM | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0044 | EUR | IBS | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG01515 | hp2 | a0001 | c0001 | t0002 | g0004 | EUR | IBS | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0028 | EUR | IBS | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG01516 | hp2 | a0001 | c0001 | t0004 | g0088 | EUR | IBS | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG01517 | hp1 | a0001 | c0001 | t0004 | g0029 | EUR | IBS | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0117 | EUR | IBS | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG01884 | hp1 | a0001 | c0001 | t0005 | g0014 | AFR | ACB | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG01884 | hp2 | a0001 | c0001 | t0002 | g0113 | AFR | ACB | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG01891 | hp1 | a0001 | c0001 | t0002 | g0045 | AFR | ACB | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG01891 | hp2 | a0001 | c0001 | t0005 | g0104 | AFR | ACB | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | PEL | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG01928 | hp2 | a0009 | c0010 | t0001 | g0251 | AMR | PEL | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG01934 | hp1 | a0001 | c0001 | t0002 | g0017 | AMR | PEL | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG01934 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | PEL | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG01952 | hp1 | a0002 | c0002 | t0002 | g0006 | AMR | PEL | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG01975 | hp1 | a0001 | c0001 | t0002 | g0080 | AMR | PEL | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PEL | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG01981 | hp1 | a0002 | c0002 | t0003 | g0177 | AMR | PEL | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PEL | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PEL | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG01993 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | PEL | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG02004 | hp1 | a0001 | c0001 | t0002 | g0166 | AMR | PEL | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG02004 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | PEL | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG02015 | hp1 | a0002 | c0002 | t0003 | g0002 | EAS | KHV | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG02015 | hp2 | a0001 | c0001 | t0002 | g0145 | EAS | KHV | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG02027 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | KHV | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | KHV | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | KHV | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG02055 | hp1 | a0001 | c0003 | t0005 | g0013 | AFR | ACB | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG02055 | hp2 | a0005 | c0012 | t0006 | g0059 | AFR | ACB | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG02056 | hp1 | a0001 | c0001 | t0003 | g0068 | EAS | KHV | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0179 | EAS | KHV | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | KHV | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG02074 | hp2 | a0001 | c0001 | t0003 | g0072 | EAS | KHV | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG02080 | hp1 | a0001 | c0001 | t0021 | g0205 | EAS | KHV | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG02080 | hp2 | a0001 | c0001 | t0003 | g0086 | EAS | KHV | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG02129 | hp1 | a0001 | c0001 | t0002 | g0038 | EAS | KHV | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG02129 | hp2 | a0010 | c0013 | t0003 | g0003 | EAS | KHV | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG02132 | hp1 | a0001 | c0001 | t0017 | g0228 | EAS | KHV | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | KHV | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG02135 | hp1 | a0001 | c0001 | t0003 | g0073 | EAS | KHV | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | ACB | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG02145 | hp2 | a0001 | c0001 | t0002 | g0252 | AFR | ACB | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0017 | AMR | PEL | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0245 | AMR | PEL | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG02155 | hp1 | a0002 | c0002 | t0003 | g0002 | EAS | CDX | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG02155 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | CDX | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG02257 | hp1 | a0001 | c0001 | t0004 | g0034 | AFR | ACB | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG02257 | hp2 | a0001 | c0001 | t0004 | g0012 | AFR | ACB | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG02258 | hp1 | a0001 | c0001 | t0007 | g0090 | AFR | ACB | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG02258 | hp2 | a0001 | c0004 | t0006 | g0027 | AFR | ACB | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG02273 | hp1 | a0002 | c0002 | t0003 | g0002 | AMR | PEL | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG02280 | hp1 | a0001 | c0001 | t0004 | g0012 | AFR | ACB | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG02280 | hp2 | a0001 | c0003 | t0005 | g0106 | AFR | ACB | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG02293 | hp1 | a0008 | c0011 | t0003 | g0178 | AMR | PEL | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0233 | AMR | PEL | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG02300 | hp1 | a0004 | c0006 | t0004 | g0093 | AMR | PEL | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG02451 | hp1 | a0001 | c0001 | t0005 | g0014 | AFR | ACB | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG02451 | hp2 | a0001 | c0001 | t0002 | g0042 | AFR | ACB | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG02523 | hp1 | a0002 | c0002 | t0025 | g0181 | EAS | KHV | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG02523 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | KHV | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG02572 | hp1 | a0001 | c0001 | t0002 | g0015 | AFR | GWD | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG02572 | hp2 | a0001 | c0004 | t0006 | g0026 | AFR | GWD | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG02602 | hp1 | a0001 | c0001 | t0008 | g0007 | SAS | PJL | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG02615 | hp1 | a0001 | c0001 | t0005 | g0112 | AFR | GWD | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG02615 | hp2 | a0001 | c0001 | t0007 | g0103 | AFR | GWD | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG02622 | hp1 | a0001 | c0004 | t0010 | g0060 | AFR | GWD | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG02622 | hp2 | a0001 | c0003 | t0002 | g0015 | AFR | GWD | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG02630 | hp1 | a0001 | c0004 | t0006 | g0026 | AFR | GWD | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG02630 | hp2 | a0001 | c0001 | t0005 | g0218 | AFR | GWD | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG02647 | hp1 | a0001 | c0004 | t0006 | g0061 | AFR | GWD | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG02647 | hp2 | a0001 | c0001 | t0002 | g0173 | AFR | GWD | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0213 | SAS | PJL | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG02698 | hp2 | a0001 | c0001 | t0004 | g0097 | SAS | PJL | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG02717 | hp1 | a0001 | c0001 | t0009 | g0188 | AFR | GWD | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | GWD | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG02723 | hp1 | a0001 | c0001 | t0010 | g0057 | AFR | GWD | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG02723 | hp2 | a0001 | c0001 | t0005 | g0014 | AFR | GWD | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG02735 | hp1 | a0001 | c0003 | t0005 | g0253 | SAS | PJL | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0048 | SAS | PJL | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG02738 | hp1 | a0007 | c0009 | t0002 | g0154 | SAS | PJL | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG02738 | hp2 | a0001 | c0001 | t0020 | g0002 | SAS | PJL | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG02809 | hp1 | a0001 | c0001 | t0002 | g0037 | AFR | GWD | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0127 | AFR | GWD | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG02818 | hp1 | a0001 | c0001 | t0011 | g0152 | AFR | GWD | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG02818 | hp2 | a0002 | c0002 | t0002 | g0147 | AFR | GWD | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG02895 | hp1 | a0001 | c0001 | t0009 | g0186 | AFR | GWD | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG02895 | hp2 | a0001 | c0001 | t0007 | g0030 | AFR | GWD | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG02896 | hp1 | a0001 | c0003 | t0005 | g0109 | AFR | GWD | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG02896 | hp2 | a0001 | c0001 | t0004 | g0035 | AFR | GWD | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG02897 | hp1 | a0001 | c0001 | t0004 | g0035 | AFR | GWD | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG02897 | hp2 | a0001 | c0001 | t0009 | g0187 | AFR | GWD | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG02922 | hp1 | a0002 | c0002 | t0002 | g0132 | AFR | ESN | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG02922 | hp2 | a0001 | c0001 | t0005 | g0014 | AFR | ESN | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG02970 | hp1 | a0001 | c0001 | t0002 | g0039 | AFR | ESN | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG02970 | hp2 | a0001 | c0001 | t0005 | g0110 | AFR | ESN | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG02976 | hp1 | a0001 | c0001 | t0007 | g0030 | AFR | ESN | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG02976 | hp2 | a0001 | c0001 | t0002 | g0042 | AFR | ESN | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG03017 | hp1 | a0006 | c0008 | t0001 | g0195 | SAS | PJL | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0250 | SAS | PJL | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG03041 | hp1 | a0001 | c0001 | t0023 | g0063 | AFR | GWD | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG03041 | hp2 | a0001 | c0001 | t0002 | g0015 | AFR | GWD | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG03130 | hp1 | a0001 | c0004 | t0006 | g0027 | AFR | ESN | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG03130 | hp2 | a0001 | c0001 | t0002 | g0041 | AFR | ESN | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG03139 | hp1 | a0001 | c0001 | t0002 | g0157 | AFR | ESN | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG03139 | hp2 | a0001 | c0001 | t0004 | g0012 | AFR | ESN | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG03195 | hp1 | a0001 | c0001 | t0004 | g0102 | AFR | ESN | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | MSL | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG03209 | hp2 | a0001 | c0001 | t0013 | g0082 | AFR | MSL | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG03225 | hp1 | a0001 | c0001 | t0002 | g0128 | AFR | MSL | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG03225 | hp2 | a0001 | c0001 | t0004 | g0034 | AFR | MSL | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG03239 | hp1 | a0001 | c0001 | t0004 | g0098 | SAS | PJL | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG03453 | hp1 | a0001 | c0001 | t0002 | g0041 | AFR | MSL | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG03453 | hp2 | a0001 | c0001 | t0011 | g0091 | AFR | MSL | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG03490 | hp1 | a0001 | c0001 | t0004 | g0031 | SAS | PJL | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG03490 | hp2 | a0001 | c0001 | t0008 | g0007 | SAS | PJL | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG03491 | hp1 | a0003 | c0005 | t0001 | g0234 | SAS | PJL | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG03492 | hp1 | a0003 | c0005 | t0001 | g0053 | SAS | PJL | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG03492 | hp2 | a0001 | c0001 | t0004 | g0031 | SAS | PJL | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG03516 | hp1 | a0001 | c0001 | t0002 | g0125 | AFR | ESN | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG03516 | hp2 | a0001 | c0001 | t0002 | g0037 | AFR | ESN | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG03540 | hp1 | a0001 | c0001 | t0002 | g0135 | AFR | GWD | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG03579 | hp1 | a0001 | c0001 | t0002 | g0144 | AFR | MSL | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG03579 | hp2 | a0001 | c0001 | t0002 | g0150 | AFR | MSL | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG03654 | hp1 | a0001 | c0001 | t0004 | g0056 | SAS | PJL | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0247 | SAS | PJL | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG03669 | hp1 | a0002 | c0002 | t0003 | g0183 | SAS | PJL | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG03669 | hp2 | a0001 | c0001 | t0002 | g0175 | SAS | PJL | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG03688 | hp1 | a0001 | c0001 | t0004 | g0095 | SAS | STU | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0203 | SAS | STU | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0220 | SAS | BEB | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG03831 | hp2 | a0001 | c0001 | t0004 | g0100 | SAS | BEB | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG03834 | hp1 | a0001 | c0001 | t0016 | g0204 | SAS | BEB | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG03834 | hp2 | a0003 | c0005 | t0001 | g0053 | SAS | BEB | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG03927 | hp1 | a0002 | c0002 | t0003 | g0182 | SAS | BEB | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | BEB | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0019 | SAS | BEB | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG03942 | hp2 | a0002 | c0007 | t0003 | g0254 | SAS | BEB | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG04115 | hp1 | a0001 | c0001 | t0004 | g0094 | SAS | STU | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0256 | SAS | STU | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG04184 | hp1 | a0004 | c0006 | t0004 | g0092 | SAS | BEB | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | BEB | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0167 | SAS | STU | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0221 | SAS | STU | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0171 | SAS | STU | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG04228 | hp2 | a0001 | c0001 | t0004 | g0237 | SAS | STU | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | YRI | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA18522 | hp2 | a0001 | c0003 | t0005 | g0107 | AFR | YRI | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA18747 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | CHB | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | CHB | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA18906 | hp1 | a0001 | c0001 | t0004 | g0012 | AFR | YRI | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA18906 | hp2 | a0001 | c0001 | t0002 | g0156 | AFR | YRI | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA18942 | hp2 | a0002 | c0002 | t0003 | g0002 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA18944 | hp1 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA18945 | hp1 | a0002 | c0002 | t0003 | g0002 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA18951 | hp1 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA18953 | hp2 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA18956 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA18956 | hp2 | a0002 | c0002 | t0003 | g0071 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA18959 | hp2 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA18962 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA18965 | hp1 | a0002 | c0002 | t0003 | g0002 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA18966 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA18969 | hp2 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA18970 | hp2 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA18972 | hp1 | a0002 | c0002 | t0003 | g0074 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA18973 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA18977 | hp1 | a0002 | c0002 | t0003 | g0002 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA18979 | hp1 | a0002 | c0002 | t0003 | g0002 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA18980 | hp1 | a0001 | c0001 | t0004 | g0033 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA18980 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA18983 | hp1 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA18985 | hp1 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA18986 | hp1 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA18986 | hp2 | a0002 | c0002 | t0003 | g0075 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA18987 | hp2 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA18988 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA18990 | hp2 | a0001 | c0001 | t0012 | g0160 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA18992 | hp2 | a0001 | c0001 | t0003 | g0087 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA18993 | hp2 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA18994 | hp1 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA18997 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA18999 | hp1 | a0002 | c0002 | t0003 | g0002 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA19000 | hp1 | a0002 | c0002 | t0003 | g0002 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA19003 | hp1 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA19005 | hp2 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA19030 | hp1 | a0001 | c0001 | t0005 | g0108 | AFR | LWK | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | LWK | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA19043 | hp1 | a0001 | c0001 | t0015 | g0189 | AFR | LWK | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA19043 | hp2 | a0001 | c0003 | t0014 | g0076 | AFR | LWK | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA19054 | hp1 | a0001 | c0001 | t0003 | g0066 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA19055 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA19055 | hp2 | a0003 | c0005 | t0001 | g0049 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA19056 | hp2 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA19057 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA19060 | hp1 | a0001 | c0014 | t0001 | g0022 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA19060 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA19062 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA19062 | hp2 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA19063 | hp1 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA19064 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA19065 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA19065 | hp2 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA19068 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA19074 | hp1 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA19075 | hp2 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA19076 | hp1 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA19077 | hp1 | a0001 | c0001 | t0002 | g0138 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA19079 | hp1 | a0002 | c0002 | t0003 | g0070 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA19082 | hp2 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA19083 | hp2 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA19086 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA19087 | hp2 | a0001 | c0001 | t0024 | g0006 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA19088 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA19090 | hp1 | a0002 | c0002 | t0003 | g0002 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA19240 | hp1 | a0001 | c0001 | t0002 | g0161 | AFR | YRI | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA19240 | hp2 | a0001 | c0003 | t0005 | g0013 | AFR | YRI | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0015 | AFR | ASW | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA20752 | hp1 | a0001 | c0001 | t0018 | g0149 | EUR | TSI | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0122 | EUR | TSI | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0148 | EUR | TSI | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | GIH | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0044 | SAS | GIH | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0242 | AMR | CLM | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG01123 | hp2 | a0004 | c0006 | t0004 | g0032 | AMR | CLM | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG02109 | hp1 | a0001 | c0001 | t0005 | g0176 | AFR | ACB | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG02109 | hp2 | a0001 | c0001 | t0002 | g0126 | AFR | ACB | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG02486 | hp1 | a0001 | c0003 | t0005 | g0013 | AFR | ACB | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG02486 | hp2 | a0001 | c0001 | t0002 | g0065 | AFR | ACB | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG02559 | hp1 | a0001 | c0001 | t0005 | g0105 | AFR | ACB | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG02559 | hp2 | a0001 | c0004 | t0010 | g0058 | AFR | ACB | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG03471 | hp1 | a0001 | c0001 | t0019 | g0215 | AFR | MSL | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
HG03471 | hp2 | a0001 | c0001 | t0002 | g0039 | AFR | MSL | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA20300 | hp1 | a0001 | c0001 | t0005 | g0111 | AFR | USA | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA20300 | hp2 | a0002 | c0002 | t0002 | g0129 | AFR | USA | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0243 | AFR | LWK | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | LWK | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0116 | REF | REF | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0137 | REF | REF | FAM98B_chr15_38449127_38492710 | FAM98B | chr15 | 38449127 | 38492710 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:38470352
|
C | T | 1 | a0010 | 1 | HG02129.hp2 | missense_variant | MODERATE | c.478C>T | p.Pro160Ser | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 4/8 | 513/4388 | 478/1302 | 160/433 | chr15 | 38470352 | ||
chr15:38470377
|
C | T | 1 | a0005 | 1 | HG02055.hp2 | missense_variant | MODERATE | c.503C>T | p.Pro168Leu | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 4/8 | 538/4388 | 503/1302 | 168/433 | chr15 | 38470377 | ||
chr15:38484433
|
G | C | 1 | a0006 | 1 | HG03017.hp1 | missense_variant | MODERATE | c.1076G>C | p.Trp359Ser | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 8/8 | 1111/4388 | 1076/1302 | 359/433 | chr15 | 38484433 | ||
chr15:38484469
|
G | A | 1 | a0004 | 3 | HG01123.hp2 HG02300.hp1 HG04184.hp1 |
missense_variant | MODERATE | c.1112G>A | p.Gly371Glu | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 8/8 | 1147/4388 | 1112/1302 | 371/433 | chr15 | 38484469 | ||
chr15:38484483
|
T | G | 1 | a0007 | 1 | HG02738.hp1 | missense_variant | MODERATE | c.1126T>G | p.Trp376Gly | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 8/8 | 1161/4388 | 1126/1302 | 376/433 | chr15 | 38484483 | ||
chr15:38484486
|
G | A | 1 | a0009 | 1 | HG01928.hp2 | missense_variant | MODERATE | c.1129G>A | p.Gly377Arg | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 8/8 | 1164/4388 | 1129/1302 | 377/433 | chr15 | 38484486 | ||
chr15:38484532
|
ATTATGGT others(11): Show |
A | 1 | a0003 | 4 | HG03491.hp1 HG03492.hp1 HG03834.hp2 others(1): Show |
disruptive_inframe_deletion | MODERATE | c.1194_1211delTTATGG others(12): Show |
p.Tyr399_Gly404del | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 8/8 | 1229/4388 | 1194/1302 | 398/433 | INFO_REALIGN_3_PRIME | chr15 | 38484532 | |
chr15:38484551
|
TTATGGTG others(11): Show |
T | 1 | a0008 | 1 | HG02293.hp1 | disruptive_inframe_deletion | MODERATE | c.1209_1226delGGGCTA others(12): Show |
p.Gly404_Gly409del | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 8/8 | 1244/4388 | 1209/1302 | 403/433 | INFO_REALIGN_3_PRIME | chr15 | 38484551 | |
chr15:38484605
|
AGGTGGTG others(2): Show |
A | 2 | a0002a0008 | 31 | HG00642.hp1 HG00738.hp2 HG01169.hp1 others(28): Show |
disruptive_inframe_deletion | MODERATE | c.1269_1277delTGGTGG others(3): Show |
p.Gly424_Gly426del | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 8/8 | 1304/4388 | 1269/1302 | 423/433 | INFO_REALIGN_3_PRIME | chr15 | 38484605 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:38454188
|
A | G | 1 | a0001c0014 | 1 | NA19060.hp1 | synonymous_variant | LOW | c.27A>G | p.Gln9Gln | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/8 | 62/4388 | 27/1302 | 9/433 | chr15 | 38454188 | ||
chr15:38484368
|
T | C | 2 | a0001c0003a0002c0007 | 13 | HG01069.hp1 HG01071.hp1 HG01109.hp2 others(10): Show |
synonymous_variant | LOW | c.1011T>C | p.Gly337Gly | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 8/8 | 1046/4388 | 1011/1302 | 337/433 | chr15 | 38484368 | ||
chr15:38484440
|
T | C | 2 | a0001c0004a0005c0012 | 8 | HG02055.hp2 HG02258.hp2 HG02559.hp2 others(5): Show |
synonymous_variant | LOW | c.1083T>C | p.Gly361Gly | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 8/8 | 1118/4388 | 1083/1302 | 361/433 | chr15 | 38484440 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:38484675
|
G | A | 1 | a0001c0001t0012 | 1 | NA18990.hp2 | 3_prime_UTR_variant | MODIFIER | c.*16G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 8/8 | 16 | chr15 | 38484675 | |||||
chr15:38484810
|
A | G | 1 | a0002c0002t0025 | 1 | HG02523.hp1 | 3_prime_UTR_variant | MODIFIER | c.*151A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 8/8 | 151 | chr15 | 38484810 | |||||
chr15:38484970
|
A | G | 2 | a0001c0001t0012a0001c0001t0024 | 2 | NA18990.hp2 NA19087.hp2 |
3_prime_UTR_variant | MODIFIER | c.*311A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 8/8 | 311 | chr15 | 38484970 | |||||
chr15:38485057
|
A | G | 1 | a0001c0001t0023 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*398A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 8/8 | 398 | chr15 | 38485057 | |||||
chr15:38485088
|
C | T | 1 | a0001c0001t0022 | 1 | HG01106.hp1 | 3_prime_UTR_variant | MODIFIER | c.*429C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 8/8 | 429 | chr15 | 38485088 | |||||
chr15:38485142
|
C | T | 2 | a0001c0004t0006a0005c0012t0006 | 6 | HG02055.hp2 HG02258.hp2 HG02572.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*483C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 8/8 | 483 | chr15 | 38485142 | |||||
chr15:38485173
|
G | A | 1 | a0001c0001t0013 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*514G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 8/8 | 514 | chr15 | 38485173 | |||||
chr15:38485180
|
T | C | 1 | a0001c0001t0022 | 1 | HG01106.hp1 | 3_prime_UTR_variant | MODIFIER | c.*521T>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 8/8 | 521 | chr15 | 38485180 | |||||
chr15:38485264
|
G | A | 1 | a0001c0003t0014 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*605G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 8/8 | 605 | chr15 | 38485264 | |||||
chr15:38485272
|
T | A | 1 | a0001c0001t0015 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*613T>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 8/8 | 613 | chr15 | 38485272 | |||||
chr15:38485622
|
C | T | 1 | a0001c0001t0021 | 1 | HG02080.hp1 | 3_prime_UTR_variant | MODIFIER | c.*963C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 8/8 | 963 | chr15 | 38485622 | |||||
chr15:38485632
|
A | C | 9 | a0001c0001t0003a0001c0001t0020a0001c0001t0023others(6): Show | 52 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*973A>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 8/8 | 973 | chr15 | 38485632 | |||||
chr15:38486037
|
T | G | 1 | a0001c0001t0016 | 1 | HG03834.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1378T>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 8/8 | 1378 | chr15 | 38486037 | |||||
chr15:38486273
|
GA | G | 2 | a0001c0001t0007a0001c0001t0022 | 5 | HG01106.hp1 HG02258.hp1 HG02615.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1621delA | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 8/8 | 1621 | INFO_REALIGN_3_PRIME | chr15 | 38486273 | ||||
chr15:38486331
|
A | C | 1 | a0001c0001t0019 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1672A>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 8/8 | 1672 | chr15 | 38486331 | |||||
chr15:38486691
|
T | C | 1 | a0001c0001t0017 | 1 | HG02132.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2032T>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 8/8 | 2032 | chr15 | 38486691 | |||||
chr15:38486839
|
G | A | 1 | a0001c0001t0008 | 3 | HG00140.hp1 HG02602.hp1 HG03490.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2180G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 8/8 | 2180 | chr15 | 38486839 | |||||
chr15:38486896
|
G | A | 1 | a0001c0001t0023 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2237G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 8/8 | 2237 | chr15 | 38486896 | |||||
chr15:38487116
|
C | T | 1 | a0001c0001t0022 | 1 | HG01106.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2457C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 8/8 | 2457 | chr15 | 38487116 | |||||
chr15:38487121
|
G | A | 1 | a0001c0001t0007 | 4 | HG02258.hp1 HG02615.hp2 HG02895.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2462G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 8/8 | 2462 | chr15 | 38487121 | |||||
chr15:38487206
|
T | C | 1 | a0001c0001t0020 | 1 | HG02738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2547T>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 8/8 | 2547 | chr15 | 38487206 | |||||
chr15:38487335
|
A | C | 2 | a0001c0001t0005a0001c0003t0005 | 22 | HG01069.hp1 HG01071.hp1 HG01109.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*2676A>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 8/8 | 2676 | chr15 | 38487335 | |||||
chr15:38487339
|
G | T | 2 | a0001c0001t0010a0001c0004t0010 | 3 | HG02559.hp2 HG02622.hp1 HG02723.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2680G>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 8/8 | 2680 | chr15 | 38487339 | |||||
chr15:38487425
|
A | G | 33 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(30): Show | 278 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(275): Show |
3_prime_UTR_variant | MODIFIER | c.*2766A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 8/8 | 2766 | chr15 | 38487425 | |||||
chr15:38487537
|
T | C | 10 | a0001c0001t0001a0001c0001t0008a0001c0001t0016others(7): Show | 150 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(147): Show |
3_prime_UTR_variant | MODIFIER | c.*2878T>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 8/8 | 2878 | chr15 | 38487537 | |||||
chr15:38487556
|
C | G | 1 | a0001c0001t0018 | 1 | NA20752.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2897C>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 8/8 | 2897 | chr15 | 38487556 | |||||
chr15:38487589
|
T | C | 6 | a0001c0001t0007a0001c0001t0010a0001c0001t0011others(3): Show | 15 | HG02055.hp2 HG02258.hp1 HG02258.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*2930T>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 8/8 | 2930 | chr15 | 38487589 | |||||
chr15:38487701
|
G | A | 2 | a0001c0001t0009a0001c0001t0015 | 4 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3042G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 8/8 | 3042 | chr15 | 38487701 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:38454243
|
T | C | 1 | a0001c0001t0004g0056 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.71+11T>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38454243 | ||||||
chr15:38454407
|
T | C | 7 | a0001c0001t0010g0057a0001c0004t0006g0026a0001c0004t0006g0027others(4): Show | 9 | HG02055.hp2 HG02258.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.71+175T>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38454407 | ||||||
chr15:38454449
|
C | G | 1 | a0001c0001t0001g0256 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.71+217C>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38454449 | ||||||
chr15:38454548
|
G | T | 1 | a0001c0004t0006g0027 | 2 | HG02258.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.71+316G>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38454548 | ||||||
chr15:38454671
|
A | G | 1 | a0001c0001t0001g0255 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.71+439A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38454671 | ||||||
chr15:38454696
|
A | G | 3 | a0001c0003t0005g0055a0001c0003t0005g0253a0002c0007t0003g0254 | 4 | HG01069.hp1 HG01071.hp1 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.71+464A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38454696 | ||||||
chr15:38454870
|
C | G | 1 | a0001c0001t0002g0252 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.71+638C>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38454870 | ||||||
chr15:38455077
|
G | A | 1 | a0001c0001t0002g0062 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.71+845G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38455077 | ||||||
chr15:38455114
|
A | G | 84 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(81): Show | 141 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.71+882A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38455114 | ||||||
chr15:38455223
|
G | T | 1 | a0001c0001t0002g0190 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.71+991G>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38455223 | ||||||
chr15:38455343
|
C | T | 4 | a0001c0001t0009g0186a0001c0001t0009g0187a0001c0001t0009g0188others(1): Show | 4 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.71+1111C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38455343 | ||||||
chr15:38455437
|
C | CT | 5 | a0002c0002t0003g0182a0002c0002t0003g0183a0002c0002t0003g0184others(2): Show | 5 | HG00642.hp1 HG00738.hp2 HG02523.hp1 others(2): Show |
intron_variant | MODIFIER | c.71+1206dupT | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr15 | 38455437 | |||||
chr15:38455477
|
T | C | 1 | a0001c0001t0001g0028 | 2 | HG00735.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.71+1245T>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38455477 | ||||||
chr15:38455671
|
C | T | 1 | a0001c0001t0001g0054 | 2 | NA18979.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.71+1439C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38455671 | ||||||
chr15:38455685
|
C | G | 1 | a0001c0001t0022g0180 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.71+1453C>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38455685 | ||||||
chr15:38456318
|
C | T | 4 | a0001c0001t0009g0186a0001c0001t0009g0187a0001c0001t0009g0188others(1): Show | 4 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.71+2086C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38456318 | ||||||
chr15:38456362
|
G | A | 2 | a0001c0001t0001g0191a0001c0001t0001g0192 | 2 | NA18944.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.71+2130G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38456362 | ||||||
chr15:38456385
|
G | A | 1 | a0001c0001t0023g0063 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.71+2153G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38456385 | ||||||
chr15:38456479
|
G | A | 1 | a0001c0001t0022g0180 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.71+2247G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38456479 | ||||||
chr15:38456782
|
A | G | 1 | a0001c0001t0002g0179 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.71+2550A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38456782 | ||||||
chr15:38457058
|
T | A | 1 | a0001c0001t0002g0064 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.71+2826T>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38457058 | ||||||
chr15:38457171
|
T | C | 1 | a0001c0001t0022g0180 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.71+2939T>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38457171 | ||||||
chr15:38457188
|
T | A | 1 | a0001c0001t0002g0065 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.71+2956T>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38457188 | ||||||
chr15:38457215
|
G | T | 2 | a0002c0002t0003g0177a0008c0011t0003g0178 | 2 | HG01981.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.71+2983G>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38457215 | ||||||
chr15:38457225
|
C | T | 1 | a0009c0010t0001g0251 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.71+2993C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38457225 | ||||||
chr15:38457411
|
A | G | 1 | a0001c0001t0005g0176 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.71+3179A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38457411 | ||||||
chr15:38457560
|
T | C | 55 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0020others(52): Show | 95 | HG00099.hp1 HG00323.hp1 HG00621.hp1 others(92): Show |
intron_variant | MODIFIER | c.71+3328T>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38457560 | ||||||
chr15:38457654
|
G | A | 1 | a0001c0001t0002g0252 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.71+3422G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38457654 | ||||||
chr15:38457957
|
C | CT | 27 | a0001c0001t0001g0229a0001c0001t0002g0006a0001c0001t0002g0018others(24): Show | 36 | HG00597.hp1 HG00673.hp1 HG01192.hp2 others(33): Show |
intron_variant | MODIFIER | c.71+3742dupT | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr15 | 38457957 | |||||
chr15:38457957
|
CT | C | 44 | a0001c0001t0001g0020a0001c0001t0001g0048a0001c0001t0001g0193others(41): Show | 70 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.71+3742delT | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr15 | 38457957 | |||||
chr15:38457978
|
A | G | 3 | a0001c0003t0005g0055a0001c0003t0005g0253a0002c0007t0003g0254 | 4 | HG01069.hp1 HG01071.hp1 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.71+3746A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38457978 | ||||||
chr15:38458158
|
G | A | 25 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0011others(22): Show | 48 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(45): Show |
intron_variant | MODIFIER | c.71+3926G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458158 | ||||||
chr15:38458541
|
A | G | 1 | a0002c0002t0003g0075 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.71+4309A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458541 | ||||||
chr15:38458581
|
T | C | 1 | a0001c0001t0001g0193 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4349T>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458581 | ||||||
chr15:38458619
|
C | G | 3 | a0001c0001t0001g0250a0003c0005t0001g0053a0003c0005t0001g0234 | 4 | HG03017.hp2 HG03491.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.71+4387C>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458619 | ||||||
chr15:38458733
|
GCTTGGAA others(8): Show |
G | 1 | a0001c0001t0001g0193 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4502_71+4516del others(15): Show |
FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458733 | ||||||
chr15:38458749
|
G | T | 1 | a0001c0001t0001g0193 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4517G>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458749 | ||||||
chr15:38458750
|
G | T | 4 | a0001c0001t0009g0186a0001c0001t0009g0187a0001c0001t0009g0188others(1): Show | 4 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.71+4518G>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458750 | ||||||
chr15:38458764
|
C | T | 1 | a0001c0001t0001g0193 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4532C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458764 | ||||||
chr15:38458765
|
C | T | 1 | a0001c0001t0001g0193 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4533C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458765 | ||||||
chr15:38458766
|
C | G | 1 | a0001c0001t0001g0193 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4534C>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458766 | ||||||
chr15:38458771
|
C | A | 1 | a0001c0001t0001g0193 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4539C>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458771 | ||||||
chr15:38458772
|
A | T | 1 | a0001c0001t0001g0193 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4540A>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458772 | ||||||
chr15:38458774
|
G | T | 1 | a0001c0001t0001g0193 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4542G>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458774 | ||||||
chr15:38458776
|
C | T | 1 | a0001c0001t0001g0193 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4544C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458776 | ||||||
chr15:38458778
|
G | T | 1 | a0001c0001t0001g0193 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4546G>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458778 | ||||||
chr15:38458781
|
A | T | 1 | a0001c0001t0001g0193 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4549A>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458781 | ||||||
chr15:38458784
|
G | T | 1 | a0001c0001t0001g0193 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4552G>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458784 | ||||||
chr15:38458786
|
T | C | 164 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(161): Show | 262 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(259): Show |
intron_variant | MODIFIER | c.71+4554T>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458786 | ||||||
chr15:38458787
|
G | A | 1 | a0001c0001t0001g0193 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4555G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458787 | ||||||
chr15:38458789
|
C | T | 1 | a0001c0001t0001g0193 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4557C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458789 | ||||||
chr15:38458790
|
C | A | 25 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0011others(22): Show | 48 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(45): Show |
intron_variant | MODIFIER | c.71+4558C>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458790 | ||||||
chr15:38458792
|
C | T | 1 | a0001c0001t0001g0193 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4560C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458792 | ||||||
chr15:38458794
|
G | A | 1 | a0001c0001t0001g0193 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4562G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458794 | ||||||
chr15:38458796
|
T | A | 1 | a0001c0001t0001g0193 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4564T>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458796 | ||||||
chr15:38458797
|
C | A | 1 | a0001c0001t0001g0193 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4565C>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458797 | ||||||
chr15:38458799
|
G | T | 1 | a0001c0001t0001g0193 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4567G>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458799 | ||||||
chr15:38458800
|
C | A | 1 | a0001c0001t0001g0193 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4568C>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458800 | ||||||
chr15:38458802
|
T | C | 1 | a0001c0001t0001g0193 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4570T>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458802 | ||||||
chr15:38458805
|
C | T | 1 | a0001c0001t0001g0193 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4573C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458805 | ||||||
chr15:38458807
|
A | T | 1 | a0001c0001t0001g0193 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4575A>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458807 | ||||||
chr15:38458811
|
C | T | 1 | a0001c0001t0001g0193 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4579C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458811 | ||||||
chr15:38458812
|
T | G | 1 | a0001c0001t0001g0193 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4580T>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458812 | ||||||
chr15:38458813
|
G | A | 1 | a0001c0001t0001g0193 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4581G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458813 | ||||||
chr15:38458817
|
A | T | 1 | a0001c0001t0022g0180 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.71+4585A>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458817 | ||||||
chr15:38458818
|
C | G | 1 | a0001c0001t0001g0193 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4586C>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458818 | ||||||
chr15:38458820
|
G | A | 1 | a0001c0001t0001g0193 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4588G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458820 | ||||||
chr15:38458821
|
G | A | 1 | a0001c0001t0001g0193 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4589G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458821 | ||||||
chr15:38458824
|
C | G | 1 | a0001c0001t0001g0193 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4592C>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458824 | ||||||
chr15:38458830
|
C | G | 1 | a0001c0001t0001g0193 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4598C>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458830 | ||||||
chr15:38458832
|
C | T | 1 | a0001c0001t0001g0193 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4600C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458832 | ||||||
chr15:38458837
|
T | A | 1 | a0001c0001t0001g0193 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4605T>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458837 | ||||||
chr15:38458840
|
G | T | 1 | a0001c0001t0001g0193 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4608G>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458840 | ||||||
chr15:38458842
|
C | A | 1 | a0001c0001t0001g0193 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4610C>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458842 | ||||||
chr15:38458844
|
T | G | 1 | a0001c0001t0001g0193 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4612T>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458844 | ||||||
chr15:38458846
|
T | C | 1 | a0001c0001t0001g0193 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4614T>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458846 | ||||||
chr15:38458849
|
T | C | 1 | a0001c0001t0001g0193 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4617T>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458849 | ||||||
chr15:38458851
|
A | T | 1 | a0001c0001t0001g0193 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4619A>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458851 | ||||||
chr15:38458853
|
A | G | 1 | a0001c0001t0001g0193 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4621A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458853 | ||||||
chr15:38458855
|
C | T | 1 | a0001c0001t0001g0193 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4623C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458855 | ||||||
chr15:38458858
|
G | T | 1 | a0001c0001t0001g0193 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4626G>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458858 | ||||||
chr15:38458860
|
C | A | 1 | a0001c0001t0001g0193 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4628C>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458860 | ||||||
chr15:38458861
|
T | A | 1 | a0001c0001t0001g0193 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4629T>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458861 | ||||||
chr15:38458862
|
G | A | 1 | a0001c0001t0001g0193 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4630G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458862 | ||||||
chr15:38458863
|
C | G | 1 | a0001c0001t0001g0193 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4631C>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458863 | ||||||
chr15:38458864
|
A | T | 1 | a0001c0001t0001g0193 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4632A>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458864 | ||||||
chr15:38458866
|
A | G | 1 | a0001c0001t0001g0193 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4634A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458866 | ||||||
chr15:38458874
|
C | G | 1 | a0001c0001t0001g0193 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4642C>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458874 | ||||||
chr15:38458876
|
T | G | 1 | a0001c0001t0001g0193 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4644T>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458876 | ||||||
chr15:38458879
|
T | A | 1 | a0001c0001t0001g0193 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4647T>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458879 | ||||||
chr15:38458887
|
G | T | 1 | a0001c0001t0001g0193 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4655G>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458887 | ||||||
chr15:38458888
|
A | C | 1 | a0001c0001t0001g0193 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4656A>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458888 | ||||||
chr15:38458892
|
T | A | 1 | a0001c0001t0001g0193 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4660T>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458892 | ||||||
chr15:38458894
|
T | C | 1 | a0001c0001t0001g0193 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4662T>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458894 | ||||||
chr15:38458898
|
A | T | 1 | a0001c0001t0001g0193 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4666A>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458898 | ||||||
chr15:38458899
|
A | C | 1 | a0001c0001t0001g0193 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4667A>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458899 | ||||||
chr15:38458900
|
G | C | 1 | a0001c0001t0001g0193 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4668G>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458900 | ||||||
chr15:38458902
|
A | G | 1 | a0001c0001t0001g0193 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4670A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458902 | ||||||
chr15:38458904
|
A | G | 1 | a0001c0001t0001g0193 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4672A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458904 | ||||||
chr15:38458906
|
A | T | 1 | a0001c0001t0001g0193 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4674A>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458906 | ||||||
chr15:38458912
|
T | C | 1 | a0001c0001t0001g0193 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4680T>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458912 | ||||||
chr15:38458914
|
C | T | 1 | a0001c0001t0001g0193 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4682C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458914 | ||||||
chr15:38458920
|
G | A | 2 | a0001c0001t0001g0051a0001c0001t0001g0235 | 3 | NA18945.hp2 NA18994.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.71+4688G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458920 | ||||||
chr15:38458920
|
G | C | 1 | a0001c0001t0001g0193 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4688G>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458920 | ||||||
chr15:38458921
|
A | C | 1 | a0001c0001t0001g0193 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4689A>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458921 | ||||||
chr15:38458922
|
G | A | 1 | a0001c0001t0001g0028 | 2 | HG00735.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.71+4690G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458922 | ||||||
chr15:38458927
|
T | A | 1 | a0001c0001t0001g0193 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4695T>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458927 | ||||||
chr15:38458930
|
C | T | 1 | a0001c0001t0001g0193 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4698C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458930 | ||||||
chr15:38458931
|
T | C | 1 | a0001c0001t0001g0193 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.71+4699T>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458931 | ||||||
chr15:38458949
|
G | A | 25 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0011others(22): Show | 48 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(45): Show |
intron_variant | MODIFIER | c.71+4717G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458949 | ||||||
chr15:38458956
|
G | A | 3 | a0001c0001t0004g0029a0001c0001t0004g0088a0001c0001t0004g0089 | 4 | HG00280.hp2 HG00735.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.71+4724G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38458956 | ||||||
chr15:38459017
|
C | G | 1 | a0001c0001t0002g0158 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.71+4785C>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38459017 | ||||||
chr15:38459025
|
C | T | 1 | a0001c0001t0023g0063 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.71+4793C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38459025 | ||||||
chr15:38459038
|
C | T | 15 | a0001c0001t0005g0014a0001c0001t0005g0104a0001c0001t0005g0105others(12): Show | 22 | HG01069.hp1 HG01071.hp1 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.71+4806C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38459038 | ||||||
chr15:38459105
|
C | T | 1 | a0001c0004t0010g0060 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.71+4873C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38459105 | ||||||
chr15:38459124
|
T | C | 1 | a0001c0001t0022g0180 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.71+4892T>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38459124 | ||||||
chr15:38459277
|
C | A | 2 | a0001c0001t0007g0030a0001c0001t0007g0090 | 3 | HG02258.hp1 HG02895.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.72-4755C>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38459277 | ||||||
chr15:38459296
|
C | T | 2 | a0001c0001t0002g0156a0001c0001t0002g0157 | 2 | HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.72-4736C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38459296 | ||||||
chr15:38459330
|
C | T | 3 | a0001c0001t0007g0030a0001c0001t0007g0090a0001c0001t0007g0103 | 4 | HG02258.hp1 HG02615.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.72-4702C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38459330 | ||||||
chr15:38459461
|
G | A | 1 | a0001c0001t0023g0063 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.72-4571G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38459461 | ||||||
chr15:38459556
|
C | T | 83 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(80): Show | 140 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.72-4476C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38459556 | ||||||
chr15:38459569
|
T | G | 1 | a0001c0001t0005g0176 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.72-4463T>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38459569 | ||||||
chr15:38459597
|
G | T | 1 | a0001c0001t0001g0249 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.72-4435G>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38459597 | ||||||
chr15:38459752
|
C | G | 1 | a0001c0001t0004g0056 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.72-4280C>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38459752 | ||||||
chr15:38459815
|
A | C | 25 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0011others(22): Show | 48 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(45): Show |
intron_variant | MODIFIER | c.72-4217A>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38459815 | ||||||
chr15:38459844
|
C | G | 2 | a0001c0001t0002g0155a0007c0009t0002g0154 | 2 | HG00642.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.72-4188C>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38459844 | ||||||
chr15:38459886
|
T | C | 1 | a0001c0001t0002g0113 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.72-4146T>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38459886 | ||||||
chr15:38459954
|
A | G | 6 | a0001c0001t0002g0045a0001c0001t0002g0065a0001c0001t0002g0083others(3): Show | 7 | HG00639.hp1 HG01070.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.72-4078A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38459954 | ||||||
chr15:38459961
|
G | A | 4 | a0001c0001t0009g0186a0001c0001t0009g0187a0001c0001t0009g0188others(1): Show | 4 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.72-4071G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38459961 | ||||||
chr15:38460072
|
T | C | 1 | a0001c0001t0001g0196 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.72-3960T>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38460072 | ||||||
chr15:38460168
|
G | C | 3 | a0001c0001t0007g0030a0001c0001t0007g0090a0001c0001t0007g0103 | 4 | HG02258.hp1 HG02615.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.72-3864G>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38460168 | ||||||
chr15:38460209
|
A | C | 3 | a0001c0001t0007g0030a0001c0001t0007g0090a0001c0001t0007g0103 | 4 | HG02258.hp1 HG02615.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.72-3823A>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38460209 | ||||||
chr15:38460382
|
GAGA | G | 82 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(79): Show | 139 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.72-3647_72-3645del others(3): Show |
FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr15 | 38460382 | |||||
chr15:38460408
|
A | G | 1 | a0001c0001t0022g0180 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.72-3624A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38460408 | ||||||
chr15:38460409
|
GT | G | 26 | a0001c0001t0002g0114a0001c0001t0003g0002a0001c0001t0003g0003others(23): Show | 49 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(46): Show |
intron_variant | MODIFIER | c.72-3612delT | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr15 | 38460409 | |||||
chr15:38460433
|
A | G | 1 | a0001c0001t0017g0228 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.72-3599A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38460433 | ||||||
chr15:38460498
|
T | C | 2 | a0001c0001t0005g0104a0001c0001t0005g0105 | 2 | HG01891.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.72-3534T>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38460498 | ||||||
chr15:38460584
|
A | G | 4 | a0001c0001t0009g0186a0001c0001t0009g0187a0001c0001t0009g0188others(1): Show | 4 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.72-3448A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38460584 | ||||||
chr15:38460594
|
A | G | 1 | a0001c0001t0022g0180 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.72-3438A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38460594 | ||||||
chr15:38460600
|
T | C | 1 | a0001c0001t0022g0180 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.72-3432T>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38460600 | ||||||
chr15:38460619
|
G | C | 1 | a0001c0001t0022g0180 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.72-3413G>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38460619 | ||||||
chr15:38460664
|
C | T | 3 | a0001c0001t0001g0247a0001c0001t0001g0248a0001c0001t0001g0249 | 3 | HG01069.hp2 HG03654.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.72-3368C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38460664 | ||||||
chr15:38460675
|
C | T | 4 | a0001c0001t0009g0186a0001c0001t0009g0187a0001c0001t0009g0188others(1): Show | 4 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.72-3357C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38460675 | ||||||
chr15:38460765
|
C | T | 1 | a0001c0001t0011g0152 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.72-3267C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38460765 | ||||||
chr15:38460927
|
C | T | 3 | a0001c0004t0006g0026a0001c0004t0006g0061a0005c0012t0006g0059 | 4 | HG02055.hp2 HG02572.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.72-3105C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38460927 | ||||||
chr15:38461180
|
GTT | G | 39 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0021others(36): Show | 68 | HG00323.hp1 HG00621.hp1 HG00673.hp2 others(65): Show |
intron_variant | MODIFIER | c.72-2850_72-2849del others(2): Show |
FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr15 | 38461180 | |||||
chr15:38461309
|
C | T | 1 | a0001c0001t0004g0012 | 4 | HG02257.hp2 HG02280.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.72-2723C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38461309 | ||||||
chr15:38461539
|
A | AAT | 16 | a0001c0001t0001g0016a0001c0001t0001g0028a0001c0001t0001g0116others(13): Show | 20 | HG00280.hp1 HG00735.hp1 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.72-2476_72-2475dup others(2): Show |
FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr15 | 38461539 | |||||
chr15:38461539
|
A | AATAT | 2 | a0001c0001t0001g0036a0002c0002t0002g0115 | 3 | HG01257.hp1 HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.72-2478_72-2475dup others(4): Show |
FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr15 | 38461539 | |||||
chr15:38461575
|
G | A | 15 | a0001c0001t0005g0014a0001c0001t0005g0104a0001c0001t0005g0105others(12): Show | 22 | HG01069.hp1 HG01071.hp1 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.72-2457G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38461575 | ||||||
chr15:38461593
|
G | C | 1 | a0001c0001t0005g0218 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.72-2439G>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38461593 | ||||||
chr15:38461618
|
G | C | 1 | a0001c0001t0007g0090 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.72-2414G>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38461618 | ||||||
chr15:38461676
|
T | C | 1 | a0001c0001t0023g0063 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.72-2356T>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38461676 | ||||||
chr15:38461739
|
C | T | 1 | a0002c0002t0003g0185 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.72-2293C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38461739 | ||||||
chr15:38461792
|
C | G | 1 | a0001c0001t0001g0217 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.72-2240C>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38461792 | ||||||
chr15:38461812
|
A | C | 1 | a0001c0001t0022g0180 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.72-2220A>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38461812 | ||||||
chr15:38461877
|
A | C | 1 | a0001c0001t0001g0192 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.72-2155A>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38461877 | ||||||
chr15:38461978
|
A | G | 1 | a0001c0001t0022g0180 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.72-2054A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38461978 | ||||||
chr15:38462123
|
T | A | 1 | a0001c0001t0001g0238 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.72-1909T>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38462123 | ||||||
chr15:38462126
|
A | AAATGTAT others(11): Show |
11 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0025others(8): Show | 22 | HG00423.hp1 HG00609.hp2 HG01168.hp2 others(19): Show |
intron_variant | MODIFIER | c.72-1905_72-1888dup others(18): Show |
FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr15 | 38462126 | |||||
chr15:38462223
|
A | G | 26 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0011others(23): Show | 49 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.72-1809A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38462223 | ||||||
chr15:38462431
|
C | A | 1 | a0001c0001t0007g0103 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.72-1601C>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38462431 | ||||||
chr15:38462657
|
A | C | 2 | a0001c0001t0005g0111a0001c0001t0005g0112 | 2 | HG02615.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.72-1375A>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38462657 | ||||||
chr15:38462694
|
T | C | 100 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(97): Show | 167 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.72-1338T>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38462694 | ||||||
chr15:38462735
|
A | G | 1 | a0001c0001t0023g0063 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.72-1297A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38462735 | ||||||
chr15:38462798
|
A | G | 1 | a0001c0001t0001g0216 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.72-1234A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38462798 | ||||||
chr15:38462835
|
A | G | 100 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(97): Show | 167 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.72-1197A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38462835 | ||||||
chr15:38462858
|
A | G | 1 | a0001c0001t0002g0175 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.72-1174A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38462858 | ||||||
chr15:38463018
|
A | G | 1 | a0001c0001t0002g0064 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.72-1014A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38463018 | ||||||
chr15:38463132
|
A | T | 1 | a0001c0001t0023g0063 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.72-900A>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38463132 | ||||||
chr15:38463284
|
C | T | 1 | a0006c0008t0001g0195 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.72-748C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38463284 | ||||||
chr15:38463322
|
T | A | 1 | a0001c0001t0005g0176 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.72-710T>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38463322 | ||||||
chr15:38463446
|
G | A | 54 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0020others(51): Show | 94 | HG00099.hp1 HG00323.hp1 HG00621.hp1 others(91): Show |
intron_variant | MODIFIER | c.72-586G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38463446 | ||||||
chr15:38463487
|
C | T | 1 | a0002c0007t0003g0254 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.72-545C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38463487 | ||||||
chr15:38463491
|
A | AAAAAT | 44 | a0001c0001t0002g0017a0001c0001t0002g0037a0001c0001t0002g0038others(41): Show | 66 | HG00323.hp2 HG00544.hp1 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.72-499_72-495dupAA others(3): Show |
FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr15 | 38463491 | |||||
chr15:38463491
|
A | AAAAATAA others(3): Show |
33 | a0001c0001t0003g0003a0001c0001t0003g0011a0001c0001t0003g0066others(30): Show | 44 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(41): Show |
intron_variant | MODIFIER | c.72-504_72-495dupAA others(8): Show |
FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr15 | 38463491 | |||||
chr15:38463491
|
A | AAAAATAA others(8): Show |
6 | a0001c0001t0004g0029a0001c0001t0004g0031a0001c0001t0004g0088others(3): Show | 8 | HG00735.hp2 HG00738.hp2 HG01516.hp2 others(5): Show |
intron_variant | MODIFIER | c.72-509_72-495dupAA others(13): Show |
FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr15 | 38463491 | |||||
chr15:38463491
|
AAAAAT | A | 82 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(79): Show | 138 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.72-499_72-495delAA others(3): Show |
FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr15 | 38463491 | |||||
chr15:38463491
|
AAAAATAA others(8): Show |
A | 5 | a0001c0001t0001g0024a0001c0001t0005g0014a0001c0001t0005g0110others(2): Show | 10 | HG01884.hp1 HG02451.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.72-509_72-495delAA others(13): Show |
FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr15 | 38463491 | |||||
chr15:38463523
|
A | AAATAGAA others(3): Show |
1 | a0001c0001t0022g0180 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.72-505_72-504insGA others(8): Show |
FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr15 | 38463523 | |||||
chr15:38463528
|
A | G | 1 | a0001c0001t0022g0180 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.72-504A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38463528 | ||||||
chr15:38463533
|
A | G | 1 | a0001c0001t0022g0180 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.72-499A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38463533 | ||||||
chr15:38463667
|
G | T | 1 | a0001c0001t0018g0149 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.72-365G>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38463667 | ||||||
chr15:38463700
|
A | G | 8 | a0001c0001t0001g0005a0001c0001t0001g0024a0001c0001t0001g0054others(5): Show | 17 | HG02273.hp2 NA18747.hp2 NA18950.hp2 others(14): Show |
intron_variant | MODIFIER | c.72-332A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38463700 | ||||||
chr15:38463913
|
G | T | 1 | a0001c0001t0011g0091 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.72-119G>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38463913 | ||||||
chr15:38464009
|
A | G | 2 | a0001c0001t0001g0214a0001c0001t0019g0215 | 2 | HG02717.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.72-23A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 1/7 | chr15 | 38464009 | ||||||
chr15:38464232
|
C | T | 2 | a0001c0001t0001g0212a0001c0001t0001g0213 | 2 | HG01168.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.217+55C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 2/7 | chr15 | 38464232 | ||||||
chr15:38464233
|
G | A | 15 | a0001c0001t0005g0014a0001c0001t0005g0104a0001c0001t0005g0105others(12): Show | 22 | HG01069.hp1 HG01071.hp1 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.217+56G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 2/7 | chr15 | 38464233 | ||||||
chr15:38464419
|
T | C | 2 | a0001c0001t0001g0219a0001c0001t0001g0220 | 2 | HG00099.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.217+242T>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 2/7 | chr15 | 38464419 | ||||||
chr15:38464452
|
T | C | 1 | a0001c0001t0002g0161 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.217+275T>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 2/7 | chr15 | 38464452 | ||||||
chr15:38464710
|
A | G | 53 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0020others(50): Show | 93 | HG00099.hp1 HG00323.hp1 HG00621.hp1 others(90): Show |
intron_variant | MODIFIER | c.217+533A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 2/7 | chr15 | 38464710 | ||||||
chr15:38464725
|
A | G | 1 | a0001c0001t0022g0180 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.218-544A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 2/7 | chr15 | 38464725 | ||||||
chr15:38464730
|
A | G | 1 | a0001c0001t0022g0180 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.218-539A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 2/7 | chr15 | 38464730 | ||||||
chr15:38464749
|
G | T | 1 | a0001c0001t0022g0180 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.218-520G>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 2/7 | chr15 | 38464749 | ||||||
chr15:38464841
|
A | G | 5 | a0001c0001t0009g0186a0001c0001t0009g0187a0001c0001t0009g0188others(2): Show | 5 | HG02717.hp1 HG02818.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.218-428A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 2/7 | chr15 | 38464841 | ||||||
chr15:38464861
|
C | T | 6 | a0001c0001t0009g0186a0001c0001t0009g0187a0001c0001t0009g0188others(3): Show | 6 | HG01106.hp1 HG02717.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.218-408C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 2/7 | chr15 | 38464861 | ||||||
chr15:38464922
|
C | T | 114 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(111): Show | 178 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(175): Show |
intron_variant | MODIFIER | c.218-347C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 2/7 | chr15 | 38464922 | ||||||
chr15:38464959
|
C | T | 1 | a0001c0001t0001g0148 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.218-310C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 2/7 | chr15 | 38464959 | ||||||
chr15:38465112
|
A | G | 1 | a0001c0001t0005g0218 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.218-157A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 2/7 | chr15 | 38465112 | ||||||
chr15:38465586
|
C | T | 1 | a0001c0001t0002g0174 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.352+183C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38465586 | ||||||
chr15:38465718
|
C | T | 1 | a0001c0001t0004g0012 | 4 | HG02257.hp2 HG02280.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.352+315C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38465718 | ||||||
chr15:38465736
|
A | T | 1 | a0001c0001t0022g0180 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.352+333A>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38465736 | ||||||
chr15:38465761
|
G | A | 1 | a0001c0001t0022g0180 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.352+358G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38465761 | ||||||
chr15:38465765
|
A | G | 1 | a0001c0001t0011g0091 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.352+362A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38465765 | ||||||
chr15:38465827
|
G | A | 53 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0020others(50): Show | 93 | HG00099.hp1 HG00323.hp1 HG00621.hp1 others(90): Show |
intron_variant | MODIFIER | c.352+424G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38465827 | ||||||
chr15:38465848
|
T | A | 22 | a0001c0001t0002g0018a0001c0001t0002g0046a0001c0001t0002g0064others(19): Show | 32 | HG00558.hp2 HG01069.hp1 HG01071.hp1 others(29): Show |
intron_variant | MODIFIER | c.352+445T>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38465848 | ||||||
chr15:38465849
|
A | T | 6 | a0001c0001t0001g0044a0001c0001t0001g0117a0001c0001t0003g0073others(3): Show | 7 | HG01106.hp1 HG01515.hp1 HG01517.hp2 others(4): Show |
intron_variant | MODIFIER | c.352+446A>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38465849 | ||||||
chr15:38465872
|
T | G | 1 | a0002c0002t0002g0132 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.352+469T>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38465872 | ||||||
chr15:38465928
|
A | G | 1 | a0001c0001t0011g0152 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.352+525A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38465928 | ||||||
chr15:38466136
|
C | G | 100 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(97): Show | 167 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.352+733C>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38466136 | ||||||
chr15:38466165
|
T | G | 1 | a0001c0001t0004g0012 | 4 | HG02257.hp2 HG02280.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.352+762T>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38466165 | ||||||
chr15:38466182
|
T | TTG | 12 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0039others(9): Show | 20 | HG01106.hp2 HG01934.hp1 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.352+815_352+816dup others(2): Show |
FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr15 | 38466182 | |||||
chr15:38466182
|
T | TTGTG | 3 | a0001c0001t0005g0108a0001c0001t0011g0152a0001c0003t0005g0109 | 3 | HG02818.hp1 HG02896.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.352+813_352+816dup others(4): Show |
FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr15 | 38466182 | |||||
chr15:38466182
|
T | TTGTGTG | 8 | a0001c0001t0002g0047a0001c0001t0002g0164a0001c0001t0002g0165others(5): Show | 12 | HG00597.hp1 HG01109.hp2 HG02040.hp1 others(9): Show |
intron_variant | MODIFIER | c.352+811_352+816dup others(6): Show |
FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr15 | 38466182 | |||||
chr15:38466182
|
T | TTGTGTGT others(1): Show |
2 | a0001c0003t0005g0055a0002c0007t0003g0254 | 3 | HG01069.hp1 HG01071.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.352+809_352+816dup others(8): Show |
FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr15 | 38466182 | |||||
chr15:38466182
|
T | TTGTGTGT others(3): Show |
3 | a0001c0001t0005g0014a0001c0001t0005g0110a0001c0001t0005g0176 | 6 | HG01884.hp1 HG02109.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.352+807_352+816dup others(10): Show |
FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr15 | 38466182 | |||||
chr15:38466182
|
T | TTGTGTGT others(5): Show |
3 | a0001c0001t0005g0104a0001c0001t0005g0105a0001c0001t0005g0111 | 3 | HG01891.hp2 HG02559.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.352+805_352+816dup others(12): Show |
FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr15 | 38466182 | |||||
chr15:38466182
|
TTG | T | 61 | a0001c0001t0002g0045a0001c0001t0002g0065a0001c0001t0002g0173others(58): Show | 91 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.352+815_352+816del others(2): Show |
FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr15 | 38466182 | |||||
chr15:38466182
|
TTGTG | T | 7 | a0001c0001t0001g0116a0001c0001t0002g0163a0001c0001t0007g0030others(4): Show | 8 | HG02258.hp1 HG02818.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.352+813_352+816del others(4): Show |
FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr15 | 38466182 | |||||
chr15:38466182
|
TTGTGTG | T | 4 | a0001c0001t0023g0063a0001c0004t0006g0027a0002c0002t0003g0183others(1): Show | 5 | HG00642.hp1 HG02258.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.352+811_352+816del others(6): Show |
FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr15 | 38466182 | |||||
chr15:38466182
|
TTGTGTGT others(3): Show |
T | 2 | a0001c0001t0001g0242a0001c0001t0022g0180 | 2 | HG01106.hp1 HG01123.hp1 |
intron_variant | MODIFIER | c.352+807_352+816del others(10): Show |
FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr15 | 38466182 | |||||
chr15:38466182
|
TTGTGTGT others(5): Show |
T | 82 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(79): Show | 139 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.352+805_352+816del others(12): Show |
FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr15 | 38466182 | |||||
chr15:38466264
|
T | C | 1 | a0001c0001t0001g0199 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.352+861T>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38466264 | ||||||
chr15:38466425
|
C | T | 4 | a0001c0001t0002g0125a0001c0001t0002g0126a0001c0001t0002g0127others(1): Show | 4 | HG02109.hp2 HG02809.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.352+1022C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38466425 | ||||||
chr15:38466550
|
A | G | 1 | a0001c0001t0001g0246 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.352+1147A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38466550 | ||||||
chr15:38466699
|
G | A | 1 | a0001c0001t0011g0152 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.352+1296G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38466699 | ||||||
chr15:38466813
|
T | C | 1 | a0001c0001t0002g0083 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.352+1410T>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38466813 | ||||||
chr15:38466824
|
C | T | 1 | a0001c0003t0014g0076 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.352+1421C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38466824 | ||||||
chr15:38466955
|
C | T | 6 | a0001c0001t0001g0010a0001c0001t0001g0051a0001c0001t0001g0232others(3): Show | 11 | HG00423.hp1 HG00609.hp2 NA18939.hp2 others(8): Show |
intron_variant | MODIFIER | c.352+1552C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38466955 | ||||||
chr15:38467026
|
A | T | 1 | a0001c0001t0001g0194 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.352+1623A>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38467026 | ||||||
chr15:38467108
|
T | G | 1 | a0001c0001t0022g0180 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.352+1705T>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38467108 | ||||||
chr15:38467150
|
T | C | 2 | a0001c0003t0005g0055a0002c0007t0003g0254 | 3 | HG01069.hp1 HG01071.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.352+1747T>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38467150 | ||||||
chr15:38467153
|
A | T | 1 | a0001c0001t0002g0161 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.352+1750A>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38467153 | ||||||
chr15:38467202
|
C | G | 2 | a0001c0001t0001g0212a0001c0001t0001g0213 | 2 | HG01168.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.352+1799C>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38467202 | ||||||
chr15:38467307
|
C | A | 2 | a0001c0001t0007g0030a0001c0001t0007g0090 | 3 | HG02258.hp1 HG02895.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.352+1904C>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38467307 | ||||||
chr15:38467335
|
T | C | 1 | a0001c0001t0004g0031 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.352+1932T>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38467335 | ||||||
chr15:38467337
|
T | A | 5 | a0001c0001t0009g0186a0001c0001t0009g0187a0001c0001t0009g0188others(2): Show | 5 | HG02717.hp1 HG02818.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.352+1934T>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38467337 | ||||||
chr15:38467655
|
T | C | 1 | a0001c0001t0013g0082 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.352+2252T>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38467655 | ||||||
chr15:38467774
|
A | G | 5 | a0001c0001t0009g0186a0001c0001t0009g0187a0001c0001t0009g0188others(2): Show | 5 | HG02717.hp1 HG02818.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.352+2371A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38467774 | ||||||
chr15:38467837
|
A | T | 1 | a0001c0001t0001g0198 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.353-2390A>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38467837 | ||||||
chr15:38467937
|
G | A | 1 | a0001c0001t0023g0063 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.353-2290G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38467937 | ||||||
chr15:38467972
|
C | A | 1 | a0001c0001t0011g0091 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.353-2255C>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38467972 | ||||||
chr15:38468027
|
A | G | 1 | a0001c0001t0002g0172 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.353-2200A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38468027 | ||||||
chr15:38468299
|
G | A | 18 | a0001c0001t0005g0014a0001c0001t0005g0104a0001c0001t0005g0105others(15): Show | 26 | HG01069.hp1 HG01071.hp1 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.353-1928G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38468299 | ||||||
chr15:38468383
|
C | A | 4 | a0001c0001t0009g0186a0001c0001t0009g0187a0001c0001t0009g0188others(1): Show | 4 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.353-1844C>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38468383 | ||||||
chr15:38468389
|
A | T | 168 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(165): Show | 266 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(263): Show |
intron_variant | MODIFIER | c.353-1838A>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38468389 | ||||||
chr15:38468419
|
G | T | 84 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(81): Show | 143 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.353-1808G>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38468419 | ||||||
chr15:38468462
|
G | C | 1 | a0001c0001t0004g0056 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.353-1765G>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38468462 | ||||||
chr15:38468490
|
T | G | 1 | a0001c0001t0005g0110 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.353-1737T>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38468490 | ||||||
chr15:38468707
|
T | C | 1 | a0001c0001t0022g0180 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.353-1520T>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38468707 | ||||||
chr15:38468755
|
G | A | 2 | a0001c0001t0004g0094a0001c0001t0004g0095 | 2 | HG03688.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.353-1472G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38468755 | ||||||
chr15:38468816
|
C | T | 1 | a0001c0003t0014g0076 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.353-1411C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38468816 | ||||||
chr15:38468871
|
G | A | 5 | a0001c0001t0002g0045a0001c0001t0002g0065a0001c0001t0002g0083others(2): Show | 6 | HG01070.hp2 HG01071.hp2 HG01081.hp1 others(3): Show |
intron_variant | MODIFIER | c.353-1356G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38468871 | ||||||
chr15:38468904
|
GTATT | G | 4 | a0001c0001t0009g0186a0001c0001t0009g0187a0001c0001t0009g0188others(1): Show | 4 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.353-1315_353-1312d others(6): Show |
FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr15 | 38468904 | |||||
chr15:38468988
|
C | A | 15 | a0001c0001t0005g0014a0001c0001t0005g0104a0001c0001t0005g0105others(12): Show | 22 | HG01069.hp1 HG01071.hp1 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.353-1239C>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38468988 | ||||||
chr15:38469027
|
T | C | 1 | a0001c0001t0022g0180 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.353-1200T>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38469027 | ||||||
chr15:38469053
|
A | G | 1 | a0001c0001t0022g0180 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.353-1174A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38469053 | ||||||
chr15:38469095
|
G | A | 1 | a0001c0001t0022g0180 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.353-1132G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38469095 | ||||||
chr15:38469145
|
A | G | 1 | a0001c0001t0019g0215 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.353-1082A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38469145 | ||||||
chr15:38469152
|
T | C | 1 | a0001c0001t0001g0224 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.353-1075T>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38469152 | ||||||
chr15:38469198
|
T | G | 1 | a0001c0001t0022g0180 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.353-1029T>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38469198 | ||||||
chr15:38469211
|
C | CCTACCGT others(11): Show |
83 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(80): Show | 140 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.353-1016_353-1015i others(20): Show |
FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38469211 | ||||||
chr15:38469212
|
A | G | 83 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(80): Show | 140 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.353-1015A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38469212 | ||||||
chr15:38469319
|
G | T | 1 | a0001c0003t0005g0107 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.353-908G>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38469319 | ||||||
chr15:38469586
|
C | T | 31 | a0001c0001t0004g0029a0001c0001t0004g0031a0001c0001t0004g0032others(28): Show | 38 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.353-641C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38469586 | ||||||
chr15:38469587
|
G | A | 1 | a0001c0001t0002g0157 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.353-640G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38469587 | ||||||
chr15:38469588
|
TTCCTGGC others(10): Show |
T | 1 | a0001c0003t0014g0076 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.353-634_353-618del others(17): Show |
FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr15 | 38469588 | |||||
chr15:38469868
|
G | C | 1 | a0001c0001t0001g0221 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.353-359G>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38469868 | ||||||
chr15:38470179
|
G | A | 2 | a0001c0001t0002g0133a0001c0001t0002g0190 | 2 | HG00140.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.353-48G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38470179 | ||||||
chr15:38470192
|
A | G | 15 | a0001c0001t0005g0014a0001c0001t0005g0104a0001c0001t0005g0105others(12): Show | 22 | HG01069.hp1 HG01071.hp1 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.353-35A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38470192 | ||||||
chr15:38470204
|
T | C | 1 | a0001c0001t0002g0083 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.353-23T>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 3/7 | chr15 | 38470204 | ||||||
chr15:38470447
|
G | T | 1 | a0001c0001t0004g0012 | 4 | HG02257.hp2 HG02280.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.531+42G>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 4/7 | chr15 | 38470447 | ||||||
chr15:38470500
|
A | G | 84 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(81): Show | 141 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.531+95A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 4/7 | chr15 | 38470500 | ||||||
chr15:38470528
|
A | G | 1 | a0001c0001t0002g0145 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.531+123A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 4/7 | chr15 | 38470528 | ||||||
chr15:38470677
|
A | G | 1 | a0001c0001t0001g0211 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.531+272A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 4/7 | chr15 | 38470677 | ||||||
chr15:38470682
|
C | T | 1 | a0001c0001t0002g0144 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.531+277C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 4/7 | chr15 | 38470682 | ||||||
chr15:38470800
|
G | C | 1 | a0001c0001t0022g0180 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.531+395G>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 4/7 | chr15 | 38470800 | ||||||
chr15:38470815
|
G | A | 31 | a0001c0001t0004g0029a0001c0001t0004g0031a0001c0001t0004g0032others(28): Show | 38 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.531+410G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 4/7 | chr15 | 38470815 | ||||||
chr15:38470950
|
AT | A | 15 | a0001c0001t0005g0014a0001c0001t0005g0104a0001c0001t0005g0105others(12): Show | 22 | HG01069.hp1 HG01071.hp1 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.531+558delT | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr15 | 38470950 | |||||
chr15:38471074
|
C | T | 2 | a0001c0001t0003g0011a0001c0001t0003g0087 | 5 | NA18969.hp2 NA18985.hp1 NA18992.hp2 others(2): Show |
intron_variant | MODIFIER | c.531+669C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 4/7 | chr15 | 38471074 | ||||||
chr15:38471167
|
G | A | 1 | a0002c0002t0003g0071 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.531+762G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 4/7 | chr15 | 38471167 | ||||||
chr15:38471209
|
G | A | 28 | a0001c0001t0002g0006a0001c0001t0002g0018a0001c0001t0002g0019others(25): Show | 37 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.531+804G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 4/7 | chr15 | 38471209 | ||||||
chr15:38471296
|
A | T | 1 | a0001c0001t0022g0180 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.531+891A>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 4/7 | chr15 | 38471296 | ||||||
chr15:38471324
|
A | G | 1 | a0001c0001t0015g0189 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.531+919A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 4/7 | chr15 | 38471324 | ||||||
chr15:38471462
|
C | T | 1 | a0001c0001t0003g0086 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.531+1057C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 4/7 | chr15 | 38471462 | ||||||
chr15:38471501
|
A | G | 267 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(264): Show | 399 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(396): Show |
intron_variant | MODIFIER | c.531+1096A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 4/7 | chr15 | 38471501 | ||||||
chr15:38471507
|
T | C | 10 | a0001c0001t0002g0040a0001c0001t0002g0062a0001c0001t0002g0080others(7): Show | 11 | HG00438.hp1 HG00544.hp1 HG01975.hp1 others(8): Show |
intron_variant | MODIFIER | c.531+1102T>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 4/7 | chr15 | 38471507 | ||||||
chr15:38471575
|
G | A | 2 | a0001c0001t0001g0238a0001c0001t0001g0243 | 2 | HG01081.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.531+1170G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 4/7 | chr15 | 38471575 | ||||||
chr15:38471592
|
A | G | 30 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(27): Show | 47 | HG00140.hp1 HG00423.hp1 HG00609.hp2 others(44): Show |
intron_variant | MODIFIER | c.531+1187A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 4/7 | chr15 | 38471592 | ||||||
chr15:38471614
|
C | T | 24 | a0001c0001t0004g0029a0001c0001t0004g0031a0001c0001t0004g0032others(21): Show | 29 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.531+1209C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 4/7 | chr15 | 38471614 | ||||||
chr15:38471616
|
A | G | 1 | a0001c0001t0001g0210 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.531+1211A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 4/7 | chr15 | 38471616 | ||||||
chr15:38471657
|
C | T | 1 | a0001c0001t0022g0180 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.531+1252C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 4/7 | chr15 | 38471657 | ||||||
chr15:38471677
|
A | G | 2 | a0001c0001t0009g0186a0001c0001t0009g0187 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.531+1272A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 4/7 | chr15 | 38471677 | ||||||
chr15:38471739
|
C | T | 1 | a0001c0001t0001g0209 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.531+1334C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 4/7 | chr15 | 38471739 | ||||||
chr15:38471926
|
A | G | 1 | a0001c0001t0004g0012 | 4 | HG02257.hp2 HG02280.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.531+1521A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 4/7 | chr15 | 38471926 | ||||||
chr15:38472221
|
A | T | 1 | a0001c0003t0014g0076 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.532-1284A>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 4/7 | chr15 | 38472221 | ||||||
chr15:38472226
|
T | G | 1 | a0001c0001t0001g0200 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.532-1279T>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 4/7 | chr15 | 38472226 | ||||||
chr15:38472297
|
T | G | 1 | a0001c0001t0022g0180 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.532-1208T>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 4/7 | chr15 | 38472297 | ||||||
chr15:38472346
|
ATAAAT | A | 2 | a0001c0001t0007g0030a0001c0001t0007g0090 | 3 | HG02258.hp1 HG02895.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.532-1155_532-1151d others(7): Show |
FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr15 | 38472346 | |||||
chr15:38472389
|
A | G | 1 | a0001c0001t0002g0171 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.532-1116A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 4/7 | chr15 | 38472389 | ||||||
chr15:38472555
|
T | A | 2 | a0001c0001t0001g0052a0001c0001t0001g0244 | 3 | NA18951.hp2 NA18962.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.532-950T>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 4/7 | chr15 | 38472555 | ||||||
chr15:38472642
|
C | T | 26 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(23): Show | 42 | HG00140.hp1 HG00423.hp1 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.532-863C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 4/7 | chr15 | 38472642 | ||||||
chr15:38473078
|
A | G | 1 | a0001c0001t0022g0180 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.532-427A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 4/7 | chr15 | 38473078 | ||||||
chr15:38473133
|
G | A | 1 | a0001c0001t0001g0201 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.532-372G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 4/7 | chr15 | 38473133 | ||||||
chr15:38473437
|
T | G | 1 | a0001c0001t0002g0125 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.532-68T>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 4/7 | chr15 | 38473437 | ||||||
chr15:38473729
|
T | C | 1 | a0001c0001t0002g0179 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.612+144T>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 5/7 | chr15 | 38473729 | ||||||
chr15:38473782
|
G | A | 1 | a0001c0001t0023g0063 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.612+197G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 5/7 | chr15 | 38473782 | ||||||
chr15:38473826
|
A | G | 1 | a0001c0001t0022g0180 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.612+241A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 5/7 | chr15 | 38473826 | ||||||
chr15:38474377
|
C | A | 1 | a0001c0001t0022g0180 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.729+79C>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38474377 | ||||||
chr15:38474603
|
G | C | 1 | a0001c0001t0022g0180 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.729+305G>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38474603 | ||||||
chr15:38474809
|
G | A | 1 | a0001c0001t0004g0077 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.729+511G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38474809 | ||||||
chr15:38474814
|
G | T | 26 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0011others(23): Show | 49 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.729+516G>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38474814 | ||||||
chr15:38475066
|
T | TTATTTTT others(321): Show |
1 | a0001c0001t0022g0180 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.729+784_729+785ins others(328): Show |
FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr15 | 38475066 | |||||
chr15:38475220
|
G | A | 1 | a0002c0002t0003g0177 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.729+922G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38475220 | ||||||
chr15:38475221
|
G | A | 1 | a0001c0001t0022g0180 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.729+923G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38475221 | ||||||
chr15:38475341
|
T | C | 1 | a0001c0001t0011g0091 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.729+1043T>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38475341 | ||||||
chr15:38475398
|
C | A | 1 | a0001c0001t0002g0179 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.729+1100C>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38475398 | ||||||
chr15:38475470
|
G | C | 1 | a0001c0001t0001g0222 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.729+1172G>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38475470 | ||||||
chr15:38475564
|
C | T | 12 | a0001c0001t0001g0005a0001c0001t0001g0023a0001c0001t0001g0024others(9): Show | 23 | HG02273.hp2 HG02602.hp2 HG04204.hp2 others(20): Show |
intron_variant | MODIFIER | c.729+1266C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38475564 | ||||||
chr15:38475665
|
A | G | 1 | a0001c0001t0001g0221 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.729+1367A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38475665 | ||||||
chr15:38475730
|
C | T | 54 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0020others(51): Show | 94 | HG00099.hp1 HG00323.hp1 HG00621.hp1 others(91): Show |
intron_variant | MODIFIER | c.729+1432C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38475730 | ||||||
chr15:38475759
|
C | T | 1 | a0001c0003t0014g0076 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.729+1461C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38475759 | ||||||
chr15:38475800
|
T | C | 1 | a0001c0001t0022g0180 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.729+1502T>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38475800 | ||||||
chr15:38475842
|
G | T | 25 | a0001c0001t0004g0029a0001c0001t0004g0031a0001c0001t0004g0032others(22): Show | 30 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.729+1544G>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38475842 | ||||||
chr15:38475866
|
C | CT | 34 | a0001c0001t0004g0029a0001c0001t0004g0031a0001c0001t0004g0032others(31): Show | 41 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.729+1576dupT | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr15 | 38475866 | |||||
chr15:38476280
|
T | C | 1 | a0001c0001t0001g0239 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.729+1982T>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38476280 | ||||||
chr15:38476465
|
C | G | 82 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(79): Show | 139 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.729+2167C>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38476465 | ||||||
chr15:38476488
|
T | A | 1 | a0001c0003t0014g0076 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.729+2190T>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38476488 | ||||||
chr15:38476496
|
C | T | 1 | a0001c0001t0022g0180 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.729+2198C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38476496 | ||||||
chr15:38476514
|
T | A | 1 | a0001c0001t0001g0230 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.729+2216T>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38476514 | ||||||
chr15:38476617
|
T | TAAATTTC others(327): Show |
1 | a0001c0001t0005g0105 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.729+2335_729+2336i others(336): Show |
FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr15 | 38476617 | |||||
chr15:38476703
|
C | CT | 35 | a0001c0001t0001g0241a0001c0001t0003g0002a0001c0001t0003g0003others(32): Show | 59 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.729+2419dupT | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr15 | 38476703 | |||||
chr15:38476703
|
CT | C | 32 | a0001c0001t0002g0164a0001c0001t0004g0029a0001c0001t0004g0031others(29): Show | 39 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.729+2419delT | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr15 | 38476703 | |||||
chr15:38476785
|
C | T | 1 | a0001c0001t0022g0180 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.729+2487C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38476785 | ||||||
chr15:38476795
|
C | T | 167 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(164): Show | 265 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(262): Show |
intron_variant | MODIFIER | c.729+2497C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38476795 | ||||||
chr15:38476868
|
A | G | 1 | a0001c0001t0022g0180 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.729+2570A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38476868 | ||||||
chr15:38476896
|
C | T | 1 | a0001c0003t0014g0076 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.729+2598C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38476896 | ||||||
chr15:38477127
|
G | A | 2 | a0001c0001t0001g0025a0001c0001t0001g0230 | 4 | NA18978.hp1 NA18997.hp2 NA19079.hp2 others(1): Show |
intron_variant | MODIFIER | c.729+2829G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38477127 | ||||||
chr15:38477225
|
G | A | 1 | a0001c0001t0004g0012 | 4 | HG02257.hp2 HG02280.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.729+2927G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38477225 | ||||||
chr15:38477227
|
T | TGTGCTGT others(318): Show |
1 | a0001c0001t0004g0101 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.729+2946_729+2947i others(327): Show |
FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr15 | 38477227 | |||||
chr15:38477227
|
T | TGTGCTGT others(328): Show |
1 | a0002c0002t0004g0096 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.729+2946_729+2947i others(337): Show |
FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr15 | 38477227 | |||||
chr15:38477227
|
T | TGTGCTGT others(329): Show |
2 | a0001c0001t0004g0097a0001c0001t0004g0098 | 2 | HG02698.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.729+2946_729+2947i others(338): Show |
FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr15 | 38477227 | |||||
chr15:38477227
|
T | TGTGCTGT others(330): Show |
8 | a0001c0001t0004g0031a0001c0001t0004g0032a0001c0001t0004g0035others(5): Show | 10 | HG00280.hp2 HG01099.hp2 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.729+2946_729+2947i others(339): Show |
FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr15 | 38477227 | |||||
chr15:38477227
|
T | TGTGCTGT others(331): Show |
6 | a0001c0001t0004g0029a0001c0001t0004g0033a0001c0001t0004g0034others(3): Show | 9 | HG00639.hp2 HG00735.hp2 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.729+2946_729+2947i others(340): Show |
FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr15 | 38477227 | |||||
chr15:38477227
|
T | TGTGCTGT others(332): Show |
6 | a0001c0001t0004g0056a0001c0001t0004g0077a0001c0001t0004g0094others(3): Show | 6 | HG00733.hp2 HG02055.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.729+2946_729+2947i others(341): Show |
FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr15 | 38477227 | |||||
chr15:38477227
|
T | TGTGCTGT others(333): Show |
4 | a0001c0001t0004g0095a0001c0001t0004g0100a0001c0004t0006g0026others(1): Show | 5 | HG02300.hp1 HG02572.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.729+2946_729+2947i others(342): Show |
FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr15 | 38477227 | |||||
chr15:38477227
|
T | TGTGCTGT others(334): Show |
2 | a0001c0001t0010g0057a0001c0004t0006g0027 | 3 | HG02258.hp2 HG02723.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.729+2946_729+2947i others(343): Show |
FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr15 | 38477227 | |||||
chr15:38477227
|
T | TGTGCTGT others(335): Show |
1 | a0001c0004t0010g0060 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.729+2946_729+2947i others(344): Show |
FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr15 | 38477227 | |||||
chr15:38477227
|
T | TGTGCTGT others(337): Show |
1 | a0001c0004t0010g0058 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.729+2946_729+2947i others(346): Show |
FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr15 | 38477227 | |||||
chr15:38477252
|
A | G | 1 | a0002c0002t0003g0070 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.729+2954A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38477252 | ||||||
chr15:38477311
|
A | G | 1 | a0001c0001t0022g0180 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.729+3013A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38477311 | ||||||
chr15:38477454
|
T | C | 1 | a0001c0001t0002g0126 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.729+3156T>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38477454 | ||||||
chr15:38477521
|
G | A | 1 | a0001c0001t0001g0202 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.729+3223G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38477521 | ||||||
chr15:38477770
|
A | G | 26 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0011others(23): Show | 49 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.729+3472A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38477770 | ||||||
chr15:38477775
|
T | C | 5 | a0001c0001t0009g0186a0001c0001t0009g0187a0001c0001t0009g0188others(2): Show | 5 | HG01106.hp1 HG02717.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.729+3477T>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38477775 | ||||||
chr15:38477857
|
G | A | 1 | a0001c0001t0022g0180 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.730-3435G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38477857 | ||||||
chr15:38477890
|
T | A | 1 | a0001c0001t0002g0121 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.730-3402T>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38477890 | ||||||
chr15:38477957
|
T | G | 26 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0011others(23): Show | 49 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.730-3335T>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38477957 | ||||||
chr15:38477986
|
C | A | 1 | a0001c0001t0002g0126 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.730-3306C>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38477986 | ||||||
chr15:38478025
|
G | A | 1 | a0001c0001t0004g0097 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.730-3267G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38478025 | ||||||
chr15:38478063
|
A | G | 1 | a0001c0001t0011g0152 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.730-3229A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38478063 | ||||||
chr15:38478131
|
T | C | 2 | a0001c0001t0011g0091a0001c0001t0011g0152 | 2 | HG02818.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.730-3161T>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38478131 | ||||||
chr15:38478172
|
C | G | 2 | a0001c0001t0002g0155a0007c0009t0002g0154 | 2 | HG00642.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.730-3120C>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38478172 | ||||||
chr15:38478196
|
T | C | 1 | a0001c0001t0022g0180 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.730-3096T>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38478196 | ||||||
chr15:38478364
|
G | C | 1 | a0001c0001t0002g0165 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.730-2928G>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38478364 | ||||||
chr15:38478427
|
C | G | 1 | a0001c0001t0003g0069 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.730-2865C>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38478427 | ||||||
chr15:38478433
|
T | G | 1 | a0005c0012t0006g0059 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.730-2859T>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38478433 | ||||||
chr15:38478473
|
A | T | 1 | a0001c0001t0011g0152 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.730-2819A>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38478473 | ||||||
chr15:38478763
|
C | A | 2 | a0004c0006t0004g0092a0004c0006t0004g0093 | 2 | HG02300.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.730-2529C>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38478763 | ||||||
chr15:38478879
|
C | T | 1 | a0001c0003t0014g0076 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.730-2413C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38478879 | ||||||
chr15:38478915
|
A | T | 1 | a0002c0002t0003g0182 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.730-2377A>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38478915 | ||||||
chr15:38479099
|
C | T | 1 | a0001c0001t0002g0139 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.730-2193C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38479099 | ||||||
chr15:38479156
|
C | T | 3 | a0001c0001t0001g0207a0001c0001t0001g0210a0001c0001t0001g0211 | 3 | HG02132.hp2 NA19009.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.730-2136C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38479156 | ||||||
chr15:38479209
|
G | C | 169 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(166): Show | 267 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(264): Show |
intron_variant | MODIFIER | c.730-2083G>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38479209 | ||||||
chr15:38479225
|
C | G | 1 | a0001c0001t0003g0068 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.730-2067C>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38479225 | ||||||
chr15:38479229
|
A | G | 83 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(80): Show | 140 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.730-2063A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38479229 | ||||||
chr15:38479403
|
T | C | 169 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(166): Show | 267 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(264): Show |
intron_variant | MODIFIER | c.730-1889T>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38479403 | ||||||
chr15:38479870
|
G | C | 1 | a0001c0001t0022g0180 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.730-1422G>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38479870 | ||||||
chr15:38480030
|
A | G | 170 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(167): Show | 268 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(265): Show |
intron_variant | MODIFIER | c.730-1262A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38480030 | ||||||
chr15:38480063
|
A | G | 1 | a0001c0004t0006g0027 | 2 | HG02258.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.730-1229A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38480063 | ||||||
chr15:38480222
|
T | A | 83 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(80): Show | 140 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.730-1070T>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38480222 | ||||||
chr15:38480223
|
C | T | 83 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(80): Show | 140 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.730-1069C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38480223 | ||||||
chr15:38480430
|
A | G | 2 | a0001c0001t0001g0025a0001c0001t0001g0230 | 4 | NA18978.hp1 NA18997.hp2 NA19079.hp2 others(1): Show |
intron_variant | MODIFIER | c.730-862A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38480430 | ||||||
chr15:38480522
|
G | C | 1 | a0001c0001t0001g0241 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.730-770G>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38480522 | ||||||
chr15:38480572
|
A | G | 1 | a0001c0001t0015g0189 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.730-720A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38480572 | ||||||
chr15:38480573
|
T | C | 1 | a0001c0001t0004g0012 | 4 | HG02257.hp2 HG02280.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.730-719T>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38480573 | ||||||
chr15:38480579
|
A | AT | 51 | a0001c0001t0001g0016a0001c0001t0001g0028a0001c0001t0001g0036others(48): Show | 70 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(67): Show |
intron_variant | MODIFIER | c.730-703dupT | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr15 | 38480579 | |||||
chr15:38480684
|
C | A | 1 | a0001c0001t0001g0203 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.730-608C>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38480684 | ||||||
chr15:38480743
|
A | G | 39 | a0001c0001t0004g0029a0001c0001t0004g0031a0001c0001t0004g0032others(36): Show | 47 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.730-549A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38480743 | ||||||
chr15:38480813
|
T | A | 1 | a0001c0001t0001g0193 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.730-479T>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38480813 | ||||||
chr15:38480845
|
A | T | 1 | a0001c0001t0001g0227 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.730-447A>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38480845 | ||||||
chr15:38480996
|
G | T | 1 | a0001c0001t0002g0179 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.730-296G>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38480996 | ||||||
chr15:38481008
|
G | A | 1 | a0002c0002t0003g0182 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.730-284G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38481008 | ||||||
chr15:38481019
|
T | C | 2 | a0001c0001t0002g0038a0001c0001t0002g0119 | 3 | HG02129.hp1 HG02523.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.730-273T>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38481019 | ||||||
chr15:38481080
|
G | A | 2 | a0001c0001t0007g0030a0001c0001t0007g0090 | 3 | HG02258.hp1 HG02895.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.730-212G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 6/7 | chr15 | 38481080 | ||||||
chr15:38481583
|
G | T | 1 | a0001c0003t0014g0076 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.897+124G>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 7/7 | chr15 | 38481583 | ||||||
chr15:38481793
|
G | A | 1 | a0001c0001t0011g0152 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.897+334G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 7/7 | chr15 | 38481793 | ||||||
chr15:38482239
|
G | A | 2 | a0003c0005t0001g0053a0003c0005t0001g0234 | 3 | HG03491.hp1 HG03492.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.897+780G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 7/7 | chr15 | 38482239 | ||||||
chr15:38482310
|
A | G | 3 | a0001c0001t0009g0186a0001c0001t0009g0187a0001c0001t0009g0188 | 3 | HG02717.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.897+851A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 7/7 | chr15 | 38482310 | ||||||
chr15:38482441
|
A | G | 2 | a0001c0001t0001g0206a0001c0001t0017g0228 | 2 | HG00621.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.897+982A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 7/7 | chr15 | 38482441 | ||||||
chr15:38482498
|
C | G | 1 | a0001c0001t0002g0170 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.897+1039C>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 7/7 | chr15 | 38482498 | ||||||
chr15:38482850
|
T | C | 4 | a0001c0001t0009g0186a0001c0001t0009g0187a0001c0001t0009g0188others(1): Show | 4 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.897+1391T>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 7/7 | chr15 | 38482850 | ||||||
chr15:38482863
|
C | T | 2 | a0001c0003t0005g0106a0001c0003t0005g0109 | 2 | HG02280.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.898-1392C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 7/7 | chr15 | 38482863 | ||||||
chr15:38483129
|
A | G | 1 | a0001c0001t0001g0050 | 2 | NA18998.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.898-1126A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 7/7 | chr15 | 38483129 | ||||||
chr15:38483134
|
T | C | 1 | a0002c0002t0003g0183 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.898-1121T>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 7/7 | chr15 | 38483134 | ||||||
chr15:38483159
|
C | G | 1 | a0001c0001t0022g0180 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.898-1096C>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 7/7 | chr15 | 38483159 | ||||||
chr15:38483205
|
A | G | 2 | a0001c0001t0002g0155a0007c0009t0002g0154 | 2 | HG00642.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.898-1050A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 7/7 | chr15 | 38483205 | ||||||
chr15:38483256
|
A | T | 1 | a0001c0001t0022g0180 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.898-999A>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 7/7 | chr15 | 38483256 | ||||||
chr15:38483277
|
G | C | 1 | a0001c0001t0011g0152 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.898-978G>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 7/7 | chr15 | 38483277 | ||||||
chr15:38483417
|
A | AGCAC | 4 | a0001c0001t0009g0186a0001c0001t0009g0187a0001c0001t0009g0188others(1): Show | 4 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.898-837_898-834dup others(4): Show |
FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr15 | 38483417 | |||||
chr15:38483448
|
C | T | 1 | a0001c0001t0003g0073 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.898-807C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 7/7 | chr15 | 38483448 | ||||||
chr15:38483483
|
G | A | 1 | a0001c0001t0011g0091 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.898-772G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 7/7 | chr15 | 38483483 | ||||||
chr15:38483484
|
T | C | 1 | a0001c0001t0022g0180 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.898-771T>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 7/7 | chr15 | 38483484 | ||||||
chr15:38483543
|
G | A | 54 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0020others(51): Show | 94 | HG00099.hp1 HG00323.hp1 HG00621.hp1 others(91): Show |
intron_variant | MODIFIER | c.898-712G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 7/7 | chr15 | 38483543 | ||||||
chr15:38483552
|
A | G | 15 | a0001c0001t0005g0014a0001c0001t0005g0104a0001c0001t0005g0105others(12): Show | 22 | HG01069.hp1 HG01071.hp1 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.898-703A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 7/7 | chr15 | 38483552 | ||||||
chr15:38483558
|
C | T | 2 | a0001c0001t0005g0104a0001c0001t0005g0105 | 2 | HG01891.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.898-697C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 7/7 | chr15 | 38483558 | ||||||
chr15:38483665
|
CAA | C | 17 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(14): Show | 30 | HG00140.hp1 HG00423.hp1 HG00609.hp2 others(27): Show |
intron_variant | MODIFIER | c.898-571_898-570del others(2): Show |
FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr15 | 38483665 | |||||
chr15:38483682
|
AAAAT | A | 8 | a0001c0001t0001g0052a0001c0001t0001g0238a0001c0001t0001g0243others(5): Show | 11 | HG01069.hp2 HG01081.hp2 HG01358.hp1 others(8): Show |
intron_variant | MODIFIER | c.898-571_898-568del others(4): Show |
FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr15 | 38483682 | |||||
chr15:38483682
|
AAAATATA others(5): Show |
A | 2 | a0001c0001t0005g0218a0001c0001t0023g0063 | 2 | HG02630.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.898-571_898-560del others(12): Show |
FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr15 | 38483682 | |||||
chr15:38483683
|
AAATAT | A | 5 | a0001c0001t0002g0004a0001c0001t0002g0045a0001c0001t0002g0065others(2): Show | 12 | HG00099.hp2 HG00738.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.898-570_898-566del others(5): Show |
FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr15 | 38483683 | |||||
chr15:38483684
|
A | T | 4 | a0001c0001t0001g0245a0001c0001t0002g0042a0001c0001t0002g0113others(1): Show | 5 | HG01884.hp2 HG02148.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.898-571A>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 7/7 | chr15 | 38483684 | ||||||
chr15:38483684
|
AAT | A | 4 | a0001c0001t0001g0025a0001c0001t0001g0230a0001c0001t0002g0141others(1): Show | 6 | HG02145.hp2 NA18978.hp1 NA18997.hp2 others(3): Show |
intron_variant | MODIFIER | c.898-545_898-544del others(2): Show |
FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr15 | 38483684 | |||||
chr15:38483684
|
AATAT | A | 67 | a0001c0001t0001g0016a0001c0001t0001g0028a0001c0001t0001g0036others(64): Show | 91 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.898-547_898-544del others(4): Show |
FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr15 | 38483684 | |||||
chr15:38483684
|
AATATATA others(1): Show |
A | 65 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0193others(62): Show | 83 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.898-551_898-544del others(8): Show |
FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr15 | 38483684 | |||||
chr15:38483684
|
AATATATA others(3): Show |
A | 2 | a0001c0001t0003g0067a0001c0001t0003g0087 | 2 | HG00544.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.898-553_898-544del others(10): Show |
FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr15 | 38483684 | |||||
chr15:38483685
|
ATAT | A | 3 | a0001c0001t0001g0043a0001c0001t0002g0043a0001c0001t0011g0152 | 3 | HG01255.hp2 HG01981.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.898-569_898-567del others(3): Show |
FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 7/7 | chr15 | 38483685 | ||||||
chr15:38483685
|
ATATAT | A | 4 | a0001c0001t0002g0159a0001c0001t0002g0166a0001c0001t0013g0082others(1): Show | 4 | HG02004.hp1 HG03209.hp2 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.898-569_898-565del others(5): Show |
FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 7/7 | chr15 | 38483685 | ||||||
chr15:38483685
|
ATATATAT | A | 45 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0020others(42): Show | 85 | HG00099.hp1 HG00621.hp1 HG00673.hp2 others(82): Show |
intron_variant | MODIFIER | c.898-569_898-563del others(7): Show |
FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 7/7 | chr15 | 38483685 | ||||||
chr15:38483685
|
ATATATAT others(2): Show |
A | 25 | a0001c0001t0002g0062a0001c0001t0002g0122a0001c0001t0003g0002others(22): Show | 48 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.898-569_898-561del others(9): Show |
FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 7/7 | chr15 | 38483685 | ||||||
chr15:38483690
|
T | A | 4 | a0001c0001t0001g0148a0001c0001t0002g0039a0001c0001t0002g0130others(1): Show | 5 | HG02818.hp1 HG02970.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.898-565T>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 7/7 | chr15 | 38483690 | ||||||
chr15:38483692
|
T | A | 3 | a0001c0001t0001g0220a0001c0001t0004g0237a0001c0001t0011g0152 | 3 | HG02818.hp1 HG03831.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.898-563T>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 7/7 | chr15 | 38483692 | ||||||
chr15:38483694
|
T | A | 106 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0020others(103): Show | 160 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.898-561T>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 7/7 | chr15 | 38483694 | ||||||
chr15:38483696
|
T | A | 35 | a0001c0001t0001g0225a0001c0001t0002g0040a0001c0001t0002g0062others(32): Show | 41 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(38): Show |
intron_variant | MODIFIER | c.898-559T>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 7/7 | chr15 | 38483696 | ||||||
chr15:38483698
|
T | A | 30 | a0001c0001t0002g0040a0001c0001t0002g0062a0001c0001t0002g0081others(27): Show | 36 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(33): Show |
intron_variant | MODIFIER | c.898-557T>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 7/7 | chr15 | 38483698 | ||||||
chr15:38483708
|
T | C | 1 | a0001c0001t0022g0180 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.898-547T>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 7/7 | chr15 | 38483708 | ||||||
chr15:38483710
|
T | C | 1 | a0001c0001t0022g0180 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.898-545T>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 7/7 | chr15 | 38483710 | ||||||
chr15:38483772
|
C | A | 2 | a0001c0001t0002g0126a0001c0001t0022g0180 | 2 | HG01106.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.898-483C>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 7/7 | chr15 | 38483772 | ||||||
chr15:38483897
|
A | G | 1 | a0001c0001t0021g0205 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.898-358A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 7/7 | chr15 | 38483897 | ||||||
chr15:38483927
|
C | T | 29 | a0001c0001t0002g0122a0001c0001t0003g0002a0001c0001t0003g0003others(26): Show | 52 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.898-328C>T | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 7/7 | chr15 | 38483927 | ||||||
chr15:38483952
|
G | C | 1 | a0001c0001t0003g0073 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.898-303G>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 7/7 | chr15 | 38483952 | ||||||
chr15:38484015
|
A | G | 1 | a0001c0001t0022g0180 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.898-240A>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 7/7 | chr15 | 38484015 | ||||||
chr15:38484059
|
G | A | 14 | a0001c0001t0005g0014a0001c0001t0005g0104a0001c0001t0005g0105others(11): Show | 21 | HG01069.hp1 HG01071.hp1 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.898-196G>A | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 7/7 | chr15 | 38484059 | ||||||
chr15:38484129
|
T | G | 74 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0020others(71): Show | 124 | HG00099.hp1 HG00323.hp1 HG00621.hp1 others(121): Show |
intron_variant | MODIFIER | c.898-126T>G | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 7/7 | chr15 | 38484129 | ||||||
chr15:38484161
|
T | C | 3 | a0001c0001t0001g0198a0001c0001t0001g0212a0001c0001t0001g0213 | 3 | HG01168.hp1 HG01433.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.898-94T>C | FAM98B | ENSG00000171262.11 | transcript | ENST00000397609.6 | protein_coding | 7/7 | chr15 | 38484161 |