geneid | 165215 |
---|---|
ensemblid | ENSG00000144369.14 |
hgncid | 29412 |
symbol | FAM171B |
name | family with sequence similarity 171 member B |
refseq_nuc | NM_177454.4 |
refseq_prot | NP_803237.3 |
ensembl_nuc | ENST00000304698.10 |
ensembl_prot | ENSP00000304108.5 |
mane_status | MANE Select |
chr | chr2 |
start | 186694060 |
end | 186765959 |
strand | + |
ver | v1.2 |
region | chr2:186694060-186765959 |
region5000 | chr2:186689060-186770959 |
regionname0 | FAM171B_chr2_186694060_186765959 |
regionname5000 | FAM171B_chr2_186689060_186770959 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 827 | 239 | 66 | 48 | 81 | 10 | 33 | 52 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
a0002 | 0/0 | 828 | 68 | 14 | 19 | 22 | 4 | 9 | 16 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
a0003 | 0/0 | 827 | 7 | 4 | 2 | 0 | 0 | 1 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
a0004 | 1/0 | 826 | 6 | 5 | 0 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
a0005 | 0/0 | 829 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
a0006 | 0/0 | 827 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
a0007 | 0/0 | 826 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
a0008 | 0/0 | 827 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
a0009 | 0/0 | 827 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
a0010 | 0/0 | 827 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
a0011 | 0/0 | 827 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
a0012 | 0/0 | 827 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 2484 | 78 | 3 | 19 | 44 | 4 | 8 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
c0002 | 0/1 | 2484 | 73 | 35 | 12 | 9 | 3 | 13 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
c0003 | 0/0 | 2487 | 56 | 13 | 10 | 22 | 3 | 8 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
c0004 | 0/0 | 2484 | 43 | 20 | 4 | 17 | 0 | 2 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
c0005 | 0/0 | 2484 | 37 | 0 | 13 | 11 | 3 | 10 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
c0006 | 0/0 | 2487 | 7 | 0 | 6 | 0 | 1 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
c0007 | 1/0 | 2481 | 6 | 5 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
c0008 | 0/0 | 2484 | 5 | 4 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
c0009 | 0/0 | 2484 | 3 | 3 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
c0010 | 0/0 | 2487 | 3 | 0 | 2 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
c0011 | 0/0 | 2490 | 3 | 3 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
c0012 | 0/0 | 2484 | 2 | 2 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
c0013 | 0/0 | 2484 | 2 | 2 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
c0014 | 0/0 | 2484 | 2 | 2 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
c0015 | 0/0 | 2484 | 2 | 0 | 1 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
c0016 | 0/0 | 2484 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
c0017 | 0/0 | 2484 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
c0018 | 0/0 | 2484 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
c0019 | 0/0 | 2484 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
c0020 | 0/0 | 2484 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
c0021 | 0/0 | 2484 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
c0022 | 0/0 | 2487 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
c0023 | 0/0 | 2487 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
c0024 | 0/0 | 2490 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
c0025 | 0/0 | 2481 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 3249 | 110 | 20 | 29 | 37 | 6 | 18 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
t0002 | 0/0 | 3250 | 57 | 0 | 15 | 33 | 3 | 6 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
t0003 | 1/0 | 3251 | 33 | 19 | 5 | 8 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
t0004 | 0/0 | 3250 | 29 | 14 | 5 | 7 | 0 | 3 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
t0005 | 0/0 | 3251 | 15 | 4 | 3 | 0 | 1 | 7 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
t0006 | 0/0 | 3252 | 10 | 2 | 1 | 0 | 2 | 5 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
t0007 | 0/0 | 3248 | 9 | 2 | 3 | 2 | 1 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
t0008 | 0/0 | 3250 | 9 | 9 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
t0009 | 0/0 | 3247 | 8 | 6 | 2 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
t0010 | 0/0 | 3251 | 8 | 0 | 2 | 4 | 0 | 2 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
t0011 | 0/0 | 3250 | 5 | 0 | 0 | 5 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
t0012 | 0/0 | 3249 | 4 | 0 | 0 | 4 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
t0013 | 0/0 | 3250 | 3 | 2 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
t0014 | 0/0 | 3249 | 3 | 0 | 0 | 3 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
t0015 | 0/0 | 3252 | 3 | 1 | 0 | 2 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
t0016 | 0/1 | 3252 | 3 | 1 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
t0017 | 0/0 | 3249 | 2 | 0 | 1 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
t0018 | 0/0 | 3251 | 2 | 2 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
t0019 | 0/0 | 3248 | 2 | 2 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
t0020 | 0/0 | 3250 | 2 | 2 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
t0021 | 0/0 | 3250 | 2 | 0 | 1 | 0 | 1 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
t0022 | 0/0 | 3249 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
t0023 | 0/0 | 3252 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
t0024 | 0/0 | 3249 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
t0025 | 0/0 | 3250 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
t0026 | 0/0 | 3250 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
t0027 | 0/0 | 3251 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
t0028 | 0/0 | 3226 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
t0029 | 0/0 | 3249 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
t0030 | 0/0 | 3249 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
t0031 | 0/0 | 3249 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
t0032 | 0/0 | 3251 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
t0033 | 0/0 | 3252 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
t0034 | 0/0 | 3249 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0002 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0003 | 0/0 | 4 | 0 | 0 | 1 | 1 | 2 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0008 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0011 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0021 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0028 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0244 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 2484 | 78 | 3 | 19 | 44 | 4 | 8 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
a0001c0002 | 0/1 | 2484 | 73 | 35 | 12 | 9 | 3 | 13 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
a0001c0004 | 0/0 | 2484 | 43 | 20 | 4 | 17 | 0 | 2 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
a0001c0005 | 0/0 | 2484 | 37 | 0 | 13 | 11 | 3 | 10 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
a0001c0009 | 0/0 | 2484 | 3 | 3 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
a0001c0012 | 0/0 | 2484 | 2 | 2 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
a0001c0013 | 0/0 | 2484 | 2 | 2 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
a0001c0020 | 0/0 | 2484 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
a0002c0003 | 0/0 | 2487 | 56 | 13 | 10 | 22 | 3 | 8 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
a0002c0006 | 0/0 | 2487 | 7 | 0 | 6 | 0 | 1 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
a0002c0010 | 0/0 | 2487 | 3 | 0 | 2 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
a0002c0022 | 0/0 | 2487 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
a0002c0023 | 0/0 | 2487 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
a0003c0008 | 0/0 | 2484 | 5 | 4 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
a0003c0015 | 0/0 | 2484 | 2 | 0 | 1 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
a0004c0007 | 1/0 | 2481 | 6 | 5 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
a0005c0011 | 0/0 | 2490 | 3 | 3 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
a0005c0024 | 0/0 | 2490 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
a0006c0014 | 0/0 | 2484 | 2 | 2 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
a0007c0025 | 0/0 | 2481 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
a0008c0019 | 0/0 | 2484 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
a0009c0018 | 0/0 | 2484 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
a0010c0016 | 0/0 | 2484 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
a0011c0021 | 0/0 | 2484 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
a0012c0017 | 0/0 | 2484 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002 | 0/0 | 5733 | 53 | 0 | 14 | 30 | 3 | 6 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
a0001c0001t0004 | 0/0 | 5733 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
a0001c0001t0010 | 0/0 | 5734 | 8 | 0 | 2 | 4 | 0 | 2 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
a0001c0001t0011 | 0/0 | 5733 | 5 | 0 | 0 | 5 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
a0001c0001t0014 | 0/0 | 5732 | 3 | 0 | 0 | 3 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
a0001c0001t0020 | 0/0 | 5733 | 2 | 2 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
a0001c0001t0021 | 0/0 | 5733 | 2 | 0 | 1 | 0 | 1 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
a0001c0001t0022 | 0/0 | 5732 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
a0001c0001t0025 | 0/0 | 5733 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
a0001c0001t0032 | 0/0 | 5734 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
a0001c0001t0033 | 0/0 | 5735 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
a0001c0002t0001 | 0/0 | 5732 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
a0001c0002t0003 | 0/0 | 5734 | 23 | 12 | 5 | 6 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
a0001c0002t0004 | 0/0 | 5733 | 7 | 6 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
a0001c0002t0005 | 0/0 | 5734 | 14 | 3 | 3 | 0 | 1 | 7 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
a0001c0002t0006 | 0/0 | 5735 | 10 | 2 | 1 | 0 | 2 | 5 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
a0001c0002t0008 | 0/0 | 5733 | 5 | 5 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
a0001c0002t0013 | 0/0 | 5733 | 2 | 1 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
a0001c0002t0015 | 0/0 | 5735 | 2 | 0 | 0 | 2 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
a0001c0002t0016 | 0/1 | 5735 | 3 | 1 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
a0001c0002t0017 | 0/0 | 5732 | 2 | 0 | 1 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
a0001c0002t0018 | 0/0 | 5734 | 2 | 2 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
a0001c0002t0023 | 0/0 | 5735 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
a0001c0002t0028 | 0/0 | 5709 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
a0001c0004t0001 | 0/0 | 5732 | 19 | 5 | 2 | 11 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
a0001c0004t0003 | 0/0 | 5734 | 2 | 1 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
a0001c0004t0004 | 0/0 | 5733 | 8 | 3 | 0 | 4 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
a0001c0004t0005 | 0/0 | 5734 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
a0001c0004t0007 | 0/0 | 5731 | 2 | 0 | 1 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
a0001c0004t0009 | 0/0 | 5730 | 7 | 6 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
a0001c0004t0019 | 0/0 | 5731 | 2 | 2 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
a0001c0004t0029 | 0/0 | 5732 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
a0001c0004t0031 | 0/0 | 5732 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
a0001c0005t0001 | 0/0 | 5732 | 31 | 0 | 10 | 10 | 2 | 9 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
a0001c0005t0004 | 0/0 | 5733 | 3 | 0 | 2 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
a0001c0005t0007 | 0/0 | 5731 | 2 | 0 | 1 | 0 | 1 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
a0001c0005t0030 | 0/0 | 5732 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
a0001c0009t0003 | 0/0 | 5734 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
a0001c0009t0013 | 0/0 | 5733 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
a0001c0009t0015 | 0/0 | 5735 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
a0001c0012t0008 | 0/0 | 5733 | 2 | 2 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
a0001c0013t0008 | 0/0 | 5733 | 2 | 2 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
a0001c0020t0007 | 0/0 | 5731 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
a0002c0003t0001 | 0/0 | 5735 | 41 | 9 | 8 | 16 | 3 | 5 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
a0002c0003t0002 | 0/0 | 5736 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
a0002c0003t0004 | 0/0 | 5736 | 3 | 1 | 0 | 1 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
a0002c0003t0007 | 0/0 | 5734 | 3 | 0 | 1 | 1 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
a0002c0003t0012 | 0/0 | 5735 | 4 | 0 | 0 | 4 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
a0002c0003t0024 | 0/0 | 5735 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
a0002c0003t0026 | 0/0 | 5736 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
a0002c0003t0027 | 0/0 | 5737 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
a0002c0003t0034 | 0/0 | 5735 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
a0002c0006t0001 | 0/0 | 5735 | 6 | 0 | 5 | 0 | 1 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
a0002c0006t0009 | 0/0 | 5733 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
a0002c0010t0001 | 0/0 | 5735 | 3 | 0 | 2 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
a0002c0022t0007 | 0/0 | 5734 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
a0002c0023t0004 | 0/0 | 5736 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
a0003c0008t0004 | 0/0 | 5733 | 5 | 4 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
a0003c0015t0001 | 0/0 | 5732 | 2 | 0 | 1 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
a0004c0007t0003 | 1/0 | 5731 | 6 | 5 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
a0005c0011t0001 | 0/0 | 5738 | 3 | 3 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
a0005c0024t0001 | 0/0 | 5738 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
a0006c0014t0001 | 0/0 | 5732 | 2 | 2 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
a0007c0025t0003 | 0/0 | 5731 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
a0008c0019t0001 | 0/0 | 5732 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
a0009c0018t0002 | 0/0 | 5733 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
a0010c0016t0002 | 0/0 | 5733 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
a0011c0021t0004 | 0/0 | 5733 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
a0012c0017t0002 | 0/0 | 5733 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | copy fasta | chr2 | 186689060 | 186770959 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0002g0008 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0002g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0002g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0002g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0002g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0002g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0002g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0002g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0002g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0002g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0004g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0010g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0010g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0010g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0010g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0010g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0010g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0010g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0010g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0011g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0011g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0011g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0011g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0014g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0014g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0014g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0020g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0021g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0021g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0022g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0025g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0032g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0033g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0003g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0003g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0003g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0003g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0003g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0003g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0003g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0003g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0003g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0003g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0003g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0003g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0003g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0003g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0003g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0003g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0004g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0004g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0004g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0004g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0004g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0004g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0005g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0005g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0005g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0005g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0005g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0005g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0005g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0005g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0005g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0005g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0005g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0005g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0005g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0006g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0006g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0006g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0006g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0006g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0006g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0006g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0006g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0006g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0006g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0008g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0008g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0008g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0008g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0008g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0013g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0013g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0015g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0015g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0016g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0016g0244 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0016g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0017g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0017g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0018g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0018g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0023g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0028g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0004t0001g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0004t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0004t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0004t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0004t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0004t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0004t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0004t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0004t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0004t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0004t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0004t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0004t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0004t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0004t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0004t0003g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0004t0004g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0004t0004g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0004t0004g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0004t0004g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0004t0004g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0004t0004g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0004t0004g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0004t0005g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0004t0007g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0004t0007g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0004t0009g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0004t0009g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0004t0009g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0004t0009g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0004t0009g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0004t0009g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0004t0019g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0004t0019g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0004t0029g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0004t0031g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0005t0001g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0005t0001g0011 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0005t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0005t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0005t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0005t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0005t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0005t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0005t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0005t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0005t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0005t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0005t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0005t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0005t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0005t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0005t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0005t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0005t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0005t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0005t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0005t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0005t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0005t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0005t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0005t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0005t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0005t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0005t0004g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0005t0004g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0005t0004g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0005t0007g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0005t0007g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0005t0030g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0009t0003g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0009t0013g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0009t0015g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0012t0008g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0012t0008g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0013t0008g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0020t0007g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0003t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0003t0001g0003 | 0/0 | 4 | 0 | 0 | 1 | 1 | 2 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0003t0001g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0003t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0003t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0003t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0003t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0003t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0003t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0003t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0003t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0003t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0003t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0003t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0003t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0003t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0003t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0003t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0003t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0003t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0003t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0003t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0003t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0003t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0003t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0003t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0003t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0003t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0003t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0003t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0003t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0003t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0003t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0003t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0003t0004g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0003t0004g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0003t0004g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0003t0007g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0003t0007g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0003t0007g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0003t0012g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0003t0012g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0003t0012g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0003t0012g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0003t0024g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0003t0026g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0003t0027g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0003t0034g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0006t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0006t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0006t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0006t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0006t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0006t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0006t0009g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0010t0001g0002 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0010t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0022t0007g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0023t0004g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0003c0008t0004g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0003c0008t0004g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0003c0008t0004g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0003c0008t0004g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0003c0008t0004g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0003c0015t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0003c0015t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0004c0007t0003g0021 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0004c0007t0003g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0004c0007t0003g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0004c0007t0003g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0004c0007t0003g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0005c0011t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0005c0011t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0005c0011t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0005c0024t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0006c0014t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0006c0014t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0007c0025t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0008c0019t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0009c0018t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0010c0016t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0011c0021t0004g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0012c0017t0002g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0002 | c0003 | t0001 | g0032 | EUR | GBR | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0265 | EUR | GBR | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG00280 | hp1 | a0002 | c0003 | t0001 | g0118 | EUR | FIN | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG00280 | hp2 | a0001 | c0001 | t0002 | g0247 | EUR | FIN | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG00323 | hp1 | a0001 | c0005 | t0001 | g0130 | EUR | FIN | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG00323 | hp2 | a0001 | c0001 | t0002 | g0256 | EUR | FIN | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0278 | EAS | CHS | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG00408 | hp2 | a0002 | c0003 | t0001 | g0085 | EAS | CHS | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG00423 | hp1 | a0001 | c0002 | t0015 | g0161 | EAS | CHS | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG00423 | hp2 | a0001 | c0001 | t0002 | g0030 | EAS | CHS | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG00544 | hp1 | a0001 | c0005 | t0001 | g0103 | EAS | CHS | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG00544 | hp2 | a0001 | c0001 | t0002 | g0258 | EAS | CHS | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG00558 | hp1 | a0010 | c0016 | t0002 | g0257 | EAS | CHS | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG00558 | hp2 | a0001 | c0005 | t0001 | g0105 | EAS | CHS | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0268 | EAS | CHS | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG00597 | hp2 | a0002 | c0003 | t0001 | g0003 | EAS | CHS | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG00609 | hp1 | a0001 | c0001 | t0011 | g0027 | EAS | CHS | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG00609 | hp2 | a0001 | c0004 | t0001 | g0123 | EAS | CHS | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG00639 | hp1 | a0001 | c0005 | t0001 | g0041 | AMR | PUR | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG00639 | hp2 | a0002 | c0023 | t0004 | g0089 | AMR | PUR | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0022 | AMR | PUR | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG00642 | hp2 | a0002 | c0010 | t0001 | g0113 | AMR | PUR | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0253 | EAS | CHS | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG00673 | hp2 | a0001 | c0004 | t0004 | g0036 | EAS | CHS | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG00733 | hp1 | a0001 | c0004 | t0001 | g0128 | AMR | PUR | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG00733 | hp2 | a0001 | c0002 | t0005 | g0228 | AMR | PUR | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG00735 | hp1 | a0001 | c0002 | t0017 | g0177 | AMR | PUR | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG00735 | hp2 | a0001 | c0005 | t0001 | g0071 | AMR | PUR | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG00738 | hp1 | a0001 | c0002 | t0016 | g0274 | AMR | PUR | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG00738 | hp2 | a0003 | c0015 | t0001 | g0031 | AMR | PUR | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG00741 | hp1 | a0001 | c0005 | t0004 | g0095 | AMR | PUR | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG00741 | hp2 | a0002 | c0010 | t0001 | g0002 | AMR | PUR | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01069 | hp1 | a0002 | c0003 | t0001 | g0111 | AMR | PUR | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01069 | hp2 | a0001 | c0005 | t0001 | g0097 | AMR | PUR | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01070 | hp1 | a0002 | c0003 | t0001 | g0002 | AMR | PUR | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01070 | hp2 | a0001 | c0005 | t0007 | g0069 | AMR | PUR | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01071 | hp1 | a0001 | c0005 | t0001 | g0098 | AMR | PUR | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01071 | hp2 | a0002 | c0003 | t0001 | g0002 | AMR | PUR | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01074 | hp1 | a0001 | c0001 | t0021 | g0212 | AMR | PUR | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01074 | hp2 | a0001 | c0005 | t0001 | g0040 | AMR | PUR | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01081 | hp1 | a0001 | c0004 | t0009 | g0134 | AMR | PUR | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01081 | hp2 | a0002 | c0003 | t0001 | g0136 | AMR | PUR | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01099 | hp1 | a0003 | c0008 | t0004 | g0191 | AMR | PUR | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01099 | hp2 | a0002 | c0003 | t0002 | g0109 | AMR | PUR | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01106 | hp1 | a0001 | c0001 | t0010 | g0022 | AMR | PUR | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01106 | hp2 | a0001 | c0005 | t0001 | g0011 | AMR | PUR | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01168 | hp1 | a0001 | c0002 | t0005 | g0238 | AMR | PUR | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01168 | hp2 | a0002 | c0003 | t0001 | g0057 | AMR | PUR | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01169 | hp1 | a0002 | c0003 | t0007 | g0056 | AMR | PUR | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0287 | AMR | PUR | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01175 | hp1 | a0001 | c0005 | t0001 | g0080 | AMR | PUR | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01175 | hp2 | a0002 | c0003 | t0001 | g0055 | AMR | PUR | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01243 | hp1 | a0001 | c0002 | t0005 | g0289 | AMR | PUR | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01243 | hp2 | a0005 | c0024 | t0001 | g0072 | AMR | PUR | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01255 | hp1 | a0001 | c0002 | t0006 | g0202 | AMR | CLM | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0249 | AMR | CLM | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01256 | hp1 | a0001 | c0005 | t0001 | g0078 | AMR | CLM | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01256 | hp2 | a0001 | c0002 | t0004 | g0028 | AMR | CLM | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01258 | hp1 | a0001 | c0005 | t0001 | g0073 | AMR | CLM | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0251 | AMR | CLM | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01261 | hp1 | a0001 | c0002 | t0003 | g0150 | AMR | CLM | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01261 | hp2 | a0001 | c0002 | t0003 | g0174 | AMR | CLM | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01358 | hp1 | a0001 | c0005 | t0004 | g0035 | AMR | CLM | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01358 | hp2 | a0001 | c0001 | t0025 | g0214 | AMR | CLM | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01361 | hp1 | a0002 | c0003 | t0001 | g0135 | AMR | CLM | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01361 | hp2 | a0001 | c0001 | t0010 | g0208 | AMR | CLM | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01496 | hp1 | a0001 | c0005 | t0001 | g0125 | AMR | CLM | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0192 | AMR | CLM | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01515 | hp1 | a0001 | c0001 | t0021 | g0213 | EUR | IBS | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01515 | hp2 | a0001 | c0002 | t0006 | g0178 | EUR | IBS | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01516 | hp1 | a0001 | c0005 | t0007 | g0068 | EUR | IBS | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01516 | hp2 | a0002 | c0003 | t0001 | g0003 | EUR | IBS | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01517 | hp1 | a0001 | c0002 | t0006 | g0179 | EUR | IBS | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01517 | hp2 | a0001 | c0005 | t0001 | g0076 | EUR | IBS | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01884 | hp1 | a0001 | c0020 | t0007 | g0142 | AFR | ACB | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01884 | hp2 | a0001 | c0002 | t0003 | g0216 | AFR | ACB | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01891 | hp1 | a0001 | c0002 | t0006 | g0187 | AFR | ACB | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01891 | hp2 | a0002 | c0003 | t0001 | g0004 | AFR | ACB | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0008 | AMR | PEL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01928 | hp2 | a0002 | c0006 | t0009 | g0020 | AMR | PEL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01934 | hp1 | a0002 | c0006 | t0001 | g0160 | AMR | PEL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01934 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | PEL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0008 | AMR | PEL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01943 | hp2 | a0002 | c0006 | t0001 | g0020 | AMR | PEL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01952 | hp1 | a0001 | c0002 | t0003 | g0183 | AMR | PEL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01952 | hp2 | a0001 | c0001 | t0033 | g0266 | AMR | PEL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01975 | hp1 | a0001 | c0001 | t0002 | g0221 | AMR | PEL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01975 | hp2 | a0001 | c0002 | t0003 | g0164 | AMR | PEL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01981 | hp1 | a0002 | c0006 | t0001 | g0193 | AMR | PEL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0276 | AMR | PEL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01993 | hp1 | a0002 | c0006 | t0001 | g0172 | AMR | PEL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01993 | hp2 | a0001 | c0001 | t0002 | g0264 | AMR | PEL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02004 | hp1 | a0001 | c0004 | t0007 | g0039 | AMR | PEL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02004 | hp2 | a0001 | c0001 | t0002 | g0237 | AMR | PEL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02015 | hp1 | a0002 | c0003 | t0001 | g0112 | EAS | KHV | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02015 | hp2 | a0001 | c0001 | t0014 | g0277 | EAS | KHV | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02040 | hp1 | a0001 | c0004 | t0001 | g0047 | EAS | KHV | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02040 | hp2 | a0001 | c0001 | t0011 | g0234 | EAS | KHV | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02055 | hp1 | a0001 | c0001 | t0020 | g0006 | AFR | ACB | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02055 | hp2 | a0002 | c0003 | t0001 | g0092 | AFR | ACB | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02056 | hp1 | a0009 | c0018 | t0002 | g0284 | EAS | KHV | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02056 | hp2 | a0001 | c0005 | t0001 | g0012 | EAS | KHV | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0235 | EAS | KHV | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02074 | hp2 | a0001 | c0005 | t0001 | g0104 | EAS | KHV | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02083 | hp1 | a0002 | c0003 | t0001 | g0054 | EAS | KHV | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02083 | hp2 | a0001 | c0001 | t0011 | g0225 | EAS | KHV | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02129 | hp1 | a0001 | c0004 | t0001 | g0017 | EAS | KHV | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0261 | EAS | KHV | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02132 | hp1 | a0002 | c0003 | t0001 | g0133 | EAS | KHV | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02132 | hp2 | a0001 | c0004 | t0001 | g0001 | EAS | KHV | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02135 | hp1 | a0001 | c0001 | t0002 | g0275 | EAS | KHV | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02135 | hp2 | a0011 | c0021 | t0004 | g0066 | EAS | KHV | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02145 | hp1 | a0001 | c0002 | t0005 | g0029 | AFR | ACB | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02145 | hp2 | a0001 | c0004 | t0004 | g0046 | AFR | ACB | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02148 | hp1 | a0001 | c0002 | t0003 | g0149 | AMR | PEL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02148 | hp2 | a0002 | c0006 | t0001 | g0173 | AMR | PEL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02155 | hp1 | a0001 | c0001 | t0011 | g0224 | EAS | CDX | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02155 | hp2 | a0001 | c0001 | t0002 | g0269 | EAS | CDX | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02165 | hp1 | a0002 | c0003 | t0001 | g0115 | EAS | CDX | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0270 | EAS | CDX | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02257 | hp1 | a0001 | c0004 | t0004 | g0010 | AFR | ACB | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02257 | hp2 | a0001 | c0012 | t0008 | g0243 | AFR | ACB | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02258 | hp1 | a0001 | c0001 | t0020 | g0006 | AFR | ACB | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02258 | hp2 | a0001 | c0002 | t0018 | g0196 | AFR | ACB | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02293 | hp1 | a0001 | c0004 | t0001 | g0038 | AMR | PEL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02293 | hp2 | a0001 | c0001 | t0002 | g0227 | AMR | PEL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0263 | AMR | PEL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02300 | hp2 | a0002 | c0003 | t0001 | g0120 | AMR | PEL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02451 | hp1 | a0001 | c0002 | t0001 | g0025 | AFR | ACB | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02451 | hp2 | a0001 | c0002 | t0003 | g0184 | AFR | ACB | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02523 | hp1 | a0001 | c0005 | t0001 | g0012 | EAS | KHV | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02523 | hp2 | a0001 | c0001 | t0002 | g0030 | EAS | KHV | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02572 | hp1 | a0001 | c0001 | t0032 | g0006 | AFR | GWD | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02572 | hp2 | a0001 | c0002 | t0003 | g0005 | AFR | GWD | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02602 | hp1 | a0002 | c0003 | t0001 | g0084 | SAS | PJL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02602 | hp2 | a0001 | c0005 | t0001 | g0009 | SAS | PJL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02622 | hp1 | a0001 | c0004 | t0019 | g0139 | AFR | GWD | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02622 | hp2 | a0001 | c0002 | t0005 | g0029 | AFR | GWD | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02630 | hp1 | a0001 | c0002 | t0003 | g0182 | AFR | GWD | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02630 | hp2 | a0001 | c0002 | t0004 | g0171 | AFR | GWD | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02647 | hp1 | a0001 | c0002 | t0003 | g0148 | AFR | GWD | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02647 | hp2 | a0001 | c0002 | t0004 | g0025 | AFR | GWD | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02683 | hp1 | a0001 | c0001 | t0002 | g0273 | SAS | PJL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02683 | hp2 | a0001 | c0005 | t0004 | g0037 | SAS | PJL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02698 | hp1 | a0002 | c0003 | t0007 | g0110 | SAS | PJL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02698 | hp2 | a0001 | c0002 | t0006 | g0201 | SAS | PJL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02717 | hp1 | a0005 | c0011 | t0001 | g0119 | AFR | GWD | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02717 | hp2 | a0001 | c0002 | t0003 | g0162 | AFR | GWD | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02723 | hp1 | a0004 | c0007 | t0003 | g0210 | AFR | GWD | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02723 | hp2 | a0006 | c0014 | t0001 | g0205 | AFR | GWD | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0211 | SAS | PJL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02735 | hp2 | a0001 | c0002 | t0005 | g0240 | SAS | PJL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02738 | hp1 | a0001 | c0005 | t0001 | g0049 | SAS | PJL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02738 | hp2 | a0002 | c0003 | t0001 | g0086 | SAS | PJL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02809 | hp1 | a0001 | c0004 | t0009 | g0137 | AFR | GWD | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02809 | hp2 | a0002 | c0003 | t0001 | g0091 | AFR | GWD | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02818 | hp1 | a0001 | c0002 | t0003 | g0154 | AFR | GWD | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02818 | hp2 | a0001 | c0004 | t0009 | g0141 | AFR | GWD | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02886 | hp1 | a0002 | c0003 | t0001 | g0034 | AFR | GWD | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02886 | hp2 | a0001 | c0002 | t0003 | g0207 | AFR | GWD | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02895 | hp1 | a0001 | c0004 | t0009 | g0140 | AFR | GWD | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02895 | hp2 | a0003 | c0008 | t0004 | g0189 | AFR | GWD | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02896 | hp1 | a0001 | c0009 | t0013 | g0158 | AFR | GWD | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02896 | hp2 | a0001 | c0002 | t0004 | g0026 | AFR | GWD | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02897 | hp1 | a0003 | c0008 | t0004 | g0190 | AFR | GWD | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02897 | hp2 | a0001 | c0002 | t0004 | g0026 | AFR | GWD | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02922 | hp1 | a0001 | c0002 | t0008 | g0195 | AFR | ESN | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02922 | hp2 | a0005 | c0011 | t0001 | g0063 | AFR | ESN | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02965 | hp1 | a0001 | c0002 | t0004 | g0223 | AFR | ESN | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02965 | hp2 | a0002 | c0003 | t0001 | g0004 | AFR | ESN | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02970 | hp1 | a0001 | c0013 | t0008 | g0024 | AFR | ESN | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02970 | hp2 | a0001 | c0002 | t0003 | g0005 | AFR | ESN | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02976 | hp1 | a0001 | c0004 | t0001 | g0101 | AFR | ESN | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02976 | hp2 | a0004 | c0007 | t0003 | g0165 | AFR | ESN | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG03017 | hp1 | a0001 | c0002 | t0005 | g0246 | SAS | PJL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG03017 | hp2 | a0001 | c0005 | t0001 | g0051 | SAS | PJL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG03041 | hp1 | a0003 | c0008 | t0004 | g0170 | AFR | GWD | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG03041 | hp2 | a0001 | c0002 | t0003 | g0163 | AFR | GWD | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG03098 | hp1 | a0001 | c0004 | t0005 | g0053 | AFR | MSL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG03098 | hp2 | a0001 | c0002 | t0005 | g0217 | AFR | MSL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG03130 | hp1 | a0001 | c0002 | t0008 | g0194 | AFR | ESN | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG03130 | hp2 | a0002 | c0003 | t0026 | g0107 | AFR | ESN | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG03139 | hp1 | a0001 | c0002 | t0008 | g0200 | AFR | ESN | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG03139 | hp2 | a0002 | c0003 | t0027 | g0108 | AFR | ESN | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG03195 | hp1 | a0002 | c0003 | t0001 | g0117 | AFR | ESN | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG03195 | hp2 | a0001 | c0002 | t0018 | g0209 | AFR | ESN | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG03209 | hp1 | a0001 | c0013 | t0008 | g0024 | AFR | MSL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG03209 | hp2 | a0001 | c0002 | t0008 | g0199 | AFR | MSL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG03225 | hp1 | a0001 | c0002 | t0028 | g0005 | AFR | MSL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG03225 | hp2 | a0001 | c0012 | t0008 | g0242 | AFR | MSL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG03239 | hp1 | a0001 | c0004 | t0004 | g0124 | SAS | PJL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG03239 | hp2 | a0001 | c0002 | t0005 | g0241 | SAS | PJL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG03453 | hp1 | a0004 | c0007 | t0003 | g0185 | AFR | MSL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG03453 | hp2 | a0001 | c0004 | t0031 | g0018 | AFR | MSL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG03486 | hp1 | a0001 | c0004 | t0001 | g0048 | AFR | MSL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG03486 | hp2 | a0001 | c0004 | t0019 | g0018 | AFR | MSL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG03490 | hp1 | a0001 | c0002 | t0006 | g0180 | SAS | PJL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG03490 | hp2 | a0008 | c0019 | t0001 | g0082 | SAS | PJL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG03492 | hp1 | a0001 | c0001 | t0010 | g0248 | SAS | PJL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG03492 | hp2 | a0001 | c0002 | t0006 | g0169 | SAS | PJL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG03516 | hp1 | a0004 | c0007 | t0003 | g0021 | AFR | ESN | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG03516 | hp2 | a0002 | c0003 | t0034 | g0045 | AFR | ESN | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG03540 | hp1 | a0001 | c0002 | t0013 | g0152 | AFR | GWD | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG03540 | hp2 | a0001 | c0002 | t0003 | g0157 | AFR | GWD | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG03579 | hp1 | a0001 | c0002 | t0023 | g0197 | AFR | MSL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG03579 | hp2 | a0001 | c0009 | t0003 | g0175 | AFR | MSL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG03654 | hp1 | a0001 | c0002 | t0005 | g0239 | SAS | PJL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG03654 | hp2 | a0001 | c0005 | t0001 | g0009 | SAS | PJL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0286 | SAS | PJL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG03669 | hp2 | a0001 | c0002 | t0005 | g0229 | SAS | PJL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG03688 | hp1 | a0002 | c0003 | t0001 | g0093 | SAS | STU | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG03688 | hp2 | a0001 | c0005 | t0001 | g0070 | SAS | STU | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG03704 | hp1 | a0001 | c0002 | t0006 | g0203 | SAS | PJL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG03704 | hp2 | a0001 | c0005 | t0001 | g0011 | SAS | PJL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG03710 | hp1 | a0002 | c0003 | t0001 | g0003 | SAS | PJL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0267 | SAS | PJL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG03831 | hp1 | a0002 | c0003 | t0001 | g0003 | SAS | BEB | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG03831 | hp2 | a0001 | c0002 | t0005 | g0218 | SAS | BEB | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG03927 | hp1 | a0001 | c0002 | t0017 | g0168 | SAS | BEB | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG03927 | hp2 | a0003 | c0015 | t0001 | g0126 | SAS | BEB | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG04115 | hp1 | a0002 | c0003 | t0004 | g0083 | SAS | STU | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG04115 | hp2 | a0001 | c0005 | t0001 | g0033 | SAS | STU | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0272 | SAS | BEB | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG04184 | hp2 | a0001 | c0002 | t0006 | g0204 | SAS | BEB | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG04199 | hp1 | a0001 | c0001 | t0010 | g0279 | SAS | STU | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG04199 | hp2 | a0001 | c0004 | t0001 | g0077 | SAS | STU | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG04204 | hp1 | a0002 | c0010 | t0001 | g0002 | SAS | STU | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG04204 | hp2 | a0001 | c0005 | t0001 | g0065 | SAS | STU | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0254 | SAS | STU | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG04228 | hp2 | a0001 | c0005 | t0001 | g0096 | SAS | STU | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA18522 | hp1 | a0004 | c0007 | t0003 | g0156 | AFR | YRI | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA18522 | hp2 | a0006 | c0014 | t0001 | g0206 | AFR | YRI | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0280 | EAS | CHB | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA18612 | hp2 | a0001 | c0004 | t0001 | g0094 | EAS | CHB | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA18906 | hp1 | a0005 | c0011 | t0001 | g0121 | AFR | YRI | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA18906 | hp2 | a0001 | c0002 | t0003 | g0147 | AFR | YRI | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA18940 | hp1 | a0001 | c0005 | t0001 | g0081 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA18940 | hp2 | a0001 | c0001 | t0004 | g0219 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA18942 | hp1 | a0001 | c0004 | t0007 | g0067 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA18942 | hp2 | a0001 | c0001 | t0014 | g0231 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA18944 | hp1 | a0001 | c0001 | t0014 | g0220 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA18944 | hp2 | a0002 | c0003 | t0001 | g0061 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA18947 | hp1 | a0002 | c0003 | t0001 | g0014 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA18947 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA18948 | hp1 | a0001 | c0002 | t0003 | g0145 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0288 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA18949 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA18949 | hp2 | a0001 | c0005 | t0030 | g0131 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA18950 | hp1 | a0001 | c0002 | t0003 | g0143 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA18950 | hp2 | a0001 | c0001 | t0010 | g0283 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA18951 | hp1 | a0001 | c0002 | t0003 | g0153 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA18951 | hp2 | a0002 | c0003 | t0001 | g0116 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA18952 | hp1 | a0002 | c0003 | t0001 | g0114 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA18952 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA18954 | hp1 | a0001 | c0004 | t0001 | g0017 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA18954 | hp2 | a0001 | c0001 | t0010 | g0291 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA18964 | hp1 | a0001 | c0002 | t0013 | g0167 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0281 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA18966 | hp1 | a0001 | c0001 | t0010 | g0236 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA18966 | hp2 | a0001 | c0004 | t0001 | g0122 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA18967 | hp1 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA18967 | hp2 | a0002 | c0003 | t0012 | g0059 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA18972 | hp1 | a0001 | c0001 | t0002 | g0285 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA18972 | hp2 | a0001 | c0002 | t0003 | g0144 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA18979 | hp1 | a0001 | c0004 | t0004 | g0075 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA18979 | hp2 | a0001 | c0001 | t0002 | g0262 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA18980 | hp1 | a0001 | c0004 | t0001 | g0001 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA18980 | hp2 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA18989 | hp1 | a0001 | c0005 | t0001 | g0102 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA18989 | hp2 | a0001 | c0002 | t0003 | g0151 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA18992 | hp1 | a0001 | c0005 | t0001 | g0129 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA18992 | hp2 | a0001 | c0001 | t0002 | g0245 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA18993 | hp1 | a0001 | c0001 | t0011 | g0027 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA18993 | hp2 | a0007 | c0025 | t0003 | g0166 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA18994 | hp1 | a0001 | c0004 | t0004 | g0127 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA18994 | hp2 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA19000 | hp1 | a0002 | c0003 | t0001 | g0014 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA19000 | hp2 | a0001 | c0001 | t0010 | g0282 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA19001 | hp1 | a0001 | c0001 | t0002 | g0259 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA19001 | hp2 | a0002 | c0003 | t0001 | g0042 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA19002 | hp1 | a0001 | c0004 | t0001 | g0001 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA19002 | hp2 | a0012 | c0017 | t0002 | g0007 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA19004 | hp1 | a0002 | c0003 | t0001 | g0015 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA19004 | hp2 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA19007 | hp2 | a0001 | c0004 | t0003 | g0079 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA19009 | hp2 | a0001 | c0004 | t0001 | g0099 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA19030 | hp1 | a0003 | c0008 | t0004 | g0181 | AFR | LWK | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA19030 | hp2 | a0001 | c0002 | t0008 | g0188 | AFR | LWK | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA19060 | hp1 | a0002 | c0003 | t0004 | g0015 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA19060 | hp2 | a0001 | c0004 | t0004 | g0074 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA19070 | hp1 | a0001 | c0005 | t0001 | g0132 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA19070 | hp2 | a0001 | c0001 | t0022 | g0271 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA19075 | hp1 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA19075 | hp2 | a0002 | c0003 | t0012 | g0044 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA19080 | hp1 | a0002 | c0003 | t0012 | g0060 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA19080 | hp2 | a0001 | c0005 | t0001 | g0050 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA19083 | hp1 | a0002 | c0003 | t0012 | g0043 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA19083 | hp2 | a0001 | c0001 | t0002 | g0232 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA19085 | hp1 | a0001 | c0002 | t0015 | g0155 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA19085 | hp2 | a0002 | c0003 | t0007 | g0058 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA19086 | hp1 | a0002 | c0003 | t0001 | g0013 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA19086 | hp2 | a0001 | c0001 | t0002 | g0255 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA19088 | hp1 | a0001 | c0004 | t0001 | g0001 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA19088 | hp2 | a0002 | c0003 | t0001 | g0088 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA19240 | hp1 | a0001 | c0004 | t0009 | g0019 | AFR | YRI | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA19240 | hp2 | a0001 | c0004 | t0004 | g0010 | AFR | YRI | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA20129 | hp1 | a0001 | c0004 | t0009 | g0138 | AFR | ASW | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA20129 | hp2 | a0001 | c0004 | t0029 | g0052 | AFR | ASW | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA20752 | hp1 | a0001 | c0002 | t0005 | g0028 | EUR | TSI | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA20752 | hp2 | a0002 | c0006 | t0001 | g0159 | EUR | TSI | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA20905 | hp1 | a0002 | c0003 | t0024 | g0087 | SAS | GIH | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA20905 | hp2 | a0001 | c0002 | t0005 | g0290 | SAS | GIH | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02109 | hp1 | a0002 | c0003 | t0004 | g0090 | AFR | ACB | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02109 | hp2 | a0001 | c0002 | t0006 | g0198 | AFR | ACB | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02486 | hp1 | a0001 | c0009 | t0015 | g0176 | AFR | ACB | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02486 | hp2 | a0002 | c0003 | t0001 | g0064 | AFR | ACB | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02559 | hp1 | a0002 | c0003 | t0001 | g0062 | AFR | ACB | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02559 | hp2 | a0001 | c0004 | t0003 | g0186 | AFR | ACB | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG03471 | hp1 | a0001 | c0004 | t0001 | g0016 | AFR | MSL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG03471 | hp2 | a0001 | c0002 | t0004 | g0222 | AFR | MSL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG06807 | hp1 | a0001 | c0004 | t0009 | g0019 | AFR | USA | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG06807 | hp2 | a0001 | c0004 | t0001 | g0016 | AFR | USA | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA18955 | hp1 | a0002 | c0003 | t0001 | g0013 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA18955 | hp2 | a0001 | c0002 | t0003 | g0146 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA20300 | hp1 | a0002 | c0022 | t0007 | g0106 | AFR | USA | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA20300 | hp2 | a0002 | c0003 | t0001 | g0004 | AFR | USA | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA21309 | hp1 | a0001 | c0002 | t0016 | g0226 | AFR | LWK | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA21309 | hp2 | a0001 | c0004 | t0001 | g0100 | AFR | LWK | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0016 | g0244 | REF | REF | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
homoSapiens_grch38 | hp1 | a0004 | c0007 | t0003 | g0021 | REF | REF | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:186694249
|
G | T | 1 | a0007 | 1 | NA18993.hp2 | missense_variant | MODERATE | c.76G>T | p.Val26Phe | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/8 | 190/5731 | 76/2481 | 26/826 | chr2 | 186694249 | ||
chr2:186694250
|
T | C | 1 | a0007 | 1 | NA18993.hp2 | missense_variant | MODERATE | c.77T>C | p.Val26Ala | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/8 | 191/5731 | 77/2481 | 26/826 | chr2 | 186694250 | ||
chr2:186694302
|
A | ACAG | 4 | a0001a0003a0008others(1): Show | 85 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(82): Show |
disruptive_inframe_insertion | MODERATE | c.147_149dupGCA | p.Gln50dup | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/8 | 264/5731 | 150/2481 | 50/826 | INFO_REALIGN_3_PRIME | chr2 | 186694302 | |
chr2:186694302
|
A | ACAGCAG | 1 | a0002 | 68 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(65): Show |
disruptive_inframe_insertion | MODERATE | c.144_149dupGCAGCA | p.Gln49_Gln50dup | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/8 | 264/5731 | 150/2481 | 50/826 | INFO_REALIGN_3_PRIME | chr2 | 186694302 | |
chr2:186694302
|
A | ACAGCAGC others(2): Show |
1 | a0005 | 4 | HG01243.hp2 HG02717.hp1 HG02922.hp2 others(1): Show |
disruptive_inframe_insertion | MODERATE | c.141_149dupGCAGCAGC others(1): Show |
p.Gln48_Gln50dup | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/8 | 264/5731 | 150/2481 | 50/826 | INFO_REALIGN_3_PRIME | chr2 | 186694302 | |
chr2:186694320
|
G | GCAA | 6 | a0001a0003a0006others(3): Show | 168 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(165): Show |
disruptive_inframe_insertion | MODERATE | c.162_164dupACA | p.Gln55dup | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/8 | 279/5731 | 165/2481 | 55/826 | INFO_REALIGN_3_PRIME | chr2 | 186694320 | |
chr2:186740273
|
G | A | 1 | a0003 | 7 | HG00738.hp2 HG01099.hp1 HG02895.hp2 others(4): Show |
missense_variant | MODERATE | c.284G>A | p.Arg95His | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 2/8 | 398/5731 | 284/2481 | 95/826 | chr2 | 186740273 | ||
chr2:186740278
|
T | C | 1 | a0008 | 1 | HG03490.hp2 | missense_variant | MODERATE | c.289T>C | p.Tyr97His | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 2/8 | 403/5731 | 289/2481 | 97/826 | chr2 | 186740278 | ||
chr2:186740323
|
A | T | 1 | a0009 | 1 | HG02056.hp1 | missense_variant | MODERATE | c.334A>T | p.Thr112Ser | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 2/8 | 448/5731 | 334/2481 | 112/826 | chr2 | 186740323 | ||
chr2:186751157
|
C | T | 1 | a0006 | 2 | HG02723.hp2 NA18522.hp2 |
missense_variant | MODERATE | c.748C>T | p.Pro250Ser | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 5/8 | 862/5731 | 748/2481 | 250/826 | chr2 | 186751157 | ||
chr2:186751272
|
G | A | 1 | a0010 | 1 | HG00558.hp1 | missense_variant | MODERATE | c.863G>A | p.Arg288His | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 5/8 | 977/5731 | 863/2481 | 288/826 | chr2 | 186751272 | ||
chr2:186762414
|
A | C | 1 | a0011 | 1 | HG02135.hp2 | missense_variant | MODERATE | c.2072A>C | p.Asp691Ala | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 8/8 | 2186/5731 | 2072/2481 | 691/826 | chr2 | 186762414 | ||
chr2:186762800
|
C | T | 1 | a0012 | 1 | NA19002.hp2 | missense_variant | MODERATE | c.2458C>T | p.Arg820Cys | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 8/8 | 2572/5731 | 2458/2481 | 820/826 | chr2 | 186762800 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:186694233
|
G | A | 5 | a0001c0001a0001c0012a0009c0018others(2): Show | 83 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(80): Show |
synonymous_variant | LOW | c.60G>A | p.Leu20Leu | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/8 | 174/5731 | 60/2481 | 20/826 | chr2 | 186694233 | ||
chr2:186740319
|
G | A | 1 | a0002c0022 | 1 | NA20300.hp1 | synonymous_variant | LOW | c.330G>A | p.Thr110Thr | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 2/8 | 444/5731 | 330/2481 | 110/826 | chr2 | 186740319 | ||
chr2:186761611
|
C | T | 5 | a0001c0005a0002c0006a0003c0015others(2): Show | 48 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(45): Show |
synonymous_variant | LOW | c.1269C>T | p.Asp423Asp | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 8/8 | 1383/5731 | 1269/2481 | 423/826 | chr2 | 186761611 | ||
chr2:186761617
|
G | A | 1 | a0002c0010 | 3 | HG00642.hp2 HG00741.hp2 HG04204.hp1 |
synonymous_variant | LOW | c.1275G>A | p.Ser425Ser | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 8/8 | 1389/5731 | 1275/2481 | 425/826 | chr2 | 186761617 | ||
chr2:186761812
|
G | A | 1 | a0001c0020 | 1 | HG01884.hp1 | synonymous_variant | LOW | c.1470G>A | p.Gly490Gly | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 8/8 | 1584/5731 | 1470/2481 | 490/826 | chr2 | 186761812 | ||
chr2:186761905
|
G | A | 2 | a0001c0012a0001c0013 | 4 | HG02257.hp2 HG02970.hp1 HG03209.hp1 others(1): Show |
synonymous_variant | LOW | c.1563G>A | p.Ala521Ala | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 8/8 | 1677/5731 | 1563/2481 | 521/826 | chr2 | 186761905 | ||
chr2:186762610
|
G | A | 1 | a0002c0023 | 1 | HG00639.hp2 | synonymous_variant | LOW | c.2268G>A | p.Glu756Glu | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 8/8 | 2382/5731 | 2268/2481 | 756/826 | chr2 | 186762610 | ||
chr2:186762814
|
C | T | 1 | a0001c0009 | 3 | HG02486.hp1 HG02896.hp1 HG03579.hp2 |
synonymous_variant | LOW | c.2472C>T | p.Pro824Pro | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 8/8 | 2586/5731 | 2472/2481 | 824/826 | chr2 | 186762814 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:186694065
|
T | C | 1 | a0001c0001t0022 | 1 | NA19070.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-109T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/8 | chr2 | 186694065 | ||||||
chr2:186762840
|
G | A | 3 | a0001c0002t0006a0001c0002t0017a0001c0002t0023 | 13 | HG00735.hp1 HG01255.hp1 HG01515.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*17G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 8/8 | 17 | chr2 | 186762840 | |||||
chr2:186762849
|
G | A | 1 | a0002c0003t0024 | 1 | NA20905.hp1 | 3_prime_UTR_variant | MODIFIER | c.*26G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 8/8 | 26 | chr2 | 186762849 | |||||
chr2:186763258
|
G | A | 1 | a0001c0002t0018 | 2 | HG02258.hp2 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*435G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 8/8 | 435 | chr2 | 186763258 | |||||
chr2:186763595
|
T | A | 3 | a0001c0002t0006a0001c0002t0017a0001c0002t0023 | 13 | HG00735.hp1 HG01255.hp1 HG01515.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*772T>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 8/8 | 772 | chr2 | 186763595 | |||||
chr2:186763607
|
T | G | 1 | a0001c0001t0025 | 1 | HG01358.hp2 | 3_prime_UTR_variant | MODIFIER | c.*784T>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 8/8 | 784 | chr2 | 186763607 | |||||
chr2:186763631
|
G | A | 1 | a0002c0003t0012 | 4 | NA18967.hp2 NA19075.hp2 NA19080.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*808G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 8/8 | 808 | chr2 | 186763631 | |||||
chr2:186764047
|
A | G | 1 | a0002c0003t0034 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1224A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 8/8 | 1224 | chr2 | 186764047 | |||||
chr2:186764281
|
C | A | 2 | a0002c0003t0026a0002c0003t0027 | 2 | HG03130.hp2 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1458C>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 8/8 | 1458 | chr2 | 186764281 | |||||
chr2:186764463
|
C | CT | 24 | a0001c0001t0002a0001c0001t0004a0001c0001t0011others(21): Show | 111 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(108): Show |
3_prime_UTR_variant | MODIFIER | c.*1665dupT | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 8/8 | 1666 | INFO_REALIGN_3_PRIME | chr2 | 186764463 | ||||
chr2:186764463
|
C | CTT | 7 | a0001c0001t0010a0001c0001t0032a0001c0002t0005others(4): Show | 28 | HG00733.hp2 HG01106.hp1 HG01168.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*1664_*1665dupTT | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 8/8 | 1666 | INFO_REALIGN_3_PRIME | chr2 | 186764463 | ||||
chr2:186764463
|
C | CTTT | 4 | a0001c0001t0033a0001c0002t0006a0001c0002t0016others(1): Show | 15 | HG00738.hp1 HG01255.hp1 HG01515.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1663_*1665dupTTT | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 8/8 | 1666 | INFO_REALIGN_3_PRIME | chr2 | 186764463 | ||||
chr2:186764463
|
CT | C | 7 | a0001c0002t0013a0001c0004t0007a0001c0005t0007others(4): Show | 12 | HG01070.hp2 HG01169.hp1 HG01516.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1665delT | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 8/8 | 1665 | INFO_REALIGN_3_PRIME | chr2 | 186764463 | ||||
chr2:186764506
|
CAATT | C | 59 | a0001c0001t0002a0001c0001t0004a0001c0001t0010others(56): Show | 292 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(289): Show |
3_prime_UTR_variant | MODIFIER | c.*1689_*1692delATTA | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 8/8 | 1689 | INFO_REALIGN_3_PRIME | chr2 | 186764506 | ||||
chr2:186764623
|
T | C | 1 | a0001c0004t0029 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1800T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 8/8 | 1800 | chr2 | 186764623 | |||||
chr2:186764768
|
T | G | 7 | a0001c0002t0006a0001c0002t0008a0001c0002t0017others(4): Show | 24 | HG00735.hp1 HG01255.hp1 HG01515.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*1945T>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 8/8 | 1945 | chr2 | 186764768 | |||||
chr2:186765039
|
C | T | 1 | a0001c0001t0021 | 2 | HG01074.hp1 HG01515.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2216C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 8/8 | 2216 | chr2 | 186765039 | |||||
chr2:186765417
|
G | T | 2 | a0001c0001t0020a0001c0001t0032 | 3 | HG02055.hp1 HG02258.hp1 HG02572.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2594G>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 8/8 | 2594 | chr2 | 186765417 | |||||
chr2:186765453
|
GTATAGGG others(18): Show |
G | 1 | a0001c0002t0028 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2650_*2674delCAGT others(21): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 8/8 | 2650 | INFO_REALIGN_3_PRIME | chr2 | 186765453 | ||||
chr2:186765691
|
C | CAT | 55 | a0001c0001t0002a0001c0001t0004a0001c0001t0010others(52): Show | 281 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(278): Show |
3_prime_UTR_variant | MODIFIER | c.*2868_*2869insAT | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 8/8 | 2869 | chr2 | 186765691 | |||||
chr2:186765700
|
C | T | 2 | a0002c0003t0026a0002c0003t0027 | 2 | HG03130.hp2 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2877C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 8/8 | 2877 | chr2 | 186765700 | |||||
chr2:186765701
|
G | A | 1 | a0001c0005t0030 | 1 | NA18949.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2878G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 8/8 | 2878 | chr2 | 186765701 | |||||
chr2:186765728
|
G | A | 1 | a0001c0002t0023 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2905G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 8/8 | 2905 | chr2 | 186765728 | |||||
chr2:186765763
|
A | G | 1 | a0001c0001t0011 | 5 | HG00609.hp1 HG02040.hp2 HG02083.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2940A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 8/8 | 2940 | chr2 | 186765763 | |||||
chr2:186765819
|
G | C | 14 | a0001c0001t0002a0001c0001t0010a0001c0001t0011others(11): Show | 81 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*2996G>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 8/8 | 2996 | chr2 | 186765819 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:186694495
|
T | G | 130 | a0001c0004t0001g0001a0001c0004t0001g0016a0001c0004t0001g0017others(127): Show | 149 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.238+84T>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186694495 | ||||||
chr2:186694748
|
A | AAC | 39 | a0001c0002t0003g0174a0001c0002t0003g0182a0001c0002t0006g0178others(36): Show | 46 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.238+382_238+383dup others(2): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186694748 | |||||
chr2:186694748
|
A | AACAC | 49 | a0001c0002t0003g0005a0001c0002t0003g0162a0001c0002t0003g0163others(46): Show | 53 | HG00423.hp1 HG00735.hp2 HG01070.hp2 others(50): Show |
intron_variant | MODIFIER | c.238+380_238+383dup others(4): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186694748 | |||||
chr2:186694748
|
A | AACACAC | 22 | a0001c0002t0003g0153a0001c0002t0003g0154a0001c0002t0003g0157others(19): Show | 23 | HG01934.hp1 HG02040.hp1 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.238+378_238+383dup others(6): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186694748 | |||||
chr2:186694748
|
A | AACACACA others(1): Show |
8 | a0001c0004t0001g0038a0001c0004t0004g0036a0001c0004t0007g0039others(5): Show | 8 | HG00639.hp1 HG00673.hp2 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.238+376_238+383dup others(8): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186694748 | |||||
chr2:186694748
|
A | AACACACA others(3): Show |
7 | a0001c0002t0003g0147a0001c0002t0003g0148a0001c0002t0003g0149others(4): Show | 7 | HG00140.hp1 HG01261.hp1 HG02148.hp1 others(4): Show |
intron_variant | MODIFIER | c.238+374_238+383dup others(10): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186694748 | |||||
chr2:186694748
|
A | AACACACA others(5): Show |
2 | a0001c0002t0003g0145a0001c0002t0003g0146 | 2 | NA18948.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.238+372_238+383dup others(12): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186694748 | |||||
chr2:186694748
|
A | AACACACA others(7): Show |
1 | a0003c0015t0001g0031 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.238+370_238+383dup others(14): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186694748 | |||||
chr2:186694748
|
A | AACACACA others(9): Show |
1 | a0001c0002t0003g0144 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.238+368_238+383dup others(16): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186694748 | |||||
chr2:186694748
|
A | AACACACA others(15): Show |
1 | a0001c0002t0003g0143 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.238+362_238+383dup others(22): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186694748 | |||||
chr2:186694748
|
AAC | A | 14 | a0001c0002t0006g0198a0001c0002t0006g0201a0001c0002t0006g0202others(11): Show | 14 | HG00323.hp1 HG01255.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.238+382_238+383del others(2): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186694748 | |||||
chr2:186694748
|
AACAC | A | 7 | a0001c0001t0010g0208a0001c0002t0003g0207a0001c0002t0018g0209others(4): Show | 7 | HG01081.hp1 HG01361.hp2 HG02132.hp1 others(4): Show |
intron_variant | MODIFIER | c.238+380_238+383del others(4): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186694748 | |||||
chr2:186694748
|
AACACAC | A | 18 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0211others(15): Show | 21 | HG00642.hp1 HG01074.hp1 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.238+378_238+383del others(6): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186694748 | |||||
chr2:186694748
|
AACACACA others(1): Show |
A | 7 | a0001c0001t0004g0219a0001c0001t0014g0220a0001c0002t0001g0025others(4): Show | 7 | HG01884.hp2 HG02451.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.238+376_238+383del others(8): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186694748 | |||||
chr2:186694748
|
AACACACA others(3): Show |
A | 80 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0030others(77): Show | 88 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.238+374_238+383del others(10): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186694748 | |||||
chr2:186694748
|
AACACACA others(5): Show |
A | 2 | a0001c0002t0005g0290a0001c0020t0007g0142 | 2 | HG01884.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.238+372_238+383del others(12): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186694748 | |||||
chr2:186694748
|
AACACACA others(7): Show |
A | 1 | a0001c0001t0010g0291 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.238+370_238+383del others(14): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186694748 | |||||
chr2:186694793
|
A | C | 4 | a0001c0002t0008g0194a0001c0002t0008g0195a0001c0002t0018g0209others(1): Show | 5 | HG02922.hp1 HG02970.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.238+382A>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186694793 | ||||||
chr2:186694843
|
G | T | 1 | a0008c0019t0001g0082 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.238+432G>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186694843 | ||||||
chr2:186695046
|
C | T | 85 | a0001c0004t0001g0001a0001c0004t0001g0016a0001c0004t0001g0017others(82): Show | 95 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.238+635C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186695046 | ||||||
chr2:186695255
|
C | T | 1 | a0005c0011t0001g0121 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.238+844C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186695255 | ||||||
chr2:186695485
|
A | G | 51 | a0002c0003t0001g0002a0002c0003t0001g0003a0002c0003t0001g0004others(48): Show | 60 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(57): Show |
intron_variant | MODIFIER | c.238+1074A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186695485 | ||||||
chr2:186695554
|
C | T | 1 | a0001c0002t0003g0182 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.238+1143C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186695554 | ||||||
chr2:186695581
|
A | C | 76 | a0001c0004t0001g0001a0001c0004t0001g0016a0001c0004t0001g0017others(73): Show | 85 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.238+1170A>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186695581 | ||||||
chr2:186695657
|
T | C | 1 | a0001c0005t0001g0065 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.238+1246T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186695657 | ||||||
chr2:186695747
|
T | C | 1 | a0001c0001t0002g0221 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.238+1336T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186695747 | ||||||
chr2:186695900
|
C | A | 136 | a0001c0004t0001g0001a0001c0004t0001g0016a0001c0004t0001g0017others(133): Show | 155 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.238+1489C>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186695900 | ||||||
chr2:186695995
|
AAT | A | 180 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0022others(177): Show | 199 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.238+1597_238+1598d others(4): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186695995 | |||||
chr2:186696093
|
G | A | 16 | a0001c0002t0006g0169a0001c0002t0006g0178a0001c0002t0006g0179others(13): Show | 16 | HG00735.hp1 HG01255.hp1 HG01515.hp2 others(13): Show |
intron_variant | MODIFIER | c.238+1682G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186696093 | ||||||
chr2:186696372
|
C | T | 1 | a0001c0002t0005g0289 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.238+1961C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186696372 | ||||||
chr2:186696457
|
T | TAA | 195 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0022others(192): Show | 214 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.238+2059_238+2060d others(4): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186696457 | |||||
chr2:186696875
|
GT | G | 256 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0022others(253): Show | 284 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(281): Show |
intron_variant | MODIFIER | c.238+2469delT | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186696875 | |||||
chr2:186696995
|
AATGGATG others(5): Show |
A | 4 | a0001c0005t0001g0065a0002c0003t0001g0084a0002c0003t0004g0083others(1): Show | 4 | HG02602.hp1 HG03490.hp2 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.238+2594_238+2605d others(14): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186696995 | |||||
chr2:186696997
|
TGGATGGA others(1): Show |
T | 121 | a0001c0002t0003g0216a0001c0002t0004g0026a0001c0002t0004g0222others(118): Show | 139 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.238+2594_238+2601d others(10): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186696997 | |||||
chr2:186697001
|
TGGAC | T | 64 | a0001c0001t0002g0211a0001c0001t0002g0221a0001c0001t0002g0227others(61): Show | 69 | HG00609.hp1 HG00733.hp2 HG00735.hp1 others(66): Show |
intron_variant | MODIFIER | c.238+2594_238+2597d others(6): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186697001 | |||||
chr2:186697005
|
C | CGGAT | 4 | a0001c0002t0003g0157a0001c0009t0003g0175a0001c0009t0013g0158others(1): Show | 4 | HG02486.hp1 HG02896.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.238+2628_238+2631d others(6): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186697005 | |||||
chr2:186697005
|
C | CGGATGGA others(1): Show |
3 | a0001c0004t0009g0140a0001c0004t0019g0018a0001c0004t0031g0018 | 3 | HG02895.hp1 HG03453.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.238+2624_238+2631d others(10): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186697005 | |||||
chr2:186697005
|
C | CGGATGGA others(5): Show |
2 | a0001c0004t0009g0134a0001c0004t0009g0141 | 2 | HG01081.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.238+2620_238+2631d others(14): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186697005 | |||||
chr2:186697005
|
C | T | 67 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0022others(64): Show | 72 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(69): Show |
intron_variant | MODIFIER | c.238+2594C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186697005 | ||||||
chr2:186697039
|
G | A | 1 | a0001c0004t0001g0016 | 2 | HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.238+2628G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186697039 | ||||||
chr2:186697079
|
G | A | 181 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0022others(178): Show | 200 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.238+2668G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186697079 | ||||||
chr2:186697320
|
C | T | 1 | a0001c0005t0001g0051 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.238+2909C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186697320 | ||||||
chr2:186697393
|
G | A | 265 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0022others(262): Show | 294 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(291): Show |
intron_variant | MODIFIER | c.238+2982G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186697393 | ||||||
chr2:186697409
|
T | A | 3 | a0002c0003t0001g0042a0002c0003t0001g0054a0002c0003t0001g0085 | 3 | HG00408.hp2 HG02083.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.238+2998T>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186697409 | ||||||
chr2:186697628
|
A | G | 50 | a0002c0003t0001g0002a0002c0003t0001g0003a0002c0003t0001g0004others(47): Show | 59 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.238+3217A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186697628 | ||||||
chr2:186697947
|
A | G | 1 | a0001c0004t0003g0079 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.238+3536A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186697947 | ||||||
chr2:186698239
|
A | G | 1 | a0002c0022t0007g0106 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.238+3828A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186698239 | ||||||
chr2:186698259
|
A | G | 9 | a0001c0005t0001g0012a0001c0005t0001g0081a0001c0005t0001g0102others(6): Show | 10 | HG00544.hp1 HG00558.hp2 HG02056.hp2 others(7): Show |
intron_variant | MODIFIER | c.238+3848A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186698259 | ||||||
chr2:186698329
|
T | A | 1 | a0001c0001t0010g0208 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.238+3918T>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186698329 | ||||||
chr2:186698729
|
C | T | 72 | a0001c0004t0001g0001a0001c0004t0001g0016a0001c0004t0001g0017others(69): Show | 81 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.238+4318C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186698729 | ||||||
chr2:186698771
|
C | T | 1 | a0002c0022t0007g0106 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.238+4360C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186698771 | ||||||
chr2:186698833
|
C | T | 7 | a0002c0006t0001g0020a0002c0006t0001g0159a0002c0006t0001g0160others(4): Show | 7 | HG01928.hp2 HG01934.hp1 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.238+4422C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186698833 | ||||||
chr2:186698962
|
T | A | 1 | a0001c0001t0002g0247 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.238+4551T>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186698962 | ||||||
chr2:186698999
|
T | C | 1 | a0001c0002t0003g0183 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.238+4588T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186698999 | ||||||
chr2:186699162
|
T | C | 3 | a0001c0001t0011g0027a0001c0001t0011g0224a0001c0001t0011g0225 | 4 | HG00609.hp1 HG02083.hp2 HG02155.hp1 others(1): Show |
intron_variant | MODIFIER | c.238+4751T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186699162 | ||||||
chr2:186699291
|
T | G | 1 | a0001c0001t0004g0219 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.238+4880T>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186699291 | ||||||
chr2:186699478
|
G | T | 1 | a0002c0022t0007g0106 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.238+5067G>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186699478 | ||||||
chr2:186699540
|
A | C | 4 | a0001c0004t0009g0019a0001c0004t0009g0137a0001c0004t0009g0138others(1): Show | 5 | HG02622.hp1 HG02809.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.238+5129A>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186699540 | ||||||
chr2:186699572
|
A | G | 1 | a0001c0001t0002g0286 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.238+5161A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186699572 | ||||||
chr2:186699857
|
C | A | 2 | a0002c0003t0026g0107a0002c0003t0027g0108 | 2 | HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.238+5446C>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186699857 | ||||||
chr2:186699925
|
T | A | 73 | a0001c0004t0001g0001a0001c0004t0001g0016a0001c0004t0001g0017others(70): Show | 82 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.238+5514T>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186699925 | ||||||
chr2:186700076
|
G | GT | 73 | a0001c0004t0001g0001a0001c0004t0001g0016a0001c0004t0001g0017others(70): Show | 82 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.238+5675dupT | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186700076 | |||||
chr2:186700115
|
C | T | 1 | a0001c0004t0009g0140 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.238+5704C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186700115 | ||||||
chr2:186700217
|
G | A | 1 | a0001c0002t0005g0218 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.238+5806G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186700217 | ||||||
chr2:186700268
|
G | A | 2 | a0001c0004t0019g0018a0001c0004t0031g0018 | 2 | HG03453.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.238+5857G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186700268 | ||||||
chr2:186700321
|
A | C | 2 | a0006c0014t0001g0205a0006c0014t0001g0206 | 2 | HG02723.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.238+5910A>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186700321 | ||||||
chr2:186700321
|
A | T | 263 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0022others(260): Show | 292 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.238+5910A>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186700321 | ||||||
chr2:186700368
|
A | G | 1 | a0001c0004t0001g0101 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.238+5957A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186700368 | ||||||
chr2:186700500
|
C | T | 1 | a0002c0003t0001g0135 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.238+6089C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186700500 | ||||||
chr2:186700638
|
G | A | 1 | a0002c0022t0007g0106 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.238+6227G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186700638 | ||||||
chr2:186700785
|
G | A | 3 | a0001c0002t0004g0028a0001c0002t0005g0028a0001c0002t0016g0226 | 3 | HG01256.hp2 NA20752.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.238+6374G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186700785 | ||||||
chr2:186700819
|
T | C | 1 | a0001c0001t0011g0224 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.238+6408T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186700819 | ||||||
chr2:186700833
|
C | T | 1 | a0002c0022t0007g0106 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.238+6422C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186700833 | ||||||
chr2:186701005
|
G | C | 265 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0022others(262): Show | 294 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(291): Show |
intron_variant | MODIFIER | c.238+6594G>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186701005 | ||||||
chr2:186701007
|
C | T | 1 | a0001c0002t0006g0204 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.238+6596C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186701007 | ||||||
chr2:186701089
|
G | T | 1 | a0001c0005t0001g0040 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.238+6678G>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186701089 | ||||||
chr2:186701099
|
T | G | 1 | a0001c0002t0004g0171 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.238+6688T>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186701099 | ||||||
chr2:186701175
|
C | T | 1 | a0002c0003t0001g0118 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.238+6764C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186701175 | ||||||
chr2:186701381
|
C | T | 5 | a0003c0008t0004g0170a0003c0008t0004g0181a0003c0008t0004g0189others(2): Show | 5 | HG01099.hp1 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.238+6970C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186701381 | ||||||
chr2:186701929
|
T | A | 39 | a0002c0003t0001g0002a0002c0003t0001g0003a0002c0003t0001g0013others(36): Show | 46 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(43): Show |
intron_variant | MODIFIER | c.238+7518T>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186701929 | ||||||
chr2:186702005
|
T | C | 2 | a0002c0003t0026g0107a0002c0003t0027g0108 | 2 | HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.238+7594T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186702005 | ||||||
chr2:186702063
|
C | G | 131 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0022others(128): Show | 141 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.238+7652C>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186702063 | ||||||
chr2:186702073
|
T | C | 1 | a0001c0001t0010g0248 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.238+7662T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186702073 | ||||||
chr2:186702077
|
G | A | 39 | a0002c0003t0001g0002a0002c0003t0001g0003a0002c0003t0001g0013others(36): Show | 46 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(43): Show |
intron_variant | MODIFIER | c.238+7666G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186702077 | ||||||
chr2:186702301
|
G | A | 1 | a0001c0001t0010g0248 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.238+7890G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186702301 | ||||||
chr2:186702481
|
C | T | 1 | a0001c0004t0001g0101 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.238+8070C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186702481 | ||||||
chr2:186702518
|
T | C | 1 | a0002c0003t0001g0055 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.238+8107T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186702518 | ||||||
chr2:186702561
|
G | A | 52 | a0002c0003t0001g0002a0002c0003t0001g0003a0002c0003t0001g0004others(49): Show | 61 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(58): Show |
intron_variant | MODIFIER | c.238+8150G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186702561 | ||||||
chr2:186702636
|
C | T | 2 | a0001c0001t0002g0285a0009c0018t0002g0284 | 2 | HG02056.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.238+8225C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186702636 | ||||||
chr2:186702911
|
T | G | 72 | a0001c0004t0001g0001a0001c0004t0001g0016a0001c0004t0001g0017others(69): Show | 81 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.238+8500T>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186702911 | ||||||
chr2:186703065
|
A | G | 1 | a0001c0002t0003g0174 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.238+8654A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186703065 | ||||||
chr2:186703074
|
T | TACAC | 9 | a0001c0001t0002g0227a0001c0001t0002g0249a0001c0001t0002g0250others(6): Show | 10 | HG01255.hp2 HG02293.hp2 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.238+8664_238+8665i others(6): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186703074 | |||||
chr2:186703076
|
T | C | 10 | a0001c0001t0002g0192a0001c0001t0002g0227a0001c0001t0002g0249others(7): Show | 11 | HG01255.hp2 HG01496.hp2 HG02293.hp2 others(8): Show |
intron_variant | MODIFIER | c.238+8665T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186703076 | ||||||
chr2:186703076
|
T | TAC | 3 | a0001c0004t0001g0100a0001c0005t0004g0037a0002c0022t0007g0106 | 3 | HG02683.hp2 NA20300.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.238+8689_238+8690d others(4): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186703076 | |||||
chr2:186703076
|
T | TACAC | 126 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0022others(123): Show | 136 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.238+8687_238+8690d others(6): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186703076 | |||||
chr2:186703076
|
T | TACACAC | 7 | a0001c0001t0010g0283a0001c0002t0005g0246a0001c0004t0009g0140others(4): Show | 7 | HG02818.hp2 HG02895.hp1 HG03017.hp1 others(4): Show |
intron_variant | MODIFIER | c.238+8685_238+8690d others(8): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186703076 | |||||
chr2:186703078
|
C | T | 1 | a0001c0004t0001g0016 | 2 | HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.238+8667C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186703078 | ||||||
chr2:186703100
|
C | A | 1 | a0001c0002t0003g0174 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.238+8689C>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186703100 | ||||||
chr2:186703123
|
A | G | 52 | a0002c0003t0001g0002a0002c0003t0001g0003a0002c0003t0001g0004others(49): Show | 61 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(58): Show |
intron_variant | MODIFIER | c.238+8712A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186703123 | ||||||
chr2:186703511
|
C | T | 1 | a0001c0002t0005g0217 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.238+9100C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186703511 | ||||||
chr2:186703623
|
G | A | 1 | a0001c0001t0002g0251 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.238+9212G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186703623 | ||||||
chr2:186703696
|
T | C | 1 | a0002c0022t0007g0106 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.238+9285T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186703696 | ||||||
chr2:186703838
|
A | G | 1 | a0001c0002t0005g0289 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.238+9427A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186703838 | ||||||
chr2:186703876
|
T | C | 5 | a0003c0008t0004g0170a0003c0008t0004g0181a0003c0008t0004g0189others(2): Show | 5 | HG01099.hp1 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.238+9465T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186703876 | ||||||
chr2:186704033
|
C | G | 1 | a0001c0004t0004g0127 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.238+9622C>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186704033 | ||||||
chr2:186704082
|
A | G | 2 | a0001c0002t0013g0167a0007c0025t0003g0166 | 2 | NA18964.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.238+9671A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186704082 | ||||||
chr2:186704276
|
C | T | 16 | a0001c0002t0006g0169a0001c0002t0006g0178a0001c0002t0006g0179others(13): Show | 16 | HG00735.hp1 HG01255.hp1 HG01515.hp2 others(13): Show |
intron_variant | MODIFIER | c.238+9865C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186704276 | ||||||
chr2:186704364
|
C | T | 2 | a0001c0004t0019g0018a0001c0004t0031g0018 | 2 | HG03453.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.238+9953C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186704364 | ||||||
chr2:186704471
|
A | C | 71 | a0001c0004t0001g0001a0001c0004t0001g0016a0001c0004t0001g0017others(68): Show | 80 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.238+10060A>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186704471 | ||||||
chr2:186704493
|
C | T | 1 | a0001c0001t0002g0245 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.238+10082C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186704493 | ||||||
chr2:186704765
|
T | C | 10 | a0001c0002t0006g0169a0001c0002t0006g0178a0001c0002t0006g0179others(7): Show | 10 | HG00735.hp1 HG01255.hp1 HG01515.hp2 others(7): Show |
intron_variant | MODIFIER | c.238+10354T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186704765 | ||||||
chr2:186704859
|
A | AG | 5 | a0002c0003t0001g0004a0002c0003t0001g0034a0002c0003t0001g0062others(2): Show | 7 | HG01891.hp2 HG02559.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.238+10449dupG | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186704859 | |||||
chr2:186705024
|
C | T | 6 | a0002c0003t0001g0061a0003c0008t0004g0170a0003c0008t0004g0181others(3): Show | 6 | HG01099.hp1 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.238+10613C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186705024 | ||||||
chr2:186705081
|
T | G | 1 | a0001c0002t0004g0171 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.238+10670T>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186705081 | ||||||
chr2:186705120
|
C | T | 1 | a0001c0001t0010g0282 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.238+10709C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186705120 | ||||||
chr2:186705790
|
A | T | 122 | a0001c0004t0001g0001a0001c0004t0001g0016a0001c0004t0001g0017others(119): Show | 140 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.238+11379A>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186705790 | ||||||
chr2:186705859
|
T | C | 255 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0022others(252): Show | 283 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.238+11448T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186705859 | ||||||
chr2:186706153
|
T | C | 255 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0022others(252): Show | 283 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.238+11742T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186706153 | ||||||
chr2:186706277
|
C | T | 3 | a0001c0009t0003g0175a0001c0009t0013g0158a0001c0009t0015g0176 | 3 | HG02486.hp1 HG02896.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.238+11866C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186706277 | ||||||
chr2:186706380
|
C | T | 1 | a0001c0002t0003g0151 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.238+11969C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186706380 | ||||||
chr2:186706394
|
C | T | 1 | a0002c0023t0004g0089 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.238+11983C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186706394 | ||||||
chr2:186706402
|
A | G | 1 | a0002c0003t0001g0088 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.238+11991A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186706402 | ||||||
chr2:186706461
|
A | C | 2 | a0002c0003t0001g0064a0002c0003t0034g0045 | 2 | HG02486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.238+12050A>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186706461 | ||||||
chr2:186706548
|
C | T | 1 | a0001c0001t0002g0281 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.238+12137C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186706548 | ||||||
chr2:186706584
|
T | C | 1 | a0001c0002t0015g0161 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.238+12173T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186706584 | ||||||
chr2:186706730
|
T | C | 295 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0022others(292): Show | 325 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.238+12319T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186706730 | ||||||
chr2:186706741
|
G | A | 2 | a0001c0004t0005g0053a0001c0004t0029g0052 | 2 | HG03098.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.238+12330G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186706741 | ||||||
chr2:186706972
|
C | T | 50 | a0002c0003t0001g0002a0002c0003t0001g0003a0002c0003t0001g0004others(47): Show | 59 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.238+12561C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186706972 | ||||||
chr2:186707094
|
T | C | 50 | a0002c0003t0001g0002a0002c0003t0001g0003a0002c0003t0001g0004others(47): Show | 59 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.238+12683T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186707094 | ||||||
chr2:186707135
|
A | C | 9 | a0001c0004t0009g0019a0001c0004t0009g0134a0001c0004t0009g0137others(6): Show | 10 | HG01081.hp1 HG02622.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.238+12724A>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186707135 | ||||||
chr2:186707184
|
C | A | 2 | a0002c0003t0026g0107a0002c0003t0027g0108 | 2 | HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.238+12773C>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186707184 | ||||||
chr2:186707330
|
G | A | 1 | a0001c0004t0009g0140 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.238+12919G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186707330 | ||||||
chr2:186707377
|
C | T | 1 | a0002c0022t0007g0106 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.238+12966C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186707377 | ||||||
chr2:186707567
|
T | C | 2 | a0002c0003t0026g0107a0002c0003t0027g0108 | 2 | HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.238+13156T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186707567 | ||||||
chr2:186707612
|
A | G | 1 | a0001c0001t0002g0280 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.238+13201A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186707612 | ||||||
chr2:186707688
|
G | A | 1 | a0002c0003t0007g0110 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.238+13277G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186707688 | ||||||
chr2:186707840
|
T | A | 6 | a0001c0002t0003g0005a0001c0002t0003g0147a0001c0002t0003g0162others(3): Show | 7 | HG02451.hp2 HG02572.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.238+13429T>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186707840 | ||||||
chr2:186707841
|
T | A | 20 | a0001c0002t0003g0005a0001c0002t0003g0147a0001c0002t0003g0162others(17): Show | 23 | HG01081.hp1 HG02257.hp1 HG02451.hp2 others(20): Show |
intron_variant | MODIFIER | c.238+13430T>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186707841 | ||||||
chr2:186707841
|
TA | T | 162 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0022others(159): Show | 181 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.238+13443delA | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186707841 | |||||
chr2:186707842
|
A | T | 20 | a0001c0001t0002g0278a0001c0002t0006g0169a0001c0002t0006g0179others(17): Show | 20 | HG00408.hp1 HG00735.hp1 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.238+13431A>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186707842 | ||||||
chr2:186707843
|
A | T | 166 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0022others(163): Show | 184 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.238+13432A>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186707843 | ||||||
chr2:186707844
|
A | T | 25 | a0001c0001t0002g0250a0001c0001t0010g0279a0001c0002t0004g0171others(22): Show | 25 | HG00735.hp1 HG01099.hp1 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.238+13433A>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186707844 | ||||||
chr2:186707845
|
A | T | 5 | a0003c0008t0004g0170a0003c0008t0004g0181a0003c0008t0004g0189others(2): Show | 5 | HG01099.hp1 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.238+13434A>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186707845 | ||||||
chr2:186707846
|
A | T | 5 | a0003c0008t0004g0170a0003c0008t0004g0181a0003c0008t0004g0189others(2): Show | 5 | HG01099.hp1 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.238+13435A>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186707846 | ||||||
chr2:186707966
|
T | C | 1 | a0001c0005t0001g0065 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.238+13555T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186707966 | ||||||
chr2:186708278
|
A | G | 1 | a0001c0001t0014g0277 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.238+13867A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186708278 | ||||||
chr2:186708355
|
AT | A | 131 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0022others(128): Show | 141 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.238+13953delT | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186708355 | |||||
chr2:186708408
|
T | A | 7 | a0002c0003t0001g0002a0002c0003t0001g0055a0002c0003t0001g0111others(4): Show | 9 | HG00280.hp1 HG00642.hp2 HG00741.hp2 others(6): Show |
intron_variant | MODIFIER | c.238+13997T>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186708408 | ||||||
chr2:186708437
|
T | C | 1 | a0001c0002t0006g0202 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.238+14026T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186708437 | ||||||
chr2:186708470
|
G | A | 2 | a0001c0004t0001g0122a0001c0004t0001g0123 | 2 | HG00609.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.238+14059G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186708470 | ||||||
chr2:186708527
|
G | T | 1 | a0001c0001t0002g0276 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.238+14116G>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186708527 | ||||||
chr2:186708751
|
G | A | 102 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0022others(99): Show | 111 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(108): Show |
intron_variant | MODIFIER | c.238+14340G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186708751 | ||||||
chr2:186708796
|
A | G | 2 | a0002c0003t0026g0107a0002c0003t0027g0108 | 2 | HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.238+14385A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186708796 | ||||||
chr2:186708959
|
G | T | 9 | a0001c0004t0009g0019a0001c0004t0009g0134a0001c0004t0009g0137others(6): Show | 10 | HG01081.hp1 HG02622.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.238+14548G>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186708959 | ||||||
chr2:186709286
|
A | C | 1 | a0003c0008t0004g0191 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.238+14875A>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186709286 | ||||||
chr2:186709343
|
C | T | 131 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0022others(128): Show | 141 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.238+14932C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186709343 | ||||||
chr2:186709345
|
T | G | 131 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0022others(128): Show | 141 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.238+14934T>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186709345 | ||||||
chr2:186709986
|
C | T | 1 | a0002c0003t0001g0055 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.238+15575C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186709986 | ||||||
chr2:186710022
|
A | C | 4 | a0003c0008t0004g0170a0003c0008t0004g0189a0003c0008t0004g0190others(1): Show | 4 | HG01099.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.238+15611A>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186710022 | ||||||
chr2:186710040
|
A | G | 1 | a0001c0020t0007g0142 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.238+15629A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186710040 | ||||||
chr2:186710170
|
C | G | 7 | a0002c0006t0001g0020a0002c0006t0001g0159a0002c0006t0001g0160others(4): Show | 7 | HG01928.hp2 HG01934.hp1 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.238+15759C>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186710170 | ||||||
chr2:186710313
|
G | A | 1 | a0001c0001t0002g0252 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.238+15902G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186710313 | ||||||
chr2:186710384
|
G | A | 1 | a0002c0003t0001g0088 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.238+15973G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186710384 | ||||||
chr2:186710509
|
T | C | 1 | a0002c0023t0004g0089 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.238+16098T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186710509 | ||||||
chr2:186710592
|
G | A | 5 | a0002c0003t0001g0004a0002c0003t0001g0034a0002c0003t0001g0062others(2): Show | 7 | HG01891.hp2 HG02559.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.238+16181G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186710592 | ||||||
chr2:186710883
|
T | TAC | 6 | a0001c0002t0008g0188a0001c0002t0008g0194a0001c0002t0008g0195others(3): Show | 6 | HG02922.hp1 HG03130.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.238+16488_238+1648 others(6): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186710883 | |||||
chr2:186711252
|
C | T | 1 | a0001c0002t0003g0157 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.238+16841C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186711252 | ||||||
chr2:186711331
|
G | T | 1 | a0001c0002t0018g0196 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.238+16920G>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186711331 | ||||||
chr2:186711427
|
A | C | 1 | a0002c0022t0007g0106 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.238+17016A>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186711427 | ||||||
chr2:186711437
|
A | G | 2 | a0001c0001t0002g0247a0001c0001t0010g0248 | 2 | HG00280.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.238+17026A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186711437 | ||||||
chr2:186711462
|
G | A | 1 | a0002c0003t0004g0083 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.238+17051G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186711462 | ||||||
chr2:186711651
|
A | AT | 18 | a0001c0001t0002g0275a0001c0002t0006g0169a0001c0002t0006g0178others(15): Show | 18 | HG00735.hp1 HG01255.hp1 HG01515.hp2 others(15): Show |
intron_variant | MODIFIER | c.238+17249dupT | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186711651 | |||||
chr2:186711795
|
G | T | 1 | a0002c0003t0001g0042 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.238+17384G>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186711795 | ||||||
chr2:186712150
|
T | C | 74 | a0001c0002t0004g0026a0001c0002t0004g0222a0001c0002t0004g0223others(71): Show | 84 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.238+17739T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186712150 | ||||||
chr2:186712320
|
A | T | 1 | a0001c0001t0002g0252 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.238+17909A>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186712320 | ||||||
chr2:186712430
|
T | A | 1 | a0001c0004t0001g0100 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.238+18019T>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186712430 | ||||||
chr2:186712477
|
T | C | 7 | a0003c0008t0004g0170a0003c0008t0004g0181a0003c0008t0004g0189others(4): Show | 7 | HG01099.hp1 HG02723.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.238+18066T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186712477 | ||||||
chr2:186712767
|
C | T | 1 | a0002c0003t0001g0061 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.238+18356C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186712767 | ||||||
chr2:186713083
|
G | A | 7 | a0002c0003t0001g0002a0002c0003t0001g0055a0002c0003t0001g0111others(4): Show | 9 | HG00280.hp1 HG00642.hp2 HG00741.hp2 others(6): Show |
intron_variant | MODIFIER | c.238+18672G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186713083 | ||||||
chr2:186713133
|
C | T | 1 | a0001c0002t0003g0174 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.238+18722C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186713133 | ||||||
chr2:186713135
|
G | T | 67 | a0001c0004t0001g0001a0001c0004t0001g0016a0001c0004t0001g0017others(64): Show | 76 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.238+18724G>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186713135 | ||||||
chr2:186713206
|
G | A | 1 | a0001c0002t0003g0174 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.238+18795G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186713206 | ||||||
chr2:186713212
|
G | A | 1 | a0001c0002t0004g0171 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.238+18801G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186713212 | ||||||
chr2:186713272
|
C | T | 1 | a0001c0004t0001g0122 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.238+18861C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186713272 | ||||||
chr2:186713300
|
C | G | 5 | a0001c0002t0008g0188a0001c0002t0008g0194a0001c0002t0008g0195others(2): Show | 6 | HG02922.hp1 HG02970.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.238+18889C>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186713300 | ||||||
chr2:186713300
|
C | T | 1 | a0001c0005t0001g0033 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.238+18889C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186713300 | ||||||
chr2:186713306
|
T | C | 2 | a0002c0003t0001g0057a0002c0003t0007g0056 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.238+18895T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186713306 | ||||||
chr2:186713350
|
G | A | 1 | a0001c0001t0002g0253 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.238+18939G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186713350 | ||||||
chr2:186713360
|
G | A | 71 | a0001c0004t0001g0001a0001c0004t0001g0016a0001c0004t0001g0017others(68): Show | 80 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.238+18949G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186713360 | ||||||
chr2:186713529
|
T | G | 1 | a0001c0002t0005g0218 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.238+19118T>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186713529 | ||||||
chr2:186714121
|
A | AT | 248 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0022others(245): Show | 276 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.238+19723dupT | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186714121 | |||||
chr2:186714349
|
T | A | 2 | a0001c0005t0001g0033a0001c0005t0001g0080 | 2 | HG01175.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.238+19938T>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186714349 | ||||||
chr2:186714739
|
C | T | 2 | a0001c0002t0006g0201a0001c0002t0006g0203 | 2 | HG02698.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.238+20328C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186714739 | ||||||
chr2:186714787
|
G | A | 1 | a0001c0005t0004g0035 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.238+20376G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186714787 | ||||||
chr2:186714968
|
A | G | 1 | a0001c0001t0002g0286 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.238+20557A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186714968 | ||||||
chr2:186715967
|
A | C | 102 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0022others(99): Show | 111 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(108): Show |
intron_variant | MODIFIER | c.238+21556A>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186715967 | ||||||
chr2:186716032
|
T | A | 295 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0022others(292): Show | 325 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.238+21621T>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186716032 | ||||||
chr2:186716272
|
C | T | 1 | a0001c0004t0001g0101 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.238+21861C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186716272 | ||||||
chr2:186716370
|
T | C | 2 | a0001c0001t0002g0247a0001c0001t0010g0248 | 2 | HG00280.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.238+21959T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186716370 | ||||||
chr2:186716382
|
A | G | 8 | a0001c0002t0004g0171a0003c0008t0004g0170a0003c0008t0004g0181others(5): Show | 8 | HG01099.hp1 HG02630.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.238+21971A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186716382 | ||||||
chr2:186716397
|
C | T | 2 | a0001c0002t0003g0151a0001c0004t0003g0079 | 2 | NA18989.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.238+21986C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186716397 | ||||||
chr2:186716771
|
G | A | 1 | a0002c0003t0001g0091 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.238+22360G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186716771 | ||||||
chr2:186716796
|
A | G | 247 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0022others(244): Show | 275 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.238+22385A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186716796 | ||||||
chr2:186716796
|
A | T | 8 | a0001c0002t0004g0171a0003c0008t0004g0170a0003c0008t0004g0181others(5): Show | 8 | HG01099.hp1 HG02630.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.238+22385A>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186716796 | ||||||
chr2:186716960
|
A | G | 2 | a0002c0003t0026g0107a0002c0003t0027g0108 | 2 | HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.238+22549A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186716960 | ||||||
chr2:186716980
|
C | A | 1 | a0001c0001t0002g0211 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.238+22569C>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186716980 | ||||||
chr2:186717001
|
T | C | 73 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0022others(70): Show | 79 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(76): Show |
intron_variant | MODIFIER | c.238+22590T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186717001 | ||||||
chr2:186717516
|
C | T | 8 | a0001c0002t0004g0171a0003c0008t0004g0170a0003c0008t0004g0181others(5): Show | 8 | HG01099.hp1 HG02630.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.239-22712C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186717516 | ||||||
chr2:186717722
|
C | T | 2 | a0001c0001t0020g0006a0001c0001t0032g0006 | 3 | HG02055.hp1 HG02258.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.239-22506C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186717722 | ||||||
chr2:186717831
|
T | G | 2 | a0002c0003t0026g0107a0002c0003t0027g0108 | 2 | HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.239-22397T>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186717831 | ||||||
chr2:186717842
|
T | C | 264 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0022others(261): Show | 293 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.239-22386T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186717842 | ||||||
chr2:186718196
|
ACTGT | A | 131 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0022others(128): Show | 141 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.239-22029_239-2202 others(8): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186718196 | |||||
chr2:186718363
|
A | G | 1 | a0006c0014t0001g0205 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.239-21865A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186718363 | ||||||
chr2:186718388
|
T | G | 2 | a0002c0003t0026g0107a0002c0003t0027g0108 | 2 | HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.239-21840T>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186718388 | ||||||
chr2:186718431
|
A | T | 2 | a0001c0001t0002g0251a0001c0001t0002g0287 | 2 | HG01169.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.239-21797A>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186718431 | ||||||
chr2:186718587
|
A | C | 2 | a0001c0002t0005g0290a0001c0002t0016g0244 | 2 | NA20905.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.239-21641A>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186718587 | ||||||
chr2:186718620
|
A | G | 1 | a0002c0023t0004g0089 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.239-21608A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186718620 | ||||||
chr2:186718903
|
A | G | 1 | a0001c0002t0006g0187 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.239-21325A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186718903 | ||||||
chr2:186719005
|
G | A | 1 | a0001c0002t0005g0228 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.239-21223G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186719005 | ||||||
chr2:186719133
|
T | C | 7 | a0001c0002t0003g0005a0001c0002t0003g0147a0001c0002t0003g0162others(4): Show | 8 | HG02451.hp2 HG02572.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.239-21095T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186719133 | ||||||
chr2:186719324
|
G | A | 96 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0022others(93): Show | 105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.239-20904G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186719324 | ||||||
chr2:186719326
|
A | G | 71 | a0001c0004t0001g0001a0001c0004t0001g0016a0001c0004t0001g0017others(68): Show | 80 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.239-20902A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186719326 | ||||||
chr2:186719418
|
T | A | 2 | a0002c0003t0026g0107a0002c0003t0027g0108 | 2 | HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.239-20810T>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186719418 | ||||||
chr2:186719570
|
C | A | 1 | a0003c0008t0004g0181 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.239-20658C>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186719570 | ||||||
chr2:186719597
|
C | T | 2 | a0001c0002t0001g0025a0001c0002t0004g0025 | 2 | HG02451.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.239-20631C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186719597 | ||||||
chr2:186719808
|
T | A | 131 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0022others(128): Show | 141 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.239-20420T>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186719808 | ||||||
chr2:186719986
|
G | A | 1 | a0001c0005t0004g0037 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.239-20242G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186719986 | ||||||
chr2:186720014
|
T | C | 1 | a0001c0001t0002g0254 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.239-20214T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186720014 | ||||||
chr2:186720068
|
C | T | 1 | a0001c0002t0016g0226 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.239-20160C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186720068 | ||||||
chr2:186720316
|
A | G | 255 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0022others(252): Show | 283 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.239-19912A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186720316 | ||||||
chr2:186720429
|
T | C | 10 | a0001c0004t0001g0038a0001c0004t0001g0047a0001c0004t0001g0048others(7): Show | 11 | HG00609.hp2 HG00733.hp1 HG02004.hp1 others(8): Show |
intron_variant | MODIFIER | c.239-19799T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186720429 | ||||||
chr2:186720495
|
A | T | 1 | a0001c0009t0015g0176 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.239-19733A>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186720495 | ||||||
chr2:186720525
|
C | T | 1 | a0001c0005t0001g0105 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.239-19703C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186720525 | ||||||
chr2:186720558
|
A | T | 1 | a0002c0003t0001g0112 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.239-19670A>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186720558 | ||||||
chr2:186720700
|
C | CA | 119 | a0001c0001t0002g0215a0001c0001t0002g0272a0001c0001t0002g0273others(116): Show | 136 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.239-19512dupA | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186720700 | |||||
chr2:186720700
|
C | CAA | 108 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0022others(105): Show | 120 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.239-19513_239-1951 others(6): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186720700 | |||||
chr2:186720700
|
C | CAAA | 10 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0280others(7): Show | 10 | HG00323.hp2 HG00558.hp1 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.239-19514_239-1951 others(7): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186720700 | |||||
chr2:186720700
|
CA | C | 30 | a0001c0002t0003g0005a0001c0002t0003g0143a0001c0002t0003g0144others(27): Show | 31 | HG01261.hp1 HG01261.hp2 HG01952.hp1 others(28): Show |
intron_variant | MODIFIER | c.239-19512delA | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186720700 | |||||
chr2:186720722
|
G | C | 115 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0022others(112): Show | 128 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.239-19506G>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186720722 | ||||||
chr2:186720879
|
G | T | 2 | a0001c0002t0003g0150a0001c0002t0015g0155 | 2 | HG01261.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.239-19349G>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186720879 | ||||||
chr2:186721102
|
A | T | 2 | a0001c0002t0013g0167a0007c0025t0003g0166 | 2 | NA18964.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.239-19126A>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186721102 | ||||||
chr2:186721114
|
T | C | 1 | a0001c0002t0004g0171 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.239-19114T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186721114 | ||||||
chr2:186721156
|
G | T | 1 | a0001c0004t0004g0036 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.239-19072G>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186721156 | ||||||
chr2:186721171
|
C | G | 2 | a0001c0002t0013g0167a0007c0025t0003g0166 | 2 | NA18964.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.239-19057C>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186721171 | ||||||
chr2:186721246
|
G | A | 1 | a0001c0002t0023g0197 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.239-18982G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186721246 | ||||||
chr2:186721462
|
G | A | 124 | a0001c0004t0001g0001a0001c0004t0001g0016a0001c0004t0001g0017others(121): Show | 142 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.239-18766G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186721462 | ||||||
chr2:186721586
|
T | A | 1 | a0002c0003t0001g0032 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.239-18642T>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186721586 | ||||||
chr2:186721620
|
T | C | 57 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0022others(54): Show | 62 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.239-18608T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186721620 | ||||||
chr2:186721856
|
C | T | 1 | a0001c0005t0001g0065 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.239-18372C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186721856 | ||||||
chr2:186721872
|
C | G | 57 | a0001c0004t0001g0001a0001c0004t0001g0016a0001c0004t0001g0017others(54): Show | 65 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.239-18356C>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186721872 | ||||||
chr2:186721904
|
C | A | 253 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0022others(250): Show | 281 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(278): Show |
intron_variant | MODIFIER | c.239-18324C>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186721904 | ||||||
chr2:186722225
|
A | G | 1 | a0001c0001t0002g0227 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.239-18003A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186722225 | ||||||
chr2:186722372
|
G | T | 1 | a0002c0003t0001g0062 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.239-17856G>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186722372 | ||||||
chr2:186722689
|
G | C | 122 | a0001c0004t0001g0001a0001c0004t0001g0016a0001c0004t0001g0017others(119): Show | 140 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.239-17539G>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186722689 | ||||||
chr2:186722730
|
G | C | 2 | a0001c0001t0002g0258a0001c0001t0002g0259 | 2 | HG00544.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.239-17498G>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186722730 | ||||||
chr2:186722850
|
G | A | 255 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0022others(252): Show | 283 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.239-17378G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186722850 | ||||||
chr2:186722948
|
G | A | 2 | a0001c0002t0006g0202a0001c0002t0006g0204 | 2 | HG01255.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.239-17280G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186722948 | ||||||
chr2:186723319
|
C | T | 8 | a0001c0002t0004g0171a0003c0008t0004g0170a0003c0008t0004g0181others(5): Show | 8 | HG01099.hp1 HG02630.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.239-16909C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186723319 | ||||||
chr2:186723329
|
A | G | 16 | a0001c0001t0002g0023a0001c0001t0002g0192a0001c0001t0002g0227others(13): Show | 17 | HG00558.hp1 HG01099.hp2 HG01496.hp2 others(14): Show |
intron_variant | MODIFIER | c.239-16899A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186723329 | ||||||
chr2:186723334
|
A | G | 1 | a0001c0001t0002g0268 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.239-16894A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186723334 | ||||||
chr2:186723451
|
CT | C | 5 | a0001c0002t0008g0188a0001c0002t0008g0194a0001c0002t0008g0195others(2): Show | 6 | HG02922.hp1 HG02970.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.239-16769delT | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186723451 | |||||
chr2:186723457
|
T | A | 123 | a0001c0004t0001g0001a0001c0004t0001g0016a0001c0004t0001g0017others(120): Show | 141 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.239-16771T>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186723457 | ||||||
chr2:186723611
|
A | G | 1 | a0011c0021t0004g0066 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.239-16617A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186723611 | ||||||
chr2:186723656
|
A | C | 2 | a0001c0002t0008g0199a0001c0002t0008g0200 | 2 | HG03139.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.239-16572A>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186723656 | ||||||
chr2:186723925
|
G | A | 16 | a0001c0002t0006g0169a0001c0002t0006g0178a0001c0002t0006g0179others(13): Show | 16 | HG00735.hp1 HG01255.hp1 HG01515.hp2 others(13): Show |
intron_variant | MODIFIER | c.239-16303G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186723925 | ||||||
chr2:186723935
|
A | C | 2 | a0001c0002t0006g0169a0001c0002t0006g0180 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.239-16293A>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186723935 | ||||||
chr2:186723983
|
A | G | 6 | a0001c0004t0001g0001a0001c0004t0001g0017a0001c0004t0001g0094others(3): Show | 10 | HG02129.hp1 HG02132.hp2 NA18612.hp2 others(7): Show |
intron_variant | MODIFIER | c.239-16245A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186723983 | ||||||
chr2:186724110
|
G | A | 2 | a0001c0002t0003g0162a0001c0002t0003g0163 | 2 | HG02717.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.239-16118G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186724110 | ||||||
chr2:186724114
|
G | C | 1 | a0002c0003t0001g0085 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.239-16114G>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186724114 | ||||||
chr2:186724128
|
G | T | 24 | a0001c0002t0003g0143a0001c0002t0003g0144a0001c0002t0003g0145others(21): Show | 24 | HG00423.hp1 HG01261.hp1 HG01261.hp2 others(21): Show |
intron_variant | MODIFIER | c.239-16100G>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186724128 | ||||||
chr2:186724153
|
A | G | 57 | a0001c0004t0001g0001a0001c0004t0001g0016a0001c0004t0001g0017others(54): Show | 65 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.239-16075A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186724153 | ||||||
chr2:186724232
|
GAT | G | 70 | a0001c0004t0001g0001a0001c0004t0001g0016a0001c0004t0001g0017others(67): Show | 79 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.239-15993_239-1599 others(6): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186724232 | |||||
chr2:186724361
|
G | A | 1 | a0001c0002t0003g0157 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.239-15867G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186724361 | ||||||
chr2:186724531
|
A | G | 2 | a0001c0001t0002g0192a0001c0001t0002g0227 | 2 | HG01496.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.239-15697A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186724531 | ||||||
chr2:186724657
|
T | A | 1 | a0001c0005t0004g0037 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.239-15571T>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186724657 | ||||||
chr2:186724673
|
T | G | 16 | a0001c0002t0006g0169a0001c0002t0006g0178a0001c0002t0006g0179others(13): Show | 16 | HG00735.hp1 HG01255.hp1 HG01515.hp2 others(13): Show |
intron_variant | MODIFIER | c.239-15555T>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186724673 | ||||||
chr2:186724729
|
G | A | 255 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0022others(252): Show | 283 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.239-15499G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186724729 | ||||||
chr2:186724743
|
A | G | 1 | a0001c0001t0002g0256 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.239-15485A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186724743 | ||||||
chr2:186724755
|
G | A | 1 | a0001c0004t0001g0100 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.239-15473G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186724755 | ||||||
chr2:186725071
|
G | A | 1 | a0001c0001t0010g0282 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.239-15157G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186725071 | ||||||
chr2:186725072
|
C | T | 125 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0022others(122): Show | 135 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.239-15156C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186725072 | ||||||
chr2:186725188
|
CA | C | 103 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0022others(100): Show | 112 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.239-15034delA | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186725188 | |||||
chr2:186725213
|
A | G | 27 | a0001c0001t0002g0252a0001c0001t0010g0208a0001c0002t0003g0207others(24): Show | 27 | HG00735.hp1 HG01081.hp2 HG01099.hp1 others(24): Show |
intron_variant | MODIFIER | c.239-15015A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186725213 | ||||||
chr2:186725216
|
C | T | 2 | a0001c0005t0001g0081a0001c0005t0001g0132 | 2 | NA18940.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.239-15012C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186725216 | ||||||
chr2:186725217
|
A | G | 2 | a0001c0005t0001g0081a0001c0005t0001g0132 | 2 | NA18940.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.239-15011A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186725217 | ||||||
chr2:186725258
|
G | T | 2 | a0001c0002t0013g0167a0007c0025t0003g0166 | 2 | NA18964.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.239-14970G>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186725258 | ||||||
chr2:186725263
|
T | G | 7 | a0002c0003t0001g0013a0002c0003t0001g0014a0002c0003t0001g0015others(4): Show | 9 | NA18944.hp2 NA18947.hp1 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.239-14965T>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186725263 | ||||||
chr2:186725272
|
A | G | 20 | a0001c0002t0003g0143a0001c0002t0003g0144a0001c0002t0003g0145others(17): Show | 20 | HG00423.hp1 HG01261.hp1 HG01261.hp2 others(17): Show |
intron_variant | MODIFIER | c.239-14956A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186725272 | ||||||
chr2:186725297
|
C | T | 4 | a0001c0002t0006g0187a0001c0002t0006g0198a0001c0002t0018g0196others(1): Show | 4 | HG01891.hp1 HG02109.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.239-14931C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186725297 | ||||||
chr2:186725299
|
A | C | 4 | a0001c0002t0006g0187a0001c0002t0006g0198a0001c0002t0018g0196others(1): Show | 4 | HG01891.hp1 HG02109.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.239-14929A>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186725299 | ||||||
chr2:186725302
|
C | A | 1 | a0005c0011t0001g0121 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.239-14926C>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186725302 | ||||||
chr2:186725315
|
A | G | 4 | a0001c0002t0006g0187a0001c0002t0006g0198a0001c0002t0018g0196others(1): Show | 4 | HG01891.hp1 HG02109.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.239-14913A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186725315 | ||||||
chr2:186725338
|
T | C | 5 | a0003c0008t0004g0170a0003c0008t0004g0181a0003c0008t0004g0189others(2): Show | 5 | HG01099.hp1 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.239-14890T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186725338 | ||||||
chr2:186725343
|
C | CA | 134 | a0001c0001t0002g0230a0001c0001t0002g0232a0001c0001t0002g0233others(131): Show | 152 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.239-14870dupA | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186725343 | |||||
chr2:186725358
|
A | AG | 4 | a0001c0004t0009g0019a0001c0004t0009g0137a0001c0004t0009g0138others(1): Show | 5 | HG02622.hp1 HG02809.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.239-14869dupG | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186725358 | |||||
chr2:186725443
|
G | A | 1 | a0001c0001t0010g0279 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.239-14785G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186725443 | ||||||
chr2:186725464
|
A | G | 1 | a0001c0001t0002g0233 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.239-14764A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186725464 | ||||||
chr2:186725546
|
G | A | 1 | a0001c0002t0003g0207 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.239-14682G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186725546 | ||||||
chr2:186725968
|
C | T | 2 | a0001c0005t0001g0097a0001c0005t0001g0098 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.239-14260C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186725968 | ||||||
chr2:186726130
|
T | C | 50 | a0002c0003t0001g0002a0002c0003t0001g0003a0002c0003t0001g0004others(47): Show | 59 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.239-14098T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186726130 | ||||||
chr2:186726308
|
A | G | 2 | a0006c0014t0001g0205a0006c0014t0001g0206 | 2 | HG02723.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.239-13920A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186726308 | ||||||
chr2:186726444
|
G | A | 99 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0022others(96): Show | 108 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.239-13784G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186726444 | ||||||
chr2:186726571
|
A | G | 1 | a0001c0004t0004g0036 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.239-13657A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186726571 | ||||||
chr2:186727131
|
C | T | 295 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0022others(292): Show | 325 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.239-13097C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186727131 | ||||||
chr2:186727263
|
A | G | 2 | a0002c0003t0001g0064a0002c0003t0034g0045 | 2 | HG02486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.239-12965A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186727263 | ||||||
chr2:186727420
|
T | G | 1 | a0001c0001t0002g0260 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.239-12808T>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186727420 | ||||||
chr2:186727579
|
G | C | 1 | a0001c0001t0002g0258 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.239-12649G>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186727579 | ||||||
chr2:186727597
|
A | C | 1 | a0001c0002t0005g0029 | 2 | HG02145.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.239-12631A>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186727597 | ||||||
chr2:186727722
|
G | A | 5 | a0001c0002t0005g0228a0001c0002t0005g0238a0001c0002t0005g0239others(2): Show | 5 | HG00733.hp2 HG00738.hp1 HG01168.hp1 others(2): Show |
intron_variant | MODIFIER | c.239-12506G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186727722 | ||||||
chr2:186728421
|
C | A | 1 | a0001c0002t0003g0148 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.239-11807C>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186728421 | ||||||
chr2:186728452
|
G | A | 50 | a0002c0003t0001g0002a0002c0003t0001g0003a0002c0003t0001g0004others(47): Show | 59 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.239-11776G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186728452 | ||||||
chr2:186728511
|
C | G | 1 | a0001c0002t0005g0217 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.239-11717C>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186728511 | ||||||
chr2:186728689
|
A | C | 1 | a0006c0014t0001g0206 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.239-11539A>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186728689 | ||||||
chr2:186728716
|
A | G | 1 | a0002c0022t0007g0106 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.239-11512A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186728716 | ||||||
chr2:186728869
|
G | A | 5 | a0003c0008t0004g0170a0003c0008t0004g0181a0003c0008t0004g0189others(2): Show | 5 | HG01099.hp1 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.239-11359G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186728869 | ||||||
chr2:186728874
|
A | T | 1 | a0001c0005t0001g0050 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.239-11354A>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186728874 | ||||||
chr2:186728985
|
TA | T | 3 | a0001c0001t0004g0219a0001c0004t0004g0036a0001c0004t0004g0075 | 3 | HG00673.hp2 NA18940.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.239-11242delA | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186728985 | ||||||
chr2:186729097
|
A | T | 2 | a0006c0014t0001g0205a0006c0014t0001g0206 | 2 | HG02723.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.239-11131A>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186729097 | ||||||
chr2:186729108
|
A | G | 127 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0022others(124): Show | 137 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.239-11120A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186729108 | ||||||
chr2:186729163
|
T | C | 104 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0022others(101): Show | 113 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(110): Show |
intron_variant | MODIFIER | c.239-11065T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186729163 | ||||||
chr2:186729236
|
C | T | 4 | a0001c0002t0003g0148a0001c0002t0003g0154a0001c0002t0003g0182others(1): Show | 4 | HG01884.hp2 HG02630.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.239-10992C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186729236 | ||||||
chr2:186729271
|
A | G | 1 | a0001c0002t0004g0171 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.239-10957A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186729271 | ||||||
chr2:186729337
|
T | TA | 50 | a0002c0003t0001g0002a0002c0003t0001g0003a0002c0003t0001g0004others(47): Show | 59 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.239-10884dupA | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186729337 | |||||
chr2:186729380
|
C | T | 1 | a0001c0002t0005g0289 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.239-10848C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186729380 | ||||||
chr2:186729400
|
A | C | 14 | a0001c0002t0006g0169a0001c0002t0006g0178a0001c0002t0006g0179others(11): Show | 14 | HG00735.hp1 HG01255.hp1 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.239-10828A>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186729400 | ||||||
chr2:186729433
|
TA | T | 19 | a0001c0005t0001g0040a0001c0005t0001g0049a0001c0005t0001g0070others(16): Show | 19 | HG00323.hp1 HG00735.hp2 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.239-10794delA | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186729433 | ||||||
chr2:186729434
|
A | T | 55 | a0001c0001t0004g0219a0001c0004t0001g0001a0001c0004t0001g0016others(52): Show | 64 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.239-10794A>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186729434 | ||||||
chr2:186729438
|
T | C | 2 | a0001c0005t0001g0076a0001c0005t0007g0068 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.239-10790T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186729438 | ||||||
chr2:186729731
|
C | T | 1 | a0002c0003t0004g0090 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.239-10497C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186729731 | ||||||
chr2:186729949
|
T | G | 2 | a0001c0001t0002g0022a0001c0001t0010g0022 | 2 | HG00642.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.239-10279T>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186729949 | ||||||
chr2:186729969
|
GT | G | 9 | a0001c0002t0008g0188a0001c0002t0008g0194a0001c0002t0008g0195others(6): Show | 10 | HG02257.hp2 HG02922.hp1 HG02970.hp1 others(7): Show |
intron_variant | MODIFIER | c.239-10254delT | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186729969 | |||||
chr2:186729983
|
G | GTC | 12 | a0001c0001t0004g0219a0001c0004t0001g0001a0001c0004t0001g0017others(9): Show | 16 | HG00673.hp2 HG02129.hp1 HG02132.hp2 others(13): Show |
intron_variant | MODIFIER | c.239-10234_239-1023 others(6): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186729983 | |||||
chr2:186730154
|
T | C | 1 | a0002c0022t0007g0106 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.239-10074T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186730154 | ||||||
chr2:186730257
|
C | T | 1 | a0001c0001t0002g0278 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.239-9971C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186730257 | ||||||
chr2:186730574
|
C | T | 1 | a0001c0005t0001g0130 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.239-9654C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186730574 | ||||||
chr2:186730602
|
A | G | 2 | a0001c0001t0014g0220a0001c0001t0022g0271 | 2 | NA18944.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.239-9626A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186730602 | ||||||
chr2:186730640
|
A | G | 74 | a0001c0001t0004g0219a0001c0004t0001g0001a0001c0004t0001g0016others(71): Show | 83 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(80): Show |
intron_variant | MODIFIER | c.239-9588A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186730640 | ||||||
chr2:186730879
|
A | G | 1 | a0001c0004t0001g0094 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.239-9349A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186730879 | ||||||
chr2:186731366
|
T | C | 2 | a0002c0003t0026g0107a0002c0003t0027g0108 | 2 | HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.239-8862T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186731366 | ||||||
chr2:186731643
|
G | T | 1 | a0001c0004t0009g0140 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.239-8585G>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186731643 | ||||||
chr2:186731872
|
T | C | 1 | a0002c0003t0001g0115 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.239-8356T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186731872 | ||||||
chr2:186731932
|
C | T | 1 | a0001c0002t0005g0228 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.239-8296C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186731932 | ||||||
chr2:186732128
|
C | T | 2 | a0002c0003t0001g0064a0002c0003t0034g0045 | 2 | HG02486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.239-8100C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186732128 | ||||||
chr2:186732168
|
A | AC | 263 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0022others(260): Show | 292 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.239-8059dupC | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186732168 | |||||
chr2:186732170
|
T | A | 2 | a0002c0003t0026g0107a0002c0003t0027g0108 | 2 | HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.239-8058T>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186732170 | ||||||
chr2:186732389
|
C | T | 1 | a0002c0022t0007g0106 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.239-7839C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186732389 | ||||||
chr2:186733058
|
T | C | 1 | a0001c0004t0001g0100 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.239-7170T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186733058 | ||||||
chr2:186733194
|
A | G | 127 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0022others(124): Show | 137 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.239-7034A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186733194 | ||||||
chr2:186733857
|
C | G | 1 | a0002c0003t0001g0133 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.239-6371C>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186733857 | ||||||
chr2:186733975
|
C | A | 1 | a0002c0006t0001g0159 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.239-6253C>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186733975 | ||||||
chr2:186734425
|
C | T | 9 | a0001c0002t0008g0188a0001c0002t0008g0194a0001c0002t0008g0195others(6): Show | 10 | HG02257.hp2 HG02922.hp1 HG02970.hp1 others(7): Show |
intron_variant | MODIFIER | c.239-5803C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186734425 | ||||||
chr2:186734519
|
C | T | 2 | a0001c0001t0020g0006a0001c0001t0032g0006 | 3 | HG02055.hp1 HG02258.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.239-5709C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186734519 | ||||||
chr2:186734613
|
C | T | 2 | a0002c0003t0001g0064a0002c0003t0034g0045 | 2 | HG02486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.239-5615C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186734613 | ||||||
chr2:186734741
|
C | T | 1 | a0001c0005t0001g0049 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.239-5487C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186734741 | ||||||
chr2:186734844
|
A | C | 1 | a0001c0004t0001g0101 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.239-5384A>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186734844 | ||||||
chr2:186735009
|
G | C | 5 | a0001c0001t0004g0219a0001c0004t0004g0036a0001c0004t0004g0074others(2): Show | 5 | HG00673.hp2 HG02135.hp2 NA18940.hp2 others(2): Show |
intron_variant | MODIFIER | c.239-5219G>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186735009 | ||||||
chr2:186735091
|
C | A | 1 | a0001c0002t0003g0207 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.239-5137C>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186735091 | ||||||
chr2:186735187
|
G | A | 1 | a0001c0004t0009g0140 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.239-5041G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186735187 | ||||||
chr2:186735304
|
C | T | 9 | a0001c0002t0008g0188a0001c0002t0008g0194a0001c0002t0008g0195others(6): Show | 10 | HG02257.hp2 HG02922.hp1 HG02970.hp1 others(7): Show |
intron_variant | MODIFIER | c.239-4924C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186735304 | ||||||
chr2:186735608
|
A | C | 101 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0022others(98): Show | 110 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.239-4620A>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186735608 | ||||||
chr2:186735623
|
T | G | 2 | a0001c0004t0005g0053a0001c0004t0029g0052 | 2 | HG03098.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.239-4605T>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186735623 | ||||||
chr2:186735746
|
T | A | 254 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0022others(251): Show | 282 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.239-4482T>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186735746 | ||||||
chr2:186736011
|
A | G | 1 | a0002c0003t0001g0032 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.239-4217A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186736011 | ||||||
chr2:186736024
|
A | C | 32 | a0001c0002t0003g0005a0001c0002t0003g0143a0001c0002t0003g0144others(29): Show | 33 | HG00423.hp1 HG01261.hp1 HG01261.hp2 others(30): Show |
intron_variant | MODIFIER | c.239-4204A>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186736024 | ||||||
chr2:186736340
|
C | T | 1 | a0001c0001t0002g0286 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.239-3888C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186736340 | ||||||
chr2:186736452
|
C | T | 254 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0022others(251): Show | 282 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.239-3776C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186736452 | ||||||
chr2:186736538
|
C | CTCTGTGT others(3): Show |
1 | a0001c0001t0002g0230 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.239-3689_239-3688i others(12): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186736538 | |||||
chr2:186736538
|
C | CTG | 71 | a0001c0002t0003g0207a0001c0004t0001g0001a0001c0004t0001g0016others(68): Show | 81 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.239-3663_239-3662d others(4): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186736538 | |||||
chr2:186736538
|
C | CTGTG | 4 | a0001c0005t0004g0037a0003c0008t0004g0170a0003c0008t0004g0189others(1): Show | 4 | HG02683.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.239-3665_239-3662d others(6): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186736538 | |||||
chr2:186736538
|
C | CTGTGTG | 5 | a0001c0004t0005g0053a0001c0004t0019g0139a0001c0004t0029g0052others(2): Show | 5 | HG01516.hp1 HG01517.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.239-3667_239-3662d others(8): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186736538 | |||||
chr2:186736538
|
C | CTGTGTGT others(3): Show |
2 | a0001c0001t0002g0286a0001c0002t0005g0029 | 3 | HG02145.hp1 HG02622.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.239-3671_239-3662d others(12): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186736538 | |||||
chr2:186736538
|
C | CTGTGTGT others(11): Show |
1 | a0001c0001t0002g0267 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.239-3679_239-3662d others(20): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186736538 | |||||
chr2:186736565
|
T | G | 1 | a0001c0002t0004g0222 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.239-3663T>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186736565 | ||||||
chr2:186736565
|
T | TGTGG | 4 | a0001c0002t0008g0199a0001c0002t0008g0200a0006c0014t0001g0205others(1): Show | 4 | HG02723.hp2 HG03139.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.239-3662_239-3661i others(6): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186736565 | |||||
chr2:186736565
|
T | TGTGTGG | 9 | a0001c0002t0008g0188a0001c0002t0008g0194a0001c0002t0008g0195others(6): Show | 10 | HG01099.hp1 HG02257.hp2 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.239-3662_239-3661i others(8): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186736565 | |||||
chr2:186736565
|
T | TGTGTGTG others(1): Show |
14 | a0001c0001t0002g0211a0001c0001t0002g0254a0001c0001t0002g0255others(11): Show | 14 | HG00323.hp2 HG00735.hp1 HG01255.hp1 others(11): Show |
intron_variant | MODIFIER | c.239-3662_239-3661i others(10): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186736565 | |||||
chr2:186736565
|
T | TGTGTGTG others(3): Show |
10 | a0001c0001t0002g0252a0001c0001t0020g0006a0001c0001t0021g0212others(7): Show | 12 | HG01074.hp1 HG01891.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.239-3662_239-3661i others(12): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186736565 | |||||
chr2:186736565
|
T | TGTGTGTG others(5): Show |
1 | a0001c0001t0002g0261 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.239-3662_239-3661i others(14): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186736565 | |||||
chr2:186736565
|
T | TGTGTGTG others(5): Show |
70 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0022others(67): Show | 76 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(73): Show |
intron_variant | MODIFIER | c.239-3662_239-3661i others(14): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186736565 | |||||
chr2:186736565
|
T | TGTGTGTG others(7): Show |
3 | a0001c0001t0002g0232a0001c0001t0002g0233a0001c0001t0014g0231 | 3 | NA18942.hp2 NA19004.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.239-3662_239-3661i others(16): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186736565 | |||||
chr2:186736565
|
T | TGTGTGTG others(7): Show |
8 | a0001c0001t0002g0278a0001c0002t0001g0025a0001c0002t0004g0025others(5): Show | 8 | HG00408.hp1 HG00558.hp1 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.239-3662_239-3661i others(16): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186736565 | |||||
chr2:186736565
|
T | TGTGTGTG others(9): Show |
5 | a0001c0001t0002g0247a0001c0001t0002g0265a0001c0001t0010g0248others(2): Show | 5 | HG00140.hp2 HG00280.hp2 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.239-3662_239-3661i others(18): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186736565 | |||||
chr2:186736567
|
G | A | 127 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0022others(124): Show | 137 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.239-3661G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186736567 | ||||||
chr2:186736618
|
C | T | 2 | a0001c0002t0006g0169a0001c0002t0006g0180 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.239-3610C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186736618 | ||||||
chr2:186736645
|
C | CT | 46 | a0001c0005t0001g0071a0001c0005t0001g0104a0001c0005t0004g0035others(43): Show | 55 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(52): Show |
intron_variant | MODIFIER | c.239-3557dupT | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186736645 | |||||
chr2:186736645
|
CT | C | 126 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0022others(123): Show | 134 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.239-3557delT | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186736645 | |||||
chr2:186736645
|
CTT | C | 15 | a0001c0001t0002g0269a0001c0001t0002g0287a0001c0001t0002g0288others(12): Show | 16 | HG00609.hp1 HG01169.hp2 HG01515.hp1 others(13): Show |
intron_variant | MODIFIER | c.239-3558_239-3557d others(4): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186736645 | |||||
chr2:186736645
|
CTTTTTTT others(8): Show |
C | 1 | a0005c0011t0001g0121 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.239-3571_239-3557d others(17): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186736645 | |||||
chr2:186736912
|
G | A | 50 | a0002c0003t0001g0002a0002c0003t0001g0003a0002c0003t0001g0004others(47): Show | 59 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.239-3316G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186736912 | ||||||
chr2:186736920
|
A | G | 2 | a0001c0002t0017g0168a0001c0002t0017g0177 | 2 | HG00735.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.239-3308A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186736920 | ||||||
chr2:186737061
|
GCTAA | G | 3 | a0001c0005t0001g0050a0002c0003t0001g0064a0002c0003t0034g0045 | 3 | HG02486.hp2 HG03516.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.239-3163_239-3160d others(6): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186737061 | |||||
chr2:186737160
|
G | T | 1 | a0001c0004t0009g0141 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.239-3068G>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186737160 | ||||||
chr2:186737165
|
C | T | 1 | a0002c0003t0024g0087 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.239-3063C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186737165 | ||||||
chr2:186737214
|
A | G | 1 | a0001c0001t0022g0271 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.239-3014A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186737214 | ||||||
chr2:186737286
|
A | G | 9 | a0001c0002t0008g0188a0001c0002t0008g0194a0001c0002t0008g0195others(6): Show | 10 | HG02257.hp2 HG02922.hp1 HG02970.hp1 others(7): Show |
intron_variant | MODIFIER | c.239-2942A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186737286 | ||||||
chr2:186737345
|
T | C | 1 | a0002c0003t0004g0083 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.239-2883T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186737345 | ||||||
chr2:186737432
|
C | A | 2 | a0001c0001t0020g0006a0001c0001t0032g0006 | 3 | HG02055.hp1 HG02258.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.239-2796C>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186737432 | ||||||
chr2:186737461
|
T | G | 116 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0022others(113): Show | 126 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.239-2767T>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186737461 | ||||||
chr2:186737503
|
C | T | 14 | a0001c0002t0006g0169a0001c0002t0006g0178a0001c0002t0006g0179others(11): Show | 14 | HG00735.hp1 HG01255.hp1 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.239-2725C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186737503 | ||||||
chr2:186737796
|
A | C | 124 | a0001c0001t0004g0219a0001c0004t0001g0001a0001c0004t0001g0016others(121): Show | 142 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.239-2432A>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186737796 | ||||||
chr2:186737901
|
C | T | 1 | a0001c0002t0003g0183 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.239-2327C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186737901 | ||||||
chr2:186737936
|
G | A | 3 | a0001c0002t0004g0026a0001c0002t0004g0222a0001c0002t0004g0223 | 4 | HG02896.hp2 HG02897.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.239-2292G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186737936 | ||||||
chr2:186737942
|
C | T | 5 | a0001c0001t0014g0277a0001c0002t0004g0026a0001c0002t0004g0222others(2): Show | 6 | HG02015.hp1 HG02015.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.239-2286C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186737942 | ||||||
chr2:186737976
|
C | T | 1 | a0003c0008t0004g0181 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.239-2252C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186737976 | ||||||
chr2:186738049
|
A | G | 8 | a0002c0003t0001g0013a0002c0003t0001g0014a0002c0003t0001g0015others(5): Show | 10 | NA18944.hp2 NA18947.hp1 NA18951.hp2 others(7): Show |
intron_variant | MODIFIER | c.239-2179A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186738049 | ||||||
chr2:186738100
|
G | T | 1 | a0001c0004t0001g0100 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.239-2128G>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186738100 | ||||||
chr2:186738341
|
G | A | 2 | a0002c0003t0026g0107a0002c0003t0027g0108 | 2 | HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.239-1887G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186738341 | ||||||
chr2:186739007
|
T | A | 50 | a0002c0003t0001g0002a0002c0003t0001g0003a0002c0003t0001g0004others(47): Show | 59 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.239-1221T>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186739007 | ||||||
chr2:186739026
|
T | G | 50 | a0002c0003t0001g0002a0002c0003t0001g0003a0002c0003t0001g0004others(47): Show | 59 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.239-1202T>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186739026 | ||||||
chr2:186739093
|
T | C | 1 | a0001c0004t0001g0101 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.239-1135T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186739093 | ||||||
chr2:186739146
|
A | T | 2 | a0002c0003t0026g0107a0002c0003t0027g0108 | 2 | HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.239-1082A>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186739146 | ||||||
chr2:186739155
|
C | G | 1 | a0002c0022t0007g0106 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.239-1073C>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186739155 | ||||||
chr2:186739242
|
G | A | 127 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0022others(124): Show | 137 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.239-986G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186739242 | ||||||
chr2:186739401
|
C | T | 1 | a0001c0002t0004g0223 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.239-827C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186739401 | ||||||
chr2:186739404
|
A | T | 2 | a0002c0003t0026g0107a0002c0003t0027g0108 | 2 | HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.239-824A>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186739404 | ||||||
chr2:186739538
|
A | G | 1 | a0001c0004t0001g0048 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.239-690A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186739538 | ||||||
chr2:186739799
|
C | T | 1 | a0002c0003t0001g0054 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.239-429C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186739799 | ||||||
chr2:186739902
|
G | A | 6 | a0001c0002t0008g0188a0001c0002t0008g0194a0001c0002t0008g0195others(3): Show | 6 | HG02922.hp1 HG03130.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.239-326G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186739902 | ||||||
chr2:186739906
|
G | A | 1 | a0001c0004t0009g0141 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.239-322G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186739906 | ||||||
chr2:186739969
|
T | C | 295 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0022others(292): Show | 325 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.239-259T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186739969 | ||||||
chr2:186740136
|
C | T | 3 | a0001c0012t0008g0242a0001c0012t0008g0243a0001c0013t0008g0024 | 4 | HG02257.hp2 HG02970.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.239-92C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186740136 | ||||||
chr2:186740522
|
C | G | 1 | a0002c0003t0001g0118 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.472+61C>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 2/7 | chr2 | 186740522 | ||||||
chr2:186740682
|
A | G | 3 | a0001c0002t0001g0025a0001c0002t0004g0025a0001c0002t0005g0217 | 3 | HG02451.hp1 HG02647.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.472+221A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 2/7 | chr2 | 186740682 | ||||||
chr2:186740756
|
ATT | A | 9 | a0001c0004t0009g0019a0001c0004t0009g0134a0001c0004t0009g0137others(6): Show | 10 | HG01081.hp1 HG02622.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.472+299_472+300del others(2): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 186740756 | |||||
chr2:186741355
|
A | G | 74 | a0001c0001t0004g0219a0001c0004t0001g0001a0001c0004t0001g0016others(71): Show | 83 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(80): Show |
intron_variant | MODIFIER | c.472+894A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 2/7 | chr2 | 186741355 | ||||||
chr2:186741579
|
C | A | 1 | a0001c0004t0004g0074 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.472+1118C>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 2/7 | chr2 | 186741579 | ||||||
chr2:186741745
|
A | G | 1 | a0002c0003t0001g0064 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.472+1284A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 2/7 | chr2 | 186741745 | ||||||
chr2:186741797
|
A | G | 1 | a0001c0002t0008g0188 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.472+1336A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 2/7 | chr2 | 186741797 | ||||||
chr2:186741829
|
G | T | 16 | a0001c0002t0004g0028a0001c0002t0005g0028a0001c0002t0005g0029others(13): Show | 17 | HG00733.hp2 HG00738.hp1 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.472+1368G>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 2/7 | chr2 | 186741829 | ||||||
chr2:186741838
|
A | AATATTAA others(15): Show |
3 | a0001c0001t0002g0023a0001c0001t0002g0270a0001c0001t0002g0281 | 4 | HG02165.hp2 NA18949.hp1 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.472+1378_472+1399d others(24): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 186741838 | |||||
chr2:186741945
|
A | G | 2 | a0001c0001t0002g0192a0001c0001t0002g0227 | 2 | HG01496.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.472+1484A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 2/7 | chr2 | 186741945 | ||||||
chr2:186741955
|
C | G | 1 | a0001c0001t0002g0261 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.472+1494C>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 2/7 | chr2 | 186741955 | ||||||
chr2:186742006
|
T | A | 1 | a0002c0022t0007g0106 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.473-1477T>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 2/7 | chr2 | 186742006 | ||||||
chr2:186742026
|
T | C | 1 | a0003c0015t0001g0031 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.473-1457T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 2/7 | chr2 | 186742026 | ||||||
chr2:186742599
|
A | G | 1 | a0001c0004t0009g0138 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.473-884A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 2/7 | chr2 | 186742599 | ||||||
chr2:186742643
|
A | C | 4 | a0001c0002t0008g0188a0001c0002t0008g0194a0001c0002t0008g0195others(1): Show | 4 | HG02922.hp1 HG03130.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.473-840A>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 2/7 | chr2 | 186742643 | ||||||
chr2:186742744
|
T | C | 48 | a0002c0003t0001g0002a0002c0003t0001g0003a0002c0003t0001g0004others(45): Show | 57 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(54): Show |
intron_variant | MODIFIER | c.473-739T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 2/7 | chr2 | 186742744 | ||||||
chr2:186743147
|
A | T | 1 | a0001c0001t0002g0269 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.473-336A>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 2/7 | chr2 | 186743147 | ||||||
chr2:186743149
|
TATATC | T | 7 | a0001c0001t0002g0258a0001c0001t0002g0259a0001c0001t0002g0262others(4): Show | 8 | HG00544.hp2 HG00609.hp1 HG02040.hp2 others(5): Show |
intron_variant | MODIFIER | c.473-332_473-328del others(5): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 186743149 | |||||
chr2:186743362
|
A | C | 1 | a0002c0003t0012g0044 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.473-121A>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 2/7 | chr2 | 186743362 | ||||||
chr2:186743375
|
T | TC | 14 | a0001c0002t0006g0169a0001c0002t0006g0178a0001c0002t0006g0179others(11): Show | 14 | HG00735.hp1 HG01255.hp1 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.473-101dupC | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 186743375 | |||||
chr2:186743659
|
A | G | 2 | a0001c0004t0009g0134a0001c0004t0009g0141 | 2 | HG01081.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.565+84A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 3/7 | chr2 | 186743659 | ||||||
chr2:186743827
|
G | A | 9 | a0002c0003t0001g0004a0002c0003t0001g0034a0002c0003t0001g0062others(6): Show | 11 | HG01891.hp2 HG02109.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.565+252G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 3/7 | chr2 | 186743827 | ||||||
chr2:186744080
|
C | T | 4 | a0001c0004t0009g0019a0001c0004t0009g0137a0001c0004t0009g0138others(1): Show | 5 | HG02622.hp1 HG02809.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.565+505C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 3/7 | chr2 | 186744080 | ||||||
chr2:186744146
|
C | T | 1 | a0001c0001t0010g0282 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.565+571C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 3/7 | chr2 | 186744146 | ||||||
chr2:186744446
|
T | A | 1 | a0001c0002t0006g0187 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.565+871T>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 3/7 | chr2 | 186744446 | ||||||
chr2:186744489
|
A | C | 73 | a0001c0001t0004g0219a0001c0004t0001g0001a0001c0004t0001g0016others(70): Show | 82 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.565+914A>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 3/7 | chr2 | 186744489 | ||||||
chr2:186744668
|
A | C | 254 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0022others(251): Show | 282 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.565+1093A>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 3/7 | chr2 | 186744668 | ||||||
chr2:186744830
|
A | AT | 133 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0022others(130): Show | 143 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(140): Show |
intron_variant | MODIFIER | c.565+1273dupT | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 186744830 | |||||
chr2:186744830
|
A | ATT | 13 | a0001c0001t0002g0232a0001c0001t0004g0219a0001c0002t0005g0029others(10): Show | 16 | HG00558.hp1 HG00673.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.565+1272_565+1273d others(4): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 186744830 | |||||
chr2:186744830
|
A | T | 1 | a0001c0004t0003g0186 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.565+1255A>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 3/7 | chr2 | 186744830 | ||||||
chr2:186744884
|
G | C | 9 | a0001c0005t0001g0012a0001c0005t0001g0081a0001c0005t0001g0102others(6): Show | 10 | HG00544.hp1 HG00558.hp2 HG02056.hp2 others(7): Show |
intron_variant | MODIFIER | c.565+1309G>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 3/7 | chr2 | 186744884 | ||||||
chr2:186745180
|
G | A | 2 | a0001c0002t0013g0167a0007c0025t0003g0166 | 2 | NA18964.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.565+1605G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 3/7 | chr2 | 186745180 | ||||||
chr2:186745388
|
C | T | 5 | a0001c0004t0009g0134a0001c0004t0009g0140a0001c0004t0009g0141others(2): Show | 5 | HG01081.hp1 HG02818.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.566-1704C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 3/7 | chr2 | 186745388 | ||||||
chr2:186745774
|
G | A | 254 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0022others(251): Show | 282 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.566-1318G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 3/7 | chr2 | 186745774 | ||||||
chr2:186745930
|
G | A | 2 | a0002c0003t0026g0107a0002c0003t0027g0108 | 2 | HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.566-1162G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 3/7 | chr2 | 186745930 | ||||||
chr2:186746236
|
T | C | 1 | a0001c0001t0010g0282 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.566-856T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 3/7 | chr2 | 186746236 | ||||||
chr2:186746260
|
T | A | 1 | a0001c0001t0002g0273 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.566-832T>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 3/7 | chr2 | 186746260 | ||||||
chr2:186746613
|
A | G | 1 | a0002c0003t0004g0090 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.566-479A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 3/7 | chr2 | 186746613 | ||||||
chr2:186746670
|
G | A | 254 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0022others(251): Show | 282 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.566-422G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 3/7 | chr2 | 186746670 | ||||||
chr2:186746790
|
G | A | 2 | a0001c0004t0001g0122a0001c0004t0001g0123 | 2 | HG00609.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.566-302G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 3/7 | chr2 | 186746790 | ||||||
chr2:186747021
|
G | A | 263 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0022others(260): Show | 292 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.566-71G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 3/7 | chr2 | 186747021 | ||||||
chr2:186747583
|
C | T | 263 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0022others(260): Show | 292 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.724+333C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 4/7 | chr2 | 186747583 | ||||||
chr2:186747640
|
A | G | 2 | a0002c0003t0001g0120a0002c0003t0001g0136 | 2 | HG01081.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.724+390A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 4/7 | chr2 | 186747640 | ||||||
chr2:186747924
|
C | A | 104 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0022others(101): Show | 113 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(110): Show |
intron_variant | MODIFIER | c.724+674C>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 4/7 | chr2 | 186747924 | ||||||
chr2:186747954
|
G | T | 3 | a0001c0005t0001g0073a0001c0005t0001g0078a0001c0005t0001g0096 | 3 | HG01256.hp1 HG01258.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.724+704G>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 4/7 | chr2 | 186747954 | ||||||
chr2:186748022
|
G | A | 1 | a0001c0002t0005g0229 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.724+772G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 4/7 | chr2 | 186748022 | ||||||
chr2:186748179
|
TC | T | 50 | a0002c0003t0001g0002a0002c0003t0001g0003a0002c0003t0001g0004others(47): Show | 59 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.724+932delC | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 186748179 | |||||
chr2:186748310
|
C | CT | 49 | a0002c0003t0001g0002a0002c0003t0001g0003a0002c0003t0001g0004others(46): Show | 58 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(55): Show |
intron_variant | MODIFIER | c.724+1074dupT | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 186748310 | |||||
chr2:186748416
|
G | A | 7 | a0001c0002t0003g0005a0001c0002t0003g0147a0001c0002t0003g0162others(4): Show | 8 | HG02451.hp2 HG02572.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.724+1166G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 4/7 | chr2 | 186748416 | ||||||
chr2:186748817
|
C | T | 9 | a0002c0003t0001g0004a0002c0003t0001g0034a0002c0003t0001g0062others(6): Show | 11 | HG01891.hp2 HG02109.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.724+1567C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 4/7 | chr2 | 186748817 | ||||||
chr2:186749428
|
G | T | 5 | a0001c0002t0005g0228a0001c0002t0005g0238a0001c0002t0005g0239others(2): Show | 5 | HG00733.hp2 HG00738.hp1 HG01168.hp1 others(2): Show |
intron_variant | MODIFIER | c.725-1706G>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 4/7 | chr2 | 186749428 | ||||||
chr2:186749506
|
T | C | 2 | a0006c0014t0001g0205a0006c0014t0001g0206 | 2 | HG02723.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.725-1628T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 4/7 | chr2 | 186749506 | ||||||
chr2:186749912
|
T | C | 1 | a0001c0001t0002g0235 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.725-1222T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 4/7 | chr2 | 186749912 | ||||||
chr2:186749943
|
T | G | 1 | a0001c0001t0002g0211 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.725-1191T>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 4/7 | chr2 | 186749943 | ||||||
chr2:186750065
|
T | C | 2 | a0002c0003t0026g0107a0002c0003t0027g0108 | 2 | HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.725-1069T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 4/7 | chr2 | 186750065 | ||||||
chr2:186750586
|
TACTTTTA others(29): Show |
T | 3 | a0001c0012t0008g0242a0001c0012t0008g0243a0001c0013t0008g0024 | 4 | HG02257.hp2 HG02970.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.725-475_725-440del others(36): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 186750586 | |||||
chr2:186751347
|
TG | T | 9 | a0001c0004t0009g0019a0001c0004t0009g0134a0001c0004t0009g0137others(6): Show | 10 | HG01081.hp1 HG02622.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.895+44delG | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 5/7 | chr2 | 186751347 | ||||||
chr2:186751571
|
A | G | 1 | a0001c0004t0009g0134 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.895+267A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 5/7 | chr2 | 186751571 | ||||||
chr2:186751766
|
G | A | 2 | a0001c0009t0003g0175a0001c0009t0015g0176 | 2 | HG02486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.895+462G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 5/7 | chr2 | 186751766 | ||||||
chr2:186751919
|
C | G | 254 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0022others(251): Show | 282 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.895+615C>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 5/7 | chr2 | 186751919 | ||||||
chr2:186752137
|
C | T | 9 | a0001c0004t0009g0019a0001c0004t0009g0134a0001c0004t0009g0137others(6): Show | 10 | HG01081.hp1 HG02622.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.895+833C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 5/7 | chr2 | 186752137 | ||||||
chr2:186752244
|
G | C | 48 | a0002c0003t0001g0002a0002c0003t0001g0003a0002c0003t0001g0004others(45): Show | 57 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(54): Show |
intron_variant | MODIFIER | c.895+940G>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 5/7 | chr2 | 186752244 | ||||||
chr2:186752330
|
T | C | 7 | a0003c0008t0004g0170a0003c0008t0004g0181a0003c0008t0004g0189others(4): Show | 7 | HG01099.hp1 HG02723.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.895+1026T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 5/7 | chr2 | 186752330 | ||||||
chr2:186752436
|
C | T | 2 | a0002c0003t0026g0107a0002c0003t0027g0108 | 2 | HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.895+1132C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 5/7 | chr2 | 186752436 | ||||||
chr2:186752444
|
T | C | 1 | a0001c0002t0003g0207 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.895+1140T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 5/7 | chr2 | 186752444 | ||||||
chr2:186752516
|
A | G | 2 | a0001c0002t0003g0164a0001c0002t0003g0183 | 2 | HG01952.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.895+1212A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 5/7 | chr2 | 186752516 | ||||||
chr2:186752646
|
C | T | 253 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0022others(250): Show | 281 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(278): Show |
intron_variant | MODIFIER | c.896-1287C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 5/7 | chr2 | 186752646 | ||||||
chr2:186752883
|
T | C | 2 | a0001c0002t0006g0178a0001c0002t0006g0179 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.896-1050T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 5/7 | chr2 | 186752883 | ||||||
chr2:186753066
|
T | TAAGAGCT others(306): Show |
1 | a0002c0006t0001g0173 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.896-855_896-854ins others(313): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 186753066 | |||||
chr2:186753157
|
A | AT | 9 | a0001c0002t0008g0188a0001c0002t0008g0194a0001c0002t0008g0195others(6): Show | 10 | HG02257.hp2 HG02922.hp1 HG02970.hp1 others(7): Show |
intron_variant | MODIFIER | c.896-768dupT | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 186753157 | |||||
chr2:186753258
|
C | T | 7 | a0001c0001t0002g0008a0001c0001t0002g0237a0001c0001t0002g0249others(4): Show | 9 | HG01169.hp2 HG01255.hp2 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.896-675C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 5/7 | chr2 | 186753258 | ||||||
chr2:186753316
|
T | C | 1 | a0001c0004t0009g0140 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.896-617T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 5/7 | chr2 | 186753316 | ||||||
chr2:186753402
|
T | C | 2 | a0001c0002t0004g0028a0001c0002t0005g0028 | 2 | HG01256.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.896-531T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 5/7 | chr2 | 186753402 | ||||||
chr2:186753416
|
G | T | 1 | a0001c0004t0007g0039 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.896-517G>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 5/7 | chr2 | 186753416 | ||||||
chr2:186753454
|
A | G | 1 | a0001c0004t0003g0079 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.896-479A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 5/7 | chr2 | 186753454 | ||||||
chr2:186753467
|
A | G | 2 | a0001c0012t0008g0242a0001c0012t0008g0243 | 2 | HG02257.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.896-466A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 5/7 | chr2 | 186753467 | ||||||
chr2:186753478
|
A | T | 1 | a0001c0001t0010g0248 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.896-455A>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 5/7 | chr2 | 186753478 | ||||||
chr2:186753534
|
T | C | 1 | a0001c0005t0001g0049 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.896-399T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 5/7 | chr2 | 186753534 | ||||||
chr2:186753587
|
G | T | 69 | a0001c0004t0001g0001a0001c0004t0001g0016a0001c0004t0001g0017others(66): Show | 78 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.896-346G>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 5/7 | chr2 | 186753587 | ||||||
chr2:186753603
|
C | T | 9 | a0001c0004t0009g0019a0001c0004t0009g0134a0001c0004t0009g0137others(6): Show | 10 | HG01081.hp1 HG02622.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.896-330C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 5/7 | chr2 | 186753603 | ||||||
chr2:186753703
|
G | A | 1 | a0002c0022t0007g0106 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.896-230G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 5/7 | chr2 | 186753703 | ||||||
chr2:186753837
|
T | C | 2 | a0002c0003t0001g0064a0002c0003t0034g0045 | 2 | HG02486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.896-96T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 5/7 | chr2 | 186753837 | ||||||
chr2:186754105
|
C | T | 1 | a0001c0004t0004g0010 | 2 | HG02257.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1012+56C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 6/7 | chr2 | 186754105 | ||||||
chr2:186754612
|
G | T | 2 | a0001c0001t0002g0192a0001c0001t0002g0227 | 2 | HG01496.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.1012+563G>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 6/7 | chr2 | 186754612 | ||||||
chr2:186754738
|
C | A | 2 | a0002c0003t0012g0059a0002c0003t0012g0060 | 2 | NA18967.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.1012+689C>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 6/7 | chr2 | 186754738 | ||||||
chr2:186754872
|
A | T | 2 | a0002c0003t0001g0064a0002c0003t0034g0045 | 2 | HG02486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1012+823A>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 6/7 | chr2 | 186754872 | ||||||
chr2:186754973
|
C | T | 1 | a0001c0002t0006g0202 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1012+924C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 6/7 | chr2 | 186754973 | ||||||
chr2:186755153
|
T | A | 1 | a0001c0001t0011g0224 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1012+1104T>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 6/7 | chr2 | 186755153 | ||||||
chr2:186755170
|
T | C | 1 | a0001c0004t0001g0101 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1012+1121T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 6/7 | chr2 | 186755170 | ||||||
chr2:186755171
|
C | T | 1 | a0001c0002t0004g0171 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1012+1122C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 6/7 | chr2 | 186755171 | ||||||
chr2:186755178
|
C | T | 1 | a0001c0002t0004g0171 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1012+1129C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 6/7 | chr2 | 186755178 | ||||||
chr2:186755254
|
T | C | 2 | a0002c0003t0026g0107a0002c0003t0027g0108 | 2 | HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1012+1205T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 6/7 | chr2 | 186755254 | ||||||
chr2:186755303
|
T | C | 4 | a0003c0008t0004g0170a0003c0008t0004g0189a0003c0008t0004g0190others(1): Show | 4 | HG01099.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1012+1254T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 6/7 | chr2 | 186755303 | ||||||
chr2:186755570
|
A | T | 53 | a0001c0004t0001g0001a0001c0004t0001g0016a0001c0004t0001g0017others(50): Show | 61 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.1012+1521A>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 6/7 | chr2 | 186755570 | ||||||
chr2:186755583
|
C | A | 50 | a0002c0003t0001g0002a0002c0003t0001g0003a0002c0003t0001g0004others(47): Show | 59 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.1012+1534C>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 6/7 | chr2 | 186755583 | ||||||
chr2:186755907
|
A | C | 4 | a0001c0005t0001g0071a0001c0005t0001g0097a0001c0005t0001g0098others(1): Show | 4 | HG00735.hp2 HG01069.hp2 HG01070.hp2 others(1): Show |
intron_variant | MODIFIER | c.1012+1858A>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 6/7 | chr2 | 186755907 | ||||||
chr2:186756170
|
TATTTGTT others(7): Show |
T | 4 | a0001c0005t0001g0073a0001c0005t0001g0078a0001c0005t0001g0096others(1): Show | 4 | HG01243.hp2 HG01256.hp1 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.1012+2124_1012+213 others(18): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr2 | 186756170 | |||||
chr2:186756178
|
G | GGAAAAGA others(28): Show |
50 | a0002c0003t0001g0002a0002c0003t0001g0003a0002c0003t0001g0004others(47): Show | 59 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.1012+2131_1012+216 others(39): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr2 | 186756178 | |||||
chr2:186756296
|
A | T | 2 | a0002c0003t0026g0107a0002c0003t0027g0108 | 2 | HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1012+2247A>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 6/7 | chr2 | 186756296 | ||||||
chr2:186756460
|
A | G | 2 | a0002c0003t0026g0107a0002c0003t0027g0108 | 2 | HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1012+2411A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 6/7 | chr2 | 186756460 | ||||||
chr2:186756700
|
C | A | 48 | a0002c0003t0001g0002a0002c0003t0001g0003a0002c0003t0001g0004others(45): Show | 57 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(54): Show |
intron_variant | MODIFIER | c.1012+2651C>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 6/7 | chr2 | 186756700 | ||||||
chr2:186757074
|
G | C | 1 | a0001c0002t0004g0171 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1012+3025G>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 6/7 | chr2 | 186757074 | ||||||
chr2:186757089
|
G | C | 4 | a0002c0003t0012g0043a0002c0003t0012g0044a0002c0003t0012g0059others(1): Show | 4 | NA18967.hp2 NA19075.hp2 NA19080.hp1 others(1): Show |
intron_variant | MODIFIER | c.1012+3040G>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 6/7 | chr2 | 186757089 | ||||||
chr2:186757327
|
A | G | 14 | a0001c0002t0006g0169a0001c0002t0006g0178a0001c0002t0006g0179others(11): Show | 14 | HG00735.hp1 HG01255.hp1 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.1012+3278A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 6/7 | chr2 | 186757327 | ||||||
chr2:186757403
|
A | AAT | 8 | a0001c0004t0009g0019a0001c0004t0009g0134a0001c0004t0009g0138others(5): Show | 9 | HG01081.hp1 HG02622.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.1012+3369_1012+337 others(6): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr2 | 186757403 | |||||
chr2:186758137
|
TC | T | 125 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0022others(122): Show | 135 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.1013-2975delC | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 6/7 | chr2 | 186758137 | ||||||
chr2:186758173
|
A | C | 1 | a0001c0004t0009g0141 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1013-2940A>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 6/7 | chr2 | 186758173 | ||||||
chr2:186758189
|
G | C | 254 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0022others(251): Show | 282 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.1013-2924G>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 6/7 | chr2 | 186758189 | ||||||
chr2:186758232
|
A | G | 1 | a0001c0002t0004g0171 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1013-2881A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 6/7 | chr2 | 186758232 | ||||||
chr2:186758390
|
T | C | 4 | a0001c0002t0006g0187a0001c0002t0006g0198a0001c0002t0018g0196others(1): Show | 4 | HG01891.hp1 HG02109.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1013-2723T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 6/7 | chr2 | 186758390 | ||||||
chr2:186758668
|
T | G | 1 | a0001c0002t0003g0157 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1013-2445T>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 6/7 | chr2 | 186758668 | ||||||
chr2:186758687
|
T | C | 1 | a0001c0002t0005g0029 | 2 | HG02145.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.1013-2426T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 6/7 | chr2 | 186758687 | ||||||
chr2:186758730
|
A | C | 2 | a0001c0002t0008g0199a0001c0002t0008g0200 | 2 | HG03139.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1013-2383A>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 6/7 | chr2 | 186758730 | ||||||
chr2:186759326
|
G | T | 1 | a0001c0005t0001g0065 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1013-1787G>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 6/7 | chr2 | 186759326 | ||||||
chr2:186759368
|
A | G | 1 | a0001c0001t0002g0263 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1013-1745A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 6/7 | chr2 | 186759368 | ||||||
chr2:186759433
|
T | C | 20 | a0001c0002t0003g0143a0001c0002t0003g0144a0001c0002t0003g0145others(17): Show | 20 | HG00423.hp1 HG01261.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.1013-1680T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 6/7 | chr2 | 186759433 | ||||||
chr2:186759526
|
A | G | 2 | a0002c0003t0026g0107a0002c0003t0027g0108 | 2 | HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1013-1587A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 6/7 | chr2 | 186759526 | ||||||
chr2:186759528
|
A | C | 1 | a0002c0022t0007g0106 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1013-1585A>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 6/7 | chr2 | 186759528 | ||||||
chr2:186759810
|
C | T | 1 | a0002c0003t0001g0114 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1013-1303C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 6/7 | chr2 | 186759810 | ||||||
chr2:186759920
|
T | C | 13 | a0001c0002t0006g0169a0001c0002t0006g0178a0001c0002t0006g0179others(10): Show | 13 | HG00735.hp1 HG01255.hp1 HG01515.hp2 others(10): Show |
intron_variant | MODIFIER | c.1013-1193T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 6/7 | chr2 | 186759920 | ||||||
chr2:186760605
|
G | A | 1 | a0001c0001t0010g0208 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1013-508G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 6/7 | chr2 | 186760605 | ||||||
chr2:186760624
|
C | T | 13 | a0001c0002t0006g0169a0001c0002t0006g0178a0001c0002t0006g0179others(10): Show | 13 | HG00735.hp1 HG01255.hp1 HG01515.hp2 others(10): Show |
intron_variant | MODIFIER | c.1013-489C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 6/7 | chr2 | 186760624 | ||||||
chr2:186760690
|
G | A | 1 | a0002c0022t0007g0106 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1013-423G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 6/7 | chr2 | 186760690 | ||||||
chr2:186761299
|
T | C | 1 | a0002c0022t0007g0106 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1136+63T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 7/7 | chr2 | 186761299 | ||||||
chr2:186761368
|
A | G | 4 | a0001c0002t0003g0145a0001c0002t0003g0149a0001c0002t0003g0174others(1): Show | 4 | HG01261.hp2 HG02148.hp1 NA18948.hp1 others(1): Show |
intron_variant | MODIFIER | c.1137-111A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 7/7 | chr2 | 186761368 | ||||||
chr2:186761378
|
A | G | 1 | a0001c0004t0001g0100 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1137-101A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 7/7 | chr2 | 186761378 |