geneid | 9917 |
---|---|
ensemblid | ENSG00000116199.12 |
hgncid | 23017 |
symbol | FAM20B |
name | FAM20B glycosaminoglycan xylosylkinase |
refseq_nuc | NM_014864.4 |
refseq_prot | NP_055679.1 |
ensembl_nuc | ENST00000263733.5 |
ensembl_prot | ENSP00000263733.4 |
mane_status | MANE Select |
chr | chr1 |
start | 179025894 |
end | 179076567 |
strand | + |
ver | v1.2 |
region | chr1:179025894-179076567 |
region5000 | chr1:179020894-179081567 |
regionname0 | FAM20B_chr1_179025894_179076567 |
regionname5000 | FAM20B_chr1_179020894_179081567 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 409 | 406 | 89 | 78 | 190 | 14 | 33 | 144 | FAM20B_chr1_179020894_179081567 | FAM20B | copy fasta | chr1 | 179020894 | 179081567 |
a0002 | 0/0 | 409 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | copy fasta | chr1 | 179020894 | 179081567 |
a0003 | 0/0 | 409 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | copy fasta | chr1 | 179020894 | 179081567 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1230 | 404 | 89 | 76 | 190 | 14 | 33 | FAM20B_chr1_179020894_179081567 | FAM20B | copy fasta | chr1 | 179020894 | 179081567 |
c0002 | 0/0 | 1230 | 2 | 0 | 2 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | copy fasta | chr1 | 179020894 | 179081567 |
c0003 | 0/0 | 1230 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | copy fasta | chr1 | 179020894 | 179081567 |
c0004 | 0/0 | 1230 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20B_chr1_179020894_179081567 | FAM20B | copy fasta | chr1 | 179020894 | 179081567 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 4761 | 112 | 23 | 22 | 50 | 7 | 9 | FAM20B_chr1_179020894_179081567 | FAM20B | copy fasta | chr1 | 179020894 | 179081567 |
t0002 | 1/0 | 4762 | 93 | 2 | 25 | 51 | 3 | 11 | FAM20B_chr1_179020894_179081567 | FAM20B | copy fasta | chr1 | 179020894 | 179081567 |
t0003 | 0/0 | 4761 | 65 | 8 | 6 | 47 | 0 | 4 | FAM20B_chr1_179020894_179081567 | FAM20B | copy fasta | chr1 | 179020894 | 179081567 |
t0004 | 0/0 | 4762 | 26 | 0 | 10 | 9 | 2 | 5 | FAM20B_chr1_179020894_179081567 | FAM20B | copy fasta | chr1 | 179020894 | 179081567 |
t0005 | 0/0 | 4762 | 18 | 3 | 1 | 14 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | copy fasta | chr1 | 179020894 | 179081567 |
t0006 | 0/0 | 4761 | 16 | 9 | 2 | 0 | 1 | 4 | FAM20B_chr1_179020894_179081567 | FAM20B | copy fasta | chr1 | 179020894 | 179081567 |
t0007 | 0/0 | 4761 | 10 | 9 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | copy fasta | chr1 | 179020894 | 179081567 |
t0008 | 0/0 | 4761 | 10 | 9 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | copy fasta | chr1 | 179020894 | 179081567 |
t0009 | 0/0 | 4761 | 5 | 5 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | copy fasta | chr1 | 179020894 | 179081567 |
t0010 | 0/0 | 4761 | 5 | 0 | 4 | 0 | 1 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | copy fasta | chr1 | 179020894 | 179081567 |
t0011 | 0/0 | 4761 | 4 | 3 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | copy fasta | chr1 | 179020894 | 179081567 |
t0012 | 0/0 | 4762 | 4 | 2 | 2 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | copy fasta | chr1 | 179020894 | 179081567 |
t0013 | 0/0 | 4762 | 3 | 0 | 0 | 3 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | copy fasta | chr1 | 179020894 | 179081567 |
t0014 | 0/0 | 4762 | 3 | 0 | 0 | 3 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | copy fasta | chr1 | 179020894 | 179081567 |
t0015 | 0/0 | 4761 | 3 | 3 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | copy fasta | chr1 | 179020894 | 179081567 |
t0016 | 0/0 | 4761 | 2 | 2 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | copy fasta | chr1 | 179020894 | 179081567 |
t0017 | 0/0 | 4762 | 2 | 2 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | copy fasta | chr1 | 179020894 | 179081567 |
t0018 | 0/0 | 4761 | 2 | 2 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | copy fasta | chr1 | 179020894 | 179081567 |
t0019 | 0/0 | 4761 | 2 | 2 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | copy fasta | chr1 | 179020894 | 179081567 |
t0020 | 0/0 | 4761 | 2 | 0 | 2 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | copy fasta | chr1 | 179020894 | 179081567 |
t0021 | 0/0 | 4762 | 2 | 0 | 1 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | copy fasta | chr1 | 179020894 | 179081567 |
t0022 | 0/0 | 4761 | 2 | 0 | 0 | 2 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | copy fasta | chr1 | 179020894 | 179081567 |
t0023 | 0/0 | 4761 | 2 | 0 | 0 | 2 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | copy fasta | chr1 | 179020894 | 179081567 |
t0024 | 0/0 | 4762 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | copy fasta | chr1 | 179020894 | 179081567 |
t0025 | 0/0 | 4762 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | copy fasta | chr1 | 179020894 | 179081567 |
t0026 | 0/0 | 4745 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | copy fasta | chr1 | 179020894 | 179081567 |
t0027 | 0/0 | 4762 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | copy fasta | chr1 | 179020894 | 179081567 |
t0028 | 0/0 | 4762 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | copy fasta | chr1 | 179020894 | 179081567 |
t0029 | 0/0 | 4761 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20B_chr1_179020894_179081567 | FAM20B | copy fasta | chr1 | 179020894 | 179081567 |
t0030 | 0/0 | 4761 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | copy fasta | chr1 | 179020894 | 179081567 |
t0031 | 0/0 | 4761 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | copy fasta | chr1 | 179020894 | 179081567 |
t0032 | 0/0 | 4762 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | copy fasta | chr1 | 179020894 | 179081567 |
t0033 | 0/0 | 4762 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | copy fasta | chr1 | 179020894 | 179081567 |
t0034 | 0/0 | 4761 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | copy fasta | chr1 | 179020894 | 179081567 |
t0035 | 0/0 | 4761 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | copy fasta | chr1 | 179020894 | 179081567 |
t0036 | 0/0 | 4762 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | copy fasta | chr1 | 179020894 | 179081567 |
t0037 | 0/0 | 4762 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | copy fasta | chr1 | 179020894 | 179081567 |
t0038 | 0/0 | 4761 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | copy fasta | chr1 | 179020894 | 179081567 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 13 | 0 | 2 | 11 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0002 | 0/0 | 13 | 0 | 0 | 11 | 1 | 1 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0003 | 0/0 | 9 | 0 | 1 | 3 | 0 | 5 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0004 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0005 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0006 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0007 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0008 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0009 | 0/0 | 4 | 1 | 2 | 0 | 1 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0010 | 0/0 | 4 | 0 | 2 | 1 | 0 | 1 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0012 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0014 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0015 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0018 | 0/0 | 3 | 0 | 0 | 2 | 1 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0019 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0021 | 0/1 | 3 | 0 | 1 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0023 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0028 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0032 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0034 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0046 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0048 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0194 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0281 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1230 | 404 | 89 | 76 | 190 | 14 | 33 | FAM20B_chr1_179020894_179081567 | FAM20B | copy fasta | chr1 | 179020894 | 179081567 |
a0001c0002 | 0/0 | 1230 | 2 | 0 | 2 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | copy fasta | chr1 | 179020894 | 179081567 |
a0002c0003 | 0/0 | 1230 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | copy fasta | chr1 | 179020894 | 179081567 |
a0003c0004 | 0/0 | 1230 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20B_chr1_179020894_179081567 | FAM20B | copy fasta | chr1 | 179020894 | 179081567 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 5990 | 112 | 23 | 22 | 50 | 7 | 9 | FAM20B_chr1_179020894_179081567 | FAM20B | copy fasta | chr1 | 179020894 | 179081567 |
a0001c0001t0002 | 1/0 | 5991 | 93 | 2 | 25 | 51 | 3 | 11 | FAM20B_chr1_179020894_179081567 | FAM20B | copy fasta | chr1 | 179020894 | 179081567 |
a0001c0001t0003 | 0/0 | 5990 | 65 | 8 | 6 | 47 | 0 | 4 | FAM20B_chr1_179020894_179081567 | FAM20B | copy fasta | chr1 | 179020894 | 179081567 |
a0001c0001t0004 | 0/0 | 5991 | 26 | 0 | 10 | 9 | 2 | 5 | FAM20B_chr1_179020894_179081567 | FAM20B | copy fasta | chr1 | 179020894 | 179081567 |
a0001c0001t0005 | 0/0 | 5991 | 17 | 2 | 1 | 14 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | copy fasta | chr1 | 179020894 | 179081567 |
a0001c0001t0006 | 0/0 | 5990 | 15 | 9 | 2 | 0 | 1 | 3 | FAM20B_chr1_179020894_179081567 | FAM20B | copy fasta | chr1 | 179020894 | 179081567 |
a0001c0001t0007 | 0/0 | 5990 | 10 | 9 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | copy fasta | chr1 | 179020894 | 179081567 |
a0001c0001t0008 | 0/0 | 5990 | 10 | 9 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | copy fasta | chr1 | 179020894 | 179081567 |
a0001c0001t0009 | 0/0 | 5990 | 5 | 5 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | copy fasta | chr1 | 179020894 | 179081567 |
a0001c0001t0010 | 0/0 | 5990 | 5 | 0 | 4 | 0 | 1 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | copy fasta | chr1 | 179020894 | 179081567 |
a0001c0001t0011 | 0/0 | 5990 | 4 | 3 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | copy fasta | chr1 | 179020894 | 179081567 |
a0001c0001t0012 | 0/0 | 5991 | 4 | 2 | 2 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | copy fasta | chr1 | 179020894 | 179081567 |
a0001c0001t0013 | 0/0 | 5991 | 3 | 0 | 0 | 3 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | copy fasta | chr1 | 179020894 | 179081567 |
a0001c0001t0014 | 0/0 | 5991 | 3 | 0 | 0 | 3 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | copy fasta | chr1 | 179020894 | 179081567 |
a0001c0001t0015 | 0/0 | 5990 | 3 | 3 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | copy fasta | chr1 | 179020894 | 179081567 |
a0001c0001t0016 | 0/0 | 5990 | 2 | 2 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | copy fasta | chr1 | 179020894 | 179081567 |
a0001c0001t0017 | 0/0 | 5991 | 2 | 2 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | copy fasta | chr1 | 179020894 | 179081567 |
a0001c0001t0018 | 0/0 | 5990 | 2 | 2 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | copy fasta | chr1 | 179020894 | 179081567 |
a0001c0001t0019 | 0/0 | 5990 | 2 | 2 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | copy fasta | chr1 | 179020894 | 179081567 |
a0001c0001t0021 | 0/0 | 5991 | 2 | 0 | 1 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | copy fasta | chr1 | 179020894 | 179081567 |
a0001c0001t0022 | 0/0 | 5990 | 2 | 0 | 0 | 2 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | copy fasta | chr1 | 179020894 | 179081567 |
a0001c0001t0023 | 0/0 | 5990 | 2 | 0 | 0 | 2 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | copy fasta | chr1 | 179020894 | 179081567 |
a0001c0001t0024 | 0/0 | 5991 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | copy fasta | chr1 | 179020894 | 179081567 |
a0001c0001t0025 | 0/0 | 5991 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | copy fasta | chr1 | 179020894 | 179081567 |
a0001c0001t0026 | 0/0 | 5974 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | copy fasta | chr1 | 179020894 | 179081567 |
a0001c0001t0027 | 0/0 | 5991 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | copy fasta | chr1 | 179020894 | 179081567 |
a0001c0001t0028 | 0/0 | 5991 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | copy fasta | chr1 | 179020894 | 179081567 |
a0001c0001t0029 | 0/0 | 5990 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20B_chr1_179020894_179081567 | FAM20B | copy fasta | chr1 | 179020894 | 179081567 |
a0001c0001t0030 | 0/0 | 5990 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | copy fasta | chr1 | 179020894 | 179081567 |
a0001c0001t0031 | 0/0 | 5990 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | copy fasta | chr1 | 179020894 | 179081567 |
a0001c0001t0032 | 0/0 | 5991 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | copy fasta | chr1 | 179020894 | 179081567 |
a0001c0001t0033 | 0/0 | 5991 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | copy fasta | chr1 | 179020894 | 179081567 |
a0001c0001t0034 | 0/0 | 5990 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | copy fasta | chr1 | 179020894 | 179081567 |
a0001c0001t0035 | 0/0 | 5990 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | copy fasta | chr1 | 179020894 | 179081567 |
a0001c0001t0036 | 0/0 | 5991 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | copy fasta | chr1 | 179020894 | 179081567 |
a0001c0001t0037 | 0/0 | 5991 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | copy fasta | chr1 | 179020894 | 179081567 |
a0001c0001t0038 | 0/0 | 5990 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | copy fasta | chr1 | 179020894 | 179081567 |
a0001c0002t0020 | 0/0 | 5990 | 2 | 0 | 2 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | copy fasta | chr1 | 179020894 | 179081567 |
a0002c0003t0005 | 0/0 | 5991 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | copy fasta | chr1 | 179020894 | 179081567 |
a0003c0004t0006 | 0/0 | 5990 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20B_chr1_179020894_179081567 | FAM20B | copy fasta | chr1 | 179020894 | 179081567 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 13 | 0 | 0 | 11 | 1 | 1 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0001g0010 | 0/0 | 4 | 0 | 2 | 1 | 0 | 1 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0001g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 2 | 1 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0001g0019 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0001g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0001g0021 | 0/1 | 3 | 0 | 1 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0001g0046 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0001g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0001g0048 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0001g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0002g0001 | 0/0 | 13 | 0 | 2 | 11 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0002g0003 | 0/0 | 9 | 0 | 1 | 3 | 0 | 5 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0002g0007 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0002g0009 | 0/0 | 4 | 1 | 2 | 0 | 1 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0002g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0002g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0002g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0002g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0002g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0002g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0002g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0002g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0002g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0002g0194 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0003g0004 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0003g0005 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0003g0008 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0003g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0003g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0003g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0003g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0003g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0003g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0003g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0003g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0003g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0003g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0003g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0003g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0003g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0003g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0003g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0003g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0003g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0003g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0003g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0003g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0003g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0003g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0004g0006 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0004g0032 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0004g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0004g0034 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0004g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0004g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0004g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0004g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0004g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0004g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0004g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0004g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0004g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0004g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0004g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0004g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0004g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0004g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0004g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0005g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0005g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0005g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0005g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0005g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0005g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0005g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0005g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0005g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0005g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0005g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0005g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0005g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0005g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0005g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0006g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0006g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0006g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0006g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0006g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0006g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0006g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0006g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0006g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0006g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0006g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0006g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0006g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0006g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0006g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0007g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0007g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0007g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0007g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0007g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0007g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0007g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0007g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0007g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0008g0012 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0008g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0008g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0008g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0008g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0008g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0008g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0009g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0009g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0009g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0009g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0010g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0010g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0010g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0010g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0011g0015 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0011g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0011g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0012g0014 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0012g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0013g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0013g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0013g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0014g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0014g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0014g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0015g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0015g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0015g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0016g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0016g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0017g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0017g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0018g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0019g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0019g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0021g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0021g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0022g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0023g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0023g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0024g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0025g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0026g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0027g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0028g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0029g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0030g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0031g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0032g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0033g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0034g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0035g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0036g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0037g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0001t0038g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0002t0020g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0001c0002t0020g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0002c0003t0005g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
a0003c0004t0006g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0202 | EUR | GBR | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0229 | EUR | GBR | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG00140 | hp1 | a0001 | c0001 | t0006 | g0093 | EUR | GBR | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG00140 | hp2 | a0001 | c0001 | t0004 | g0032 | EUR | GBR | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0023 | EUR | FIN | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0281 | EUR | FIN | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG00423 | hp1 | a0001 | c0001 | t0003 | g0122 | EAS | CHS | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG00438 | hp1 | a0001 | c0001 | t0003 | g0136 | EAS | CHS | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG00438 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | CHS | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG00544 | hp1 | a0001 | c0001 | t0005 | g0064 | EAS | CHS | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG00544 | hp2 | a0001 | c0001 | t0014 | g0199 | EAS | CHS | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG00558 | hp1 | a0001 | c0001 | t0003 | g0144 | EAS | CHS | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | CHS | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG00597 | hp2 | a0001 | c0001 | t0004 | g0157 | EAS | CHS | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG00609 | hp1 | a0001 | c0001 | t0003 | g0128 | EAS | CHS | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | CHS | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | CHS | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | CHS | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG00639 | hp1 | a0001 | c0001 | t0010 | g0025 | AMR | PUR | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0213 | AMR | PUR | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG00642 | hp1 | a0001 | c0001 | t0021 | g0125 | AMR | PUR | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0188 | AMR | PUR | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | CHS | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG00673 | hp2 | a0001 | c0001 | t0002 | g0218 | EAS | CHS | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG00733 | hp1 | a0001 | c0001 | t0003 | g0131 | AMR | PUR | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG00733 | hp2 | a0001 | c0001 | t0006 | g0098 | AMR | PUR | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | PUR | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG00735 | hp2 | a0001 | c0002 | t0020 | g0106 | AMR | PUR | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG00738 | hp2 | a0001 | c0001 | t0004 | g0169 | AMR | PUR | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0257 | AMR | PUR | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG01069 | hp1 | a0001 | c0001 | t0002 | g0038 | AMR | PUR | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG01069 | hp2 | a0001 | c0001 | t0011 | g0015 | AMR | PUR | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG01070 | hp1 | a0001 | c0001 | t0010 | g0097 | AMR | PUR | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG01070 | hp2 | a0001 | c0001 | t0012 | g0014 | AMR | PUR | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0038 | AMR | PUR | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG01071 | hp2 | a0001 | c0001 | t0012 | g0014 | AMR | PUR | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG01074 | hp1 | a0001 | c0001 | t0005 | g0066 | AMR | PUR | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG01081 | hp1 | a0001 | c0001 | t0003 | g0130 | AMR | PUR | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0268 | AMR | PUR | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG01099 | hp1 | a0001 | c0001 | t0003 | g0129 | AMR | PUR | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG01099 | hp2 | a0001 | c0001 | t0007 | g0109 | AMR | PUR | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG01106 | hp1 | a0001 | c0001 | t0004 | g0163 | AMR | PUR | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0040 | AMR | PUR | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0195 | AMR | PUR | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG01167 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | PUR | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG01168 | hp2 | a0001 | c0001 | t0004 | g0155 | AMR | PUR | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0192 | AMR | PUR | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG01169 | hp2 | a0001 | c0001 | t0004 | g0033 | AMR | PUR | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG01175 | hp1 | a0001 | c0002 | t0020 | g0105 | AMR | PUR | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG01175 | hp2 | a0001 | c0001 | t0010 | g0092 | AMR | PUR | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0245 | AMR | PUR | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0243 | AMR | PUR | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG01243 | hp1 | a0001 | c0001 | t0003 | g0079 | AMR | PUR | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0183 | AMR | CLM | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | CLM | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG01256 | hp1 | a0001 | c0001 | t0002 | g0193 | AMR | CLM | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG01256 | hp2 | a0001 | c0001 | t0004 | g0153 | AMR | CLM | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0171 | AMR | CLM | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | CLM | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG01258 | hp1 | a0001 | c0001 | t0004 | g0033 | AMR | CLM | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | CLM | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0203 | AMR | CLM | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG01261 | hp2 | a0001 | c0001 | t0003 | g0008 | AMR | CLM | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG01346 | hp1 | a0001 | c0001 | t0002 | g0211 | AMR | CLM | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG01346 | hp2 | a0001 | c0001 | t0008 | g0225 | AMR | CLM | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0240 | AMR | CLM | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG01358 | hp2 | a0001 | c0001 | t0003 | g0170 | AMR | CLM | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0270 | AMR | CLM | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG01361 | hp2 | a0001 | c0001 | t0002 | g0043 | AMR | CLM | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG01433 | hp1 | a0001 | c0001 | t0010 | g0025 | AMR | CLM | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG01433 | hp2 | a0001 | c0001 | t0004 | g0166 | AMR | CLM | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0177 | AMR | CLM | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG01496 | hp2 | a0001 | c0001 | t0004 | g0162 | AMR | CLM | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG01515 | hp1 | a0001 | c0001 | t0002 | g0187 | EUR | IBS | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG01515 | hp2 | a0001 | c0001 | t0010 | g0096 | EUR | IBS | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0018 | EUR | IBS | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG01516 | hp2 | a0001 | c0001 | t0002 | g0009 | EUR | IBS | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG01891 | hp1 | a0001 | c0001 | t0015 | g0102 | AFR | ACB | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG01891 | hp2 | a0001 | c0001 | t0011 | g0103 | AFR | ACB | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0249 | AMR | PEL | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG01928 | hp2 | a0001 | c0001 | t0002 | g0040 | AMR | PEL | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG01934 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PEL | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG01934 | hp2 | a0001 | c0001 | t0004 | g0034 | AMR | PEL | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0200 | AMR | PEL | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG01952 | hp1 | a0001 | c0001 | t0004 | g0006 | AMR | PEL | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG01952 | hp2 | a0001 | c0001 | t0002 | g0178 | AMR | PEL | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG01975 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0277 | AMR | PEL | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG01978 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG01978 | hp2 | a0001 | c0001 | t0006 | g0095 | AMR | PEL | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0043 | AMR | PEL | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG02015 | hp1 | a0001 | c0001 | t0005 | g0062 | EAS | KHV | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG02015 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0206 | EAS | KHV | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG02027 | hp2 | a0001 | c0001 | t0003 | g0139 | EAS | KHV | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0173 | EAS | KHV | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | KHV | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG02055 | hp1 | a0001 | c0001 | t0008 | g0224 | AFR | ACB | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | ACB | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG02056 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG02056 | hp2 | a0001 | c0001 | t0005 | g0068 | EAS | KHV | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG02071 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | KHV | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG02071 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | KHV | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG02074 | hp1 | a0001 | c0001 | t0027 | g0007 | EAS | KHV | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG02074 | hp2 | a0001 | c0001 | t0003 | g0140 | EAS | KHV | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG02080 | hp1 | a0001 | c0001 | t0005 | g0060 | EAS | KHV | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | KHV | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG02083 | hp1 | a0001 | c0001 | t0021 | g0117 | EAS | KHV | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG02083 | hp2 | a0001 | c0001 | t0035 | g0134 | EAS | KHV | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0196 | EAS | KHV | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG02132 | hp2 | a0001 | c0001 | t0004 | g0156 | EAS | KHV | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG02135 | hp1 | a0001 | c0001 | t0005 | g0072 | EAS | KHV | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG02135 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG02145 | hp1 | a0001 | c0001 | t0007 | g0110 | AFR | ACB | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0255 | AFR | ACB | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0176 | EAS | CDX | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG02155 | hp2 | a0001 | c0001 | t0003 | g0143 | EAS | CDX | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0210 | EAS | CDX | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG02165 | hp2 | a0001 | c0001 | t0026 | g0158 | EAS | CDX | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | ACB | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG02257 | hp2 | a0001 | c0001 | t0006 | g0090 | AFR | ACB | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG02258 | hp2 | a0001 | c0001 | t0003 | g0078 | AFR | ACB | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | ACB | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG02280 | hp2 | a0001 | c0001 | t0003 | g0119 | AFR | ACB | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG02451 | hp1 | a0001 | c0001 | t0006 | g0045 | AFR | ACB | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG02451 | hp2 | a0001 | c0001 | t0019 | g0075 | AFR | ACB | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0189 | EAS | KHV | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG02523 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | KHV | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG02572 | hp1 | a0001 | c0001 | t0017 | g0293 | AFR | GWD | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG02572 | hp2 | a0001 | c0001 | t0016 | g0226 | AFR | GWD | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0250 | SAS | PJL | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0174 | SAS | PJL | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG02615 | hp1 | a0001 | c0001 | t0009 | g0292 | AFR | GWD | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0264 | AFR | GWD | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG02622 | hp1 | a0001 | c0001 | t0007 | g0108 | AFR | GWD | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0233 | AFR | GWD | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG02630 | hp1 | a0001 | c0001 | t0019 | g0076 | AFR | GWD | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0280 | AFR | GWD | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG02647 | hp1 | a0001 | c0001 | t0016 | g0227 | AFR | GWD | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG02647 | hp2 | a0001 | c0001 | t0003 | g0077 | AFR | GWD | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG02717 | hp1 | a0001 | c0001 | t0007 | g0107 | AFR | GWD | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG02717 | hp2 | a0001 | c0001 | t0008 | g0012 | AFR | GWD | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG02723 | hp1 | a0001 | c0001 | t0011 | g0015 | AFR | GWD | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG02723 | hp2 | a0001 | c0001 | t0007 | g0113 | AFR | GWD | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0246 | SAS | PJL | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0057 | SAS | PJL | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG02809 | hp1 | a0001 | c0001 | t0033 | g0015 | AFR | GWD | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG02809 | hp2 | a0001 | c0001 | t0005 | g0061 | AFR | GWD | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG02818 | hp2 | a0001 | c0001 | t0003 | g0120 | AFR | GWD | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG02886 | hp1 | a0001 | c0001 | t0003 | g0024 | AFR | GWD | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG02886 | hp2 | a0002 | c0003 | t0005 | g0063 | AFR | GWD | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG02895 | hp1 | a0001 | c0001 | t0003 | g0116 | AFR | GWD | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG02895 | hp2 | a0001 | c0001 | t0018 | g0027 | AFR | GWD | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG02897 | hp1 | a0001 | c0001 | t0018 | g0027 | AFR | GWD | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG02897 | hp2 | a0001 | c0001 | t0006 | g0083 | AFR | GWD | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG02922 | hp1 | a0001 | c0001 | t0007 | g0151 | AFR | ESN | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0263 | AFR | ESN | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG02965 | hp1 | a0001 | c0001 | t0009 | g0044 | AFR | ESN | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG02965 | hp2 | a0001 | c0001 | t0008 | g0012 | AFR | ESN | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG02970 | hp1 | a0001 | c0001 | t0007 | g0026 | AFR | ESN | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0254 | AFR | ESN | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG02976 | hp1 | a0001 | c0001 | t0030 | g0262 | AFR | ESN | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG02976 | hp2 | a0001 | c0001 | t0009 | g0044 | AFR | ESN | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG03017 | hp1 | a0001 | c0001 | t0004 | g0160 | SAS | PJL | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG03017 | hp2 | a0001 | c0001 | t0029 | g0282 | SAS | PJL | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG03041 | hp1 | a0001 | c0001 | t0015 | g0081 | AFR | GWD | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0267 | AFR | GWD | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | MSL | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG03098 | hp2 | a0001 | c0001 | t0008 | g0287 | AFR | MSL | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ESN | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG03130 | hp2 | a0001 | c0001 | t0006 | g0086 | AFR | ESN | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG03195 | hp1 | a0001 | c0001 | t0006 | g0084 | AFR | ESN | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG03195 | hp2 | a0001 | c0001 | t0005 | g0069 | AFR | ESN | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG03225 | hp1 | a0001 | c0001 | t0007 | g0112 | AFR | MSL | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG03225 | hp2 | a0001 | c0001 | t0006 | g0087 | AFR | MSL | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0209 | SAS | PJL | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG03486 | hp1 | a0001 | c0001 | t0003 | g0024 | AFR | MSL | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG03486 | hp2 | a0001 | c0001 | t0017 | g0294 | AFR | MSL | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG03490 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG03491 | hp1 | a0001 | c0001 | t0004 | g0161 | SAS | PJL | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG03491 | hp2 | a0001 | c0001 | t0003 | g0114 | SAS | PJL | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG03492 | hp2 | a0001 | c0001 | t0003 | g0118 | SAS | PJL | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG03516 | hp1 | a0001 | c0001 | t0011 | g0104 | AFR | ESN | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG03516 | hp2 | a0001 | c0001 | t0006 | g0089 | AFR | ESN | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG03540 | hp1 | a0001 | c0001 | t0015 | g0082 | AFR | GWD | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0232 | AFR | GWD | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG03579 | hp1 | a0001 | c0001 | t0009 | g0223 | AFR | MSL | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | MSL | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG03669 | hp2 | a0001 | c0001 | t0003 | g0028 | SAS | PJL | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG03704 | hp1 | a0003 | c0004 | t0006 | g0080 | SAS | PJL | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0260 | SAS | PJL | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0284 | SAS | PJL | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG03831 | hp1 | a0001 | c0001 | t0006 | g0088 | SAS | BEB | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0205 | SAS | BEB | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG03927 | hp1 | a0001 | c0001 | t0004 | g0154 | SAS | BEB | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG03927 | hp2 | a0001 | c0001 | t0002 | g0190 | SAS | BEB | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0201 | SAS | BEB | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG03942 | hp2 | a0001 | c0001 | t0006 | g0085 | SAS | BEB | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG04115 | hp1 | a0001 | c0001 | t0006 | g0091 | SAS | STU | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG04115 | hp2 | a0001 | c0001 | t0003 | g0146 | SAS | STU | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG04199 | hp1 | a0001 | c0001 | t0004 | g0165 | SAS | STU | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | STU | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0179 | SAS | STU | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG04228 | hp2 | a0001 | c0001 | t0004 | g0032 | SAS | STU | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | YRI | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA18522 | hp2 | a0001 | c0001 | t0008 | g0251 | AFR | YRI | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHB | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA18612 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | CHB | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | CHB | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | CHB | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | YRI | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA18906 | hp2 | a0001 | c0001 | t0007 | g0026 | AFR | YRI | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA18941 | hp1 | a0001 | c0001 | t0003 | g0036 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA18941 | hp2 | a0001 | c0001 | t0003 | g0145 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA18942 | hp1 | a0001 | c0001 | t0005 | g0073 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA18942 | hp2 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA18943 | hp2 | a0001 | c0001 | t0004 | g0034 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA18945 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA18946 | hp1 | a0001 | c0001 | t0003 | g0115 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA18947 | hp2 | a0001 | c0001 | t0003 | g0137 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA18949 | hp2 | a0001 | c0001 | t0003 | g0135 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA18950 | hp1 | a0001 | c0001 | t0005 | g0013 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA18950 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA18951 | hp2 | a0001 | c0001 | t0005 | g0065 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA18953 | hp2 | a0001 | c0001 | t0003 | g0148 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA18954 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA18956 | hp2 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA18957 | hp1 | a0001 | c0001 | t0003 | g0029 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA18959 | hp1 | a0001 | c0001 | t0003 | g0031 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA18961 | hp2 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA18962 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA18964 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA18964 | hp2 | a0001 | c0001 | t0013 | g0006 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA18965 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA18966 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA18966 | hp2 | a0001 | c0001 | t0003 | g0036 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA18967 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA18969 | hp2 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA18970 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA18971 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA18973 | hp2 | a0001 | c0001 | t0003 | g0031 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA18974 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA18974 | hp2 | a0001 | c0001 | t0023 | g0028 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA18975 | hp1 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA18975 | hp2 | a0001 | c0001 | t0005 | g0013 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA18977 | hp2 | a0001 | c0001 | t0037 | g0008 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA18979 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA18979 | hp2 | a0001 | c0001 | t0034 | g0141 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA18980 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA18980 | hp2 | a0001 | c0001 | t0003 | g0133 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA18981 | hp1 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA18981 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA18983 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA18983 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA18985 | hp1 | a0001 | c0001 | t0003 | g0150 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA18985 | hp2 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA18986 | hp2 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA18989 | hp1 | a0001 | c0001 | t0004 | g0035 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA18989 | hp2 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA18991 | hp1 | a0001 | c0001 | t0004 | g0167 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA18991 | hp2 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA18992 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA18992 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA18993 | hp1 | a0001 | c0001 | t0003 | g0149 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA18993 | hp2 | a0001 | c0001 | t0028 | g0017 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA18994 | hp2 | a0001 | c0001 | t0014 | g0214 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA18995 | hp1 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA18998 | hp1 | a0001 | c0001 | t0013 | g0164 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA18998 | hp2 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA19000 | hp1 | a0001 | c0001 | t0005 | g0059 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA19000 | hp2 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA19001 | hp1 | a0001 | c0001 | t0022 | g0030 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA19001 | hp2 | a0001 | c0001 | t0031 | g0253 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA19004 | hp1 | a0001 | c0001 | t0005 | g0067 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA19004 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA19006 | hp1 | a0001 | c0001 | t0005 | g0071 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA19006 | hp2 | a0001 | c0001 | t0036 | g0142 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA19007 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA19009 | hp2 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA19010 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA19010 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0272 | AFR | LWK | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA19030 | hp2 | a0001 | c0001 | t0032 | g0101 | AFR | LWK | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA19043 | hp1 | a0001 | c0001 | t0025 | g0207 | AFR | LWK | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA19043 | hp2 | a0001 | c0001 | t0006 | g0099 | AFR | LWK | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA19054 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA19056 | hp1 | a0001 | c0001 | t0003 | g0127 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA19060 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA19062 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA19062 | hp2 | a0001 | c0001 | t0003 | g0168 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA19063 | hp1 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA19063 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA19064 | hp1 | a0001 | c0001 | t0005 | g0070 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA19065 | hp2 | a0001 | c0001 | t0004 | g0035 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA19066 | hp1 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA19068 | hp1 | a0001 | c0001 | t0003 | g0138 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA19070 | hp2 | a0001 | c0001 | t0003 | g0123 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA19074 | hp1 | a0001 | c0001 | t0003 | g0147 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA19074 | hp2 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA19076 | hp1 | a0001 | c0001 | t0003 | g0029 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA19076 | hp2 | a0001 | c0001 | t0005 | g0013 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA19077 | hp1 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA19078 | hp1 | a0001 | c0001 | t0014 | g0216 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA19079 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA19079 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA19080 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA19082 | hp1 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA19082 | hp2 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA19083 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA19086 | hp1 | a0001 | c0001 | t0013 | g0159 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA19086 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA19087 | hp1 | a0001 | c0001 | t0023 | g0126 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA19088 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA19090 | hp2 | a0001 | c0001 | t0003 | g0121 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA19240 | hp1 | a0001 | c0001 | t0008 | g0286 | AFR | YRI | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | YRI | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA20129 | hp1 | a0001 | c0001 | t0008 | g0012 | AFR | ASW | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA20129 | hp2 | a0001 | c0001 | t0002 | g0219 | AFR | ASW | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0053 | EUR | TSI | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA20805 | hp1 | a0001 | c0001 | t0004 | g0152 | EUR | TSI | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0289 | EUR | TSI | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | GIH | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0288 | SAS | GIH | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0236 | AMR | CLM | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0237 | AMR | CLM | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG02109 | hp1 | a0001 | c0001 | t0012 | g0100 | AFR | ACB | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG02109 | hp2 | a0001 | c0001 | t0024 | g0074 | AFR | ACB | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | ACB | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG02486 | hp2 | a0001 | c0001 | t0007 | g0111 | AFR | ACB | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG02559 | hp1 | a0001 | c0001 | t0012 | g0014 | AFR | ACB | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG02559 | hp2 | a0001 | c0001 | t0008 | g0285 | AFR | ACB | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG03471 | hp1 | a0001 | c0001 | t0008 | g0012 | AFR | MSL | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG03471 | hp2 | a0001 | c0001 | t0003 | g0295 | AFR | MSL | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG06807 | hp1 | a0001 | c0001 | t0038 | g0058 | AFR | USA | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
HG06807 | hp2 | a0001 | c0001 | t0006 | g0094 | AFR | USA | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA18955 | hp1 | a0001 | c0001 | t0022 | g0030 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA18955 | hp2 | a0001 | c0001 | t0003 | g0124 | EAS | JPT | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA20300 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | USA | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | USA | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA21309 | hp1 | a0001 | c0001 | t0009 | g0222 | AFR | LWK | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0271 | AFR | LWK | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0021 | REF | REF | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0194 | REF | REF | FAM20B_chr1_179020894_179081567 | FAM20B | chr1 | 179020894 | 179081567 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:179044186
|
A | G | 1 | a0003 | 1 | HG03704.hp1 | missense_variant | MODERATE | c.339A>G | p.Ile113Met | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 2/8 | 677/5991 | 339/1230 | 113/409 | chr1 | 179044186 | ||
chr1:179072034
|
G | A | 1 | a0002 | 1 | HG02886.hp2 | missense_variant | MODERATE | c.1120G>A | p.Ala374Thr | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 8/8 | 1458/5991 | 1120/1230 | 374/409 | chr1 | 179072034 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:179044069
|
G | A | 1 | a0001c0002 | 2 | HG00735.hp2 HG01175.hp1 |
synonymous_variant | LOW | c.222G>A | p.Arg74Arg | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 2/8 | 560/5991 | 222/1230 | 74/409 | chr1 | 179044069 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:179025943
|
G | C | 2 | a0001c0001t0009a0001c0001t0016 | 7 | HG02572.hp2 HG02615.hp1 HG02647.hp1 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-289G>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/8 | 17905 | chr1 | 179025943 | |||||
chr1:179026015
|
C | T | 1 | a0001c0001t0038 | 1 | HG06807.hp1 | 5_prime_UTR_variant | MODIFIER | c.-217C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/8 | 17833 | chr1 | 179026015 | |||||
chr1:179026033
|
G | C | 1 | a0001c0001t0007 | 10 | HG01099.hp2 HG02145.hp1 HG02486.hp2 others(7): Show |
5_prime_UTR_variant | MODIFIER | c.-199G>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/8 | 17815 | chr1 | 179026033 | |||||
chr1:179043812
|
C | G | 9 | a0001c0001t0003a0001c0001t0015a0001c0001t0021others(6): Show | 78 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(75): Show |
5_prime_UTR_variant | MODIFIER | c.-36C>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 2/8 | 36 | chr1 | 179043812 | |||||
chr1:179072164
|
G | C | 1 | a0001c0001t0016 | 2 | HG02572.hp2 HG02647.hp1 |
3_prime_UTR_variant | MODIFIER | c.*20G>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 8/8 | 20 | chr1 | 179072164 | |||||
chr1:179072175
|
T | C | 1 | a0001c0001t0008 | 10 | HG01346.hp2 HG02055.hp1 HG02559.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*31T>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 8/8 | 31 | chr1 | 179072175 | |||||
chr1:179072256
|
G | A | 4 | a0001c0001t0006a0001c0001t0010a0001c0001t0038others(1): Show | 22 | HG00140.hp1 HG00639.hp1 HG00733.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*112G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 8/8 | 112 | chr1 | 179072256 | |||||
chr1:179072263
|
A | G | 30 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(27): Show | 276 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(273): Show |
3_prime_UTR_variant | MODIFIER | c.*119A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 8/8 | 119 | chr1 | 179072263 | |||||
chr1:179072517
|
C | T | 1 | a0001c0001t0014 | 3 | HG00544.hp2 NA18994.hp2 NA19078.hp1 |
3_prime_UTR_variant | MODIFIER | c.*373C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 8/8 | 373 | chr1 | 179072517 | |||||
chr1:179072557
|
CT | C | 26 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(23): Show | 269 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(266): Show |
3_prime_UTR_variant | MODIFIER | c.*425delT | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 8/8 | 425 | INFO_REALIGN_3_PRIME | chr1 | 179072557 | ||||
chr1:179072682
|
G | C | 1 | a0001c0001t0029 | 1 | HG03017.hp2 | 3_prime_UTR_variant | MODIFIER | c.*538G>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 8/8 | 538 | chr1 | 179072682 | |||||
chr1:179072719
|
T | C | 2 | a0001c0001t0009a0001c0001t0016 | 7 | HG02572.hp2 HG02615.hp1 HG02647.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*575T>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 8/8 | 575 | chr1 | 179072719 | |||||
chr1:179072798
|
C | T | 1 | a0001c0001t0023 | 2 | NA18974.hp2 NA19087.hp1 |
3_prime_UTR_variant | MODIFIER | c.*654C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 8/8 | 654 | chr1 | 179072798 | |||||
chr1:179072835
|
G | T | 8 | a0001c0001t0005a0001c0001t0007a0001c0001t0011others(5): Show | 38 | HG00544.hp1 HG00735.hp2 HG01069.hp2 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*691G>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 8/8 | 691 | chr1 | 179072835 | |||||
chr1:179072955
|
C | A | 1 | a0001c0001t0010 | 5 | HG00639.hp1 HG01070.hp1 HG01175.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*811C>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 8/8 | 811 | chr1 | 179072955 | |||||
chr1:179072957
|
A | G | 7 | a0001c0001t0003a0001c0001t0015a0001c0001t0022others(4): Show | 75 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*813A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 8/8 | 813 | chr1 | 179072957 | |||||
chr1:179073092
|
T | C | 22 | a0001c0001t0001a0001c0001t0003a0001c0001t0006others(19): Show | 235 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(232): Show |
3_prime_UTR_variant | MODIFIER | c.*948T>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 8/8 | 948 | chr1 | 179073092 | |||||
chr1:179073135
|
T | C | 7 | a0001c0001t0005a0001c0001t0007a0001c0001t0011others(4): Show | 36 | HG00544.hp1 HG01069.hp2 HG01074.hp1 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*991T>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 8/8 | 991 | chr1 | 179073135 | |||||
chr1:179073165
|
C | A | 11 | a0001c0001t0001a0001c0001t0006a0001c0001t0008others(8): Show | 150 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(147): Show |
3_prime_UTR_variant | MODIFIER | c.*1021C>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 8/8 | 1021 | chr1 | 179073165 | |||||
chr1:179073166
|
G | A | 1 | a0001c0001t0035 | 1 | HG02083.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1022G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 8/8 | 1022 | chr1 | 179073166 | |||||
chr1:179073181
|
C | T | 7 | a0001c0001t0003a0001c0001t0015a0001c0001t0022others(4): Show | 75 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*1037C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 8/8 | 1037 | chr1 | 179073181 | |||||
chr1:179073315
|
T | G | 14 | a0001c0001t0001a0001c0001t0006a0001c0001t0008others(11): Show | 159 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(156): Show |
3_prime_UTR_variant | MODIFIER | c.*1171T>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 8/8 | 1171 | chr1 | 179073315 | |||||
chr1:179073389
|
T | C | 35 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(32): Show | 308 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(305): Show |
3_prime_UTR_variant | MODIFIER | c.*1245T>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 8/8 | 1245 | chr1 | 179073389 | |||||
chr1:179073484
|
T | C | 1 | a0001c0001t0027 | 1 | HG02074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1340T>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 8/8 | 1340 | chr1 | 179073484 | |||||
chr1:179073613
|
G | A | 1 | a0001c0001t0030 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1469G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 8/8 | 1469 | chr1 | 179073613 | |||||
chr1:179073846
|
G | C | 7 | a0001c0001t0003a0001c0001t0015a0001c0001t0022others(4): Show | 75 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*1702G>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 8/8 | 1702 | chr1 | 179073846 | |||||
chr1:179073876
|
C | A | 2 | a0001c0001t0009a0001c0001t0016 | 7 | HG02572.hp2 HG02615.hp1 HG02647.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1732C>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 8/8 | 1732 | chr1 | 179073876 | |||||
chr1:179074404
|
T | G | 30 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(27): Show | 276 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(273): Show |
3_prime_UTR_variant | MODIFIER | c.*2260T>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 8/8 | 2260 | chr1 | 179074404 | |||||
chr1:179074418
|
G | A | 7 | a0001c0001t0003a0001c0001t0012a0001c0001t0015others(4): Show | 77 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*2274G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 8/8 | 2274 | chr1 | 179074418 | |||||
chr1:179074804
|
G | A | 8 | a0001c0001t0005a0001c0001t0007a0001c0001t0011others(5): Show | 38 | HG00544.hp1 HG00735.hp2 HG01069.hp2 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*2660G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 8/8 | 2660 | chr1 | 179074804 | |||||
chr1:179074907
|
G | A | 1 | a0001c0001t0015 | 3 | HG01891.hp1 HG03041.hp1 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2763G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 8/8 | 2763 | chr1 | 179074907 | |||||
chr1:179074913
|
G | A | 1 | a0001c0001t0019 | 2 | HG02451.hp2 HG02630.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2769G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 8/8 | 2769 | chr1 | 179074913 | |||||
chr1:179074980
|
A | T | 1 | a0001c0001t0031 | 1 | NA19001.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2836A>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 8/8 | 2836 | chr1 | 179074980 | |||||
chr1:179075065
|
G | C | 1 | a0001c0001t0024 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2921G>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 8/8 | 2921 | chr1 | 179075065 | |||||
chr1:179075167
|
G | A | 8 | a0001c0001t0003a0001c0001t0012a0001c0001t0015others(5): Show | 79 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*3023G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 8/8 | 3023 | chr1 | 179075167 | |||||
chr1:179075191
|
T | TA | 4 | a0001c0001t0005a0001c0001t0017a0001c0001t0036others(1): Show | 21 | HG00544.hp1 HG01074.hp1 HG02015.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*3060dupA | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 8/8 | 3061 | INFO_REALIGN_3_PRIME | chr1 | 179075191 | ||||
chr1:179075194
|
AAAAAAAA others(10): Show |
A | 1 | a0001c0001t0026 | 1 | HG02165.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3053_*3069delAAAA others(13): Show |
FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 8/8 | 3053 | INFO_REALIGN_3_PRIME | chr1 | 179075194 | ||||
chr1:179075246
|
T | G | 1 | a0001c0001t0022 | 2 | NA18955.hp1 NA19001.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3102T>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 8/8 | 3102 | chr1 | 179075246 | |||||
chr1:179075320
|
A | G | 1 | a0001c0001t0016 | 2 | HG02572.hp2 HG02647.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3176A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 8/8 | 3176 | chr1 | 179075320 | |||||
chr1:179075437
|
C | T | 1 | a0001c0001t0012 | 4 | HG01070.hp2 HG01071.hp2 HG02109.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3293C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 8/8 | 3293 | chr1 | 179075437 | |||||
chr1:179075588
|
A | G | 3 | a0001c0001t0004a0001c0001t0013a0001c0001t0026 | 30 | HG00140.hp2 HG00597.hp2 HG00738.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*3444A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 8/8 | 3444 | chr1 | 179075588 | |||||
chr1:179075839
|
G | T | 1 | a0001c0001t0028 | 1 | NA18993.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3695G>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 8/8 | 3695 | chr1 | 179075839 | |||||
chr1:179076338
|
G | A | 8 | a0001c0001t0003a0001c0001t0012a0001c0001t0015others(5): Show | 79 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*4194G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 8/8 | 4194 | chr1 | 179076338 | |||||
chr1:179076347
|
A | C | 1 | a0001c0001t0032 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4203A>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 8/8 | 4203 | chr1 | 179076347 | |||||
chr1:179076358
|
A | C | 1 | a0001c0001t0012 | 4 | HG01070.hp2 HG01071.hp2 HG02109.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4214A>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 8/8 | 4214 | chr1 | 179076358 | |||||
chr1:179076365
|
C | A | 30 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(27): Show | 274 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(271): Show |
3_prime_UTR_variant | MODIFIER | c.*4221C>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 8/8 | 4221 | chr1 | 179076365 | |||||
chr1:179076477
|
A | G | 1 | a0001c0001t0013 | 3 | NA18964.hp2 NA18998.hp1 NA19086.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4333A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 8/8 | 4333 | chr1 | 179076477 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:179026148
|
G | A | 10 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0050others(7): Show | 12 | HG00280.hp1 HG00621.hp2 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.-134+50G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179026148 | ||||||
chr1:179026167
|
A | G | 1 | a0001c0001t0003g0295 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-134+69A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179026167 | ||||||
chr1:179026365
|
G | T | 98 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(95): Show | 134 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.-134+267G>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179026365 | ||||||
chr1:179026386
|
G | C | 211 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(208): Show | 275 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.-134+288G>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179026386 | ||||||
chr1:179026390
|
C | T | 1 | a0001c0001t0007g0151 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-134+292C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179026390 | ||||||
chr1:179026601
|
A | T | 2 | a0001c0001t0017g0293a0001c0001t0017g0294 | 2 | HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-134+503A>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179026601 | ||||||
chr1:179026746
|
G | T | 5 | a0001c0001t0003g0031a0001c0001t0003g0147a0001c0001t0003g0148others(2): Show | 6 | NA18953.hp2 NA18959.hp1 NA18973.hp2 others(3): Show |
intron_variant | MODIFIER | c.-134+648G>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179026746 | ||||||
chr1:179026753
|
C | T | 1 | a0001c0001t0003g0295 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-134+655C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179026753 | ||||||
chr1:179026781
|
C | T | 1 | a0001c0001t0009g0292 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-134+683C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179026781 | ||||||
chr1:179026821
|
G | A | 1 | a0001c0001t0038g0058 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-134+723G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179026821 | ||||||
chr1:179026901
|
G | A | 2 | a0001c0001t0009g0222a0001c0001t0009g0223 | 2 | HG03579.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-134+803G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179026901 | ||||||
chr1:179026948
|
T | C | 2 | a0001c0001t0008g0224a0001c0001t0008g0225 | 2 | HG01346.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.-134+850T>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179026948 | ||||||
chr1:179026954
|
T | G | 2 | a0001c0001t0008g0224a0001c0001t0008g0225 | 2 | HG01346.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.-134+856T>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179026954 | ||||||
chr1:179027209
|
T | G | 237 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(234): Show | 309 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(306): Show |
intron_variant | MODIFIER | c.-134+1111T>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179027209 | ||||||
chr1:179027278
|
A | G | 92 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(89): Show | 127 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.-134+1180A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179027278 | ||||||
chr1:179027526
|
G | A | 1 | a0001c0001t0001g0050 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-134+1428G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179027526 | ||||||
chr1:179027658
|
G | A | 16 | a0001c0001t0005g0013a0001c0001t0005g0059a0001c0001t0005g0060others(13): Show | 18 | HG00544.hp1 HG01074.hp1 HG02015.hp1 others(15): Show |
intron_variant | MODIFIER | c.-134+1560G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179027658 | ||||||
chr1:179027746
|
A | G | 49 | a0001c0001t0001g0132a0001c0001t0003g0004a0001c0001t0003g0005others(46): Show | 68 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.-134+1648A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179027746 | ||||||
chr1:179027763
|
G | C | 1 | a0001c0001t0024g0074 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-134+1665G>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179027763 | ||||||
chr1:179027938
|
T | C | 8 | a0001c0001t0001g0010a0001c0001t0001g0228a0001c0001t0001g0229others(5): Show | 11 | HG00099.hp2 HG00609.hp2 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.-134+1840T>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179027938 | ||||||
chr1:179027958
|
C | A | 4 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0235others(1): Show | 5 | HG01109.hp1 HG02055.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.-134+1860C>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179027958 | ||||||
chr1:179028024
|
C | T | 98 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(95): Show | 134 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.-134+1926C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179028024 | ||||||
chr1:179028040
|
A | G | 1 | a0001c0001t0018g0027 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-134+1942A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179028040 | ||||||
chr1:179028105
|
G | T | 4 | a0001c0001t0002g0017a0001c0001t0002g0220a0001c0001t0002g0221others(1): Show | 5 | HG00621.hp1 NA18942.hp2 NA18967.hp2 others(2): Show |
intron_variant | MODIFIER | c.-134+2007G>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179028105 | ||||||
chr1:179028109
|
A | G | 1 | a0001c0001t0003g0146 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-134+2011A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179028109 | ||||||
chr1:179028114
|
T | C | 2 | a0001c0001t0019g0075a0001c0001t0019g0076 | 2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.-134+2016T>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179028114 | ||||||
chr1:179028179
|
G | A | 2 | a0001c0001t0001g0236a0001c0001t0001g0237 | 2 | HG01123.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.-134+2081G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179028179 | ||||||
chr1:179028420
|
A | G | 1 | a0001c0001t0001g0057 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-134+2322A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179028420 | ||||||
chr1:179028454
|
C | T | 2 | a0001c0001t0017g0293a0001c0001t0017g0294 | 2 | HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-134+2356C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179028454 | ||||||
chr1:179028477
|
G | C | 4 | a0001c0001t0003g0024a0001c0001t0003g0077a0001c0001t0003g0078others(1): Show | 5 | HG01243.hp1 HG02258.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.-134+2379G>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179028477 | ||||||
chr1:179028549
|
T | G | 1 | a0001c0001t0018g0027 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-134+2451T>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179028549 | ||||||
chr1:179028581
|
AAAAC | A | 4 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0235others(1): Show | 5 | HG01109.hp1 HG02055.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.-134+2498_-134+250 others(8): Show |
FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 179028581 | |||||
chr1:179028648
|
C | T | 33 | a0001c0001t0005g0013a0001c0001t0005g0059a0001c0001t0005g0060others(30): Show | 37 | HG00544.hp1 HG00735.hp2 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.-134+2550C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179028648 | ||||||
chr1:179028664
|
G | T | 2 | a0001c0001t0003g0149a0001c0001t0003g0150 | 2 | NA18985.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.-134+2566G>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179028664 | ||||||
chr1:179028901
|
A | G | 1 | a0001c0001t0015g0102 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-134+2803A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179028901 | ||||||
chr1:179028912
|
G | A | 1 | a0001c0001t0018g0027 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-134+2814G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179028912 | ||||||
chr1:179028927
|
C | T | 1 | a0001c0001t0007g0113 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-134+2829C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179028927 | ||||||
chr1:179029005
|
C | T | 1 | a0001c0001t0004g0169 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-134+2907C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179029005 | ||||||
chr1:179029014
|
G | A | 1 | a0001c0001t0004g0152 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-134+2916G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179029014 | ||||||
chr1:179029103
|
C | T | 1 | a0001c0001t0003g0145 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.-134+3005C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179029103 | ||||||
chr1:179029246
|
C | G | 1 | a0001c0001t0003g0168 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-134+3148C>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179029246 | ||||||
chr1:179029281
|
A | C | 1 | a0001c0001t0002g0219 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-134+3183A>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179029281 | ||||||
chr1:179029695
|
G | A | 1 | a0001c0001t0001g0236 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-134+3597G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179029695 | ||||||
chr1:179029969
|
A | C | 1 | a0001c0001t0032g0101 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-134+3871A>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179029969 | ||||||
chr1:179030154
|
C | A | 2 | a0001c0001t0017g0293a0001c0001t0017g0294 | 2 | HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-134+4056C>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179030154 | ||||||
chr1:179030339
|
G | T | 2 | a0001c0001t0001g0233a0001c0001t0001g0234 | 2 | HG02280.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.-134+4241G>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179030339 | ||||||
chr1:179030345
|
G | T | 1 | a0001c0001t0001g0291 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-134+4247G>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179030345 | ||||||
chr1:179030822
|
G | A | 4 | a0001c0001t0011g0015a0001c0001t0011g0103a0001c0001t0011g0104others(1): Show | 5 | HG01069.hp2 HG01891.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.-134+4724G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179030822 | ||||||
chr1:179030878
|
C | CA | 6 | a0001c0001t0001g0238a0001c0001t0001g0239a0001c0001t0001g0240others(3): Show | 6 | HG01257.hp1 HG01257.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-134+4795dupA | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 179030878 | |||||
chr1:179030878
|
CA | C | 6 | a0001c0001t0009g0044a0001c0001t0009g0222a0001c0001t0009g0223others(3): Show | 7 | HG02572.hp2 HG02615.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.-134+4795delA | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 179030878 | |||||
chr1:179030922
|
A | G | 9 | a0001c0001t0007g0026a0001c0001t0007g0107a0001c0001t0007g0108others(6): Show | 10 | HG01099.hp2 HG02145.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.-134+4824A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179030922 | ||||||
chr1:179031008
|
G | A | 235 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(232): Show | 307 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(304): Show |
intron_variant | MODIFIER | c.-134+4910G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179031008 | ||||||
chr1:179031309
|
A | G | 60 | a0001c0001t0003g0024a0001c0001t0003g0077a0001c0001t0003g0078others(57): Show | 68 | HG00140.hp1 HG00544.hp1 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.-134+5211A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179031309 | ||||||
chr1:179031340
|
G | A | 38 | a0001c0001t0001g0132a0001c0001t0003g0005a0001c0001t0003g0008others(35): Show | 49 | HG00423.hp1 HG00438.hp2 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.-134+5242G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179031340 | ||||||
chr1:179031563
|
G | A | 1 | a0001c0001t0002g0172 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-134+5465G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179031563 | ||||||
chr1:179031590
|
A | C | 58 | a0001c0001t0001g0132a0001c0001t0003g0004a0001c0001t0003g0005others(55): Show | 79 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.-134+5492A>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179031590 | ||||||
chr1:179031698
|
G | C | 1 | a0001c0001t0032g0101 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-134+5600G>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179031698 | ||||||
chr1:179031764
|
T | C | 1 | a0001c0001t0032g0101 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-134+5666T>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179031764 | ||||||
chr1:179031768
|
GCTTAT | G | 20 | a0001c0001t0006g0083a0001c0001t0006g0084a0001c0001t0006g0085others(17): Show | 21 | HG00140.hp1 HG00639.hp1 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.-134+5675_-134+567 others(9): Show |
FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 179031768 | |||||
chr1:179032179
|
A | G | 1 | a0001c0001t0032g0101 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-134+6081A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179032179 | ||||||
chr1:179032305
|
G | A | 112 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(109): Show | 148 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.-134+6207G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179032305 | ||||||
chr1:179032313
|
C | CT | 13 | a0001c0001t0002g0210a0001c0001t0002g0211a0001c0001t0002g0212others(10): Show | 15 | HG00639.hp2 HG00673.hp2 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.-134+6241dupT | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 179032313 | |||||
chr1:179032313
|
C | CTTT | 14 | a0001c0001t0005g0013a0001c0001t0005g0061a0001c0001t0005g0062others(11): Show | 16 | HG00544.hp1 HG01074.hp1 HG02015.hp1 others(13): Show |
intron_variant | MODIFIER | c.-134+6239_-134+624 others(7): Show |
FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 179032313 | |||||
chr1:179032313
|
CT | C | 71 | a0001c0001t0002g0037a0001c0001t0002g0173a0001c0001t0002g0174others(68): Show | 98 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.-134+6241delT | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 179032313 | |||||
chr1:179032313
|
CTT | C | 13 | a0001c0001t0003g0114a0001c0001t0003g0115a0001c0001t0003g0116others(10): Show | 15 | HG00140.hp2 HG01099.hp2 HG01256.hp2 others(12): Show |
intron_variant | MODIFIER | c.-134+6240_-134+624 others(6): Show |
FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 179032313 | |||||
chr1:179032313
|
CTTTTTTT | C | 89 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(86): Show | 124 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.-134+6235_-134+624 others(11): Show |
FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 179032313 | |||||
chr1:179032313
|
CTTTTTTT others(1): Show |
C | 23 | a0001c0001t0001g0022a0001c0001t0001g0241a0001c0001t0001g0242others(20): Show | 25 | HG00140.hp1 HG00639.hp1 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.-134+6234_-134+624 others(12): Show |
FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 179032313 | |||||
chr1:179032313
|
CTTTTTTT others(7): Show |
C | 4 | a0001c0001t0011g0015a0001c0001t0011g0103a0001c0001t0011g0104others(1): Show | 5 | HG01069.hp2 HG01891.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.-134+6228_-134+624 others(18): Show |
FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 179032313 | |||||
chr1:179032404
|
C | T | 1 | a0001c0001t0002g0209 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-134+6306C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179032404 | ||||||
chr1:179032441
|
A | G | 1 | a0001c0001t0003g0078 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-134+6343A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179032441 | ||||||
chr1:179032453
|
T | TAGGTAAT others(4498): Show |
1 | a0001c0001t0001g0291 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-134+6371_-134+637 others(4509): Show |
FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 179032453 | |||||
chr1:179032462
|
G | A | 2 | a0001c0001t0019g0075a0001c0001t0019g0076 | 2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.-134+6364G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179032462 | ||||||
chr1:179032506
|
G | T | 8 | a0001c0001t0006g0093a0001c0001t0006g0094a0001c0001t0006g0095others(5): Show | 9 | HG00140.hp1 HG00639.hp1 HG00733.hp2 others(6): Show |
intron_variant | MODIFIER | c.-134+6408G>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179032506 | ||||||
chr1:179032673
|
T | C | 4 | a0001c0001t0003g0024a0001c0001t0003g0077a0001c0001t0003g0078others(1): Show | 5 | HG01243.hp1 HG02258.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.-134+6575T>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179032673 | ||||||
chr1:179032687
|
A | G | 2 | a0001c0001t0012g0014a0001c0001t0012g0100 | 4 | HG01070.hp2 HG01071.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.-134+6589A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179032687 | ||||||
chr1:179032756
|
C | T | 6 | a0001c0001t0008g0012a0001c0001t0008g0224a0001c0001t0008g0225others(3): Show | 9 | HG01346.hp2 HG02055.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.-134+6658C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179032756 | ||||||
chr1:179032998
|
C | T | 1 | a0001c0001t0024g0074 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-134+6900C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179032998 | ||||||
chr1:179033081
|
C | T | 16 | a0001c0001t0005g0013a0001c0001t0005g0059a0001c0001t0005g0060others(13): Show | 18 | HG00544.hp1 HG01074.hp1 HG02015.hp1 others(15): Show |
intron_variant | MODIFIER | c.-134+6983C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179033081 | ||||||
chr1:179033192
|
G | A | 1 | a0001c0001t0003g0133 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.-134+7094G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179033192 | ||||||
chr1:179033264
|
G | A | 1 | a0001c0001t0001g0288 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-134+7166G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179033264 | ||||||
chr1:179033335
|
T | C | 1 | a0001c0001t0002g0173 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-134+7237T>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179033335 | ||||||
chr1:179033540
|
G | A | 1 | a0001c0001t0008g0285 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-134+7442G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179033540 | ||||||
chr1:179033728
|
C | T | 4 | a0001c0001t0011g0015a0001c0001t0011g0103a0001c0001t0011g0104others(1): Show | 5 | HG01069.hp2 HG01891.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.-134+7630C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179033728 | ||||||
chr1:179033834
|
A | C | 124 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(121): Show | 168 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.-134+7736A>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179033834 | ||||||
chr1:179034006
|
A | G | 1 | a0001c0001t0002g0208 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-134+7908A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179034006 | ||||||
chr1:179034113
|
A | G | 2 | a0001c0001t0024g0074a0001c0001t0032g0101 | 2 | HG02109.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-134+8015A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179034113 | ||||||
chr1:179034355
|
C | T | 236 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(233): Show | 308 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(305): Show |
intron_variant | MODIFIER | c.-134+8257C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179034355 | ||||||
chr1:179034384
|
T | TTC | 5 | a0001c0001t0001g0243a0001c0001t0001g0244a0001c0001t0001g0245others(2): Show | 5 | HG00735.hp2 HG01175.hp1 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.-134+8304_-134+830 others(6): Show |
FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 179034384 | |||||
chr1:179034462
|
T | C | 1 | a0001c0001t0001g0050 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-134+8364T>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179034462 | ||||||
chr1:179034534
|
C | T | 1 | a0001c0001t0001g0284 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-134+8436C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179034534 | ||||||
chr1:179034573
|
G | T | 1 | a0001c0001t0002g0218 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-134+8475G>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179034573 | ||||||
chr1:179034631
|
A | T | 1 | a0001c0001t0003g0170 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-134+8533A>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179034631 | ||||||
chr1:179035035
|
G | C | 1 | a0001c0001t0001g0246 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-133-8680G>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179035035 | ||||||
chr1:179035047
|
G | C | 20 | a0001c0001t0006g0083a0001c0001t0006g0084a0001c0001t0006g0085others(17): Show | 21 | HG00140.hp1 HG00639.hp1 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.-133-8668G>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179035047 | ||||||
chr1:179035222
|
T | C | 2 | a0001c0001t0019g0075a0001c0001t0019g0076 | 2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.-133-8493T>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179035222 | ||||||
chr1:179035341
|
C | T | 2 | a0001c0001t0017g0293a0001c0001t0017g0294 | 2 | HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-133-8374C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179035341 | ||||||
chr1:179035356
|
C | T | 1 | a0001c0001t0006g0099 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-133-8359C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179035356 | ||||||
chr1:179035441
|
G | T | 4 | a0001c0001t0003g0024a0001c0001t0003g0077a0001c0001t0003g0078others(1): Show | 5 | HG01243.hp1 HG02258.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.-133-8274G>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179035441 | ||||||
chr1:179035467
|
A | G | 24 | a0001c0001t0003g0024a0001c0001t0003g0077a0001c0001t0003g0078others(21): Show | 26 | HG00140.hp1 HG00639.hp1 HG00733.hp2 others(23): Show |
intron_variant | MODIFIER | c.-133-8248A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179035467 | ||||||
chr1:179035500
|
C | A | 1 | a0001c0001t0017g0293 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-133-8215C>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179035500 | ||||||
chr1:179035523
|
A | G | 95 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(92): Show | 130 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.-133-8192A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179035523 | ||||||
chr1:179035630
|
T | C | 1 | a0001c0001t0021g0117 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-133-8085T>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179035630 | ||||||
chr1:179035643
|
T | A | 16 | a0001c0001t0005g0013a0001c0001t0005g0059a0001c0001t0005g0060others(13): Show | 18 | HG00544.hp1 HG01074.hp1 HG02015.hp1 others(15): Show |
intron_variant | MODIFIER | c.-133-8072T>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179035643 | ||||||
chr1:179035668
|
C | T | 1 | a0001c0002t0020g0106 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-133-8047C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179035668 | ||||||
chr1:179035810
|
T | TTG | 6 | a0001c0001t0015g0081a0001c0001t0015g0082a0001c0001t0015g0102others(3): Show | 6 | HG01891.hp1 HG02451.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-133-7889_-133-788 others(6): Show |
FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 179035810 | |||||
chr1:179035856
|
G | A | 2 | a0001c0002t0020g0105a0001c0002t0020g0106 | 2 | HG00735.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.-133-7859G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179035856 | ||||||
chr1:179035946
|
G | A | 93 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(90): Show | 128 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.-133-7769G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179035946 | ||||||
chr1:179035989
|
G | C | 1 | a0001c0001t0001g0051 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.-133-7726G>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179035989 | ||||||
chr1:179036163
|
C | G | 1 | a0001c0001t0025g0207 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-133-7552C>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179036163 | ||||||
chr1:179036413
|
A | T | 1 | a0001c0001t0001g0232 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-133-7302A>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179036413 | ||||||
chr1:179036484
|
A | G | 2 | a0001c0001t0017g0293a0001c0001t0017g0294 | 2 | HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-133-7231A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179036484 | ||||||
chr1:179036783
|
C | T | 2 | a0001c0001t0012g0014a0001c0001t0012g0100 | 4 | HG01070.hp2 HG01071.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.-133-6932C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179036783 | ||||||
chr1:179036835
|
A | G | 235 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(232): Show | 307 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(304): Show |
intron_variant | MODIFIER | c.-133-6880A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179036835 | ||||||
chr1:179036878
|
G | A | 1 | a0001c0001t0025g0207 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-133-6837G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179036878 | ||||||
chr1:179036971
|
A | G | 2 | a0001c0001t0007g0112a0001c0001t0007g0151 | 2 | HG02922.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-133-6744A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179036971 | ||||||
chr1:179036994
|
C | G | 1 | a0001c0001t0001g0283 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.-133-6721C>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179036994 | ||||||
chr1:179037248
|
G | T | 6 | a0001c0001t0009g0044a0001c0001t0009g0222a0001c0001t0009g0223others(3): Show | 7 | HG02572.hp2 HG02615.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.-133-6467G>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179037248 | ||||||
chr1:179037268
|
C | T | 1 | a0001c0001t0029g0282 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-133-6447C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179037268 | ||||||
chr1:179037327
|
G | A | 209 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(206): Show | 273 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.-133-6388G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179037327 | ||||||
chr1:179037358
|
C | CT | 206 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(203): Show | 268 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.-133-6348dupT | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 179037358 | |||||
chr1:179037475
|
C | T | 1 | a0001c0001t0001g0281 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-133-6240C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179037475 | ||||||
chr1:179037479
|
C | CT | 58 | a0001c0001t0002g0177a0001c0001t0002g0203a0001c0001t0002g0204others(55): Show | 78 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.-133-6215dupT | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 179037479 | |||||
chr1:179037479
|
C | CTT | 46 | a0001c0001t0001g0228a0001c0001t0001g0235a0001c0001t0001g0241others(43): Show | 56 | HG00544.hp1 HG00597.hp2 HG00733.hp1 others(53): Show |
intron_variant | MODIFIER | c.-133-6216_-133-621 others(6): Show |
FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 179037479 | |||||
chr1:179037479
|
C | CTTT | 77 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(74): Show | 109 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.-133-6217_-133-621 others(7): Show |
FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 179037479 | |||||
chr1:179037479
|
C | CTTTT | 44 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0046others(41): Show | 50 | HG00140.hp1 HG00673.hp1 HG00738.hp1 others(47): Show |
intron_variant | MODIFIER | c.-133-6218_-133-621 others(8): Show |
FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 179037479 | |||||
chr1:179037479
|
C | CTTTTT | 8 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0006g0089others(5): Show | 9 | HG00639.hp1 HG00733.hp2 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.-133-6219_-133-621 others(9): Show |
FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 179037479 | |||||
chr1:179037766
|
C | T | 1 | a0001c0001t0018g0027 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-133-5949C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179037766 | ||||||
chr1:179038068
|
GA | G | 2 | a0001c0001t0012g0014a0001c0001t0012g0100 | 4 | HG01070.hp2 HG01071.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.-133-5646delA | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179038068 | ||||||
chr1:179038142
|
C | T | 120 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(117): Show | 157 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.-133-5573C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179038142 | ||||||
chr1:179038317
|
A | C | 1 | a0001c0001t0003g0140 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-133-5398A>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179038317 | ||||||
chr1:179038326
|
G | A | 1 | a0001c0001t0032g0101 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-133-5389G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179038326 | ||||||
chr1:179038357
|
G | A | 1 | a0001c0001t0024g0074 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-133-5358G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179038357 | ||||||
chr1:179038411
|
C | CA | 181 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(178): Show | 243 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(240): Show |
intron_variant | MODIFIER | c.-133-5289dupA | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 179038411 | |||||
chr1:179038411
|
C | CAA | 25 | a0001c0001t0001g0268a0001c0001t0001g0279a0001c0001t0003g0114others(22): Show | 26 | HG00140.hp1 HG00639.hp1 HG00733.hp2 others(23): Show |
intron_variant | MODIFIER | c.-133-5290_-133-528 others(6): Show |
FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 179038411 | |||||
chr1:179038441
|
G | A | 6 | a0001c0001t0009g0044a0001c0001t0009g0222a0001c0001t0009g0223others(3): Show | 7 | HG02572.hp2 HG02615.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.-133-5274G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179038441 | ||||||
chr1:179038705
|
C | T | 48 | a0001c0001t0003g0004a0001c0001t0003g0005a0001c0001t0003g0008others(45): Show | 67 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.-133-5010C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179038705 | ||||||
chr1:179038725
|
A | T | 3 | a0001c0001t0012g0014a0001c0001t0012g0100a0001c0001t0032g0101 | 5 | HG01070.hp2 HG01071.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.-133-4990A>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179038725 | ||||||
chr1:179038808
|
G | A | 1 | a0001c0001t0005g0061 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-133-4907G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179038808 | ||||||
chr1:179038965
|
A | AT | 4 | a0001c0001t0003g0024a0001c0001t0003g0077a0001c0001t0003g0078others(1): Show | 5 | HG01243.hp1 HG02258.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.-133-4750_-133-474 others(5): Show |
FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179038965 | ||||||
chr1:179039143
|
G | A | 2 | a0001c0001t0002g0179a0001c0001t0002g0208 | 2 | HG04228.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.-133-4572G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179039143 | ||||||
chr1:179039190
|
T | G | 2 | a0001c0002t0020g0105a0001c0002t0020g0106 | 2 | HG00735.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.-133-4525T>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179039190 | ||||||
chr1:179039382
|
G | A | 48 | a0001c0001t0003g0004a0001c0001t0003g0005a0001c0001t0003g0008others(45): Show | 67 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.-133-4333G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179039382 | ||||||
chr1:179039568
|
G | A | 1 | a0001c0001t0002g0220 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-133-4147G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179039568 | ||||||
chr1:179039612
|
A | C | 2 | a0001c0001t0012g0014a0001c0001t0012g0100 | 4 | HG01070.hp2 HG01071.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.-133-4103A>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179039612 | ||||||
chr1:179039644
|
G | C | 1 | a0001c0001t0038g0058 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-133-4071G>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179039644 | ||||||
chr1:179039739
|
A | T | 3 | a0001c0001t0006g0083a0001c0001t0006g0089a0001c0001t0006g0090 | 3 | HG02257.hp2 HG02897.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-133-3976A>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179039739 | ||||||
chr1:179039741
|
TA | T | 89 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(86): Show | 122 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.-133-3973delA | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179039741 | ||||||
chr1:179039742
|
A | T | 28 | a0001c0001t0001g0264a0001c0001t0001g0265a0001c0001t0001g0266others(25): Show | 30 | HG00140.hp1 HG00597.hp1 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.-133-3973A>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179039742 | ||||||
chr1:179039743
|
T | A | 6 | a0001c0001t0006g0093a0001c0001t0009g0044a0001c0001t0009g0222others(3): Show | 7 | HG00140.hp1 HG02615.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.-133-3972T>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179039743 | ||||||
chr1:179039744
|
T | A | 3 | a0001c0001t0001g0229a0001c0001t0001g0241a0001c0001t0001g0248 | 3 | HG00099.hp2 NA18959.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.-133-3971T>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179039744 | ||||||
chr1:179039775
|
T | C | 37 | a0001c0001t0003g0024a0001c0001t0003g0077a0001c0001t0003g0078others(34): Show | 42 | HG00544.hp1 HG00735.hp2 HG01069.hp2 others(39): Show |
intron_variant | MODIFIER | c.-133-3940T>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179039775 | ||||||
chr1:179039800
|
T | C | 131 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(128): Show | 171 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.-133-3915T>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179039800 | ||||||
chr1:179039886
|
G | A | 4 | a0001c0001t0003g0024a0001c0001t0003g0077a0001c0001t0003g0078others(1): Show | 5 | HG01243.hp1 HG02258.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.-133-3829G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179039886 | ||||||
chr1:179039895
|
G | T | 2 | a0001c0001t0012g0014a0001c0001t0012g0100 | 4 | HG01070.hp2 HG01071.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.-133-3820G>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179039895 | ||||||
chr1:179039957
|
A | G | 5 | a0001c0001t0007g0026a0001c0001t0007g0109a0001c0001t0007g0110others(2): Show | 6 | HG01099.hp2 HG02145.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-133-3758A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179039957 | ||||||
chr1:179039986
|
C | T | 1 | a0001c0001t0007g0108 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-133-3729C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179039986 | ||||||
chr1:179040105
|
A | G | 2 | a0001c0002t0020g0105a0001c0002t0020g0106 | 2 | HG00735.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.-133-3610A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179040105 | ||||||
chr1:179040146
|
A | C | 1 | a0001c0001t0004g0163 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-133-3569A>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179040146 | ||||||
chr1:179040208
|
C | T | 1 | a0001c0001t0032g0101 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-133-3507C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179040208 | ||||||
chr1:179040227
|
C | T | 1 | a0001c0001t0004g0166 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-133-3488C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179040227 | ||||||
chr1:179040263
|
G | A | 1 | a0001c0001t0032g0101 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-133-3452G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179040263 | ||||||
chr1:179040384
|
G | A | 1 | a0001c0001t0006g0094 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-133-3331G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179040384 | ||||||
chr1:179040438
|
G | C | 1 | a0001c0001t0001g0249 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-133-3277G>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179040438 | ||||||
chr1:179040493
|
CCCCCCCA others(211): Show |
C | 32 | a0001c0001t0005g0013a0001c0001t0005g0059a0001c0001t0005g0060others(29): Show | 36 | HG00544.hp1 HG00735.hp2 HG01069.hp2 others(33): Show |
intron_variant | MODIFIER | c.-133-3187_-133-297 others(4): Show |
FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 179040493 | |||||
chr1:179040494
|
CCCCCCAC others(210): Show |
C | 1 | a0001c0001t0005g0068 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-133-3215_-133-299 others(4): Show |
FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 179040494 | |||||
chr1:179040510
|
C | T | 54 | a0001c0001t0003g0004a0001c0001t0003g0005a0001c0001t0003g0008others(51): Show | 75 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.-133-3205C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179040510 | ||||||
chr1:179040511
|
G | A | 26 | a0001c0001t0004g0006a0001c0001t0004g0032a0001c0001t0004g0033others(23): Show | 35 | HG00140.hp2 HG00597.hp2 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.-133-3204G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179040511 | ||||||
chr1:179040520
|
GGCTGGCC others(42): Show |
G | 23 | a0001c0001t0004g0006a0001c0001t0004g0032a0001c0001t0004g0033others(20): Show | 30 | HG00140.hp2 HG00597.hp2 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.-133-3183_-133-313 others(53): Show |
FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 179040520 | |||||
chr1:179040531
|
C | T | 54 | a0001c0001t0003g0004a0001c0001t0003g0005a0001c0001t0003g0008others(51): Show | 75 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.-133-3184C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179040531 | ||||||
chr1:179040572
|
TGGCCGGG others(30): Show |
T | 4 | a0001c0001t0001g0010a0001c0001t0001g0228a0001c0001t0001g0229others(1): Show | 7 | HG00099.hp2 HG00609.hp2 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.-133-3129_-133-309 others(41): Show |
FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 179040572 | |||||
chr1:179040654
|
C | T | 1 | a0001c0001t0003g0116 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-133-3061C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179040654 | ||||||
chr1:179040664
|
TCCCCCCA others(40): Show |
T | 7 | a0001c0001t0001g0018a0001c0001t0001g0021a0001c0001t0001g0246others(4): Show | 11 | HG01081.hp2 HG01167.hp2 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.-133-2998_-133-295 others(51): Show |
FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 179040664 | |||||
chr1:179040665
|
C | CCCCCCAC others(39): Show |
1 | a0001c0001t0002g0174 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-133-3044_-133-299 others(50): Show |
FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 179040665 | |||||
chr1:179040679
|
C | T | 1 | a0001c0001t0018g0027 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-133-3036C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179040679 | ||||||
chr1:179040690
|
C | T | 32 | a0001c0001t0003g0005a0001c0001t0003g0008a0001c0001t0003g0016others(29): Show | 44 | HG00423.hp1 HG00438.hp2 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.-133-3025C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179040690 | ||||||
chr1:179040691
|
G | A | 1 | a0001c0001t0002g0038 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.-133-3024G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179040691 | ||||||
chr1:179040703
|
G | A | 2 | a0001c0001t0003g0149a0001c0001t0006g0084 | 2 | HG03195.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.-133-3012G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179040703 | ||||||
chr1:179040740
|
C | T | 1 | a0001c0001t0025g0207 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-133-2975C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179040740 | ||||||
chr1:179040779
|
G | A | 1 | a0001c0001t0004g0152 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-133-2936G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179040779 | ||||||
chr1:179040948
|
G | A | 18 | a0001c0001t0001g0018a0001c0001t0001g0021a0001c0001t0001g0045others(15): Show | 26 | HG01081.hp2 HG01109.hp1 HG01167.hp2 others(23): Show |
intron_variant | MODIFIER | c.-133-2767G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179040948 | ||||||
chr1:179040964
|
C | T | 119 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(116): Show | 156 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.-133-2751C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179040964 | ||||||
chr1:179040981
|
C | A | 1 | a0001c0001t0006g0086 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-133-2734C>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179040981 | ||||||
chr1:179040981
|
C | G | 154 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(151): Show | 197 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.-133-2734C>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179040981 | ||||||
chr1:179040984
|
C | G | 209 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(206): Show | 273 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.-133-2731C>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179040984 | ||||||
chr1:179041020
|
A | G | 209 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(206): Show | 273 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.-133-2695A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179041020 | ||||||
chr1:179041089
|
TGATGGGA others(33): Show |
T | 34 | a0001c0001t0005g0013a0001c0001t0005g0059a0001c0001t0005g0060others(31): Show | 38 | HG00544.hp1 HG00735.hp2 HG01069.hp2 others(35): Show |
intron_variant | MODIFIER | c.-133-2607_-133-256 others(44): Show |
FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 179041089 | |||||
chr1:179041104
|
C | T | 2 | a0001c0001t0012g0014a0001c0001t0012g0100 | 4 | HG01070.hp2 HG01071.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.-133-2611C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179041104 | ||||||
chr1:179041115
|
G | A | 3 | a0001c0001t0015g0081a0001c0001t0015g0082a0001c0001t0015g0102 | 3 | HG01891.hp1 HG03041.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-133-2600G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179041115 | ||||||
chr1:179041144
|
C | T | 1 | a0001c0001t0001g0263 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-133-2571C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179041144 | ||||||
chr1:179041191
|
G | T | 1 | a0001c0001t0032g0101 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-133-2524G>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179041191 | ||||||
chr1:179041218
|
A | G | 1 | a0001c0001t0003g0138 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-133-2497A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179041218 | ||||||
chr1:179041233
|
T | G | 1 | a0001c0001t0018g0027 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-133-2482T>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179041233 | ||||||
chr1:179041248
|
C | CG | 9 | a0001c0001t0001g0132a0001c0001t0001g0252a0001c0001t0002g0180others(6): Show | 9 | HG01099.hp2 HG01261.hp1 HG02080.hp2 others(6): Show |
intron_variant | MODIFIER | c.-133-2463dupG | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 179041248 | |||||
chr1:179041317
|
G | A | 1 | a0001c0001t0024g0074 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-133-2398G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179041317 | ||||||
chr1:179041384
|
G | A | 2 | a0001c0001t0002g0039a0001c0001t0002g0218 | 3 | HG00673.hp2 NA18747.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.-133-2331G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179041384 | ||||||
chr1:179041391
|
C | T | 1 | a0001c0001t0004g0162 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-133-2324C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179041391 | ||||||
chr1:179041392
|
G | A | 9 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0180others(6): Show | 11 | HG01106.hp2 HG01255.hp1 HG01928.hp2 others(8): Show |
intron_variant | MODIFIER | c.-133-2323G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179041392 | ||||||
chr1:179041409
|
G | C | 208 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(205): Show | 270 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.-133-2306G>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179041409 | ||||||
chr1:179041472
|
G | A | 235 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(232): Show | 307 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(304): Show |
intron_variant | MODIFIER | c.-133-2243G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179041472 | ||||||
chr1:179041590
|
C | T | 1 | a0001c0001t0006g0099 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-133-2125C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179041590 | ||||||
chr1:179041601
|
C | CAGAGGGA others(69): Show |
20 | a0001c0001t0006g0083a0001c0001t0006g0084a0001c0001t0006g0085others(17): Show | 21 | HG00140.hp1 HG00639.hp1 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.-133-2086_-133-208 others(80): Show |
FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 179041601 | |||||
chr1:179041671
|
G | GGAGGGA | 119 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(116): Show | 156 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.-133-2029_-133-202 others(10): Show |
FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 179041671 | |||||
chr1:179041671
|
G | GGAGGGAG others(5): Show |
1 | a0001c0001t0029g0282 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-133-2035_-133-202 others(16): Show |
FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 179041671 | |||||
chr1:179041671
|
G | GGAGGGAG others(36): Show |
33 | a0001c0001t0005g0013a0001c0001t0005g0059a0001c0001t0005g0060others(30): Show | 37 | HG00544.hp1 HG00735.hp2 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.-133-2024_-133-202 others(47): Show |
FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 179041671 | |||||
chr1:179041683
|
AGAGGGAG others(12): Show |
A | 1 | a0001c0001t0004g0032 | 2 | HG00140.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.-133-2022_-133-200 others(23): Show |
FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 179041683 | |||||
chr1:179041779
|
C | T | 1 | a0001c0001t0002g0183 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-133-1936C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179041779 | ||||||
chr1:179041811
|
A | G | 31 | a0001c0001t0005g0013a0001c0001t0005g0059a0001c0001t0005g0060others(28): Show | 35 | HG00544.hp1 HG01069.hp2 HG01074.hp1 others(32): Show |
intron_variant | MODIFIER | c.-133-1904A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179041811 | ||||||
chr1:179041927
|
G | T | 1 | a0001c0001t0024g0074 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-133-1788G>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179041927 | ||||||
chr1:179041967
|
A | G | 1 | a0001c0001t0006g0088 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-133-1748A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179041967 | ||||||
chr1:179042174
|
G | A | 2 | a0001c0001t0001g0051a0001c0001t0001g0242 | 2 | NA18953.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.-133-1541G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179042174 | ||||||
chr1:179042184
|
C | T | 1 | a0001c0001t0024g0074 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-133-1531C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179042184 | ||||||
chr1:179042250
|
G | A | 2 | a0001c0001t0001g0049a0001c0001t0001g0290 | 3 | NA18956.hp1 NA18961.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.-133-1465G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179042250 | ||||||
chr1:179042289
|
C | T | 1 | a0001c0001t0001g0236 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-133-1426C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179042289 | ||||||
chr1:179042298
|
G | T | 4 | a0001c0001t0011g0015a0001c0001t0011g0103a0001c0001t0011g0104others(1): Show | 5 | HG01069.hp2 HG01891.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.-133-1417G>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179042298 | ||||||
chr1:179042344
|
C | A | 6 | a0001c0001t0009g0044a0001c0001t0009g0222a0001c0001t0009g0223others(3): Show | 7 | HG02572.hp2 HG02615.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.-133-1371C>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179042344 | ||||||
chr1:179042349
|
C | T | 56 | a0001c0001t0003g0004a0001c0001t0003g0005a0001c0001t0003g0008others(53): Show | 77 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.-133-1366C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179042349 | ||||||
chr1:179042397
|
C | T | 1 | a0001c0001t0010g0097 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.-133-1318C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179042397 | ||||||
chr1:179042741
|
T | C | 1 | a0001c0001t0002g0181 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.-133-974T>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179042741 | ||||||
chr1:179042762
|
T | A | 8 | a0001c0001t0006g0093a0001c0001t0006g0094a0001c0001t0006g0095others(5): Show | 9 | HG00140.hp1 HG00639.hp1 HG00733.hp2 others(6): Show |
intron_variant | MODIFIER | c.-133-953T>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179042762 | ||||||
chr1:179042790
|
A | C | 1 | a0001c0001t0036g0142 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.-133-925A>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179042790 | ||||||
chr1:179042960
|
G | A | 16 | a0001c0001t0005g0013a0001c0001t0005g0059a0001c0001t0005g0060others(13): Show | 18 | HG00544.hp1 HG01074.hp1 HG02015.hp1 others(15): Show |
intron_variant | MODIFIER | c.-133-755G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179042960 | ||||||
chr1:179042978
|
G | A | 2 | a0001c0001t0003g0121a0001c0001t0003g0122 | 2 | HG00423.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.-133-737G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179042978 | ||||||
chr1:179043073
|
A | G | 57 | a0001c0001t0003g0004a0001c0001t0003g0005a0001c0001t0003g0008others(54): Show | 78 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.-133-642A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179043073 | ||||||
chr1:179043090
|
C | A | 56 | a0001c0001t0003g0004a0001c0001t0003g0005a0001c0001t0003g0008others(53): Show | 77 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.-133-625C>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179043090 | ||||||
chr1:179043467
|
G | A | 4 | a0001c0001t0011g0015a0001c0001t0011g0103a0001c0001t0011g0104others(1): Show | 5 | HG01069.hp2 HG01891.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.-133-248G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179043467 | ||||||
chr1:179043504
|
A | G | 2 | a0001c0001t0005g0060a0001c0001t0005g0072 | 2 | HG02080.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.-133-211A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179043504 | ||||||
chr1:179043565
|
C | T | 2 | a0001c0001t0018g0027a0001c0001t0030g0262 | 3 | HG02895.hp2 HG02897.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-133-150C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179043565 | ||||||
chr1:179043567
|
A | G | 8 | a0001c0001t0001g0010a0001c0001t0001g0228a0001c0001t0001g0229others(5): Show | 11 | HG00099.hp2 HG00609.hp2 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.-133-148A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179043567 | ||||||
chr1:179043582
|
A | T | 2 | a0001c0001t0012g0014a0001c0001t0012g0100 | 4 | HG01070.hp2 HG01071.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.-133-133A>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 1/7 | chr1 | 179043582 | ||||||
chr1:179044291
|
G | A | 1 | a0001c0001t0001g0250 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.377+67G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 2/7 | chr1 | 179044291 | ||||||
chr1:179044397
|
A | G | 1 | a0001c0001t0006g0093 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.377+173A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 2/7 | chr1 | 179044397 | ||||||
chr1:179044851
|
C | T | 1 | a0001c0001t0001g0278 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.377+627C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 2/7 | chr1 | 179044851 | ||||||
chr1:179045080
|
T | C | 58 | a0001c0001t0001g0132a0001c0001t0003g0004a0001c0001t0003g0005others(55): Show | 79 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.377+856T>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 2/7 | chr1 | 179045080 | ||||||
chr1:179045135
|
G | A | 2 | a0001c0002t0020g0105a0001c0002t0020g0106 | 2 | HG00735.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.377+911G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 2/7 | chr1 | 179045135 | ||||||
chr1:179045277
|
C | T | 1 | a0001c0001t0032g0101 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.377+1053C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 2/7 | chr1 | 179045277 | ||||||
chr1:179045278
|
G | A | 1 | a0001c0001t0001g0269 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.377+1054G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 2/7 | chr1 | 179045278 | ||||||
chr1:179045494
|
G | T | 1 | a0001c0001t0001g0232 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.377+1270G>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 2/7 | chr1 | 179045494 | ||||||
chr1:179045643
|
G | T | 1 | a0001c0001t0001g0051 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.377+1419G>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 2/7 | chr1 | 179045643 | ||||||
chr1:179045670
|
C | T | 20 | a0001c0001t0006g0083a0001c0001t0006g0084a0001c0001t0006g0085others(17): Show | 21 | HG00140.hp1 HG00639.hp1 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.377+1446C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 2/7 | chr1 | 179045670 | ||||||
chr1:179045671
|
G | A | 2 | a0001c0001t0001g0020a0001c0001t0001g0280 | 4 | HG02258.hp1 HG02630.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.377+1447G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 2/7 | chr1 | 179045671 | ||||||
chr1:179045912
|
C | CA | 14 | a0001c0001t0001g0052a0001c0001t0001g0057a0001c0001t0001g0132others(11): Show | 14 | HG00735.hp1 HG02056.hp2 HG02738.hp2 others(11): Show |
intron_variant | MODIFIER | c.377+1697dupA | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr1 | 179045912 | |||||
chr1:179045963
|
A | T | 1 | a0001c0001t0003g0168 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.377+1739A>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 2/7 | chr1 | 179045963 | ||||||
chr1:179045993
|
T | C | 1 | a0001c0001t0001g0254 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.377+1769T>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 2/7 | chr1 | 179045993 | ||||||
chr1:179046188
|
C | G | 1 | a0001c0001t0003g0295 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.377+1964C>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 2/7 | chr1 | 179046188 | ||||||
chr1:179046372
|
C | T | 1 | a0001c0001t0018g0027 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.377+2148C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 2/7 | chr1 | 179046372 | ||||||
chr1:179046594
|
G | T | 49 | a0001c0001t0003g0004a0001c0001t0003g0005a0001c0001t0003g0008others(46): Show | 69 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.377+2370G>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 2/7 | chr1 | 179046594 | ||||||
chr1:179046680
|
G | A | 1 | a0001c0001t0002g0185 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.377+2456G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 2/7 | chr1 | 179046680 | ||||||
chr1:179046778
|
G | A | 3 | a0001c0001t0003g0123a0001c0001t0003g0124a0001c0001t0003g0145 | 3 | NA18941.hp2 NA18955.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.377+2554G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 2/7 | chr1 | 179046778 | ||||||
chr1:179046822
|
C | G | 34 | a0001c0001t0005g0013a0001c0001t0005g0059a0001c0001t0005g0060others(31): Show | 38 | HG00544.hp1 HG00735.hp2 HG01069.hp2 others(35): Show |
intron_variant | MODIFIER | c.377+2598C>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 2/7 | chr1 | 179046822 | ||||||
chr1:179046860
|
T | C | 154 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(151): Show | 195 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.377+2636T>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 2/7 | chr1 | 179046860 | ||||||
chr1:179046889
|
G | A | 2 | a0001c0001t0019g0075a0001c0001t0019g0076 | 2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.377+2665G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 2/7 | chr1 | 179046889 | ||||||
chr1:179046927
|
G | A | 2 | a0001c0001t0012g0014a0001c0001t0012g0100 | 4 | HG01070.hp2 HG01071.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.377+2703G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 2/7 | chr1 | 179046927 | ||||||
chr1:179046951
|
C | T | 1 | a0001c0001t0003g0145 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.377+2727C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 2/7 | chr1 | 179046951 | ||||||
chr1:179047257
|
C | T | 4 | a0001c0001t0011g0015a0001c0001t0011g0103a0001c0001t0011g0104others(1): Show | 5 | HG01069.hp2 HG01891.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.378-3022C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 2/7 | chr1 | 179047257 | ||||||
chr1:179047263
|
C | A | 120 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(117): Show | 157 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.378-3016C>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 2/7 | chr1 | 179047263 | ||||||
chr1:179047348
|
T | C | 57 | a0001c0001t0001g0132a0001c0001t0003g0004a0001c0001t0003g0005others(54): Show | 78 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.378-2931T>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 2/7 | chr1 | 179047348 | ||||||
chr1:179047422
|
C | T | 1 | a0001c0001t0002g0221 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.378-2857C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 2/7 | chr1 | 179047422 | ||||||
chr1:179047476
|
C | T | 9 | a0001c0001t0001g0019a0001c0001t0001g0238a0001c0001t0001g0239others(6): Show | 11 | HG01168.hp1 HG01192.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.378-2803C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 2/7 | chr1 | 179047476 | ||||||
chr1:179047512
|
G | T | 1 | a0001c0001t0006g0098 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.378-2767G>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 2/7 | chr1 | 179047512 | ||||||
chr1:179047637
|
G | C | 34 | a0001c0001t0005g0013a0001c0001t0005g0059a0001c0001t0005g0060others(31): Show | 38 | HG00544.hp1 HG00735.hp2 HG01069.hp2 others(35): Show |
intron_variant | MODIFIER | c.378-2642G>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 2/7 | chr1 | 179047637 | ||||||
chr1:179047795
|
T | A | 34 | a0001c0001t0005g0013a0001c0001t0005g0059a0001c0001t0005g0060others(31): Show | 38 | HG00544.hp1 HG00735.hp2 HG01069.hp2 others(35): Show |
intron_variant | MODIFIER | c.378-2484T>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 2/7 | chr1 | 179047795 | ||||||
chr1:179048052
|
T | A | 1 | a0001c0001t0032g0101 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.378-2227T>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 2/7 | chr1 | 179048052 | ||||||
chr1:179048195
|
G | A | 6 | a0001c0001t0009g0044a0001c0001t0009g0222a0001c0001t0009g0223others(3): Show | 7 | HG02572.hp2 HG02615.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.378-2084G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 2/7 | chr1 | 179048195 | ||||||
chr1:179048241
|
G | A | 4 | a0001c0001t0011g0015a0001c0001t0011g0103a0001c0001t0011g0104others(1): Show | 5 | HG01069.hp2 HG01891.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.378-2038G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 2/7 | chr1 | 179048241 | ||||||
chr1:179048367
|
T | C | 6 | a0001c0001t0009g0044a0001c0001t0009g0222a0001c0001t0009g0223others(3): Show | 7 | HG02572.hp2 HG02615.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.378-1912T>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 2/7 | chr1 | 179048367 | ||||||
chr1:179048380
|
C | T | 1 | a0001c0001t0002g0202 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.378-1899C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 2/7 | chr1 | 179048380 | ||||||
chr1:179048507
|
G | A | 4 | a0001c0001t0003g0024a0001c0001t0003g0077a0001c0001t0003g0078others(1): Show | 5 | HG01243.hp1 HG02258.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.378-1772G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 2/7 | chr1 | 179048507 | ||||||
chr1:179048580
|
G | GC | 3 | a0001c0001t0001g0238a0001c0001t0001g0239a0001c0001t0001g0240 | 3 | HG01257.hp2 HG01258.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.378-1697dupC | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr1 | 179048580 | |||||
chr1:179048586
|
A | G | 1 | a0001c0001t0002g0201 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.378-1693A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 2/7 | chr1 | 179048586 | ||||||
chr1:179049135
|
A | C | 7 | a0001c0001t0008g0012a0001c0001t0008g0224a0001c0001t0008g0225others(4): Show | 10 | HG01346.hp2 HG02055.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.378-1144A>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 2/7 | chr1 | 179049135 | ||||||
chr1:179049177
|
C | T | 1 | a0001c0001t0003g0130 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.378-1102C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 2/7 | chr1 | 179049177 | ||||||
chr1:179049181
|
T | C | 1 | a0001c0001t0032g0101 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.378-1098T>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 2/7 | chr1 | 179049181 | ||||||
chr1:179049344
|
C | T | 5 | a0001c0001t0002g0041a0001c0001t0002g0180a0001c0001t0002g0182others(2): Show | 6 | NA18962.hp2 NA18989.hp2 NA19000.hp2 others(3): Show |
intron_variant | MODIFIER | c.378-935C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 2/7 | chr1 | 179049344 | ||||||
chr1:179049389
|
A | G | 2 | a0001c0001t0003g0129a0001c0001t0003g0130 | 2 | HG01081.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.378-890A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 2/7 | chr1 | 179049389 | ||||||
chr1:179049441
|
C | T | 14 | a0001c0001t0003g0005a0001c0001t0003g0016a0001c0001t0003g0029others(11): Show | 24 | HG00423.hp1 HG00438.hp2 HG00609.hp1 others(21): Show |
intron_variant | MODIFIER | c.378-838C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 2/7 | chr1 | 179049441 | ||||||
chr1:179049611
|
G | C | 34 | a0001c0001t0005g0013a0001c0001t0005g0059a0001c0001t0005g0060others(31): Show | 38 | HG00544.hp1 HG00735.hp2 HG01069.hp2 others(35): Show |
intron_variant | MODIFIER | c.378-668G>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 2/7 | chr1 | 179049611 | ||||||
chr1:179049648
|
C | G | 120 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(117): Show | 157 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.378-631C>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 2/7 | chr1 | 179049648 | ||||||
chr1:179049707
|
A | T | 6 | a0001c0001t0009g0044a0001c0001t0009g0222a0001c0001t0009g0223others(3): Show | 7 | HG02572.hp2 HG02615.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.378-572A>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 2/7 | chr1 | 179049707 | ||||||
chr1:179049790
|
T | C | 154 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(151): Show | 195 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.378-489T>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 2/7 | chr1 | 179049790 | ||||||
chr1:179049884
|
C | T | 119 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(116): Show | 156 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.378-395C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 2/7 | chr1 | 179049884 | ||||||
chr1:179050051
|
A | G | 64 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0018others(61): Show | 93 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.378-228A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 2/7 | chr1 | 179050051 | ||||||
chr1:179050103
|
C | G | 34 | a0001c0001t0005g0013a0001c0001t0005g0059a0001c0001t0005g0060others(31): Show | 38 | HG00544.hp1 HG00735.hp2 HG01069.hp2 others(35): Show |
intron_variant | MODIFIER | c.378-176C>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 2/7 | chr1 | 179050103 | ||||||
chr1:179050441
|
C | G | 16 | a0001c0001t0005g0013a0001c0001t0005g0059a0001c0001t0005g0060others(13): Show | 18 | HG00544.hp1 HG01074.hp1 HG02015.hp1 others(15): Show |
intron_variant | MODIFIER | c.464+76C>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 3/7 | chr1 | 179050441 | ||||||
chr1:179050479
|
G | A | 1 | a0001c0001t0004g0156 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.464+114G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 3/7 | chr1 | 179050479 | ||||||
chr1:179050525
|
T | G | 2 | a0001c0002t0020g0105a0001c0002t0020g0106 | 2 | HG00735.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.464+160T>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 3/7 | chr1 | 179050525 | ||||||
chr1:179051053
|
C | T | 114 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(111): Show | 150 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.464+688C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 3/7 | chr1 | 179051053 | ||||||
chr1:179051055
|
C | G | 213 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(210): Show | 278 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.464+690C>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 3/7 | chr1 | 179051055 | ||||||
chr1:179051058
|
C | G | 213 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(210): Show | 278 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.464+693C>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 3/7 | chr1 | 179051058 | ||||||
chr1:179051071
|
G | A | 2 | a0001c0001t0012g0014a0001c0001t0012g0100 | 4 | HG01070.hp2 HG01071.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.464+706G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 3/7 | chr1 | 179051071 | ||||||
chr1:179051122
|
TA | T | 130 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(127): Show | 168 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.464+772delA | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 179051122 | |||||
chr1:179051242
|
C | G | 49 | a0001c0001t0003g0004a0001c0001t0003g0005a0001c0001t0003g0008others(46): Show | 69 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.464+877C>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 3/7 | chr1 | 179051242 | ||||||
chr1:179051560
|
G | A | 9 | a0001c0001t0007g0026a0001c0001t0007g0107a0001c0001t0007g0108others(6): Show | 10 | HG01099.hp2 HG02145.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.464+1195G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 3/7 | chr1 | 179051560 | ||||||
chr1:179051840
|
G | C | 1 | a0001c0001t0032g0101 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.464+1475G>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 3/7 | chr1 | 179051840 | ||||||
chr1:179051928
|
G | A | 2 | a0001c0001t0001g0230a0001c0001t0001g0263 | 2 | HG00609.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.464+1563G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 3/7 | chr1 | 179051928 | ||||||
chr1:179052033
|
A | G | 9 | a0001c0001t0007g0026a0001c0001t0007g0107a0001c0001t0007g0108others(6): Show | 10 | HG01099.hp2 HG02145.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.464+1668A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 3/7 | chr1 | 179052033 | ||||||
chr1:179052097
|
G | A | 203 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(200): Show | 271 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.464+1732G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 3/7 | chr1 | 179052097 | ||||||
chr1:179052123
|
C | T | 4 | a0001c0001t0011g0015a0001c0001t0011g0103a0001c0001t0011g0104others(1): Show | 5 | HG01069.hp2 HG01891.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.464+1758C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 3/7 | chr1 | 179052123 | ||||||
chr1:179052193
|
T | A | 1 | a0001c0001t0001g0256 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.464+1828T>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 3/7 | chr1 | 179052193 | ||||||
chr1:179052218
|
CAT | C | 4 | a0001c0001t0001g0261a0001c0001t0015g0081a0001c0001t0015g0082others(1): Show | 4 | HG01891.hp1 HG02040.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.464+1856_464+1857d others(4): Show |
FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 179052218 | |||||
chr1:179052442
|
T | G | 1 | a0001c0001t0001g0243 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.464+2077T>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 3/7 | chr1 | 179052442 | ||||||
chr1:179052516
|
G | A | 23 | a0001c0001t0004g0006a0001c0001t0004g0032a0001c0001t0004g0033others(20): Show | 30 | HG00140.hp2 HG00597.hp2 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.465-2013G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 3/7 | chr1 | 179052516 | ||||||
chr1:179052601
|
T | G | 120 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(117): Show | 157 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.465-1928T>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 3/7 | chr1 | 179052601 | ||||||
chr1:179052611
|
T | C | 143 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(140): Show | 187 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(184): Show |
intron_variant | MODIFIER | c.465-1918T>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 3/7 | chr1 | 179052611 | ||||||
chr1:179052676
|
A | G | 1 | a0001c0001t0005g0067 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.465-1853A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 3/7 | chr1 | 179052676 | ||||||
chr1:179052823
|
C | T | 23 | a0001c0001t0004g0006a0001c0001t0004g0032a0001c0001t0004g0033others(20): Show | 30 | HG00140.hp2 HG00597.hp2 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.465-1706C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 3/7 | chr1 | 179052823 | ||||||
chr1:179052940
|
A | C | 1 | a0001c0001t0003g0131 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.465-1589A>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 3/7 | chr1 | 179052940 | ||||||
chr1:179052946
|
A | G | 16 | a0001c0001t0005g0013a0001c0001t0005g0059a0001c0001t0005g0060others(13): Show | 18 | HG00544.hp1 HG01074.hp1 HG02015.hp1 others(15): Show |
intron_variant | MODIFIER | c.465-1583A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 3/7 | chr1 | 179052946 | ||||||
chr1:179052993
|
C | T | 2 | a0001c0002t0020g0105a0001c0002t0020g0106 | 2 | HG00735.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.465-1536C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 3/7 | chr1 | 179052993 | ||||||
chr1:179053101
|
G | T | 92 | a0001c0001t0003g0004a0001c0001t0003g0005a0001c0001t0003g0008others(89): Show | 119 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.465-1428G>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 3/7 | chr1 | 179053101 | ||||||
chr1:179053232
|
T | C | 7 | a0001c0001t0008g0012a0001c0001t0008g0224a0001c0001t0008g0225others(4): Show | 10 | HG01346.hp2 HG02055.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.465-1297T>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 3/7 | chr1 | 179053232 | ||||||
chr1:179053293
|
T | C | 58 | a0001c0001t0003g0004a0001c0001t0003g0005a0001c0001t0003g0008others(55): Show | 81 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.465-1236T>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 3/7 | chr1 | 179053293 | ||||||
chr1:179053443
|
CCAAA | C | 114 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(111): Show | 150 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.465-1061_465-1058d others(6): Show |
FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 179053443 | |||||
chr1:179053444
|
C | G | 32 | a0001c0001t0005g0013a0001c0001t0005g0059a0001c0001t0005g0060others(29): Show | 36 | HG00544.hp1 HG01069.hp2 HG01074.hp1 others(33): Show |
intron_variant | MODIFIER | c.465-1085C>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 3/7 | chr1 | 179053444 | ||||||
chr1:179053495
|
A | G | 121 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(118): Show | 159 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.465-1034A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 3/7 | chr1 | 179053495 | ||||||
chr1:179053515
|
T | C | 213 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(210): Show | 278 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.465-1014T>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 3/7 | chr1 | 179053515 | ||||||
chr1:179053547
|
T | G | 3 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234 | 3 | HG02280.hp1 HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.465-982T>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 3/7 | chr1 | 179053547 | ||||||
chr1:179053582
|
C | T | 2 | a0001c0002t0020g0105a0001c0002t0020g0106 | 2 | HG00735.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.465-947C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 3/7 | chr1 | 179053582 | ||||||
chr1:179053933
|
G | C | 2 | a0001c0002t0020g0105a0001c0002t0020g0106 | 2 | HG00735.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.465-596G>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 3/7 | chr1 | 179053933 | ||||||
chr1:179054017
|
C | T | 213 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(210): Show | 278 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.465-512C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 3/7 | chr1 | 179054017 | ||||||
chr1:179054108
|
C | CT | 16 | a0001c0001t0005g0013a0001c0001t0005g0059a0001c0001t0005g0060others(13): Show | 18 | HG00544.hp1 HG01074.hp1 HG02015.hp1 others(15): Show |
intron_variant | MODIFIER | c.465-409dupT | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 179054108 | |||||
chr1:179054275
|
C | T | 1 | a0001c0001t0032g0101 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.465-254C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 3/7 | chr1 | 179054275 | ||||||
chr1:179054390
|
G | A | 7 | a0001c0001t0001g0010a0001c0001t0001g0228a0001c0001t0001g0229others(4): Show | 10 | HG00099.hp2 HG00609.hp2 HG01074.hp2 others(7): Show |
intron_variant | MODIFIER | c.465-139G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 3/7 | chr1 | 179054390 | ||||||
chr1:179054466
|
G | T | 58 | a0001c0001t0003g0004a0001c0001t0003g0005a0001c0001t0003g0008others(55): Show | 81 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.465-63G>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 3/7 | chr1 | 179054466 | ||||||
chr1:179054502
|
C | T | 1 | a0001c0001t0001g0256 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.465-27C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 3/7 | chr1 | 179054502 | ||||||
chr1:179054744
|
T | G | 94 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(91): Show | 129 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.574+106T>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179054744 | ||||||
chr1:179054841
|
G | A | 3 | a0001c0001t0004g0156a0001c0001t0004g0157a0001c0001t0026g0158 | 3 | HG00597.hp2 HG02132.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.574+203G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179054841 | ||||||
chr1:179055221
|
G | C | 2 | a0001c0001t0012g0014a0001c0001t0012g0100 | 4 | HG01070.hp2 HG01071.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.574+583G>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179055221 | ||||||
chr1:179055418
|
T | G | 7 | a0001c0001t0001g0018a0001c0001t0001g0021a0001c0001t0001g0246others(4): Show | 11 | HG01081.hp2 HG01167.hp2 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.574+780T>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179055418 | ||||||
chr1:179055444
|
A | T | 1 | a0001c0001t0001g0261 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.574+806A>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179055444 | ||||||
chr1:179055558
|
A | C | 1 | a0001c0001t0001g0290 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.574+920A>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179055558 | ||||||
chr1:179055628
|
T | C | 1 | a0001c0001t0038g0058 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.574+990T>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179055628 | ||||||
chr1:179055688
|
C | T | 1 | a0001c0001t0006g0086 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.574+1050C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179055688 | ||||||
chr1:179055697
|
A | T | 1 | a0001c0001t0007g0151 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.574+1059A>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179055697 | ||||||
chr1:179055750
|
A | G | 213 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(210): Show | 278 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.574+1112A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179055750 | ||||||
chr1:179056048
|
G | A | 1 | a0001c0001t0002g0186 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.574+1410G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179056048 | ||||||
chr1:179056234
|
A | G | 34 | a0001c0001t0005g0013a0001c0001t0005g0059a0001c0001t0005g0060others(31): Show | 38 | HG00544.hp1 HG00735.hp2 HG01069.hp2 others(35): Show |
intron_variant | MODIFIER | c.574+1596A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179056234 | ||||||
chr1:179056314
|
A | G | 1 | a0001c0001t0018g0027 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.574+1676A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179056314 | ||||||
chr1:179056334
|
C | G | 56 | a0001c0001t0003g0004a0001c0001t0003g0005a0001c0001t0003g0008others(53): Show | 77 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.574+1696C>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179056334 | ||||||
chr1:179056463
|
A | G | 1 | a0001c0001t0002g0176 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.574+1825A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179056463 | ||||||
chr1:179056538
|
C | G | 2 | a0001c0002t0020g0105a0001c0002t0020g0106 | 2 | HG00735.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.574+1900C>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179056538 | ||||||
chr1:179056661
|
G | A | 2 | a0001c0001t0006g0095a0001c0001t0006g0098 | 2 | HG00733.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.574+2023G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179056661 | ||||||
chr1:179056805
|
A | G | 3 | a0001c0001t0016g0226a0001c0001t0016g0227a0001c0001t0018g0027 | 4 | HG02572.hp2 HG02647.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.574+2167A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179056805 | ||||||
chr1:179056982
|
T | G | 1 | a0001c0001t0006g0085 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.574+2344T>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179056982 | ||||||
chr1:179057020
|
C | T | 1 | a0001c0001t0001g0277 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.574+2382C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179057020 | ||||||
chr1:179057025
|
G | A | 1 | a0001c0001t0002g0187 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.574+2387G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179057025 | ||||||
chr1:179057134
|
C | T | 3 | a0001c0001t0023g0126a0001c0002t0020g0105a0001c0002t0020g0106 | 3 | HG00735.hp2 HG01175.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.574+2496C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179057134 | ||||||
chr1:179057142
|
C | G | 2 | a0001c0001t0012g0014a0001c0001t0012g0100 | 4 | HG01070.hp2 HG01071.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.574+2504C>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179057142 | ||||||
chr1:179057288
|
T | A | 2 | a0001c0001t0016g0226a0001c0001t0016g0227 | 2 | HG02572.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.574+2650T>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179057288 | ||||||
chr1:179057354
|
A | G | 213 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(210): Show | 278 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.574+2716A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179057354 | ||||||
chr1:179057392
|
C | T | 120 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(117): Show | 157 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.574+2754C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179057392 | ||||||
chr1:179057432
|
C | A | 213 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(210): Show | 278 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.574+2794C>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179057432 | ||||||
chr1:179057535
|
T | G | 121 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(118): Show | 159 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.574+2897T>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179057535 | ||||||
chr1:179057678
|
G | C | 1 | a0001c0001t0002g0219 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.574+3040G>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179057678 | ||||||
chr1:179057762
|
T | C | 9 | a0001c0001t0007g0026a0001c0001t0007g0107a0001c0001t0007g0108others(6): Show | 10 | HG01099.hp2 HG02145.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.574+3124T>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179057762 | ||||||
chr1:179057825
|
G | T | 121 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(118): Show | 159 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.574+3187G>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179057825 | ||||||
chr1:179058005
|
C | A | 121 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(118): Show | 159 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.574+3367C>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179058005 | ||||||
chr1:179058217
|
A | G | 24 | a0001c0001t0003g0130a0001c0001t0004g0006a0001c0001t0004g0032others(21): Show | 31 | HG00140.hp2 HG00597.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.574+3579A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179058217 | ||||||
chr1:179058415
|
G | A | 6 | a0001c0001t0004g0032a0001c0001t0004g0033a0001c0001t0004g0153others(3): Show | 8 | HG00140.hp2 HG00738.hp2 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.574+3777G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179058415 | ||||||
chr1:179058647
|
T | A | 1 | a0001c0001t0001g0273 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.574+4009T>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179058647 | ||||||
chr1:179058685
|
A | G | 6 | a0001c0001t0005g0013a0001c0001t0005g0059a0001c0001t0005g0060others(3): Show | 8 | HG02080.hp1 HG02135.hp1 NA18942.hp1 others(5): Show |
intron_variant | MODIFIER | c.574+4047A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179058685 | ||||||
chr1:179058777
|
G | C | 4 | a0001c0001t0003g0116a0001c0001t0003g0119a0001c0001t0003g0120others(1): Show | 4 | HG02280.hp2 HG02818.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.574+4139G>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179058777 | ||||||
chr1:179058834
|
G | A | 1 | a0001c0001t0002g0179 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.574+4196G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179058834 | ||||||
chr1:179058836
|
A | G | 1 | a0001c0001t0018g0027 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.574+4198A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179058836 | ||||||
chr1:179058870
|
T | A | 1 | a0001c0001t0002g0188 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.574+4232T>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179058870 | ||||||
chr1:179058879
|
A | T | 1 | a0001c0001t0003g0295 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.574+4241A>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179058879 | ||||||
chr1:179058957
|
T | A | 16 | a0001c0001t0005g0013a0001c0001t0005g0059a0001c0001t0005g0060others(13): Show | 18 | HG00544.hp1 HG01074.hp1 HG02015.hp1 others(15): Show |
intron_variant | MODIFIER | c.574+4319T>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179058957 | ||||||
chr1:179058999
|
A | G | 1 | a0001c0001t0001g0260 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.574+4361A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179058999 | ||||||
chr1:179059003
|
T | C | 1 | a0001c0001t0002g0189 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.574+4365T>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179059003 | ||||||
chr1:179059017
|
G | C | 1 | a0001c0001t0002g0188 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.574+4379G>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179059017 | ||||||
chr1:179059038
|
G | A | 1 | a0001c0001t0001g0257 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.574+4400G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179059038 | ||||||
chr1:179059311
|
T | C | 56 | a0001c0001t0003g0004a0001c0001t0003g0005a0001c0001t0003g0008others(53): Show | 77 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.575-4616T>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179059311 | ||||||
chr1:179059528
|
C | G | 1 | a0001c0001t0006g0086 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.575-4399C>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179059528 | ||||||
chr1:179059700
|
G | A | 11 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0050others(8): Show | 13 | HG00280.hp1 HG00621.hp2 HG00735.hp1 others(10): Show |
intron_variant | MODIFIER | c.575-4227G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179059700 | ||||||
chr1:179059801
|
A | G | 216 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(213): Show | 281 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(278): Show |
intron_variant | MODIFIER | c.575-4126A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179059801 | ||||||
chr1:179059919
|
C | T | 1 | a0001c0001t0001g0264 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.575-4008C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179059919 | ||||||
chr1:179059971
|
C | CA | 9 | a0001c0001t0001g0132a0001c0001t0001g0263a0001c0001t0001g0274others(6): Show | 9 | HG02922.hp2 HG03927.hp2 HG03942.hp2 others(6): Show |
intron_variant | MODIFIER | c.575-3940dupA | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 179059971 | |||||
chr1:179059971
|
CA | C | 57 | a0001c0001t0003g0004a0001c0001t0003g0005a0001c0001t0003g0008others(54): Show | 78 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.575-3940delA | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 179059971 | |||||
chr1:179059990
|
C | A | 2 | a0001c0002t0020g0105a0001c0002t0020g0106 | 2 | HG00735.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.575-3937C>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179059990 | ||||||
chr1:179060101
|
A | AT | 212 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(209): Show | 283 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.575-3819dupT | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 179060101 | |||||
chr1:179060101
|
A | T | 21 | a0001c0001t0003g0128a0001c0001t0006g0083a0001c0001t0006g0084others(18): Show | 22 | HG00140.hp1 HG00609.hp1 HG00639.hp1 others(19): Show |
intron_variant | MODIFIER | c.575-3826A>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179060101 | ||||||
chr1:179060102
|
T | TA | 5 | a0001c0001t0001g0263a0001c0001t0001g0275a0001c0001t0002g0191others(2): Show | 5 | HG02083.hp2 HG02922.hp2 NA18975.hp1 others(2): Show |
intron_variant | MODIFIER | c.575-3825_575-3824i others(3): Show |
FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179060102 | ||||||
chr1:179060304
|
T | C | 1 | a0001c0001t0003g0135 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.575-3623T>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179060304 | ||||||
chr1:179060586
|
G | C | 4 | a0001c0001t0011g0015a0001c0001t0011g0103a0001c0001t0011g0104others(1): Show | 5 | HG01069.hp2 HG01891.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.575-3341G>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179060586 | ||||||
chr1:179061010
|
C | A | 1 | a0001c0001t0001g0278 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.575-2917C>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179061010 | ||||||
chr1:179061011
|
G | A | 1 | a0001c0001t0025g0207 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.575-2916G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179061011 | ||||||
chr1:179061076
|
A | AT | 125 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(122): Show | 168 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.575-2831dupT | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 179061076 | |||||
chr1:179061076
|
A | ATT | 16 | a0001c0001t0001g0048a0001c0001t0001g0057a0001c0001t0001g0234others(13): Show | 17 | HG01175.hp2 HG01346.hp2 HG01358.hp1 others(14): Show |
intron_variant | MODIFIER | c.575-2832_575-2831d others(4): Show |
FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 179061076 | |||||
chr1:179061076
|
AT | A | 42 | a0001c0001t0002g0042a0001c0001t0002g0192a0001c0001t0002g0193others(39): Show | 49 | HG00544.hp1 HG00735.hp2 HG01069.hp2 others(46): Show |
intron_variant | MODIFIER | c.575-2831delT | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 179061076 | |||||
chr1:179061076
|
ATT | A | 53 | a0001c0001t0003g0004a0001c0001t0003g0005a0001c0001t0003g0008others(50): Show | 74 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.575-2832_575-2831d others(4): Show |
FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 179061076 | |||||
chr1:179061166
|
C | T | 1 | a0001c0001t0002g0219 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.575-2761C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179061166 | ||||||
chr1:179061190
|
C | T | 56 | a0001c0001t0003g0004a0001c0001t0003g0005a0001c0001t0003g0008others(53): Show | 77 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.575-2737C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179061190 | ||||||
chr1:179061234
|
G | A | 238 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(235): Show | 310 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(307): Show |
intron_variant | MODIFIER | c.575-2693G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179061234 | ||||||
chr1:179061549
|
A | G | 34 | a0001c0001t0005g0013a0001c0001t0005g0059a0001c0001t0005g0060others(31): Show | 38 | HG00544.hp1 HG00735.hp2 HG01069.hp2 others(35): Show |
intron_variant | MODIFIER | c.575-2378A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179061549 | ||||||
chr1:179061642
|
C | G | 1 | a0001c0001t0003g0295 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.575-2285C>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179061642 | ||||||
chr1:179061648
|
A | T | 4 | a0001c0001t0011g0015a0001c0001t0011g0103a0001c0001t0011g0104others(1): Show | 5 | HG01069.hp2 HG01891.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.575-2279A>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179061648 | ||||||
chr1:179061807
|
C | T | 124 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(121): Show | 162 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.575-2120C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179061807 | ||||||
chr1:179061960
|
T | C | 32 | a0001c0001t0005g0013a0001c0001t0005g0059a0001c0001t0005g0060others(29): Show | 36 | HG00544.hp1 HG01069.hp2 HG01074.hp1 others(33): Show |
intron_variant | MODIFIER | c.575-1967T>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179061960 | ||||||
chr1:179062014
|
C | CT | 34 | a0001c0001t0005g0013a0001c0001t0005g0059a0001c0001t0005g0060others(31): Show | 38 | HG00544.hp1 HG00735.hp2 HG01069.hp2 others(35): Show |
intron_variant | MODIFIER | c.575-1903dupT | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 179062014 | |||||
chr1:179062076
|
G | A | 1 | a0001c0001t0018g0027 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.575-1851G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179062076 | ||||||
chr1:179062154
|
A | G | 7 | a0001c0001t0001g0018a0001c0001t0001g0021a0001c0001t0001g0246others(4): Show | 11 | HG01081.hp2 HG01167.hp2 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.575-1773A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179062154 | ||||||
chr1:179062162
|
A | C | 2 | a0001c0001t0019g0075a0001c0001t0019g0076 | 2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.575-1765A>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179062162 | ||||||
chr1:179062170
|
A | T | 2 | a0001c0001t0012g0014a0001c0001t0012g0100 | 4 | HG01070.hp2 HG01071.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.575-1757A>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179062170 | ||||||
chr1:179062212
|
C | G | 2 | a0001c0001t0012g0014a0001c0001t0012g0100 | 4 | HG01070.hp2 HG01071.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.575-1715C>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179062212 | ||||||
chr1:179062467
|
A | C | 1 | a0001c0001t0006g0099 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.575-1460A>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179062467 | ||||||
chr1:179062478
|
C | T | 14 | a0001c0001t0001g0018a0001c0001t0001g0021a0001c0001t0001g0246others(11): Show | 21 | HG01081.hp2 HG01167.hp2 HG01346.hp2 others(18): Show |
intron_variant | MODIFIER | c.575-1449C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179062478 | ||||||
chr1:179062588
|
T | C | 2 | a0001c0001t0012g0014a0001c0001t0012g0100 | 4 | HG01070.hp2 HG01071.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.575-1339T>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179062588 | ||||||
chr1:179062669
|
A | G | 1 | a0001c0001t0022g0030 | 2 | NA18955.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.575-1258A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179062669 | ||||||
chr1:179062752
|
C | A | 23 | a0001c0001t0004g0006a0001c0001t0004g0032a0001c0001t0004g0033others(20): Show | 30 | HG00140.hp2 HG00597.hp2 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.575-1175C>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179062752 | ||||||
chr1:179062789
|
A | G | 1 | a0001c0001t0024g0074 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.575-1138A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179062789 | ||||||
chr1:179062868
|
A | G | 4 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0235others(1): Show | 5 | HG01109.hp1 HG02055.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.575-1059A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179062868 | ||||||
chr1:179062928
|
C | G | 1 | a0001c0001t0002g0190 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.575-999C>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179062928 | ||||||
chr1:179062948
|
A | G | 124 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(121): Show | 162 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.575-979A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179062948 | ||||||
chr1:179063013
|
A | G | 2 | a0001c0001t0012g0014a0001c0001t0012g0100 | 4 | HG01070.hp2 HG01071.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.575-914A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179063013 | ||||||
chr1:179063080
|
C | T | 16 | a0001c0001t0005g0013a0001c0001t0005g0059a0001c0001t0005g0060others(13): Show | 18 | HG00544.hp1 HG01074.hp1 HG02015.hp1 others(15): Show |
intron_variant | MODIFIER | c.575-847C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179063080 | ||||||
chr1:179063183
|
G | A | 1 | a0001c0001t0024g0074 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.575-744G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179063183 | ||||||
chr1:179063206
|
G | A | 6 | a0001c0001t0009g0044a0001c0001t0009g0222a0001c0001t0009g0223others(3): Show | 7 | HG02572.hp2 HG02615.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.575-721G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179063206 | ||||||
chr1:179063217
|
C | G | 7 | a0001c0001t0001g0047a0001c0001t0001g0254a0001c0001t0001g0255others(4): Show | 8 | HG02145.hp2 HG02818.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.575-710C>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179063217 | ||||||
chr1:179063448
|
C | T | 4 | a0001c0001t0011g0015a0001c0001t0011g0103a0001c0001t0011g0104others(1): Show | 5 | HG01069.hp2 HG01891.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.575-479C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179063448 | ||||||
chr1:179063479
|
T | A | 56 | a0001c0001t0003g0004a0001c0001t0003g0005a0001c0001t0003g0008others(53): Show | 77 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.575-448T>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179063479 | ||||||
chr1:179063845
|
T | A | 1 | a0001c0001t0002g0183 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.575-82T>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 4/7 | chr1 | 179063845 | ||||||
chr1:179064649
|
T | C | 23 | a0001c0001t0004g0006a0001c0001t0004g0032a0001c0001t0004g0033others(20): Show | 30 | HG00140.hp2 HG00597.hp2 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.938+153T>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 6/7 | chr1 | 179064649 | ||||||
chr1:179064852
|
G | A | 213 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(210): Show | 278 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.938+356G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 6/7 | chr1 | 179064852 | ||||||
chr1:179065020
|
T | A | 1 | a0001c0001t0002g0172 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.938+524T>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 6/7 | chr1 | 179065020 | ||||||
chr1:179065094
|
T | A | 23 | a0001c0001t0004g0006a0001c0001t0004g0032a0001c0001t0004g0033others(20): Show | 30 | HG00140.hp2 HG00597.hp2 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.938+598T>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 6/7 | chr1 | 179065094 | ||||||
chr1:179065147
|
C | CT | 5 | a0001c0001t0011g0015a0001c0001t0011g0103a0001c0001t0011g0104others(2): Show | 6 | HG01069.hp2 HG01891.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.938+662dupT | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr1 | 179065147 | |||||
chr1:179065174
|
G | A | 2 | a0001c0001t0004g0160a0001c0001t0004g0161 | 2 | HG03017.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.938+678G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 6/7 | chr1 | 179065174 | ||||||
chr1:179065253
|
C | T | 1 | a0001c0001t0001g0237 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.938+757C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 6/7 | chr1 | 179065253 | ||||||
chr1:179065346
|
A | G | 56 | a0001c0001t0003g0004a0001c0001t0003g0005a0001c0001t0003g0008others(53): Show | 77 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.938+850A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 6/7 | chr1 | 179065346 | ||||||
chr1:179065416
|
T | C | 3 | a0001c0001t0005g0061a0001c0001t0005g0069a0002c0003t0005g0063 | 3 | HG02809.hp2 HG02886.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.938+920T>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 6/7 | chr1 | 179065416 | ||||||
chr1:179065649
|
A | C | 56 | a0001c0001t0003g0004a0001c0001t0003g0005a0001c0001t0003g0008others(53): Show | 77 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.939-1151A>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 6/7 | chr1 | 179065649 | ||||||
chr1:179065683
|
C | G | 1 | a0001c0001t0025g0207 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.939-1117C>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 6/7 | chr1 | 179065683 | ||||||
chr1:179065836
|
A | G | 1 | a0001c0001t0002g0221 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.939-964A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 6/7 | chr1 | 179065836 | ||||||
chr1:179065916
|
T | C | 1 | a0001c0001t0024g0074 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.939-884T>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 6/7 | chr1 | 179065916 | ||||||
chr1:179066008
|
C | G | 1 | a0001c0001t0032g0101 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.939-792C>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 6/7 | chr1 | 179066008 | ||||||
chr1:179066141
|
A | G | 9 | a0001c0001t0007g0026a0001c0001t0007g0107a0001c0001t0007g0108others(6): Show | 10 | HG01099.hp2 HG02145.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.939-659A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 6/7 | chr1 | 179066141 | ||||||
chr1:179066196
|
T | C | 56 | a0001c0001t0003g0004a0001c0001t0003g0005a0001c0001t0003g0008others(53): Show | 77 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.939-604T>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 6/7 | chr1 | 179066196 | ||||||
chr1:179066294
|
T | G | 56 | a0001c0001t0003g0004a0001c0001t0003g0005a0001c0001t0003g0008others(53): Show | 77 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.939-506T>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 6/7 | chr1 | 179066294 | ||||||
chr1:179066327
|
T | G | 216 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(213): Show | 281 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(278): Show |
intron_variant | MODIFIER | c.939-473T>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 6/7 | chr1 | 179066327 | ||||||
chr1:179066527
|
C | G | 9 | a0001c0001t0007g0026a0001c0001t0007g0107a0001c0001t0007g0108others(6): Show | 10 | HG01099.hp2 HG02145.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.939-273C>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 6/7 | chr1 | 179066527 | ||||||
chr1:179067150
|
C | A | 1 | a0001c0001t0003g0146 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.998+291C>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179067150 | ||||||
chr1:179067267
|
C | A | 1 | a0001c0001t0024g0074 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.998+408C>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179067267 | ||||||
chr1:179067402
|
C | T | 1 | a0001c0001t0015g0102 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.998+543C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179067402 | ||||||
chr1:179067537
|
G | C | 2 | a0001c0001t0012g0014a0001c0001t0012g0100 | 4 | HG01070.hp2 HG01071.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.998+678G>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179067537 | ||||||
chr1:179067639
|
T | A | 215 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(212): Show | 280 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.998+780T>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179067639 | ||||||
chr1:179067696
|
T | G | 2 | a0001c0002t0020g0105a0001c0002t0020g0106 | 2 | HG00735.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.998+837T>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179067696 | ||||||
chr1:179067854
|
T | C | 241 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(238): Show | 313 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(310): Show |
intron_variant | MODIFIER | c.998+995T>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179067854 | ||||||
chr1:179067895
|
C | G | 1 | a0001c0001t0003g0144 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.998+1036C>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179067895 | ||||||
chr1:179067983
|
A | G | 291 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(288): Show | 393 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(390): Show |
intron_variant | MODIFIER | c.998+1124A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179067983 | ||||||
chr1:179068043
|
G | A | 56 | a0001c0001t0003g0004a0001c0001t0003g0005a0001c0001t0003g0008others(53): Show | 77 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.998+1184G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179068043 | ||||||
chr1:179068085
|
C | T | 3 | a0001c0001t0015g0081a0001c0001t0015g0082a0001c0001t0015g0102 | 3 | HG01891.hp1 HG03041.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.998+1226C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179068085 | ||||||
chr1:179068331
|
T | C | 8 | a0001c0001t0006g0093a0001c0001t0006g0094a0001c0001t0006g0095others(5): Show | 9 | HG00140.hp1 HG00639.hp1 HG00733.hp2 others(6): Show |
intron_variant | MODIFIER | c.998+1472T>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179068331 | ||||||
chr1:179068440
|
A | AT | 6 | a0001c0001t0009g0044a0001c0001t0009g0222a0001c0001t0009g0223others(3): Show | 7 | HG02572.hp2 HG02615.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.998+1593dupT | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 179068440 | |||||
chr1:179068456
|
G | T | 117 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(114): Show | 153 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.998+1597G>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179068456 | ||||||
chr1:179068536
|
A | G | 1 | a0001c0001t0002g0181 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.998+1677A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179068536 | ||||||
chr1:179068980
|
T | C | 2 | a0001c0001t0019g0075a0001c0001t0019g0076 | 2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.998+2121T>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179068980 | ||||||
chr1:179069020
|
T | C | 40 | a0001c0001t0001g0271a0001c0001t0005g0013a0001c0001t0005g0059others(37): Show | 45 | HG00544.hp1 HG00735.hp2 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.998+2161T>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179069020 | ||||||
chr1:179069032
|
G | A | 1 | a0001c0001t0001g0281 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.998+2173G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179069032 | ||||||
chr1:179069061
|
T | C | 2 | a0001c0002t0020g0105a0001c0002t0020g0106 | 2 | HG00735.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.998+2202T>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179069061 | ||||||
chr1:179069115
|
G | A | 1 | a0001c0001t0001g0274 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.998+2256G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179069115 | ||||||
chr1:179069143
|
C | T | 4 | a0001c0001t0003g0024a0001c0001t0003g0077a0001c0001t0003g0078others(1): Show | 5 | HG01243.hp1 HG02258.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.998+2284C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179069143 | ||||||
chr1:179069402
|
G | A | 55 | a0001c0001t0003g0004a0001c0001t0003g0005a0001c0001t0003g0008others(52): Show | 76 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.999-2511G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179069402 | ||||||
chr1:179069463
|
C | T | 1 | a0001c0001t0006g0087 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.999-2450C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179069463 | ||||||
chr1:179069474
|
G | A | 56 | a0001c0001t0003g0004a0001c0001t0003g0005a0001c0001t0003g0008others(53): Show | 77 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.999-2439G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179069474 | ||||||
chr1:179069591
|
C | T | 2 | a0001c0001t0001g0243a0001c0001t0001g0244 | 2 | HG01192.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.999-2322C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179069591 | ||||||
chr1:179069904
|
A | C | 5 | a0001c0001t0002g0172a0001c0001t0002g0186a0001c0001t0002g0197others(2): Show | 5 | NA18969.hp2 NA18991.hp2 NA19063.hp1 others(2): Show |
intron_variant | MODIFIER | c.999-2009A>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179069904 | ||||||
chr1:179069909
|
C | T | 114 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0045others(111): Show | 148 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.999-2004C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179069909 | ||||||
chr1:179069920
|
C | T | 24 | a0001c0001t0002g0188a0001c0001t0006g0083a0001c0001t0006g0084others(21): Show | 25 | HG00140.hp1 HG00639.hp1 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.999-1993C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179069920 | ||||||
chr1:179069951
|
T | A | 2 | a0001c0001t0001g0231a0001c0001t0001g0259 | 2 | NA18995.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.999-1962T>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179069951 | ||||||
chr1:179070054
|
A | G | 4 | a0001c0001t0011g0015a0001c0001t0011g0103a0001c0001t0011g0104others(1): Show | 5 | HG01069.hp2 HG01891.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.999-1859A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179070054 | ||||||
chr1:179070084
|
T | C | 29 | a0001c0001t0004g0006a0001c0001t0004g0032a0001c0001t0004g0033others(26): Show | 37 | HG00140.hp2 HG00597.hp2 HG00738.hp2 others(34): Show |
intron_variant | MODIFIER | c.999-1829T>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179070084 | ||||||
chr1:179070109
|
G | A | 1 | a0001c0001t0024g0074 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.999-1804G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179070109 | ||||||
chr1:179070148
|
T | C | 17 | a0001c0001t0004g0006a0001c0001t0004g0034a0001c0001t0004g0035others(14): Show | 22 | HG00597.hp2 HG01106.hp1 HG01433.hp2 others(19): Show |
intron_variant | MODIFIER | c.999-1765T>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179070148 | ||||||
chr1:179070507
|
G | A | 6 | a0001c0001t0009g0044a0001c0001t0009g0222a0001c0001t0009g0223others(3): Show | 7 | HG02572.hp2 HG02615.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.999-1406G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179070507 | ||||||
chr1:179070510
|
C | T | 1 | a0001c0001t0001g0248 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.999-1403C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179070510 | ||||||
chr1:179070515
|
C | CT | 39 | a0001c0001t0001g0011a0001c0001t0001g0245a0001c0001t0001g0249others(36): Show | 51 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.999-1371dupT | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 179070515 | |||||
chr1:179070515
|
CT | C | 76 | a0001c0001t0001g0010a0001c0001t0001g0018a0001c0001t0001g0021others(73): Show | 95 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.999-1371delT | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 179070515 | |||||
chr1:179070515
|
CTT | C | 59 | a0001c0001t0002g0205a0001c0001t0003g0004a0001c0001t0003g0005others(56): Show | 80 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.999-1372_999-1371d others(4): Show |
FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 179070515 | |||||
chr1:179070515
|
CTTT | C | 12 | a0001c0001t0002g0219a0001c0001t0007g0026a0001c0001t0007g0107others(9): Show | 13 | HG00735.hp2 HG01099.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.999-1373_999-1371d others(5): Show |
FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 179070515 | |||||
chr1:179070558
|
T | C | 213 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(210): Show | 278 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.999-1355T>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179070558 | ||||||
chr1:179070738
|
T | G | 1 | a0001c0001t0004g0163 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.999-1175T>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179070738 | ||||||
chr1:179070934
|
G | A | 1 | a0001c0001t0038g0058 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.999-979G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179070934 | ||||||
chr1:179070942
|
T | G | 213 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(210): Show | 278 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.999-971T>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179070942 | ||||||
chr1:179071023
|
A | G | 236 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(233): Show | 308 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(305): Show |
intron_variant | MODIFIER | c.999-890A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179071023 | ||||||
chr1:179071061
|
G | A | 3 | a0001c0001t0001g0243a0001c0001t0001g0244a0001c0001t0001g0264 | 3 | HG01192.hp2 HG02615.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.999-852G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179071061 | ||||||
chr1:179071076
|
C | T | 9 | a0001c0001t0007g0026a0001c0001t0007g0107a0001c0001t0007g0108others(6): Show | 10 | HG01099.hp2 HG02145.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.999-837C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179071076 | ||||||
chr1:179071118
|
A | C | 212 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(209): Show | 277 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.999-795A>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179071118 | ||||||
chr1:179071212
|
C | T | 1 | a0001c0001t0002g0201 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.999-701C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179071212 | ||||||
chr1:179071213
|
G | A | 1 | a0001c0001t0006g0083 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.999-700G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179071213 | ||||||
chr1:179071220
|
C | T | 1 | a0001c0002t0020g0105 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.999-693C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179071220 | ||||||
chr1:179071274
|
C | T | 2 | a0001c0001t0019g0075a0001c0001t0019g0076 | 2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.999-639C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179071274 | ||||||
chr1:179071303
|
A | T | 115 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(112): Show | 151 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.999-610A>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179071303 | ||||||
chr1:179071306
|
T | A | 1 | a0001c0001t0002g0206 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.999-607T>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179071306 | ||||||
chr1:179071405
|
G | A | 22 | a0001c0001t0006g0083a0001c0001t0006g0084a0001c0001t0006g0085others(19): Show | 25 | HG00140.hp1 HG00639.hp1 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.999-508G>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179071405 | ||||||
chr1:179071442
|
A | C | 1 | a0001c0001t0003g0148 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.999-471A>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179071442 | ||||||
chr1:179071511
|
C | T | 211 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(208): Show | 276 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.999-402C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179071511 | ||||||
chr1:179071601
|
A | G | 1 | a0001c0001t0003g0127 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.999-312A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179071601 | ||||||
chr1:179071679
|
C | T | 1 | a0001c0001t0007g0108 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.999-234C>T | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179071679 | ||||||
chr1:179071711
|
T | A | 15 | a0001c0001t0007g0026a0001c0001t0007g0107a0001c0001t0007g0108others(12): Show | 17 | HG01069.hp2 HG01099.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.999-202T>A | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179071711 | ||||||
chr1:179071795
|
T | C | 71 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(68): Show | 103 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.999-118T>C | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179071795 | ||||||
chr1:179071876
|
A | G | 211 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(208): Show | 276 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.999-37A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179071876 | ||||||
chr1:179071896
|
A | G | 6 | a0001c0001t0009g0044a0001c0001t0009g0222a0001c0001t0009g0223others(3): Show | 7 | HG02572.hp2 HG02615.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.999-17A>G | FAM20B | ENSG00000116199.12 | transcript | ENST00000263733.5 | protein_coding | 7/7 | chr1 | 179071896 |