geneid | 10827 |
---|---|
ensemblid | ENSG00000055147.19 |
hgncid | 1333 |
symbol | FAM114A2 |
name | family with sequence similarity 114 member A2 |
refseq_nuc | NM_018691.4 |
refseq_prot | NP_061161.2 |
ensembl_nuc | ENST00000351797.9 |
ensembl_prot | ENSP00000341597.4 |
mane_status | MANE Select |
chr | chr5 |
start | 153990148 |
end | 154038910 |
strand | - |
ver | v1.2 |
region | chr5:153990148-154038910 |
region5000 | chr5:153985148-154043910 |
regionname0 | FAM114A2_chr5_153990148_154038910 |
regionname5000 | FAM114A2_chr5_153985148_154043910 |
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 | 0/0 | 505 | 220 | 51 | 34 | 102 | 5 | 28 | 71 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
a0002 | 1/1 | 505 | 104 | 28 | 24 | 33 | 5 | 12 | 26 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
a0003 | 0/0 | 505 | 8 | 0 | 4 | 0 | 2 | 2 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
a0004 | 0/0 | 505 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
a0005 | 0/0 | 505 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
a0006 | 0/0 | 505 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
a0007 | 0/0 | 505 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
a0008 | 0/0 | 505 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
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 | 0/0 | 1518 | 215 | 49 | 34 | 99 | 5 | 28 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
c0002 | 1/1 | 1518 | 75 | 15 | 17 | 29 | 1 | 11 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
c0003 | 0/0 | 1518 | 29 | 13 | 7 | 4 | 4 | 1 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
c0004 | 0/0 | 1518 | 8 | 0 | 4 | 0 | 2 | 2 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
c0005 | 0/0 | 1518 | 7 | 7 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
c0006 | 0/0 | 1518 | 2 | 0 | 0 | 2 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
c0007 | 0/0 | 1518 | 2 | 2 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
c0008 | 0/0 | 1518 | 2 | 2 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
c0009 | 0/0 | 1518 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
c0010 | 0/0 | 1518 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
c0011 | 0/0 | 1518 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
c0012 | 0/0 | 1518 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
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 | 0/0 | 2895 | 91 | 14 | 13 | 57 | 2 | 5 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
t0002 | 0/0 | 2896 | 45 | 8 | 14 | 12 | 2 | 9 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
t0003 | 0/0 | 2897 | 32 | 0 | 3 | 26 | 0 | 3 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
t0004 | 0/0 | 2897 | 24 | 14 | 5 | 3 | 2 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
t0005 | 0/0 | 2896 | 22 | 7 | 6 | 2 | 2 | 5 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
t0006 | 0/0 | 2896 | 21 | 0 | 0 | 21 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
t0007 | 0/0 | 2897 | 13 | 5 | 3 | 0 | 0 | 5 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
t0008 | 1/1 | 2897 | 10 | 1 | 7 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
t0009 | 0/0 | 2900 | 7 | 7 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
t0010 | 0/0 | 2896 | 7 | 3 | 1 | 0 | 1 | 2 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
t0011 | 0/0 | 2900 | 7 | 6 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
t0012 | 0/0 | 2900 | 6 | 2 | 1 | 0 | 0 | 3 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
t0013 | 0/0 | 2897 | 6 | 5 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
t0014 | 0/0 | 2896 | 6 | 2 | 0 | 0 | 0 | 4 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
t0015 | 0/0 | 2894 | 6 | 1 | 0 | 5 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
t0016 | 0/0 | 2897 | 4 | 0 | 1 | 0 | 2 | 1 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
t0017 | 0/0 | 2897 | 4 | 0 | 2 | 0 | 0 | 2 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
t0018 | 0/0 | 2894 | 4 | 4 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
t0019 | 0/0 | 2898 | 2 | 1 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
t0020 | 0/0 | 2894 | 2 | 2 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
t0021 | 0/0 | 2897 | 2 | 2 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
t0022 | 0/0 | 2897 | 2 | 0 | 0 | 2 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
t0023 | 0/0 | 2897 | 2 | 1 | 0 | 0 | 1 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
t0024 | 0/0 | 2895 | 2 | 0 | 0 | 0 | 0 | 2 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
t0025 | 0/0 | 2895 | 2 | 2 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
t0026 | 0/0 | 2896 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
t0027 | 0/0 | 2898 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
t0028 | 0/0 | 2896 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
t0029 | 0/0 | 2896 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
t0030 | 0/0 | 2899 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
t0031 | 0/0 | 2898 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
t0032 | 0/0 | 2896 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
t0033 | 0/0 | 2896 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
t0034 | 0/0 | 2895 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
t0035 | 0/0 | 2896 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
t0036 | 0/0 | 2895 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
t0037 | 0/0 | 2898 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
t0038 | 0/0 | 2895 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
t0039 | 0/0 | 2897 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
t0040 | 0/0 | 2895 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
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 | 10 | 0 | 4 | 4 | 0 | 2 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0002 | 0/0 | 9 | 1 | 1 | 7 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0003 | 0/0 | 8 | 2 | 2 | 0 | 0 | 4 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0004 | 0/0 | 7 | 0 | 3 | 4 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0005 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0006 | 0/0 | 6 | 2 | 1 | 3 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0007 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0008 | 1/1 | 5 | 0 | 3 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0009 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0013 | 0/0 | 4 | 0 | 1 | 0 | 1 | 2 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0014 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0015 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0016 | 0/0 | 3 | 1 | 0 | 0 | 2 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0018 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0025 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0027 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0032 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0033 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0034 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0036 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0037 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
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 | 0/0 | 1518 | 215 | 49 | 34 | 99 | 5 | 28 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
a0001c0006 | 0/0 | 1518 | 2 | 0 | 0 | 2 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
a0001c0007 | 0/0 | 1518 | 2 | 2 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
a0001c0009 | 0/0 | 1518 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
a0002c0002 | 1/1 | 1518 | 75 | 15 | 17 | 29 | 1 | 11 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
a0002c0003 | 0/0 | 1518 | 29 | 13 | 7 | 4 | 4 | 1 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
a0003c0004 | 0/0 | 1518 | 8 | 0 | 4 | 0 | 2 | 2 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
a0004c0005 | 0/0 | 1518 | 7 | 7 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
a0005c0008 | 0/0 | 1518 | 2 | 2 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
a0006c0011 | 0/0 | 1518 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
a0007c0010 | 0/0 | 1518 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
a0008c0012 | 0/0 | 1518 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 4412 | 87 | 13 | 13 | 55 | 1 | 5 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
a0001c0001t0002 | 0/0 | 4413 | 40 | 8 | 10 | 12 | 2 | 8 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
a0001c0001t0005 | 0/0 | 4413 | 22 | 7 | 6 | 2 | 2 | 5 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
a0001c0001t0006 | 0/0 | 4413 | 19 | 0 | 0 | 19 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
a0001c0001t0011 | 0/0 | 4417 | 7 | 6 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
a0001c0001t0012 | 0/0 | 4417 | 6 | 2 | 1 | 0 | 0 | 3 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
a0001c0001t0014 | 0/0 | 4413 | 4 | 0 | 0 | 0 | 0 | 4 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
a0001c0001t0015 | 0/0 | 4411 | 6 | 1 | 0 | 5 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
a0001c0001t0017 | 0/0 | 4414 | 3 | 0 | 2 | 0 | 0 | 1 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
a0001c0001t0018 | 0/0 | 4411 | 4 | 4 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
a0001c0001t0020 | 0/0 | 4411 | 2 | 2 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
a0001c0001t0022 | 0/0 | 4414 | 2 | 0 | 0 | 2 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
a0001c0001t0023 | 0/0 | 4414 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
a0001c0001t0024 | 0/0 | 4412 | 2 | 0 | 0 | 0 | 0 | 2 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
a0001c0001t0025 | 0/0 | 4412 | 2 | 2 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
a0001c0001t0026 | 0/0 | 4413 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
a0001c0001t0034 | 0/0 | 4412 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
a0001c0001t0035 | 0/0 | 4413 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
a0001c0001t0036 | 0/0 | 4412 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
a0001c0001t0037 | 0/0 | 4415 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
a0001c0001t0038 | 0/0 | 4412 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
a0001c0001t0039 | 0/0 | 4414 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
a0001c0001t0040 | 0/0 | 4412 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
a0001c0006t0006 | 0/0 | 4413 | 2 | 0 | 0 | 2 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
a0001c0007t0014 | 0/0 | 4413 | 2 | 2 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
a0001c0009t0001 | 0/0 | 4412 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
a0002c0002t0003 | 0/0 | 4414 | 32 | 0 | 3 | 26 | 0 | 3 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
a0002c0002t0004 | 0/0 | 4414 | 7 | 6 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
a0002c0002t0007 | 0/0 | 4414 | 13 | 5 | 3 | 0 | 0 | 5 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
a0002c0002t0008 | 1/1 | 4414 | 10 | 1 | 7 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
a0002c0002t0010 | 0/0 | 4413 | 7 | 3 | 1 | 0 | 1 | 2 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
a0002c0002t0027 | 0/0 | 4415 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
a0002c0002t0028 | 0/0 | 4413 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
a0002c0002t0029 | 0/0 | 4413 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
a0002c0002t0030 | 0/0 | 4416 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
a0002c0002t0031 | 0/0 | 4415 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
a0002c0002t0033 | 0/0 | 4413 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
a0002c0003t0004 | 0/0 | 4414 | 16 | 7 | 4 | 3 | 2 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
a0002c0003t0013 | 0/0 | 4414 | 6 | 5 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
a0002c0003t0016 | 0/0 | 4414 | 4 | 0 | 1 | 0 | 2 | 1 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
a0002c0003t0019 | 0/0 | 4415 | 2 | 1 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
a0002c0003t0032 | 0/0 | 4413 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
a0003c0004t0001 | 0/0 | 4412 | 1 | 0 | 0 | 0 | 1 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
a0003c0004t0002 | 0/0 | 4413 | 5 | 0 | 4 | 0 | 0 | 1 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
a0003c0004t0017 | 0/0 | 4414 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
a0003c0004t0023 | 0/0 | 4414 | 1 | 0 | 0 | 0 | 1 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
a0004c0005t0009 | 0/0 | 4417 | 7 | 7 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
a0005c0008t0021 | 0/0 | 4414 | 2 | 2 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
a0006c0011t0004 | 0/0 | 4414 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
a0007c0010t0001 | 0/0 | 4412 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
a0008c0012t0001 | 0/0 | 4412 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | copy fasta | chr5 | 153985148 | 154043910 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 10 | 0 | 4 | 4 | 0 | 2 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0001g0002 | 0/0 | 9 | 1 | 1 | 7 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0001g0006 | 0/0 | 6 | 2 | 1 | 3 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0001g0014 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0001g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0001g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0002g0005 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0002g0015 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0002g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0002g0033 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0002g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0002g0037 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0002g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0005g0013 | 0/0 | 4 | 0 | 1 | 0 | 1 | 2 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0005g0034 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0005g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0005g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0005g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0005g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0005g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0005g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0005g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0005g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0005g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0005g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0005g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0005g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0005g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0005g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0005g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0005g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0006g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0006g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0006g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0006g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0006g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0006g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0006g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0006g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0006g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0006g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0006g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0006g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0006g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0006g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0011g0009 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0011g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0011g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0012g0027 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0012g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0012g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0012g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0012g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0014g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0014g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0014g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0014g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0015g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0015g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0015g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0015g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0015g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0015g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0017g0032 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0017g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0018g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0018g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0018g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0020g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0020g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0022g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0022g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0023g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0024g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0024g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0025g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0025g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0026g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0034g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0035g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0036g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0037g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0038g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0039g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0001t0040g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0006t0006g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0006t0006g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0007t0014g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0001c0009t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0002t0003g0004 | 0/0 | 7 | 0 | 3 | 4 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0002t0003g0007 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0002t0003g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0002t0003g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0002t0003g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0002t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0002t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0002t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0002t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0002t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0002t0003g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0002t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0002t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0002t0003g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0002t0003g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0002t0004g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0002t0004g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0002t0004g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0002t0004g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0002t0004g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0002t0004g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0002t0004g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0002t0007g0003 | 0/0 | 8 | 2 | 2 | 0 | 0 | 4 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0002t0007g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0002t0007g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0002t0007g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0002t0007g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0002t0007g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0002t0008g0008 | 1/1 | 5 | 0 | 3 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0002t0008g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0002t0008g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0002t0008g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0002t0008g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0002t0010g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0002t0010g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0002t0010g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0002t0010g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0002t0010g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0002t0010g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0002t0010g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0002t0027g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0002t0028g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0002t0029g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0002t0030g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0002t0031g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0002t0033g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0003t0004g0016 | 0/0 | 3 | 1 | 0 | 0 | 2 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0003t0004g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0003t0004g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0003t0004g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0003t0004g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0003t0004g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0003t0004g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0003t0004g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0003t0004g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0003t0004g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0003t0004g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0003t0004g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0003t0013g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0003t0013g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0003t0013g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0003t0013g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0003t0013g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0003t0016g0025 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0003t0016g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0003t0016g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0003t0019g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0003t0019g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0002c0003t0032g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0003c0004t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0003c0004t0002g0018 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0003c0004t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0003c0004t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0003c0004t0017g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0003c0004t0023g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0004c0005t0009g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0004c0005t0009g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0004c0005t0009g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0004c0005t0009g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0004c0005t0009g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0004c0005t0009g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0004c0005t0009g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0005c0008t0021g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0005c0008t0021g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0006c0011t0004g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0007c0010t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
a0008c0012t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0005 | g0013 | EUR | GBR | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG00099 | hp2 | a0003 | c0004 | t0023 | g0166 | EUR | GBR | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG00140 | hp1 | a0001 | c0001 | t0005 | g0034 | EUR | GBR | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG00140 | hp2 | a0002 | c0002 | t0010 | g0090 | EUR | GBR | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0155 | EUR | FIN | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG00323 | hp2 | a0003 | c0004 | t0001 | g0162 | EUR | FIN | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | CHS | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | CHS | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | CHS | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | CHS | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG00438 | hp1 | a0001 | c0001 | t0022 | g0133 | EAS | CHS | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG00438 | hp2 | a0001 | c0001 | t0006 | g0120 | EAS | CHS | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | CHS | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG00597 | hp1 | a0001 | c0001 | t0015 | g0188 | EAS | CHS | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG00597 | hp2 | a0001 | c0001 | t0015 | g0227 | EAS | CHS | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | CHS | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | CHS | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | CHS | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG00621 | hp2 | a0001 | c0009 | t0001 | g0189 | EAS | CHS | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG00639 | hp1 | a0002 | c0002 | t0033 | g0096 | AMR | PUR | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG00639 | hp2 | a0001 | c0001 | t0017 | g0032 | AMR | PUR | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG00735 | hp1 | a0002 | c0002 | t0004 | g0057 | AMR | PUR | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG00738 | hp1 | a0001 | c0001 | t0039 | g0209 | AMR | PUR | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG00738 | hp2 | a0002 | c0002 | t0008 | g0060 | AMR | PUR | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01069 | hp1 | a0002 | c0002 | t0008 | g0008 | AMR | PUR | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01069 | hp2 | a0002 | c0003 | t0004 | g0024 | AMR | PUR | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01070 | hp1 | a0002 | c0002 | t0008 | g0022 | AMR | PUR | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | PUR | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01071 | hp1 | a0002 | c0003 | t0004 | g0024 | AMR | PUR | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01071 | hp2 | a0002 | c0002 | t0008 | g0008 | AMR | PUR | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01074 | hp1 | a0003 | c0004 | t0002 | g0018 | AMR | PUR | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01081 | hp1 | a0003 | c0004 | t0002 | g0018 | AMR | PUR | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01081 | hp2 | a0002 | c0002 | t0031 | g0068 | AMR | PUR | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01099 | hp1 | a0001 | c0001 | t0017 | g0146 | AMR | PUR | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01099 | hp2 | a0001 | c0001 | t0002 | g0167 | AMR | PUR | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01106 | hp1 | a0002 | c0002 | t0007 | g0003 | AMR | PUR | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01167 | hp2 | a0002 | c0003 | t0032 | g0097 | AMR | PUR | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01168 | hp1 | a0001 | c0001 | t0005 | g0013 | AMR | PUR | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01168 | hp2 | a0002 | c0002 | t0008 | g0022 | AMR | PUR | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01169 | hp1 | a0002 | c0003 | t0013 | g0098 | AMR | PUR | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01169 | hp2 | a0002 | c0002 | t0008 | g0008 | AMR | PUR | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01192 | hp1 | a0001 | c0001 | t0012 | g0103 | AMR | PUR | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01255 | hp1 | a0002 | c0002 | t0010 | g0089 | AMR | CLM | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0015 | AMR | CLM | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01256 | hp1 | a0002 | c0003 | t0016 | g0082 | AMR | CLM | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01256 | hp2 | a0001 | c0001 | t0002 | g0015 | AMR | CLM | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01257 | hp1 | a0001 | c0001 | t0005 | g0149 | AMR | CLM | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01257 | hp2 | a0002 | c0002 | t0003 | g0004 | AMR | CLM | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01258 | hp1 | a0001 | c0001 | t0005 | g0181 | AMR | CLM | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0015 | AMR | CLM | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | CLM | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01261 | hp2 | a0002 | c0002 | t0007 | g0003 | AMR | CLM | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01358 | hp1 | a0002 | c0002 | t0007 | g0100 | AMR | CLM | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | CLM | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01361 | hp1 | a0002 | c0003 | t0004 | g0026 | AMR | CLM | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01361 | hp2 | a0001 | c0001 | t0005 | g0034 | AMR | CLM | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01433 | hp1 | a0002 | c0003 | t0004 | g0026 | AMR | CLM | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | CLM | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01515 | hp1 | a0001 | c0001 | t0002 | g0164 | EUR | IBS | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01515 | hp2 | a0002 | c0003 | t0016 | g0025 | EUR | IBS | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01516 | hp1 | a0001 | c0001 | t0002 | g0234 | EUR | IBS | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01516 | hp2 | a0002 | c0003 | t0004 | g0016 | EUR | IBS | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01517 | hp1 | a0002 | c0003 | t0004 | g0016 | EUR | IBS | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01517 | hp2 | a0002 | c0003 | t0016 | g0025 | EUR | IBS | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01884 | hp1 | a0001 | c0001 | t0005 | g0232 | AFR | ACB | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01884 | hp2 | a0001 | c0001 | t0011 | g0243 | AFR | ACB | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01891 | hp1 | a0001 | c0001 | t0002 | g0238 | AFR | ACB | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01891 | hp2 | a0001 | c0001 | t0012 | g0102 | AFR | ACB | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01928 | hp1 | a0001 | c0001 | t0005 | g0147 | AMR | PEL | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01928 | hp2 | a0002 | c0002 | t0003 | g0004 | AMR | PEL | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01934 | hp1 | a0001 | c0001 | t0005 | g0176 | AMR | PEL | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01934 | hp2 | a0003 | c0004 | t0002 | g0195 | AMR | PEL | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0199 | AMR | PEL | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PEL | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01975 | hp2 | a0001 | c0001 | t0002 | g0168 | AMR | PEL | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0037 | AMR | PEL | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01981 | hp2 | a0001 | c0001 | t0011 | g0009 | AMR | PEL | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02015 | hp1 | a0001 | c0001 | t0005 | g0158 | EAS | KHV | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02015 | hp2 | a0002 | c0002 | t0003 | g0007 | EAS | KHV | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02027 | hp1 | a0002 | c0003 | t0004 | g0080 | EAS | KHV | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | KHV | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02040 | hp2 | a0001 | c0001 | t0034 | g0240 | EAS | KHV | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02055 | hp1 | a0002 | c0003 | t0004 | g0073 | AFR | ACB | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02055 | hp2 | a0001 | c0001 | t0002 | g0194 | AFR | ACB | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02071 | hp1 | a0001 | c0001 | t0006 | g0114 | EAS | KHV | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | KHV | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02074 | hp1 | a0002 | c0002 | t0003 | g0004 | EAS | KHV | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | KHV | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | KHV | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02083 | hp2 | a0002 | c0002 | t0003 | g0050 | EAS | KHV | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | KHV | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02132 | hp2 | a0001 | c0006 | t0006 | g0116 | EAS | KHV | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | KHV | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02135 | hp2 | a0002 | c0002 | t0003 | g0046 | EAS | KHV | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02145 | hp1 | a0001 | c0001 | t0037 | g0148 | AFR | ACB | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02145 | hp2 | a0005 | c0008 | t0021 | g0134 | AFR | ACB | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0225 | AMR | PEL | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02148 | hp2 | a0001 | c0001 | t0002 | g0198 | AMR | PEL | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02155 | hp1 | a0001 | c0001 | t0006 | g0012 | EAS | CDX | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | CDX | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | CDX | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02165 | hp2 | a0002 | c0002 | t0003 | g0021 | EAS | CDX | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02257 | hp1 | a0002 | c0003 | t0004 | g0079 | AFR | ACB | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | ACB | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02258 | hp1 | a0002 | c0003 | t0013 | g0072 | AFR | ACB | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02258 | hp2 | a0001 | c0001 | t0020 | g0125 | AFR | ACB | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02280 | hp1 | a0002 | c0003 | t0004 | g0016 | AFR | ACB | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02280 | hp2 | a0004 | c0005 | t0009 | g0106 | AFR | ACB | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02293 | hp1 | a0001 | c0001 | t0002 | g0015 | AMR | PEL | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02293 | hp2 | a0002 | c0002 | t0008 | g0062 | AMR | PEL | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02300 | hp2 | a0002 | c0002 | t0003 | g0004 | AMR | PEL | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | GWD | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02572 | hp2 | a0002 | c0003 | t0013 | g0023 | AFR | GWD | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0235 | SAS | PJL | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02602 | hp2 | a0002 | c0002 | t0007 | g0003 | SAS | PJL | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02615 | hp1 | a0001 | c0001 | t0018 | g0030 | AFR | GWD | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02615 | hp2 | a0002 | c0002 | t0004 | g0085 | AFR | GWD | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02622 | hp1 | a0002 | c0002 | t0010 | g0088 | AFR | GWD | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02622 | hp2 | a0007 | c0010 | t0001 | g0186 | AFR | GWD | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02630 | hp1 | a0004 | c0005 | t0009 | g0105 | AFR | GWD | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02647 | hp1 | a0001 | c0001 | t0002 | g0192 | AFR | GWD | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02647 | hp2 | a0001 | c0001 | t0035 | g0193 | AFR | GWD | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02683 | hp1 | a0001 | c0001 | t0014 | g0191 | SAS | PJL | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02683 | hp2 | a0001 | c0001 | t0012 | g0104 | SAS | PJL | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02698 | hp1 | a0001 | c0001 | t0012 | g0027 | SAS | PJL | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02698 | hp2 | a0001 | c0001 | t0005 | g0013 | SAS | PJL | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02717 | hp1 | a0002 | c0002 | t0007 | g0066 | AFR | GWD | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02717 | hp2 | a0001 | c0001 | t0011 | g0009 | AFR | GWD | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02723 | hp1 | a0002 | c0003 | t0004 | g0084 | AFR | GWD | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | GWD | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0033 | SAS | PJL | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0037 | SAS | PJL | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02738 | hp1 | a0001 | c0001 | t0005 | g0178 | SAS | PJL | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02738 | hp2 | a0002 | c0002 | t0007 | g0070 | SAS | PJL | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02809 | hp1 | a0001 | c0001 | t0011 | g0009 | AFR | GWD | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02809 | hp2 | a0001 | c0001 | t0018 | g0127 | AFR | GWD | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02818 | hp2 | a0002 | c0002 | t0004 | g0059 | AFR | GWD | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02886 | hp1 | a0001 | c0001 | t0020 | g0126 | AFR | GWD | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02886 | hp2 | a0005 | c0008 | t0021 | g0172 | AFR | GWD | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02895 | hp1 | a0001 | c0007 | t0014 | g0040 | AFR | GWD | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02895 | hp2 | a0002 | c0002 | t0004 | g0092 | AFR | GWD | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02896 | hp1 | a0001 | c0001 | t0018 | g0128 | AFR | GWD | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02896 | hp2 | a0002 | c0002 | t0010 | g0086 | AFR | GWD | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02897 | hp1 | a0002 | c0002 | t0010 | g0087 | AFR | GWD | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02897 | hp2 | a0001 | c0007 | t0014 | g0040 | AFR | GWD | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02922 | hp2 | a0004 | c0005 | t0009 | g0108 | AFR | ESN | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | ESN | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02970 | hp1 | a0001 | c0001 | t0011 | g0244 | AFR | ESN | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02976 | hp1 | a0002 | c0003 | t0019 | g0074 | AFR | ESN | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02976 | hp2 | a0001 | c0001 | t0005 | g0139 | AFR | ESN | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | GWD | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG03041 | hp2 | a0001 | c0001 | t0023 | g0131 | AFR | GWD | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG03098 | hp1 | a0004 | c0005 | t0009 | g0043 | AFR | MSL | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG03098 | hp2 | a0002 | c0003 | t0013 | g0077 | AFR | MSL | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG03130 | hp1 | a0002 | c0002 | t0007 | g0003 | AFR | ESN | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG03130 | hp2 | a0002 | c0002 | t0004 | g0091 | AFR | ESN | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG03139 | hp1 | a0001 | c0001 | t0011 | g0009 | AFR | ESN | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG03139 | hp2 | a0001 | c0001 | t0002 | g0242 | AFR | ESN | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG03195 | hp2 | a0001 | c0001 | t0011 | g0009 | AFR | ESN | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG03225 | hp1 | a0001 | c0001 | t0025 | g0129 | AFR | MSL | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG03225 | hp2 | a0002 | c0003 | t0013 | g0023 | AFR | MSL | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG03239 | hp1 | a0002 | c0002 | t0007 | g0003 | SAS | PJL | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG03239 | hp2 | a0003 | c0004 | t0002 | g0018 | SAS | PJL | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG03453 | hp1 | a0002 | c0003 | t0013 | g0076 | AFR | MSL | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG03453 | hp2 | a0001 | c0001 | t0012 | g0101 | AFR | MSL | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG03486 | hp1 | a0002 | c0003 | t0004 | g0081 | AFR | MSL | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG03486 | hp2 | a0006 | c0011 | t0004 | g0099 | AFR | MSL | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG03490 | hp1 | a0002 | c0002 | t0010 | g0095 | SAS | PJL | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG03490 | hp2 | a0002 | c0002 | t0007 | g0003 | SAS | PJL | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0237 | SAS | PJL | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG03491 | hp2 | a0001 | c0001 | t0024 | g0204 | SAS | PJL | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0236 | SAS | PJL | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG03492 | hp2 | a0002 | c0002 | t0007 | g0003 | SAS | PJL | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG03516 | hp1 | a0002 | c0002 | t0007 | g0003 | AFR | ESN | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG03516 | hp2 | a0002 | c0003 | t0004 | g0071 | AFR | ESN | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG03540 | hp1 | a0001 | c0001 | t0005 | g0174 | AFR | GWD | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG03540 | hp2 | a0002 | c0002 | t0007 | g0065 | AFR | GWD | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG03579 | hp1 | a0002 | c0003 | t0004 | g0078 | AFR | MSL | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | MSL | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG03654 | hp1 | a0003 | c0004 | t0017 | g0165 | SAS | PJL | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG03654 | hp2 | a0001 | c0001 | t0005 | g0179 | SAS | PJL | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG03688 | hp1 | a0002 | c0002 | t0030 | g0069 | SAS | STU | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG03688 | hp2 | a0001 | c0001 | t0005 | g0213 | SAS | STU | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG03704 | hp1 | a0001 | c0001 | t0014 | g0136 | SAS | PJL | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG03704 | hp2 | a0001 | c0001 | t0024 | g0222 | SAS | PJL | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG03710 | hp1 | a0001 | c0001 | t0005 | g0013 | SAS | PJL | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG03710 | hp2 | a0001 | c0001 | t0014 | g0137 | SAS | PJL | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG03831 | hp1 | a0002 | c0003 | t0016 | g0083 | SAS | BEB | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG03831 | hp2 | a0002 | c0002 | t0003 | g0056 | SAS | BEB | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG03834 | hp1 | a0002 | c0002 | t0003 | g0055 | SAS | BEB | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0132 | SAS | BEB | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0200 | SAS | BEB | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG03942 | hp2 | a0001 | c0001 | t0014 | g0171 | SAS | BEB | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG04184 | hp2 | a0001 | c0001 | t0012 | g0027 | SAS | BEB | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG04199 | hp1 | a0002 | c0002 | t0010 | g0093 | SAS | STU | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0229 | SAS | STU | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0130 | SAS | STU | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG04228 | hp1 | a0002 | c0002 | t0003 | g0051 | SAS | STU | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0031 | SAS | STU | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18522 | hp1 | a0001 | c0001 | t0005 | g0138 | AFR | YRI | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18522 | hp2 | a0001 | c0001 | t0002 | g0163 | AFR | YRI | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0226 | EAS | CHB | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18747 | hp2 | a0002 | c0003 | t0004 | g0075 | EAS | CHB | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18906 | hp1 | a0001 | c0001 | t0015 | g0157 | AFR | YRI | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18906 | hp2 | a0001 | c0001 | t0002 | g0170 | AFR | YRI | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18939 | hp1 | a0002 | c0002 | t0028 | g0048 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18939 | hp2 | a0001 | c0001 | t0015 | g0156 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18941 | hp2 | a0002 | c0002 | t0003 | g0053 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18942 | hp1 | a0002 | c0002 | t0003 | g0011 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18942 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18946 | hp2 | a0002 | c0002 | t0003 | g0010 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18947 | hp1 | a0002 | c0002 | t0003 | g0047 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18947 | hp2 | a0001 | c0001 | t0005 | g0151 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18950 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18950 | hp2 | a0008 | c0012 | t0001 | g0233 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18952 | hp1 | a0001 | c0001 | t0006 | g0029 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18952 | hp2 | a0002 | c0002 | t0003 | g0007 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18953 | hp1 | a0002 | c0002 | t0003 | g0004 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18953 | hp2 | a0001 | c0001 | t0006 | g0124 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18954 | hp1 | a0001 | c0001 | t0006 | g0028 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18954 | hp2 | a0002 | c0002 | t0003 | g0011 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18961 | hp1 | a0002 | c0002 | t0003 | g0007 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18963 | hp1 | a0001 | c0001 | t0006 | g0012 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18963 | hp2 | a0001 | c0001 | t0015 | g0152 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18965 | hp1 | a0002 | c0003 | t0019 | g0063 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18965 | hp2 | a0001 | c0001 | t0022 | g0135 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18966 | hp1 | a0001 | c0001 | t0006 | g0121 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18966 | hp2 | a0002 | c0003 | t0004 | g0064 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18967 | hp1 | a0001 | c0001 | t0006 | g0115 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18968 | hp1 | a0002 | c0002 | t0003 | g0011 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18968 | hp2 | a0001 | c0001 | t0006 | g0111 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18969 | hp2 | a0002 | c0002 | t0029 | g0045 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18970 | hp2 | a0001 | c0001 | t0006 | g0122 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18971 | hp2 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18972 | hp1 | a0001 | c0001 | t0006 | g0012 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18973 | hp2 | a0001 | c0001 | t0006 | g0112 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18974 | hp2 | a0001 | c0001 | t0036 | g0144 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18975 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18975 | hp2 | a0002 | c0002 | t0003 | g0004 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18977 | hp1 | a0001 | c0001 | t0006 | g0118 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18978 | hp1 | a0001 | c0006 | t0006 | g0119 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18980 | hp1 | a0001 | c0001 | t0015 | g0239 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18982 | hp1 | a0002 | c0002 | t0003 | g0010 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18983 | hp2 | a0001 | c0001 | t0006 | g0028 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18984 | hp2 | a0001 | c0001 | t0038 | g0216 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18987 | hp2 | a0002 | c0002 | t0003 | g0010 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA18995 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA19000 | hp2 | a0001 | c0001 | t0006 | g0012 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA19001 | hp1 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA19005 | hp2 | a0002 | c0002 | t0003 | g0044 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA19007 | hp1 | a0002 | c0002 | t0003 | g0049 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA19011 | hp1 | a0002 | c0002 | t0003 | g0007 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA19030 | hp1 | a0002 | c0002 | t0004 | g0094 | AFR | LWK | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA19030 | hp2 | a0001 | c0001 | t0002 | g0143 | AFR | LWK | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA19043 | hp1 | a0001 | c0001 | t0026 | g0041 | AFR | LWK | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA19043 | hp2 | a0001 | c0001 | t0018 | g0030 | AFR | LWK | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA19057 | hp1 | a0002 | c0002 | t0003 | g0011 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA19057 | hp2 | a0001 | c0001 | t0040 | g0117 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA19058 | hp2 | a0002 | c0002 | t0003 | g0007 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA19070 | hp1 | a0002 | c0002 | t0003 | g0021 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA19078 | hp2 | a0002 | c0002 | t0003 | g0054 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA19079 | hp2 | a0002 | c0002 | t0027 | g0052 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA19080 | hp1 | a0002 | c0002 | t0003 | g0010 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA19081 | hp2 | a0001 | c0001 | t0006 | g0029 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA19083 | hp1 | a0002 | c0002 | t0003 | g0004 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA19084 | hp2 | a0001 | c0001 | t0006 | g0113 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA19085 | hp1 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA19090 | hp1 | a0001 | c0001 | t0006 | g0123 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA20129 | hp1 | a0001 | c0001 | t0005 | g0140 | AFR | ASW | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA20129 | hp2 | a0004 | c0005 | t0009 | g0042 | AFR | ASW | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0031 | SAS | GIH | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA20905 | hp2 | a0001 | c0001 | t0017 | g0032 | SAS | GIH | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01123 | hp1 | a0003 | c0004 | t0002 | g0196 | AMR | CLM | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | CLM | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02109 | hp1 | a0001 | c0001 | t0005 | g0142 | AFR | ACB | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02109 | hp2 | a0004 | c0005 | t0009 | g0109 | AFR | ACB | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02486 | hp1 | a0001 | c0001 | t0025 | g0202 | AFR | ACB | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02486 | hp2 | a0002 | c0002 | t0007 | g0067 | AFR | ACB | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02559 | hp1 | a0002 | c0002 | t0008 | g0061 | AFR | ACB | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG02559 | hp2 | a0002 | c0002 | t0004 | g0058 | AFR | ACB | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG03471 | hp1 | a0001 | c0001 | t0002 | g0033 | AFR | MSL | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
HG03471 | hp2 | a0004 | c0005 | t0009 | g0107 | AFR | MSL | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA20300 | hp1 | a0001 | c0001 | t0005 | g0201 | AFR | USA | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | USA | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0008 | g0008 | REF | REF | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
homoSapiens_grch38 | hp1 | a0002 | c0002 | t0008 | g0008 | REF | REF | FAM114A2_chr5_153985148_154043910 | FAM114A2 | chr5 | 153985148 | 154043910 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:153993004
|
T | C | 1 | a0004 | 7 | HG02109.hp2 HG02280.hp2 HG02630.hp1 others(4): Show |
missense_variant | MODERATE | c.1490A>G | p.Gln497Arg | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 14/14 | 1558/4414 | 1490/1518 | 497/505 | chr5 | 153993004 | ||
chr5:153993010
|
T | G | 1 | a0006 | 1 | HG03486.hp2 | missense_variant | MODERATE | c.1484A>C | p.Glu495Ala | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 14/14 | 1552/4414 | 1484/1518 | 495/505 | chr5 | 153993010 | ||
chr5:154002251
|
T | C | 1 | a0007 | 1 | HG02622.hp2 | missense_variant&splice_region_variant | MODERATE | c.1256A>G | p.Gln419Arg | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 11/14 | 1324/4414 | 1256/1518 | 419/505 | chr5 | 154002251 | ||
chr5:154002288
|
C | T | 1 | a0003 | 8 | HG00099.hp2 HG00323.hp2 HG01074.hp1 others(5): Show |
missense_variant | MODERATE | c.1219G>A | p.Glu407Lys | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 11/14 | 1287/4414 | 1219/1518 | 407/505 | chr5 | 154002288 | ||
chr5:154027304
|
T | C | 1 | a0005 | 2 | HG02145.hp2 HG02886.hp2 |
missense_variant | MODERATE | c.661A>G | p.Ile221Val | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 7/14 | 729/4414 | 661/1518 | 221/505 | chr5 | 154027304 | ||
chr5:154033830
|
C | T | 6 | a0001a0003a0004others(3): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
missense_variant | MODERATE | c.364G>A | p.Gly122Ser | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 4/14 | 432/4414 | 364/1518 | 122/505 | chr5 | 154033830 | ||
chr5:154034373
|
T | C | 1 | a0008 | 1 | NA18950.hp2 | missense_variant | MODERATE | c.215A>G | p.Asn72Ser | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 3/14 | 283/4414 | 215/1518 | 72/505 | chr5 | 154034373 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:153993012
|
A | G | 1 | a0001c0009 | 1 | HG00621.hp2 | synonymous_variant | LOW | c.1482T>C | p.His494His | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 14/14 | 1550/4414 | 1482/1518 | 494/505 | chr5 | 153993012 | ||
chr5:154002313
|
T | A | 1 | a0001c0006 | 2 | HG02132.hp2 NA18978.hp1 |
synonymous_variant | LOW | c.1194A>T | p.Ala398Ala | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 11/14 | 1262/4414 | 1194/1518 | 398/505 | chr5 | 154002313 | ||
chr5:154002889
|
C | T | 1 | a0008c0012 | 1 | NA18950.hp2 | synonymous_variant | LOW | c.1074G>A | p.Ser358Ser | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 10/14 | 1142/4414 | 1074/1518 | 358/505 | chr5 | 154002889 | ||
chr5:154002958
|
G | A | 1 | a0002c0003 | 29 | HG01069.hp2 HG01071.hp1 HG01167.hp2 others(26): Show |
synonymous_variant | LOW | c.1005C>T | p.Thr335Thr | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 10/14 | 1073/4414 | 1005/1518 | 335/505 | chr5 | 154002958 | ||
chr5:154026403
|
T | C | 1 | a0001c0007 | 2 | HG02895.hp1 HG02897.hp2 |
synonymous_variant | LOW | c.909A>G | p.Lys303Lys | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/14 | 977/4414 | 909/1518 | 303/505 | chr5 | 154026403 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:153990428
|
T | C | 1 | a0001c0001t0038 | 1 | NA18984.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2548A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 14/14 | 2548 | chr5 | 153990428 | |||||
chr5:153990499
|
T | TA | 1 | a0004c0005t0009 | 7 | HG02109.hp2 HG02280.hp2 HG02630.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2476dupT | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 14/14 | 2476 | chr5 | 153990499 | |||||
chr5:153990499
|
TA | T | 12 | a0001c0001t0005a0001c0001t0014a0001c0001t0017others(9): Show | 45 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*2476delT | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 14/14 | 2476 | chr5 | 153990499 | |||||
chr5:153990499
|
TAA | T | 15 | a0001c0001t0001a0001c0001t0002a0001c0001t0015others(12): Show | 150 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(147): Show |
3_prime_UTR_variant | MODIFIER | c.*2475_*2476delTT | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 14/14 | 2475 | chr5 | 153990499 | |||||
chr5:153990739
|
A | G | 1 | a0002c0003t0016 | 4 | HG01256.hp1 HG01515.hp2 HG01517.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2237T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 14/14 | 2237 | chr5 | 153990739 | |||||
chr5:153990753
|
G | T | 1 | a0005c0008t0021 | 2 | HG02145.hp2 HG02886.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2223C>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 14/14 | 2223 | chr5 | 153990753 | |||||
chr5:153990831
|
A | C | 50 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(47): Show | 334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
3_prime_UTR_variant | MODIFIER | c.*2145T>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 14/14 | 2145 | chr5 | 153990831 | |||||
chr5:153990872
|
T | C | 3 | a0001c0001t0011a0001c0001t0012a0004c0005t0009 | 20 | HG01192.hp1 HG01884.hp2 HG01891.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*2104A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 14/14 | 2104 | chr5 | 153990872 | |||||
chr5:153991006
|
T | C | 31 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(28): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
3_prime_UTR_variant | MODIFIER | c.*1970A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 14/14 | 1970 | chr5 | 153991006 | |||||
chr5:153991389
|
C | T | 2 | a0002c0003t0013a0002c0003t0032 | 7 | HG01167.hp2 HG01169.hp1 HG02258.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1587G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 14/14 | 1587 | chr5 | 153991389 | |||||
chr5:153991433
|
T | C | 1 | a0002c0002t0033 | 1 | HG00639.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1543A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 14/14 | 1543 | chr5 | 153991433 | |||||
chr5:153991646
|
G | A | 47 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(44): Show | 319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
3_prime_UTR_variant | MODIFIER | c.*1330C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 14/14 | 1330 | chr5 | 153991646 | |||||
chr5:153991681
|
T | G | 1 | a0001c0001t0024 | 2 | HG03491.hp2 HG03704.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1295A>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 14/14 | 1295 | chr5 | 153991681 | |||||
chr5:153991692
|
A | AT | 9 | a0001c0001t0002a0001c0001t0017a0001c0001t0022others(6): Show | 56 | HG00438.hp1 HG00609.hp1 HG00639.hp2 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*1283dupA | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 14/14 | 1283 | chr5 | 153991692 | |||||
chr5:153991692
|
A | ATT | 5 | a0001c0001t0023a0001c0001t0037a0002c0002t0030others(2): Show | 11 | HG00099.hp2 HG02109.hp2 HG02145.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1282_*1283dupAA | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 14/14 | 1283 | chr5 | 153991692 | |||||
chr5:153991692
|
A | ATTT | 2 | a0001c0001t0011a0001c0001t0012 | 13 | HG01192.hp1 HG01884.hp2 HG01891.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1281_*1283dupAAA | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 14/14 | 1283 | chr5 | 153991692 | |||||
chr5:153991692
|
AT | A | 8 | a0001c0001t0006a0001c0001t0015a0001c0001t0025others(5): Show | 39 | HG00140.hp2 HG00438.hp2 HG00597.hp1 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*1283delA | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 14/14 | 1283 | chr5 | 153991692 | |||||
chr5:153991692
|
ATT | A | 3 | a0001c0001t0018a0001c0001t0020a0001c0001t0040 | 7 | HG02258.hp2 HG02615.hp1 HG02809.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1282_*1283delAA | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 14/14 | 1282 | chr5 | 153991692 | |||||
chr5:153991762
|
A | T | 1 | a0001c0001t0036 | 1 | NA18974.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1214T>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 14/14 | 1214 | chr5 | 153991762 | |||||
chr5:153991828
|
C | T | 1 | a0001c0001t0035 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1148G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 14/14 | 1148 | chr5 | 153991828 | |||||
chr5:153991845
|
C | T | 31 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(28): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
3_prime_UTR_variant | MODIFIER | c.*1131G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 14/14 | 1131 | chr5 | 153991845 | |||||
chr5:153991903
|
C | T | 34 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(31): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
3_prime_UTR_variant | MODIFIER | c.*1073G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 14/14 | 1073 | chr5 | 153991903 | |||||
chr5:153992132
|
C | G | 1 | a0001c0001t0034 | 1 | HG02040.hp2 | 3_prime_UTR_variant | MODIFIER | c.*844G>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 14/14 | 844 | chr5 | 153992132 | |||||
chr5:153992200
|
C | G | 3 | a0001c0001t0014a0001c0001t0022a0001c0007t0014 | 8 | HG00438.hp1 HG02683.hp1 HG02895.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*776G>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 14/14 | 776 | chr5 | 153992200 | |||||
chr5:153992320
|
G | T | 1 | a0005c0008t0021 | 2 | HG02145.hp2 HG02886.hp2 |
3_prime_UTR_variant | MODIFIER | c.*656C>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 14/14 | 656 | chr5 | 153992320 | |||||
chr5:153992529
|
A | T | 4 | a0002c0002t0003a0002c0002t0027a0002c0002t0028others(1): Show | 35 | HG01257.hp2 HG01928.hp2 HG02015.hp2 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*447T>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 14/14 | 447 | chr5 | 153992529 | |||||
chr5:153992616
|
T | C | 3 | a0001c0001t0006a0001c0001t0040a0001c0006t0006 | 22 | HG00438.hp2 HG02071.hp1 HG02132.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*360A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 14/14 | 360 | chr5 | 153992616 | |||||
chr5:153992657
|
C | T | 1 | a0001c0001t0020 | 2 | HG02258.hp2 HG02886.hp1 |
3_prime_UTR_variant | MODIFIER | c.*319G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 14/14 | 319 | chr5 | 153992657 | |||||
chr5:153992965
|
G | A | 31 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(28): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
3_prime_UTR_variant | MODIFIER | c.*11C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 14/14 | 11 | chr5 | 153992965 | |||||
chr5:154038885
|
A | T | 1 | a0001c0001t0026 | 1 | NA19043.hp1 | 5_prime_UTR_variant | MODIFIER | c.-43T>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 1/14 | 3932 | chr5 | 154038885 | |||||
chr5:154038887
|
G | A | 1 | a0001c0001t0011 | 7 | HG01884.hp2 HG01981.hp2 HG02717.hp2 others(4): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-45C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 1/14 | chr5 | 154038887 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:153993183
|
G | A | 174 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(171): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.1384-73C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 13/13 | chr5 | 153993183 | ||||||
chr5:153993187
|
A | T | 1 | a0001c0001t0026g0041 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1384-77T>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 13/13 | chr5 | 153993187 | ||||||
chr5:153993193
|
T | C | 17 | a0001c0001t0006g0012a0001c0001t0006g0028a0001c0001t0006g0029others(14): Show | 22 | HG00438.hp2 HG02071.hp1 HG02132.hp2 others(19): Show |
intron_variant | MODIFIER | c.1384-83A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 13/13 | chr5 | 153993193 | ||||||
chr5:153993202
|
G | A | 1 | a0002c0002t0004g0085 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1384-92C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 13/13 | chr5 | 153993202 | ||||||
chr5:153993317
|
ATGTCAGC others(13): Show |
A | 4 | a0001c0001t0001g0141a0001c0001t0005g0138a0001c0001t0005g0142others(1): Show | 4 | HG02109.hp1 HG02965.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1384-227_1384-208d others(22): Show |
FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 13/13 | chr5 | 153993317 | ||||||
chr5:153993475
|
T | C | 6 | a0004c0005t0009g0042a0004c0005t0009g0043a0004c0005t0009g0105others(3): Show | 6 | HG02109.hp2 HG02630.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1384-365A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 13/13 | chr5 | 153993475 | ||||||
chr5:153993785
|
C | G | 172 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(169): Show | 237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.1384-675G>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 13/13 | chr5 | 153993785 | ||||||
chr5:153993786
|
C | A | 2 | a0005c0008t0021g0134a0005c0008t0021g0172 | 2 | HG02145.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1384-676G>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 13/13 | chr5 | 153993786 | ||||||
chr5:153993786
|
CA | C | 7 | a0001c0001t0011g0009a0001c0001t0011g0243a0001c0001t0011g0244others(4): Show | 12 | HG01192.hp1 HG01884.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.1384-677delT | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 13/13 | chr5 | 153993786 | ||||||
chr5:153993823
|
A | G | 1 | a0001c0001t0012g0101 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1384-713T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 13/13 | chr5 | 153993823 | ||||||
chr5:153994058
|
A | G | 157 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(154): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.1383+861T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 13/13 | chr5 | 153994058 | ||||||
chr5:153994464
|
A | T | 4 | a0002c0002t0004g0085a0002c0002t0010g0086a0002c0002t0010g0087others(1): Show | 4 | HG02615.hp2 HG02622.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1383+455T>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 13/13 | chr5 | 153994464 | ||||||
chr5:153994538
|
T | C | 15 | a0001c0001t0011g0009a0001c0001t0011g0243a0001c0001t0011g0244others(12): Show | 20 | HG01192.hp1 HG01884.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.1383+381A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 13/13 | chr5 | 153994538 | ||||||
chr5:153994810
|
T | C | 2 | a0001c0001t0005g0201a0001c0001t0025g0202 | 2 | HG02486.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1383+109A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 13/13 | chr5 | 153994810 | ||||||
chr5:153994836
|
A | T | 1 | a0001c0001t0001g0153 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1383+83T>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 13/13 | chr5 | 153994836 | ||||||
chr5:153995047
|
A | AAC | 3 | a0001c0001t0011g0009a0001c0001t0011g0243a0001c0001t0011g0244 | 7 | HG01884.hp2 HG01981.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1330-77_1330-76dup others(2): Show |
FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 12/13 | chr5 | 153995047 | ||||||
chr5:153995068
|
A | G | 1 | a0002c0002t0008g0061 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1330-96T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 12/13 | chr5 | 153995068 | ||||||
chr5:153995222
|
A | G | 135 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(132): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.1330-250T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 12/13 | chr5 | 153995222 | ||||||
chr5:153995279
|
T | C | 1 | a0001c0001t0005g0201 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1330-307A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 12/13 | chr5 | 153995279 | ||||||
chr5:153995332
|
A | G | 174 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(171): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.1330-360T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 12/13 | chr5 | 153995332 | ||||||
chr5:153995338
|
C | T | 174 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(171): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.1330-366G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 12/13 | chr5 | 153995338 | ||||||
chr5:153995475
|
A | G | 17 | a0001c0001t0006g0012a0001c0001t0006g0028a0001c0001t0006g0029others(14): Show | 22 | HG00438.hp2 HG02071.hp1 HG02132.hp2 others(19): Show |
intron_variant | MODIFIER | c.1330-503T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 12/13 | chr5 | 153995475 | ||||||
chr5:153995550
|
A | T | 1 | a0002c0002t0004g0094 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1330-578T>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 12/13 | chr5 | 153995550 | ||||||
chr5:153995723
|
T | C | 1 | a0001c0001t0001g0180 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1330-751A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 12/13 | chr5 | 153995723 | ||||||
chr5:153995814
|
C | T | 3 | a0001c0001t0018g0127a0001c0001t0018g0128a0001c0001t0025g0129 | 3 | HG02809.hp2 HG02896.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1330-842G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 12/13 | chr5 | 153995814 | ||||||
chr5:153995837
|
C | T | 1 | a0001c0001t0005g0147 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1330-865G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 12/13 | chr5 | 153995837 | ||||||
chr5:153996012
|
A | G | 231 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(228): Show | 319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.1330-1040T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 12/13 | chr5 | 153996012 | ||||||
chr5:153996021
|
T | G | 1 | a0001c0001t0006g0121 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1330-1049A>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 12/13 | chr5 | 153996021 | ||||||
chr5:153996210
|
T | C | 1 | a0001c0001t0018g0128 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1330-1238A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 12/13 | chr5 | 153996210 | ||||||
chr5:153996334
|
C | T | 2 | a0002c0002t0004g0091a0002c0002t0004g0092 | 2 | HG02895.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1330-1362G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 12/13 | chr5 | 153996334 | ||||||
chr5:153996406
|
G | T | 8 | a0001c0001t0011g0009a0001c0001t0011g0243a0001c0001t0011g0244others(5): Show | 13 | HG01192.hp1 HG01884.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.1329+1397C>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 12/13 | chr5 | 153996406 | ||||||
chr5:153996455
|
A | C | 2 | a0005c0008t0021g0134a0005c0008t0021g0172 | 2 | HG02145.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1329+1348T>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 12/13 | chr5 | 153996455 | ||||||
chr5:153996484
|
C | T | 1 | a0001c0001t0012g0102 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1329+1319G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 12/13 | chr5 | 153996484 | ||||||
chr5:153996569
|
TA | T | 19 | a0001c0001t0001g0038a0001c0001t0001g0153a0001c0001t0001g0154others(16): Show | 25 | HG00735.hp1 HG01884.hp2 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.1329+1233delT | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 12/13 | chr5 | 153996569 | ||||||
chr5:153996569
|
TAA | T | 157 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(154): Show | 216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.1329+1232_1329+123 others(6): Show |
FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 12/13 | chr5 | 153996569 | ||||||
chr5:153996594
|
C | A | 1 | a0001c0001t0018g0030 | 2 | HG02615.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1329+1209G>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 12/13 | chr5 | 153996594 | ||||||
chr5:153996613
|
AAAC | A | 18 | a0002c0002t0003g0004a0002c0002t0003g0007a0002c0002t0003g0010others(15): Show | 35 | HG01257.hp2 HG01928.hp2 HG02015.hp2 others(32): Show |
intron_variant | MODIFIER | c.1329+1187_1329+118 others(7): Show |
FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 12/13 | chr5 | 153996613 | ||||||
chr5:153996636
|
G | A | 136 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(133): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.1329+1167C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 12/13 | chr5 | 153996636 | ||||||
chr5:153996754
|
TG | T | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(156): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.1329+1048delC | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 12/13 | chr5 | 153996754 | ||||||
chr5:153996967
|
A | C | 8 | a0001c0001t0011g0009a0001c0001t0011g0243a0001c0001t0011g0244others(5): Show | 13 | HG01192.hp1 HG01884.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.1329+836T>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 12/13 | chr5 | 153996967 | ||||||
chr5:153996991
|
T | TA | 8 | a0002c0002t0004g0059a0002c0002t0004g0085a0002c0002t0004g0091others(5): Show | 8 | HG02615.hp2 HG02717.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.1329+811dupT | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 12/13 | chr5 | 153996991 | ||||||
chr5:153996991
|
TA | T | 99 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(96): Show | 141 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.1329+811delT | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 12/13 | chr5 | 153996991 | ||||||
chr5:153996991
|
TAA | T | 74 | a0001c0001t0001g0132a0001c0001t0001g0155a0001c0001t0001g0159others(71): Show | 98 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.1329+810_1329+811d others(4): Show |
FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 12/13 | chr5 | 153996991 | ||||||
chr5:153997007
|
A | G | 1 | a0002c0002t0003g0053 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1329+796T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 12/13 | chr5 | 153997007 | ||||||
chr5:153997012
|
A | T | 174 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(171): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.1329+791T>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 12/13 | chr5 | 153997012 | ||||||
chr5:153997553
|
A | G | 211 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(208): Show | 282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.1329+250T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 12/13 | chr5 | 153997553 | ||||||
chr5:153997672
|
G | A | 7 | a0004c0005t0009g0042a0004c0005t0009g0043a0004c0005t0009g0105others(4): Show | 7 | HG02109.hp2 HG02280.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1329+131C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 12/13 | chr5 | 153997672 | ||||||
chr5:153997754
|
C | T | 1 | a0001c0001t0015g0239 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1329+49G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 12/13 | chr5 | 153997754 | ||||||
chr5:153997778
|
T | C | 15 | a0001c0001t0011g0009a0001c0001t0011g0243a0001c0001t0011g0244others(12): Show | 20 | HG01192.hp1 HG01884.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.1329+25A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 12/13 | chr5 | 153997778 | ||||||
chr5:153997788
|
G | C | 1 | a0003c0004t0023g0166 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1329+15C>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 12/13 | chr5 | 153997788 | ||||||
chr5:153997917
|
T | A | 3 | a0002c0002t0004g0091a0002c0002t0004g0092a0002c0002t0004g0094 | 3 | HG02895.hp2 HG03130.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1257-42A>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 11/13 | chr5 | 153997917 | ||||||
chr5:153998017
|
C | T | 1 | a0002c0002t0003g0051 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1257-142G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 11/13 | chr5 | 153998017 | ||||||
chr5:153998031
|
T | C | 1 | a0001c0001t0023g0131 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1257-156A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 11/13 | chr5 | 153998031 | ||||||
chr5:153998038
|
A | G | 172 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(169): Show | 237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.1257-163T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 11/13 | chr5 | 153998038 | ||||||
chr5:153998097
|
T | A | 2 | a0001c0001t0020g0125a0001c0001t0020g0126 | 2 | HG02258.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1257-222A>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 11/13 | chr5 | 153998097 | ||||||
chr5:153998116
|
A | G | 17 | a0001c0001t0006g0012a0001c0001t0006g0028a0001c0001t0006g0029others(14): Show | 22 | HG00438.hp2 HG02071.hp1 HG02132.hp2 others(19): Show |
intron_variant | MODIFIER | c.1257-241T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 11/13 | chr5 | 153998116 | ||||||
chr5:153998123
|
T | A | 2 | a0002c0003t0004g0075a0002c0003t0004g0080 | 2 | HG02027.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.1257-248A>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 11/13 | chr5 | 153998123 | ||||||
chr5:153998425
|
C | A | 1 | a0001c0001t0001g0221 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1257-550G>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 11/13 | chr5 | 153998425 | ||||||
chr5:153998476
|
T | G | 1 | a0001c0001t0001g0223 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1257-601A>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 11/13 | chr5 | 153998476 | ||||||
chr5:153998539
|
G | A | 1 | a0001c0007t0014g0040 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1257-664C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 11/13 | chr5 | 153998539 | ||||||
chr5:153998846
|
G | A | 15 | a0001c0001t0011g0009a0001c0001t0011g0243a0001c0001t0011g0244others(12): Show | 20 | HG01192.hp1 HG01884.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.1257-971C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 11/13 | chr5 | 153998846 | ||||||
chr5:153998858
|
G | A | 1 | a0002c0002t0010g0093 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1257-983C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 11/13 | chr5 | 153998858 | ||||||
chr5:153999055
|
G | C | 3 | a0001c0001t0001g0019a0001c0001t0001g0038a0001c0001t0002g0226 | 6 | HG00408.hp1 HG02040.hp1 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.1257-1180C>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 11/13 | chr5 | 153999055 | ||||||
chr5:153999077
|
T | C | 4 | a0001c0001t0001g0141a0001c0001t0005g0138a0001c0001t0005g0142others(1): Show | 4 | HG02109.hp1 HG02965.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1257-1202A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 11/13 | chr5 | 153999077 | ||||||
chr5:153999327
|
G | C | 11 | a0001c0001t0002g0015a0001c0001t0002g0031a0001c0001t0002g0130others(8): Show | 15 | HG01255.hp2 HG01256.hp2 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1257-1452C>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 11/13 | chr5 | 153999327 | ||||||
chr5:153999453
|
T | C | 2 | a0001c0001t0020g0125a0001c0001t0020g0126 | 2 | HG02258.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1257-1578A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 11/13 | chr5 | 153999453 | ||||||
chr5:153999491
|
T | C | 1 | a0001c0001t0026g0041 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1257-1616A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 11/13 | chr5 | 153999491 | ||||||
chr5:153999533
|
C | T | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(156): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.1257-1658G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 11/13 | chr5 | 153999533 | ||||||
chr5:153999666
|
T | A | 1 | a0001c0001t0005g0178 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1257-1791A>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 11/13 | chr5 | 153999666 | ||||||
chr5:153999686
|
T | C | 1 | a0001c0001t0015g0156 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1257-1811A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 11/13 | chr5 | 153999686 | ||||||
chr5:153999718
|
A | G | 4 | a0001c0001t0018g0030a0001c0001t0018g0127a0001c0001t0018g0128others(1): Show | 5 | HG02615.hp1 HG02809.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1257-1843T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 11/13 | chr5 | 153999718 | ||||||
chr5:153999871
|
T | C | 4 | a0002c0002t0003g0011a0002c0002t0003g0049a0002c0002t0027g0052others(1): Show | 7 | NA18939.hp1 NA18942.hp1 NA18954.hp2 others(4): Show |
intron_variant | MODIFIER | c.1257-1996A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 11/13 | chr5 | 153999871 | ||||||
chr5:153999925
|
G | A | 1 | a0001c0001t0001g0214 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1257-2050C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 11/13 | chr5 | 153999925 | ||||||
chr5:153999925
|
G | GTGTGTGT others(11): Show |
3 | a0001c0001t0012g0027a0001c0001t0012g0103a0001c0001t0012g0104 | 4 | HG01192.hp1 HG02683.hp2 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.1257-2068_1257-205 others(22): Show |
FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 11/13 | chr5 | 153999925 | ||||||
chr5:153999972
|
T | C | 15 | a0001c0001t0011g0009a0001c0001t0011g0243a0001c0001t0011g0244others(12): Show | 20 | HG01192.hp1 HG01884.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.1257-2097A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 11/13 | chr5 | 153999972 | ||||||
chr5:154000024
|
A | T | 1 | a0006c0011t0004g0099 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1257-2149T>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 11/13 | chr5 | 154000024 | ||||||
chr5:154000045
|
A | T | 1 | a0001c0001t0012g0101 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1257-2170T>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 11/13 | chr5 | 154000045 | ||||||
chr5:154000069
|
G | A | 15 | a0001c0001t0011g0009a0001c0001t0011g0243a0001c0001t0011g0244others(12): Show | 20 | HG01192.hp1 HG01884.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.1256+2182C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 11/13 | chr5 | 154000069 | ||||||
chr5:154000462
|
C | CAT | 157 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(154): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.1256+1787_1256+178 others(6): Show |
FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 11/13 | chr5 | 154000462 | ||||||
chr5:154000506
|
G | A | 8 | a0002c0002t0004g0091a0002c0002t0004g0092a0002c0002t0004g0094others(5): Show | 8 | HG00140.hp2 HG00639.hp1 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.1256+1745C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 11/13 | chr5 | 154000506 | ||||||
chr5:154000562
|
C | T | 2 | a0001c0001t0020g0125a0001c0001t0020g0126 | 2 | HG02258.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1256+1689G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 11/13 | chr5 | 154000562 | ||||||
chr5:154000817
|
A | G | 1 | a0002c0003t0004g0078 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1256+1434T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 11/13 | chr5 | 154000817 | ||||||
chr5:154001720
|
A | G | 174 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(171): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.1256+531T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 11/13 | chr5 | 154001720 | ||||||
chr5:154002060
|
G | T | 1 | a0002c0002t0010g0089 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1256+191C>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 11/13 | chr5 | 154002060 | ||||||
chr5:154002110
|
A | C | 7 | a0004c0005t0009g0042a0004c0005t0009g0043a0004c0005t0009g0105others(4): Show | 7 | HG02109.hp2 HG02280.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1256+141T>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 11/13 | chr5 | 154002110 | ||||||
chr5:154002151
|
C | T | 15 | a0001c0001t0011g0009a0001c0001t0011g0243a0001c0001t0011g0244others(12): Show | 20 | HG01192.hp1 HG01884.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.1256+100G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 11/13 | chr5 | 154002151 | ||||||
chr5:154002438
|
G | A | 17 | a0001c0001t0006g0012a0001c0001t0006g0028a0001c0001t0006g0029others(14): Show | 22 | HG00438.hp2 HG02071.hp1 HG02132.hp2 others(19): Show |
intron_variant | MODIFIER | c.1117-48C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 10/13 | chr5 | 154002438 | ||||||
chr5:154002512
|
GTCT | G | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(156): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.1117-125_1117-123d others(5): Show |
FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 10/13 | chr5 | 154002512 | ||||||
chr5:154002564
|
T | C | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(156): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.1117-174A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 10/13 | chr5 | 154002564 | ||||||
chr5:154002650
|
A | G | 2 | a0001c0001t0020g0125a0001c0001t0020g0126 | 2 | HG02258.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1116+197T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 10/13 | chr5 | 154002650 | ||||||
chr5:154002658
|
C | T | 12 | a0002c0002t0004g0085a0002c0002t0004g0091a0002c0002t0004g0092others(9): Show | 12 | HG00140.hp2 HG00639.hp1 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.1116+189G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 10/13 | chr5 | 154002658 | ||||||
chr5:154002659
|
G | A | 1 | a0001c0001t0025g0202 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1116+188C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 10/13 | chr5 | 154002659 | ||||||
chr5:154002660
|
C | T | 1 | a0001c0001t0005g0176 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1116+187G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 10/13 | chr5 | 154002660 | ||||||
chr5:154002738
|
C | T | 15 | a0001c0001t0011g0009a0001c0001t0011g0243a0001c0001t0011g0244others(12): Show | 20 | HG01192.hp1 HG01884.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.1116+109G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 10/13 | chr5 | 154002738 | ||||||
chr5:154002786
|
T | C | 1 | a0002c0003t0016g0025 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1116+61A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 10/13 | chr5 | 154002786 | ||||||
chr5:154003042
|
A | G | 6 | a0003c0004t0001g0162a0003c0004t0002g0018a0003c0004t0002g0195others(3): Show | 8 | HG00099.hp2 HG00323.hp2 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.994-73T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154003042 | ||||||
chr5:154003134
|
T | C | 1 | a0001c0001t0001g0215 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.994-165A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154003134 | ||||||
chr5:154003177
|
G | GC | 5 | a0001c0001t0001g0177a0001c0001t0002g0198a0001c0001t0002g0225others(2): Show | 5 | HG01934.hp1 HG02148.hp1 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.994-209_994-208ins others(1): Show |
FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154003177 | ||||||
chr5:154003177
|
G | GT | 5 | a0001c0001t0006g0115a0001c0001t0012g0027a0001c0001t0012g0102others(2): Show | 6 | HG01192.hp1 HG01891.hp2 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.994-209dupA | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154003177 | ||||||
chr5:154003177
|
G | GTT | 4 | a0001c0001t0011g0009a0001c0001t0011g0243a0001c0001t0011g0244others(1): Show | 8 | HG01884.hp2 HG01981.hp2 HG02683.hp2 others(5): Show |
intron_variant | MODIFIER | c.994-209_994-208ins others(2): Show |
FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154003177 | ||||||
chr5:154003178
|
T | C | 128 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(125): Show | 182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.994-209A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154003178 | ||||||
chr5:154003178
|
TA | T | 7 | a0004c0005t0009g0042a0004c0005t0009g0043a0004c0005t0009g0105others(4): Show | 7 | HG02109.hp2 HG02280.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.994-210delT | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154003178 | ||||||
chr5:154003179
|
A | C | 2 | a0001c0001t0002g0235a0001c0001t0005g0201 | 2 | HG02602.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.994-210T>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154003179 | ||||||
chr5:154003179
|
A | T | 165 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(162): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.994-210T>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154003179 | ||||||
chr5:154003228
|
G | T | 1 | a0001c0001t0002g0168 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.994-259C>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154003228 | ||||||
chr5:154003367
|
C | T | 1 | a0002c0002t0008g0060 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.994-398G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154003367 | ||||||
chr5:154003471
|
G | A | 5 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0183others(2): Show | 5 | HG02257.hp2 HG02572.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.994-502C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154003471 | ||||||
chr5:154003489
|
T | C | 18 | a0002c0002t0003g0004a0002c0002t0003g0007a0002c0002t0003g0010others(15): Show | 35 | HG01257.hp2 HG01928.hp2 HG02015.hp2 others(32): Show |
intron_variant | MODIFIER | c.994-520A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154003489 | ||||||
chr5:154003575
|
C | T | 1 | a0004c0005t0009g0105 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.994-606G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154003575 | ||||||
chr5:154003607
|
C | T | 7 | a0001c0001t0011g0009a0001c0001t0011g0243a0001c0001t0011g0244others(4): Show | 12 | HG01192.hp1 HG01884.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.994-638G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154003607 | ||||||
chr5:154003819
|
T | A | 2 | a0002c0003t0004g0024a0002c0003t0004g0071 | 3 | HG01069.hp2 HG01071.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.994-850A>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154003819 | ||||||
chr5:154003832
|
A | G | 1 | a0001c0001t0001g0229 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.994-863T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154003832 | ||||||
chr5:154003911
|
T | C | 4 | a0001c0001t0018g0030a0001c0001t0018g0127a0001c0001t0018g0128others(1): Show | 5 | HG02615.hp1 HG02809.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.994-942A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154003911 | ||||||
chr5:154004184
|
A | G | 1 | a0001c0007t0014g0040 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.994-1215T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154004184 | ||||||
chr5:154004204
|
T | C | 1 | a0001c0001t0001g0230 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.994-1235A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154004204 | ||||||
chr5:154004215
|
A | T | 1 | a0002c0002t0003g0046 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.994-1246T>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154004215 | ||||||
chr5:154004470
|
C | T | 1 | a0002c0003t0013g0072 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.994-1501G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154004470 | ||||||
chr5:154004567
|
A | AC | 231 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(228): Show | 319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.994-1599dupG | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154004567 | ||||||
chr5:154004732
|
TCCTC | T | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(156): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.994-1767_994-1764d others(6): Show |
FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154004732 | ||||||
chr5:154004885
|
T | C | 1 | a0001c0001t0002g0169 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.994-1916A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154004885 | ||||||
chr5:154004912
|
G | C | 7 | a0004c0005t0009g0042a0004c0005t0009g0043a0004c0005t0009g0105others(4): Show | 7 | HG02109.hp2 HG02280.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.994-1943C>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154004912 | ||||||
chr5:154005348
|
C | G | 1 | a0001c0001t0026g0041 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.994-2379G>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154005348 | ||||||
chr5:154005443
|
A | C | 1 | a0001c0001t0026g0041 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.994-2474T>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154005443 | ||||||
chr5:154005612
|
G | C | 7 | a0001c0001t0001g0039a0001c0001t0001g0215a0001c0001t0001g0217others(4): Show | 8 | HG00544.hp2 HG00597.hp2 HG00609.hp2 others(5): Show |
intron_variant | MODIFIER | c.994-2643C>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154005612 | ||||||
chr5:154005673
|
C | T | 174 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(171): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.994-2704G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154005673 | ||||||
chr5:154005762
|
C | T | 1 | a0001c0001t0001g0183 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.994-2793G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154005762 | ||||||
chr5:154005866
|
G | A | 1 | a0001c0001t0012g0101 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.994-2897C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154005866 | ||||||
chr5:154006092
|
C | T | 1 | a0001c0007t0014g0040 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.994-3123G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154006092 | ||||||
chr5:154006179
|
T | C | 1 | a0001c0001t0012g0101 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.994-3210A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154006179 | ||||||
chr5:154006187
|
T | A | 174 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(171): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.994-3218A>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154006187 | ||||||
chr5:154006192
|
T | A | 1 | a0001c0001t0023g0131 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.994-3223A>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154006192 | ||||||
chr5:154006203
|
C | A | 7 | a0001c0001t0011g0009a0001c0001t0011g0243a0001c0001t0011g0244others(4): Show | 12 | HG01192.hp1 HG01884.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.994-3234G>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154006203 | ||||||
chr5:154006326
|
T | C | 1 | a0002c0002t0004g0092 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.994-3357A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154006326 | ||||||
chr5:154006422
|
C | G | 3 | a0001c0001t0018g0127a0001c0001t0018g0128a0001c0001t0025g0129 | 3 | HG02809.hp2 HG02896.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.994-3453G>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154006422 | ||||||
chr5:154006444
|
A | G | 6 | a0004c0005t0009g0042a0004c0005t0009g0043a0004c0005t0009g0105others(3): Show | 6 | HG02109.hp2 HG02630.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.994-3475T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154006444 | ||||||
chr5:154006451
|
T | C | 7 | a0004c0005t0009g0042a0004c0005t0009g0043a0004c0005t0009g0105others(4): Show | 7 | HG02109.hp2 HG02280.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.994-3482A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154006451 | ||||||
chr5:154006543
|
A | G | 174 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(171): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.994-3574T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154006543 | ||||||
chr5:154006589
|
A | G | 4 | a0001c0001t0012g0027a0001c0001t0012g0102a0001c0001t0012g0103others(1): Show | 5 | HG01192.hp1 HG01891.hp2 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.994-3620T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154006589 | ||||||
chr5:154006597
|
G | A | 2 | a0001c0001t0020g0125a0001c0001t0020g0126 | 2 | HG02258.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.994-3628C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154006597 | ||||||
chr5:154006641
|
A | G | 3 | a0002c0002t0004g0091a0002c0002t0004g0092a0002c0002t0004g0094 | 3 | HG02895.hp2 HG03130.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.994-3672T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154006641 | ||||||
chr5:154006751
|
A | C | 1 | a0001c0001t0001g0159 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.994-3782T>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154006751 | ||||||
chr5:154006765
|
G | A | 17 | a0001c0001t0006g0012a0001c0001t0006g0028a0001c0001t0006g0029others(14): Show | 22 | HG00438.hp2 HG02071.hp1 HG02132.hp2 others(19): Show |
intron_variant | MODIFIER | c.994-3796C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154006765 | ||||||
chr5:154006773
|
TA | T | 7 | a0004c0005t0009g0042a0004c0005t0009g0043a0004c0005t0009g0105others(4): Show | 7 | HG02109.hp2 HG02280.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.994-3805delT | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154006773 | ||||||
chr5:154006796
|
AT | A | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(151): Show | 213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.994-3828delA | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154006796 | ||||||
chr5:154006796
|
ATT | A | 20 | a0001c0001t0001g0175a0001c0001t0005g0149a0001c0001t0005g0174others(17): Show | 26 | HG01192.hp1 HG01257.hp1 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.994-3829_994-3828d others(4): Show |
FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154006796 | ||||||
chr5:154007031
|
A | G | 174 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(171): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.994-4062T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154007031 | ||||||
chr5:154007075
|
G | C | 1 | a0001c0001t0026g0041 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.994-4106C>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154007075 | ||||||
chr5:154007131
|
T | C | 1 | a0003c0004t0002g0196 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.993+4110A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154007131 | ||||||
chr5:154007336
|
A | G | 1 | a0002c0002t0004g0059 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.993+3905T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154007336 | ||||||
chr5:154007428
|
C | T | 1 | a0001c0001t0018g0030 | 2 | HG02615.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.993+3813G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154007428 | ||||||
chr5:154007536
|
C | G | 2 | a0001c0001t0020g0125a0001c0001t0020g0126 | 2 | HG02258.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.993+3705G>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154007536 | ||||||
chr5:154007568
|
C | T | 1 | a0001c0001t0005g0201 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.993+3673G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154007568 | ||||||
chr5:154007824
|
C | A | 1 | a0001c0007t0014g0040 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.993+3417G>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154007824 | ||||||
chr5:154007839
|
A | G | 174 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(171): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.993+3402T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154007839 | ||||||
chr5:154008245
|
A | T | 2 | a0001c0001t0002g0236a0001c0001t0002g0237 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.993+2996T>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154008245 | ||||||
chr5:154008319
|
G | A | 2 | a0001c0001t0020g0125a0001c0001t0020g0126 | 2 | HG02258.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.993+2922C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154008319 | ||||||
chr5:154008330
|
G | C | 174 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(171): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.993+2911C>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154008330 | ||||||
chr5:154008356
|
C | A | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(156): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.993+2885G>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154008356 | ||||||
chr5:154008398
|
T | C | 1 | a0001c0001t0038g0216 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.993+2843A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154008398 | ||||||
chr5:154008522
|
C | T | 2 | a0002c0002t0003g0021a0002c0002t0003g0050 | 3 | HG02083.hp2 HG02165.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.993+2719G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154008522 | ||||||
chr5:154008562
|
T | A | 1 | a0004c0005t0009g0108 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.993+2679A>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154008562 | ||||||
chr5:154008646
|
T | C | 1 | a0002c0002t0008g0062 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.993+2595A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154008646 | ||||||
chr5:154008658
|
ACAG | A | 15 | a0001c0001t0011g0009a0001c0001t0011g0243a0001c0001t0011g0244others(12): Show | 20 | HG01192.hp1 HG01884.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.993+2580_993+2582d others(5): Show |
FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154008658 | ||||||
chr5:154008674
|
A | ATG | 9 | a0001c0001t0001g0145a0002c0002t0004g0091a0002c0002t0004g0092others(6): Show | 9 | HG00140.hp2 HG00639.hp1 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.993+2565_993+2566d others(4): Show |
FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154008674 | ||||||
chr5:154008881
|
T | C | 17 | a0001c0001t0006g0012a0001c0001t0006g0028a0001c0001t0006g0029others(14): Show | 22 | HG00438.hp2 HG02071.hp1 HG02132.hp2 others(19): Show |
intron_variant | MODIFIER | c.993+2360A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154008881 | ||||||
chr5:154008964
|
T | A | 2 | a0001c0001t0014g0137a0001c0001t0014g0171 | 2 | HG03710.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.993+2277A>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154008964 | ||||||
chr5:154009081
|
G | C | 1 | a0004c0005t0009g0106 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.993+2160C>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154009081 | ||||||
chr5:154009278
|
C | A | 1 | a0002c0002t0030g0069 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.993+1963G>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154009278 | ||||||
chr5:154009352
|
G | A | 174 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(171): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.993+1889C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154009352 | ||||||
chr5:154009602
|
T | C | 1 | a0002c0002t0007g0066 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.993+1639A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154009602 | ||||||
chr5:154009916
|
G | T | 1 | a0001c0001t0001g0211 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.993+1325C>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154009916 | ||||||
chr5:154009933
|
A | G | 1 | a0001c0001t0005g0232 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.993+1308T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154009933 | ||||||
chr5:154010044
|
G | A | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(156): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.993+1197C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154010044 | ||||||
chr5:154010171
|
A | G | 1 | a0001c0001t0026g0041 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.993+1070T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154010171 | ||||||
chr5:154010205
|
T | C | 7 | a0001c0001t0011g0009a0001c0001t0011g0243a0001c0001t0011g0244others(4): Show | 12 | HG01192.hp1 HG01884.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.993+1036A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154010205 | ||||||
chr5:154010221
|
G | A | 174 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(171): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.993+1020C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154010221 | ||||||
chr5:154010389
|
G | C | 1 | a0002c0002t0003g0049 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.993+852C>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154010389 | ||||||
chr5:154010434
|
T | C | 1 | a0002c0002t0003g0053 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.993+807A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154010434 | ||||||
chr5:154010569
|
T | G | 17 | a0001c0001t0006g0012a0001c0001t0006g0028a0001c0001t0006g0029others(14): Show | 22 | HG00438.hp2 HG02071.hp1 HG02132.hp2 others(19): Show |
intron_variant | MODIFIER | c.993+672A>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154010569 | ||||||
chr5:154010636
|
G | A | 4 | a0002c0002t0004g0085a0002c0002t0010g0086a0002c0002t0010g0087others(1): Show | 4 | HG02615.hp2 HG02622.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.993+605C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154010636 | ||||||
chr5:154010663
|
A | T | 1 | a0002c0002t0004g0085 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.993+578T>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154010663 | ||||||
chr5:154010761
|
G | C | 15 | a0001c0001t0011g0009a0001c0001t0011g0243a0001c0001t0011g0244others(12): Show | 20 | HG01192.hp1 HG01884.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.993+480C>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154010761 | ||||||
chr5:154010794
|
C | T | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(156): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.993+447G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154010794 | ||||||
chr5:154010856
|
G | A | 135 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(132): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.993+385C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154010856 | ||||||
chr5:154010889
|
T | A | 37 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0020others(34): Show | 53 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.993+352A>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154010889 | ||||||
chr5:154010979
|
G | A | 1 | a0001c0001t0001g0150 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.993+262C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154010979 | ||||||
chr5:154011010
|
T | A | 1 | a0001c0001t0006g0114 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.993+231A>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154011010 | ||||||
chr5:154011115
|
T | C | 1 | a0001c0001t0005g0201 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.993+126A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154011115 | ||||||
chr5:154011153
|
C | G | 4 | a0001c0001t0012g0027a0001c0001t0012g0102a0001c0001t0012g0103others(1): Show | 5 | HG01192.hp1 HG01891.hp2 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.993+88G>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154011153 | ||||||
chr5:154011155
|
C | A | 15 | a0001c0001t0011g0009a0001c0001t0011g0243a0001c0001t0011g0244others(12): Show | 20 | HG01192.hp1 HG01884.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.993+86G>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154011155 | ||||||
chr5:154011212
|
A | G | 1 | a0001c0007t0014g0040 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.993+29T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 9/13 | chr5 | 154011212 | ||||||
chr5:154011367
|
G | A | 1 | a0001c0001t0006g0112 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.914-47C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154011367 | ||||||
chr5:154011621
|
C | G | 2 | a0001c0001t0002g0167a0001c0001t0002g0192 | 2 | HG01099.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.914-301G>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154011621 | ||||||
chr5:154011715
|
TAAGC | T | 6 | a0002c0003t0013g0023a0002c0003t0013g0072a0002c0003t0013g0076others(3): Show | 7 | HG01167.hp2 HG01169.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.914-399_914-396del others(4): Show |
FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154011715 | ||||||
chr5:154011749
|
G | A | 2 | a0002c0002t0007g0065a0002c0002t0007g0066 | 2 | HG02717.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.914-429C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154011749 | ||||||
chr5:154011888
|
G | A | 2 | a0001c0001t0006g0111a0001c0001t0006g0112 | 2 | NA18968.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.914-568C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154011888 | ||||||
chr5:154011952
|
G | A | 1 | a0001c0001t0001g0217 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.914-632C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154011952 | ||||||
chr5:154012058
|
G | A | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(156): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.914-738C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154012058 | ||||||
chr5:154012069
|
T | C | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(156): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.914-749A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154012069 | ||||||
chr5:154012118
|
A | T | 1 | a0001c0001t0002g0197 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.914-798T>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154012118 | ||||||
chr5:154012122
|
A | G | 2 | a0001c0001t0001g0159a0001c0001t0001g0160 | 2 | NA18960.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.914-802T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154012122 | ||||||
chr5:154012149
|
A | G | 174 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(171): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.914-829T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154012149 | ||||||
chr5:154012218
|
G | A | 4 | a0001c0001t0001g0205a0001c0001t0001g0218a0001c0001t0001g0219others(1): Show | 4 | HG00423.hp2 HG02071.hp2 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.914-898C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154012218 | ||||||
chr5:154012555
|
T | A | 1 | a0001c0001t0011g0243 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.914-1235A>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154012555 | ||||||
chr5:154012976
|
T | C | 1 | a0001c0001t0002g0220 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.914-1656A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154012976 | ||||||
chr5:154013039
|
TTA | T | 7 | a0004c0005t0009g0042a0004c0005t0009g0043a0004c0005t0009g0105others(4): Show | 7 | HG02109.hp2 HG02280.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.914-1721_914-1720d others(4): Show |
FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154013039 | ||||||
chr5:154013084
|
C | T | 2 | a0005c0008t0021g0134a0005c0008t0021g0172 | 2 | HG02145.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.914-1764G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154013084 | ||||||
chr5:154013094
|
G | A | 2 | a0001c0001t0002g0236a0001c0001t0002g0237 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.914-1774C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154013094 | ||||||
chr5:154013903
|
C | T | 1 | a0001c0001t0002g0163 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.914-2583G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154013903 | ||||||
chr5:154014009
|
T | C | 1 | a0002c0002t0004g0059 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.914-2689A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154014009 | ||||||
chr5:154014024
|
A | T | 1 | a0002c0002t0007g0066 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.914-2704T>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154014024 | ||||||
chr5:154014034
|
C | T | 15 | a0001c0001t0011g0009a0001c0001t0011g0243a0001c0001t0011g0244others(12): Show | 20 | HG01192.hp1 HG01884.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.914-2714G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154014034 | ||||||
chr5:154014076
|
A | G | 20 | a0002c0002t0003g0004a0002c0002t0003g0007a0002c0002t0003g0010others(17): Show | 37 | HG00735.hp1 HG01257.hp2 HG01928.hp2 others(34): Show |
intron_variant | MODIFIER | c.914-2756T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154014076 | ||||||
chr5:154014359
|
G | A | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(156): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.914-3039C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154014359 | ||||||
chr5:154014363
|
A | G | 7 | a0004c0005t0009g0042a0004c0005t0009g0043a0004c0005t0009g0105others(4): Show | 7 | HG02109.hp2 HG02280.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.914-3043T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154014363 | ||||||
chr5:154014385
|
A | G | 17 | a0001c0001t0006g0012a0001c0001t0006g0028a0001c0001t0006g0029others(14): Show | 22 | HG00438.hp2 HG02071.hp1 HG02132.hp2 others(19): Show |
intron_variant | MODIFIER | c.914-3065T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154014385 | ||||||
chr5:154014604
|
G | A | 136 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(133): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.914-3284C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154014604 | ||||||
chr5:154014648
|
C | G | 1 | a0001c0001t0001g0210 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.914-3328G>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154014648 | ||||||
chr5:154014769
|
C | T | 15 | a0001c0001t0011g0009a0001c0001t0011g0243a0001c0001t0011g0244others(12): Show | 20 | HG01192.hp1 HG01884.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.914-3449G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154014769 | ||||||
chr5:154014989
|
C | T | 1 | a0001c0001t0001g0175 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.914-3669G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154014989 | ||||||
chr5:154015003
|
G | T | 1 | a0001c0001t0026g0041 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.914-3683C>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154015003 | ||||||
chr5:154015053
|
A | T | 1 | a0001c0001t0026g0041 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.914-3733T>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154015053 | ||||||
chr5:154015154
|
A | G | 17 | a0001c0001t0006g0012a0001c0001t0006g0028a0001c0001t0006g0029others(14): Show | 22 | HG00438.hp2 HG02071.hp1 HG02132.hp2 others(19): Show |
intron_variant | MODIFIER | c.914-3834T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154015154 | ||||||
chr5:154015196
|
A | T | 6 | a0004c0005t0009g0042a0004c0005t0009g0043a0004c0005t0009g0105others(3): Show | 6 | HG02109.hp2 HG02630.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.914-3876T>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154015196 | ||||||
chr5:154015295
|
C | T | 1 | a0002c0002t0003g0049 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.914-3975G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154015295 | ||||||
chr5:154015405
|
G | A | 1 | a0004c0005t0009g0108 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.914-4085C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154015405 | ||||||
chr5:154015698
|
T | C | 6 | a0003c0004t0001g0162a0003c0004t0002g0018a0003c0004t0002g0195others(3): Show | 8 | HG00099.hp2 HG00323.hp2 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.914-4378A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154015698 | ||||||
chr5:154015837
|
G | A | 1 | a0003c0004t0001g0162 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.914-4517C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154015837 | ||||||
chr5:154015912
|
T | C | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(156): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.914-4592A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154015912 | ||||||
chr5:154016002
|
T | C | 6 | a0001c0001t0001g0141a0001c0001t0005g0138a0001c0001t0005g0139others(3): Show | 6 | HG02109.hp1 HG02965.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.914-4682A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154016002 | ||||||
chr5:154016002
|
T | G | 15 | a0001c0001t0011g0009a0001c0001t0011g0243a0001c0001t0011g0244others(12): Show | 20 | HG01192.hp1 HG01884.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.914-4682A>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154016002 | ||||||
chr5:154016127
|
T | C | 174 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(171): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.914-4807A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154016127 | ||||||
chr5:154016221
|
GCCT | G | 8 | a0001c0001t0011g0009a0001c0001t0011g0243a0001c0001t0011g0244others(5): Show | 13 | HG01192.hp1 HG01884.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.914-4904_914-4902d others(5): Show |
FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154016221 | ||||||
chr5:154016239
|
G | A | 3 | a0001c0001t0001g0017a0001c0001t0001g0182a0001c0001t0036g0144 | 5 | NA18948.hp2 NA18961.hp2 NA18972.hp2 others(2): Show |
intron_variant | MODIFIER | c.914-4919C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154016239 | ||||||
chr5:154016340
|
GA | G | 7 | a0001c0001t0006g0028a0001c0001t0006g0115a0001c0001t0006g0120others(4): Show | 8 | HG00438.hp2 HG02132.hp2 NA18953.hp2 others(5): Show |
intron_variant | MODIFIER | c.914-5021delT | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154016340 | ||||||
chr5:154016343
|
A | G | 7 | a0001c0001t0006g0028a0001c0001t0006g0115a0001c0001t0006g0120others(4): Show | 8 | HG00438.hp2 HG02132.hp2 NA18953.hp2 others(5): Show |
intron_variant | MODIFIER | c.914-5023T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154016343 | ||||||
chr5:154016360
|
T | G | 174 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(171): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.914-5040A>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154016360 | ||||||
chr5:154016554
|
C | A | 17 | a0001c0001t0006g0012a0001c0001t0006g0028a0001c0001t0006g0029others(14): Show | 22 | HG00438.hp2 HG02071.hp1 HG02132.hp2 others(19): Show |
intron_variant | MODIFIER | c.914-5234G>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154016554 | ||||||
chr5:154016678
|
T | G | 1 | a0001c0001t0005g0151 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.914-5358A>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154016678 | ||||||
chr5:154016710
|
A | T | 1 | a0002c0002t0004g0059 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.914-5390T>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154016710 | ||||||
chr5:154016814
|
G | A | 1 | a0001c0001t0015g0152 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.914-5494C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154016814 | ||||||
chr5:154016972
|
G | C | 7 | a0004c0005t0009g0042a0004c0005t0009g0043a0004c0005t0009g0105others(4): Show | 7 | HG02109.hp2 HG02280.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.914-5652C>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154016972 | ||||||
chr5:154017155
|
G | T | 31 | a0001c0001t0001g0132a0001c0001t0001g0200a0001c0001t0002g0005others(28): Show | 44 | HG00099.hp2 HG00323.hp2 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.914-5835C>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154017155 | ||||||
chr5:154017214
|
A | G | 174 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(171): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.914-5894T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154017214 | ||||||
chr5:154017346
|
G | A | 1 | a0002c0003t0004g0081 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.914-6026C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154017346 | ||||||
chr5:154017373
|
C | T | 23 | a0002c0003t0004g0016a0002c0003t0004g0024a0002c0003t0004g0026others(20): Show | 29 | HG01069.hp2 HG01071.hp1 HG01167.hp2 others(26): Show |
intron_variant | MODIFIER | c.914-6053G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154017373 | ||||||
chr5:154017497
|
G | A | 1 | a0001c0001t0025g0202 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.914-6177C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154017497 | ||||||
chr5:154017503
|
C | CT | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(156): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.914-6184dupA | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154017503 | ||||||
chr5:154017518
|
G | A | 1 | a0001c0007t0014g0040 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.914-6198C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154017518 | ||||||
chr5:154017592
|
C | T | 6 | a0001c0001t0001g0141a0001c0001t0005g0138a0001c0001t0005g0139others(3): Show | 6 | HG02109.hp1 HG02965.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.914-6272G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154017592 | ||||||
chr5:154017600
|
A | G | 1 | a0001c0001t0001g0231 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.914-6280T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154017600 | ||||||
chr5:154017658
|
T | C | 8 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0183others(5): Show | 8 | HG02257.hp2 HG02258.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.914-6338A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154017658 | ||||||
chr5:154017669
|
C | T | 6 | a0003c0004t0001g0162a0003c0004t0002g0018a0003c0004t0002g0195others(3): Show | 8 | HG00099.hp2 HG00323.hp2 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.914-6349G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154017669 | ||||||
chr5:154017687
|
T | C | 3 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0039g0209 | 3 | HG00738.hp1 HG01070.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.914-6367A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154017687 | ||||||
chr5:154017688
|
A | G | 7 | a0001c0001t0011g0009a0001c0001t0011g0243a0001c0001t0011g0244others(4): Show | 12 | HG01192.hp1 HG01884.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.914-6368T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154017688 | ||||||
chr5:154017703
|
C | T | 2 | a0002c0002t0010g0090a0002c0002t0033g0096 | 2 | HG00140.hp2 HG00639.hp1 |
intron_variant | MODIFIER | c.914-6383G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154017703 | ||||||
chr5:154017711
|
A | G | 1 | a0001c0001t0001g0224 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.914-6391T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154017711 | ||||||
chr5:154017758
|
G | A | 3 | a0001c0001t0011g0009a0001c0001t0011g0243a0001c0001t0011g0244 | 7 | HG01884.hp2 HG01981.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.914-6438C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154017758 | ||||||
chr5:154017941
|
C | T | 1 | a0002c0002t0004g0057 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.914-6621G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154017941 | ||||||
chr5:154017991
|
G | A | 1 | a0005c0008t0021g0134 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.914-6671C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154017991 | ||||||
chr5:154018114
|
C | T | 174 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(171): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.914-6794G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154018114 | ||||||
chr5:154018289
|
C | G | 1 | a0002c0002t0028g0048 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.914-6969G>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154018289 | ||||||
chr5:154018349
|
G | C | 6 | a0004c0005t0009g0042a0004c0005t0009g0043a0004c0005t0009g0105others(3): Show | 6 | HG02109.hp2 HG02630.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.914-7029C>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154018349 | ||||||
chr5:154018610
|
A | G | 2 | a0002c0002t0004g0059a0006c0011t0004g0099 | 2 | HG02818.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.914-7290T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154018610 | ||||||
chr5:154018804
|
A | T | 4 | a0001c0001t0018g0030a0001c0001t0018g0127a0001c0001t0018g0128others(1): Show | 5 | HG02615.hp1 HG02809.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.914-7484T>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154018804 | ||||||
chr5:154018880
|
C | T | 17 | a0001c0001t0006g0012a0001c0001t0006g0028a0001c0001t0006g0029others(14): Show | 22 | HG00438.hp2 HG02071.hp1 HG02132.hp2 others(19): Show |
intron_variant | MODIFIER | c.913+7519G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154018880 | ||||||
chr5:154019000
|
A | T | 2 | a0001c0001t0020g0125a0001c0001t0020g0126 | 2 | HG02258.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.913+7399T>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154019000 | ||||||
chr5:154019071
|
A | C | 2 | a0002c0002t0030g0069a0002c0002t0031g0068 | 2 | HG01081.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.913+7328T>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154019071 | ||||||
chr5:154019349
|
G | T | 1 | a0001c0001t0001g0155 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.913+7050C>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154019349 | ||||||
chr5:154019359
|
A | G | 23 | a0002c0003t0004g0016a0002c0003t0004g0024a0002c0003t0004g0026others(20): Show | 29 | HG01069.hp2 HG01071.hp1 HG01167.hp2 others(26): Show |
intron_variant | MODIFIER | c.913+7040T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154019359 | ||||||
chr5:154019502
|
C | A | 1 | a0001c0001t0005g0232 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.913+6897G>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154019502 | ||||||
chr5:154019696
|
T | C | 1 | a0001c0001t0012g0101 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.913+6703A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154019696 | ||||||
chr5:154019783
|
A | C | 2 | a0001c0001t0005g0139a0001c0001t0005g0140 | 2 | HG02976.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.913+6616T>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154019783 | ||||||
chr5:154019786
|
G | A | 1 | a0001c0001t0001g0155 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.913+6613C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154019786 | ||||||
chr5:154019836
|
A | G | 4 | a0001c0001t0018g0030a0001c0001t0018g0127a0001c0001t0018g0128others(1): Show | 5 | HG02615.hp1 HG02809.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.913+6563T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154019836 | ||||||
chr5:154020162
|
C | T | 157 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(154): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.913+6237G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154020162 | ||||||
chr5:154020326
|
C | CA | 156 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(153): Show | 216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.913+6072dupT | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154020326 | ||||||
chr5:154020440
|
C | T | 1 | a0001c0001t0018g0030 | 2 | HG02615.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.913+5959G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154020440 | ||||||
chr5:154020486
|
T | A | 3 | a0001c0001t0018g0127a0001c0001t0018g0128a0001c0001t0025g0129 | 3 | HG02809.hp2 HG02896.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.913+5913A>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154020486 | ||||||
chr5:154020583
|
A | G | 1 | a0001c0001t0005g0232 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.913+5816T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154020583 | ||||||
chr5:154020757
|
A | G | 1 | a0001c0001t0005g0138 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.913+5642T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154020757 | ||||||
chr5:154020867
|
C | A | 135 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(132): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.913+5532G>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154020867 | ||||||
chr5:154020915
|
G | A | 1 | a0001c0001t0001g0229 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.913+5484C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154020915 | ||||||
chr5:154020932
|
A | G | 135 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(132): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.913+5467T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154020932 | ||||||
chr5:154021261
|
G | A | 9 | a0001c0001t0001g0187a0001c0001t0015g0156a0001c0001t0015g0188others(6): Show | 9 | HG00423.hp1 HG00597.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.913+5138C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154021261 | ||||||
chr5:154021306
|
GC | G | 17 | a0001c0001t0006g0012a0001c0001t0006g0028a0001c0001t0006g0029others(14): Show | 22 | HG00438.hp2 HG02071.hp1 HG02132.hp2 others(19): Show |
intron_variant | MODIFIER | c.913+5092delG | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154021306 | ||||||
chr5:154021448
|
G | A | 1 | a0001c0001t0012g0101 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.913+4951C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154021448 | ||||||
chr5:154021567
|
A | T | 23 | a0002c0003t0004g0016a0002c0003t0004g0024a0002c0003t0004g0026others(20): Show | 29 | HG01069.hp2 HG01071.hp1 HG01167.hp2 others(26): Show |
intron_variant | MODIFIER | c.913+4832T>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154021567 | ||||||
chr5:154021571
|
G | A | 3 | a0002c0003t0016g0025a0002c0003t0016g0082a0002c0003t0016g0083 | 4 | HG01256.hp1 HG01515.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.913+4828C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154021571 | ||||||
chr5:154021636
|
C | T | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(156): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.913+4763G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154021636 | ||||||
chr5:154021691
|
A | G | 2 | a0001c0001t0002g0163a0001c0001t0035g0193 | 2 | HG02647.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.913+4708T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154021691 | ||||||
chr5:154021728
|
T | G | 1 | a0001c0001t0012g0104 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.913+4671A>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154021728 | ||||||
chr5:154021855
|
A | C | 5 | a0002c0002t0003g0004a0002c0002t0003g0044a0002c0002t0003g0053others(2): Show | 11 | HG01257.hp2 HG01928.hp2 HG02074.hp1 others(8): Show |
intron_variant | MODIFIER | c.913+4544T>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154021855 | ||||||
chr5:154022129
|
A | C | 92 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(89): Show | 132 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.913+4270T>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154022129 | ||||||
chr5:154022272
|
A | G | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(156): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.913+4127T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154022272 | ||||||
chr5:154022400
|
G | T | 1 | a0001c0001t0001g0190 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.913+3999C>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154022400 | ||||||
chr5:154022467
|
T | C | 1 | a0001c0001t0012g0101 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.913+3932A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154022467 | ||||||
chr5:154022476
|
G | T | 1 | a0001c0001t0025g0202 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.913+3923C>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154022476 | ||||||
chr5:154022490
|
T | C | 174 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(171): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.913+3909A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154022490 | ||||||
chr5:154022495
|
C | T | 2 | a0002c0002t0004g0059a0006c0011t0004g0099 | 2 | HG02818.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.913+3904G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154022495 | ||||||
chr5:154022719
|
A | T | 1 | a0002c0002t0003g0047 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.913+3680T>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154022719 | ||||||
chr5:154022823
|
G | A | 2 | a0001c0001t0001g0014a0001c0001t0015g0157 | 5 | HG02630.hp2 HG02922.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.913+3576C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154022823 | ||||||
chr5:154022933
|
A | G | 1 | a0001c0001t0001g0223 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.913+3466T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154022933 | ||||||
chr5:154022975
|
T | C | 12 | a0002c0002t0004g0085a0002c0002t0004g0091a0002c0002t0004g0092others(9): Show | 12 | HG00140.hp2 HG00639.hp1 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.913+3424A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154022975 | ||||||
chr5:154023125
|
T | C | 17 | a0001c0001t0006g0012a0001c0001t0006g0028a0001c0001t0006g0029others(14): Show | 22 | HG00438.hp2 HG02071.hp1 HG02132.hp2 others(19): Show |
intron_variant | MODIFIER | c.913+3274A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154023125 | ||||||
chr5:154023143
|
A | G | 174 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(171): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.913+3256T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154023143 | ||||||
chr5:154023223
|
C | A | 23 | a0002c0003t0004g0016a0002c0003t0004g0024a0002c0003t0004g0026others(20): Show | 29 | HG01069.hp2 HG01071.hp1 HG01167.hp2 others(26): Show |
intron_variant | MODIFIER | c.913+3176G>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154023223 | ||||||
chr5:154023324
|
G | T | 8 | a0001c0001t0011g0009a0001c0001t0011g0243a0001c0001t0011g0244others(5): Show | 13 | HG01192.hp1 HG01884.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.913+3075C>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154023324 | ||||||
chr5:154023390
|
C | T | 1 | a0001c0001t0026g0041 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.913+3009G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154023390 | ||||||
chr5:154023463
|
T | C | 1 | a0001c0001t0012g0101 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.913+2936A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154023463 | ||||||
chr5:154023510
|
A | C | 7 | a0001c0001t0011g0009a0001c0001t0011g0243a0001c0001t0011g0244others(4): Show | 12 | HG01192.hp1 HG01884.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.913+2889T>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154023510 | ||||||
chr5:154023670
|
T | C | 84 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(81): Show | 124 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.913+2729A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154023670 | ||||||
chr5:154023863
|
C | T | 3 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0039g0209 | 3 | HG00738.hp1 HG01070.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.913+2536G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154023863 | ||||||
chr5:154023864
|
T | G | 103 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(100): Show | 144 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(141): Show |
intron_variant | MODIFIER | c.913+2535A>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154023864 | ||||||
chr5:154023992
|
G | T | 1 | a0002c0002t0007g0066 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.913+2407C>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154023992 | ||||||
chr5:154024055
|
A | G | 174 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(171): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.913+2344T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154024055 | ||||||
chr5:154024085
|
C | T | 12 | a0002c0002t0004g0085a0002c0002t0004g0091a0002c0002t0004g0092others(9): Show | 12 | HG00140.hp2 HG00639.hp1 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.913+2314G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154024085 | ||||||
chr5:154024108
|
T | A | 1 | a0001c0001t0005g0158 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.913+2291A>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154024108 | ||||||
chr5:154024327
|
A | C | 1 | a0001c0001t0001g0206 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.913+2072T>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154024327 | ||||||
chr5:154024394
|
A | T | 1 | a0001c0001t0002g0164 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.913+2005T>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154024394 | ||||||
chr5:154024467
|
A | G | 12 | a0002c0002t0004g0085a0002c0002t0004g0091a0002c0002t0004g0092others(9): Show | 12 | HG00140.hp2 HG00639.hp1 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.913+1932T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154024467 | ||||||
chr5:154024620
|
A | G | 1 | a0001c0001t0001g0173 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.913+1779T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154024620 | ||||||
chr5:154024634
|
C | A | 4 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0161others(1): Show | 4 | HG00621.hp2 NA18960.hp2 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.913+1765G>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154024634 | ||||||
chr5:154024658
|
C | T | 1 | a0002c0003t0013g0076 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.913+1741G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154024658 | ||||||
chr5:154024673
|
A | G | 1 | a0001c0001t0026g0041 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.913+1726T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154024673 | ||||||
chr5:154024842
|
C | G | 1 | a0001c0001t0001g0205 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.913+1557G>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154024842 | ||||||
chr5:154025011
|
A | C | 1 | a0001c0001t0026g0041 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.913+1388T>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154025011 | ||||||
chr5:154025139
|
C | T | 1 | a0002c0002t0007g0066 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.913+1260G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154025139 | ||||||
chr5:154025141
|
C | CA | 17 | a0001c0001t0006g0012a0001c0001t0006g0028a0001c0001t0006g0029others(14): Show | 22 | HG00438.hp2 HG02071.hp1 HG02132.hp2 others(19): Show |
intron_variant | MODIFIER | c.913+1257dupT | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154025141 | ||||||
chr5:154025291
|
C | CT | 160 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(157): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.913+1107dupA | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154025291 | ||||||
chr5:154025331
|
A | G | 15 | a0001c0001t0011g0009a0001c0001t0011g0243a0001c0001t0011g0244others(12): Show | 20 | HG01192.hp1 HG01884.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.913+1068T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154025331 | ||||||
chr5:154025428
|
G | GA | 27 | a0001c0001t0001g0132a0001c0001t0001g0200a0001c0001t0001g0241others(24): Show | 39 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(36): Show |
intron_variant | MODIFIER | c.913+970dupT | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154025428 | ||||||
chr5:154025502
|
C | CTCATAGA others(200): Show |
1 | a0001c0001t0001g0190 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.913+896_913+897ins others(207): Show |
FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154025502 | ||||||
chr5:154025525
|
C | T | 174 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(171): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.913+874G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154025525 | ||||||
chr5:154025582
|
A | T | 1 | a0001c0001t0002g0242 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.913+817T>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154025582 | ||||||
chr5:154025744
|
C | A | 1 | a0002c0002t0003g0054 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.913+655G>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154025744 | ||||||
chr5:154025854
|
T | G | 100 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(97): Show | 141 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.913+545A>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154025854 | ||||||
chr5:154026024
|
G | A | 15 | a0001c0001t0011g0009a0001c0001t0011g0243a0001c0001t0011g0244others(12): Show | 20 | HG01192.hp1 HG01884.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.913+375C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154026024 | ||||||
chr5:154026094
|
T | C | 174 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(171): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.913+305A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154026094 | ||||||
chr5:154026266
|
T | A | 7 | a0004c0005t0009g0042a0004c0005t0009g0043a0004c0005t0009g0105others(4): Show | 7 | HG02109.hp2 HG02280.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.913+133A>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154026266 | ||||||
chr5:154026360
|
C | T | 7 | a0001c0001t0014g0136a0001c0001t0014g0137a0001c0001t0014g0171others(4): Show | 8 | HG00438.hp1 HG02683.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.913+39G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 8/13 | chr5 | 154026360 | ||||||
chr5:154026588
|
G | A | 1 | a0001c0001t0026g0041 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.790-66C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 7/13 | chr5 | 154026588 | ||||||
chr5:154026750
|
CAGTGTTT | C | 17 | a0001c0001t0006g0012a0001c0001t0006g0028a0001c0001t0006g0029others(14): Show | 22 | HG00438.hp2 HG02071.hp1 HG02132.hp2 others(19): Show |
intron_variant | MODIFIER | c.790-235_790-229del others(7): Show |
FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 7/13 | chr5 | 154026750 | ||||||
chr5:154026793
|
T | C | 5 | a0002c0003t0004g0073a0002c0003t0004g0078a0002c0003t0004g0079others(2): Show | 5 | HG02055.hp1 HG02257.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.790-271A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 7/13 | chr5 | 154026793 | ||||||
chr5:154026829
|
C | A | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(156): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.790-307G>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 7/13 | chr5 | 154026829 | ||||||
chr5:154026830
|
A | C | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(156): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.790-308T>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 7/13 | chr5 | 154026830 | ||||||
chr5:154026881
|
T | TA | 165 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(162): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.789+294dupT | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 7/13 | chr5 | 154026881 | ||||||
chr5:154026881
|
T | TAAA | 5 | a0002c0002t0003g0004a0002c0002t0003g0044a0002c0002t0003g0053others(2): Show | 11 | HG01257.hp2 HG01928.hp2 HG02074.hp1 others(8): Show |
intron_variant | MODIFIER | c.789+292_789+294dup others(3): Show |
FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 7/13 | chr5 | 154026881 | ||||||
chr5:154026924
|
T | C | 1 | a0001c0007t0014g0040 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.789+252A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 7/13 | chr5 | 154026924 | ||||||
chr5:154026932
|
T | G | 1 | a0001c0001t0002g0170 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.789+244A>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 7/13 | chr5 | 154026932 | ||||||
chr5:154027010
|
A | C | 2 | a0002c0002t0010g0089a0002c0002t0010g0095 | 2 | HG01255.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.789+166T>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 7/13 | chr5 | 154027010 | ||||||
chr5:154027016
|
A | T | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(156): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.789+160T>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 7/13 | chr5 | 154027016 | ||||||
chr5:154027084
|
C | T | 173 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(170): Show | 238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.789+92G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 7/13 | chr5 | 154027084 | ||||||
chr5:154027381
|
A | C | 1 | a0001c0001t0034g0240 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.631-47T>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 6/13 | chr5 | 154027381 | ||||||
chr5:154027401
|
G | A | 1 | a0001c0001t0001g0229 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.631-67C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 6/13 | chr5 | 154027401 | ||||||
chr5:154027427
|
G | C | 174 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(171): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.631-93C>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 6/13 | chr5 | 154027427 | ||||||
chr5:154027649
|
C | T | 1 | a0001c0001t0026g0041 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.631-315G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 6/13 | chr5 | 154027649 | ||||||
chr5:154027689
|
C | T | 1 | a0001c0001t0002g0192 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.631-355G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 6/13 | chr5 | 154027689 | ||||||
chr5:154027690
|
G | A | 1 | a0001c0001t0001g0221 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.631-356C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 6/13 | chr5 | 154027690 | ||||||
chr5:154027718
|
C | T | 7 | a0004c0005t0009g0042a0004c0005t0009g0043a0004c0005t0009g0105others(4): Show | 7 | HG02109.hp2 HG02280.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.631-384G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 6/13 | chr5 | 154027718 | ||||||
chr5:154027777
|
A | G | 1 | a0003c0004t0001g0162 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.630+372T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 6/13 | chr5 | 154027777 | ||||||
chr5:154027837
|
A | G | 103 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(100): Show | 144 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(141): Show |
intron_variant | MODIFIER | c.630+312T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 6/13 | chr5 | 154027837 | ||||||
chr5:154027968
|
G | C | 2 | a0001c0001t0020g0125a0001c0001t0020g0126 | 2 | HG02258.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.630+181C>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 6/13 | chr5 | 154027968 | ||||||
chr5:154028612
|
C | T | 1 | a0001c0001t0026g0041 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.496-329G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 5/13 | chr5 | 154028612 | ||||||
chr5:154028764
|
A | G | 1 | a0002c0002t0004g0094 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.496-481T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 5/13 | chr5 | 154028764 | ||||||
chr5:154028827
|
G | A | 2 | a0001c0001t0001g0132a0001c0001t0001g0200 | 2 | HG03834.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.496-544C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 5/13 | chr5 | 154028827 | ||||||
chr5:154028871
|
C | G | 1 | a0001c0001t0001g0203 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.496-588G>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 5/13 | chr5 | 154028871 | ||||||
chr5:154028969
|
T | C | 15 | a0001c0001t0011g0009a0001c0001t0011g0243a0001c0001t0011g0244others(12): Show | 20 | HG01192.hp1 HG01884.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.495+520A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 5/13 | chr5 | 154028969 | ||||||
chr5:154028983
|
G | C | 1 | a0002c0002t0007g0066 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.495+506C>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 5/13 | chr5 | 154028983 | ||||||
chr5:154029112
|
C | T | 2 | a0005c0008t0021g0134a0005c0008t0021g0172 | 2 | HG02145.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.495+377G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 5/13 | chr5 | 154029112 | ||||||
chr5:154029423
|
G | C | 1 | a0002c0002t0003g0055 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.495+66C>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 5/13 | chr5 | 154029423 | ||||||
chr5:154029592
|
A | C | 17 | a0001c0001t0006g0012a0001c0001t0006g0028a0001c0001t0006g0029others(14): Show | 22 | HG00438.hp2 HG02071.hp1 HG02132.hp2 others(19): Show |
intron_variant | MODIFIER | c.404-12T>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 4/13 | chr5 | 154029592 | ||||||
chr5:154029635
|
C | T | 17 | a0001c0001t0006g0012a0001c0001t0006g0028a0001c0001t0006g0029others(14): Show | 22 | HG00438.hp2 HG02071.hp1 HG02132.hp2 others(19): Show |
intron_variant | MODIFIER | c.404-55G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 4/13 | chr5 | 154029635 | ||||||
chr5:154029995
|
T | C | 15 | a0001c0001t0011g0009a0001c0001t0011g0243a0001c0001t0011g0244others(12): Show | 20 | HG01192.hp1 HG01884.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.404-415A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 4/13 | chr5 | 154029995 | ||||||
chr5:154030107
|
A | G | 15 | a0001c0001t0011g0009a0001c0001t0011g0243a0001c0001t0011g0244others(12): Show | 20 | HG01192.hp1 HG01884.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.404-527T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 4/13 | chr5 | 154030107 | ||||||
chr5:154030232
|
G | A | 1 | a0001c0001t0018g0030 | 2 | HG02615.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.404-652C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 4/13 | chr5 | 154030232 | ||||||
chr5:154030383
|
C | T | 15 | a0001c0001t0011g0009a0001c0001t0011g0243a0001c0001t0011g0244others(12): Show | 20 | HG01192.hp1 HG01884.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.404-803G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 4/13 | chr5 | 154030383 | ||||||
chr5:154030460
|
G | A | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(156): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.404-880C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 4/13 | chr5 | 154030460 | ||||||
chr5:154030461
|
T | C | 32 | a0001c0001t0001g0132a0001c0001t0001g0200a0001c0001t0002g0005others(29): Show | 45 | HG00099.hp2 HG00323.hp2 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.404-881A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 4/13 | chr5 | 154030461 | ||||||
chr5:154030616
|
G | T | 2 | a0001c0001t0005g0201a0001c0001t0025g0202 | 2 | HG02486.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.404-1036C>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 4/13 | chr5 | 154030616 | ||||||
chr5:154030628
|
C | A | 1 | a0002c0002t0003g0056 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.404-1048G>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 4/13 | chr5 | 154030628 | ||||||
chr5:154030628
|
C | T | 1 | a0002c0002t0007g0067 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.404-1048G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 4/13 | chr5 | 154030628 | ||||||
chr5:154030629
|
G | A | 1 | a0001c0001t0005g0201 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.404-1049C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 4/13 | chr5 | 154030629 | ||||||
chr5:154030660
|
C | T | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(156): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.404-1080G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 4/13 | chr5 | 154030660 | ||||||
chr5:154030714
|
C | A | 1 | a0001c0001t0014g0171 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.404-1134G>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 4/13 | chr5 | 154030714 | ||||||
chr5:154030803
|
C | A | 10 | a0002c0003t0004g0016a0002c0003t0004g0026a0002c0003t0004g0064others(7): Show | 14 | HG01256.hp1 HG01361.hp1 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.404-1223G>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 4/13 | chr5 | 154030803 | ||||||
chr5:154030855
|
G | A | 7 | a0004c0005t0009g0042a0004c0005t0009g0043a0004c0005t0009g0105others(4): Show | 7 | HG02109.hp2 HG02280.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.404-1275C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 4/13 | chr5 | 154030855 | ||||||
chr5:154030862
|
TGA | T | 3 | a0001c0001t0006g0113a0001c0001t0006g0114a0001c0001t0006g0118 | 3 | HG02071.hp1 NA18977.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.404-1284_404-1283d others(4): Show |
FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 4/13 | chr5 | 154030862 | ||||||
chr5:154030937
|
G | A | 1 | a0001c0001t0026g0041 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.404-1357C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 4/13 | chr5 | 154030937 | ||||||
chr5:154030944
|
C | G | 15 | a0001c0001t0011g0009a0001c0001t0011g0243a0001c0001t0011g0244others(12): Show | 20 | HG01192.hp1 HG01884.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.404-1364G>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 4/13 | chr5 | 154030944 | ||||||
chr5:154030995
|
T | C | 3 | a0002c0003t0016g0025a0002c0003t0016g0082a0002c0003t0016g0083 | 4 | HG01256.hp1 HG01515.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.404-1415A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 4/13 | chr5 | 154030995 | ||||||
chr5:154031080
|
G | T | 1 | a0001c0001t0022g0133 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.404-1500C>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 4/13 | chr5 | 154031080 | ||||||
chr5:154031312
|
C | CA | 21 | a0002c0002t0003g0004a0002c0002t0003g0007a0002c0002t0003g0010others(18): Show | 38 | HG00735.hp1 HG01257.hp2 HG01928.hp2 others(35): Show |
intron_variant | MODIFIER | c.404-1733dupT | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 4/13 | chr5 | 154031312 | ||||||
chr5:154031312
|
C | CAAAAAAA others(2): Show |
3 | a0001c0001t0011g0009a0001c0001t0011g0243a0001c0001t0012g0101 | 7 | HG01884.hp2 HG01981.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.404-1741_404-1733d others(11): Show |
FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 4/13 | chr5 | 154031312 | ||||||
chr5:154031312
|
C | CAAAAAAA others(3): Show |
1 | a0001c0001t0011g0244 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.404-1742_404-1733d others(12): Show |
FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 4/13 | chr5 | 154031312 | ||||||
chr5:154031312
|
C | CAAAAAAA others(4): Show |
6 | a0001c0001t0001g0132a0004c0005t0009g0042a0004c0005t0009g0105others(3): Show | 6 | HG02280.hp2 HG02630.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.404-1743_404-1733d others(13): Show |
FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 4/13 | chr5 | 154031312 | ||||||
chr5:154031312
|
C | CAAAAAAA others(5): Show |
87 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(84): Show | 129 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.404-1744_404-1733d others(14): Show |
FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 4/13 | chr5 | 154031312 | ||||||
chr5:154031312
|
C | CAAAAAAA others(6): Show |
68 | a0001c0001t0001g0006a0001c0001t0001g0020a0001c0001t0001g0038others(65): Show | 81 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.404-1745_404-1733d others(15): Show |
FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 4/13 | chr5 | 154031312 | ||||||
chr5:154031312
|
C | CAAAAAAA others(7): Show |
20 | a0001c0001t0001g0036a0001c0001t0001g0039a0001c0001t0001g0203others(17): Show | 25 | HG00639.hp1 HG01123.hp2 HG01256.hp1 others(22): Show |
intron_variant | MODIFIER | c.404-1746_404-1733d others(16): Show |
FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 4/13 | chr5 | 154031312 | ||||||
chr5:154031312
|
C | CAAAAAAA others(8): Show |
3 | a0002c0003t0004g0026a0002c0003t0004g0064a0002c0003t0016g0083 | 4 | HG01361.hp1 HG01433.hp1 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.404-1747_404-1733d others(17): Show |
FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 4/13 | chr5 | 154031312 | ||||||
chr5:154031312
|
C | CAAAAAAA others(11): Show |
7 | a0001c0001t0006g0028a0001c0001t0006g0029a0001c0001t0006g0113others(4): Show | 9 | HG02071.hp1 HG02132.hp2 NA18952.hp1 others(6): Show |
intron_variant | MODIFIER | c.404-1733_404-1732i others(20): Show |
FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 4/13 | chr5 | 154031312 | ||||||
chr5:154031312
|
C | CAAAAAAA others(12): Show |
6 | a0001c0001t0006g0012a0001c0001t0006g0118a0001c0001t0006g0120others(3): Show | 9 | HG00438.hp2 HG02155.hp1 NA18963.hp1 others(6): Show |
intron_variant | MODIFIER | c.404-1733_404-1732i others(21): Show |
FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 4/13 | chr5 | 154031312 | ||||||
chr5:154031312
|
C | CAAAAAAA others(13): Show |
2 | a0001c0001t0006g0123a0001c0001t0006g0124 | 2 | NA18953.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.404-1733_404-1732i others(22): Show |
FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 4/13 | chr5 | 154031312 | ||||||
chr5:154031330
|
C | T | 1 | a0001c0001t0023g0131 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.404-1750G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 4/13 | chr5 | 154031330 | ||||||
chr5:154031374
|
G | A | 135 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(132): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.404-1794C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 4/13 | chr5 | 154031374 | ||||||
chr5:154031500
|
A | T | 1 | a0001c0001t0012g0101 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.404-1920T>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 4/13 | chr5 | 154031500 | ||||||
chr5:154031861
|
A | G | 8 | a0001c0001t0011g0009a0001c0001t0011g0243a0001c0001t0011g0244others(5): Show | 13 | HG01192.hp1 HG01884.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.403+1930T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 4/13 | chr5 | 154031861 | ||||||
chr5:154031865
|
T | G | 1 | a0001c0001t0023g0131 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.403+1926A>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 4/13 | chr5 | 154031865 | ||||||
chr5:154031980
|
C | T | 4 | a0002c0002t0004g0085a0002c0002t0010g0086a0002c0002t0010g0087others(1): Show | 4 | HG02615.hp2 HG02622.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.403+1811G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 4/13 | chr5 | 154031980 | ||||||
chr5:154032363
|
T | C | 1 | a0001c0001t0026g0041 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.403+1428A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 4/13 | chr5 | 154032363 | ||||||
chr5:154032413
|
G | A | 8 | a0002c0002t0004g0091a0002c0002t0004g0092a0002c0002t0004g0094others(5): Show | 8 | HG00140.hp2 HG00639.hp1 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.403+1378C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 4/13 | chr5 | 154032413 | ||||||
chr5:154032418
|
A | G | 4 | a0002c0002t0004g0085a0002c0002t0010g0086a0002c0002t0010g0087others(1): Show | 4 | HG02615.hp2 HG02622.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.403+1373T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 4/13 | chr5 | 154032418 | ||||||
chr5:154032421
|
T | C | 2 | a0001c0001t0020g0125a0001c0001t0020g0126 | 2 | HG02258.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.403+1370A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 4/13 | chr5 | 154032421 | ||||||
chr5:154032521
|
T | C | 1 | a0001c0001t0018g0030 | 2 | HG02615.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.403+1270A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 4/13 | chr5 | 154032521 | ||||||
chr5:154032524
|
T | C | 1 | a0002c0003t0004g0084 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.403+1267A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 4/13 | chr5 | 154032524 | ||||||
chr5:154032625
|
C | G | 174 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(171): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.403+1166G>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 4/13 | chr5 | 154032625 | ||||||
chr5:154032921
|
G | A | 20 | a0002c0002t0003g0004a0002c0002t0003g0007a0002c0002t0003g0010others(17): Show | 37 | HG00735.hp1 HG01257.hp2 HG01928.hp2 others(34): Show |
intron_variant | MODIFIER | c.403+870C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 4/13 | chr5 | 154032921 | ||||||
chr5:154032969
|
G | A | 188 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(185): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.403+822C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 4/13 | chr5 | 154032969 | ||||||
chr5:154033285
|
G | A | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(156): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.403+506C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 4/13 | chr5 | 154033285 | ||||||
chr5:154033363
|
G | A | 1 | a0001c0001t0001g0231 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.403+428C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 4/13 | chr5 | 154033363 | ||||||
chr5:154033522
|
T | C | 37 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0020others(34): Show | 53 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.403+269A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 4/13 | chr5 | 154033522 | ||||||
chr5:154033688
|
G | A | 2 | a0002c0003t0013g0098a0002c0003t0032g0097 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.403+103C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 4/13 | chr5 | 154033688 | ||||||
chr5:154033706
|
T | A | 1 | a0001c0001t0005g0232 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.403+85A>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 4/13 | chr5 | 154033706 | ||||||
chr5:154034982
|
G | GC | 15 | a0001c0001t0011g0009a0001c0001t0011g0243a0001c0001t0011g0244others(12): Show | 20 | HG01192.hp1 HG01884.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.-14-16dupG | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 1/13 | chr5 | 154034982 | ||||||
chr5:154034985
|
C | CA | 158 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(155): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.-14-19dupT | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 1/13 | chr5 | 154034985 | ||||||
chr5:154034986
|
A | C | 1 | a0004c0005t0009g0105 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-14-19T>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 1/13 | chr5 | 154034986 | ||||||
chr5:154035074
|
G | A | 1 | a0002c0002t0004g0057 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-14-107C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 1/13 | chr5 | 154035074 | ||||||
chr5:154035212
|
C | T | 15 | a0001c0001t0011g0009a0001c0001t0011g0243a0001c0001t0011g0244others(12): Show | 20 | HG01192.hp1 HG01884.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.-14-245G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 1/13 | chr5 | 154035212 | ||||||
chr5:154035273
|
C | T | 2 | a0002c0002t0007g0065a0002c0002t0007g0066 | 2 | HG02717.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-14-306G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 1/13 | chr5 | 154035273 | ||||||
chr5:154035539
|
T | G | 1 | a0006c0011t0004g0099 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-14-572A>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 1/13 | chr5 | 154035539 | ||||||
chr5:154035676
|
A | T | 1 | a0002c0002t0003g0046 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-14-709T>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 1/13 | chr5 | 154035676 | ||||||
chr5:154035759
|
T | A | 17 | a0001c0001t0006g0012a0001c0001t0006g0028a0001c0001t0006g0029others(14): Show | 22 | HG00438.hp2 HG02071.hp1 HG02132.hp2 others(19): Show |
intron_variant | MODIFIER | c.-14-792A>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 1/13 | chr5 | 154035759 | ||||||
chr5:154035915
|
T | A | 15 | a0001c0001t0011g0009a0001c0001t0011g0243a0001c0001t0011g0244others(12): Show | 20 | HG01192.hp1 HG01884.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.-14-948A>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 1/13 | chr5 | 154035915 | ||||||
chr5:154035922
|
T | C | 174 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(171): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.-14-955A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 1/13 | chr5 | 154035922 | ||||||
chr5:154036045
|
G | T | 2 | a0002c0003t0004g0064a0002c0003t0019g0063 | 2 | NA18965.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.-14-1078C>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 1/13 | chr5 | 154036045 | ||||||
chr5:154036137
|
T | C | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(152): Show | 214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.-14-1170A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 1/13 | chr5 | 154036137 | ||||||
chr5:154036269
|
T | A | 5 | a0001c0001t0002g0234a0001c0001t0002g0235a0001c0001t0002g0236others(2): Show | 5 | HG01516.hp1 HG01891.hp1 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.-14-1302A>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 1/13 | chr5 | 154036269 | ||||||
chr5:154036283
|
T | A | 239 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(236): Show | 334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.-14-1316A>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 1/13 | chr5 | 154036283 | ||||||
chr5:154036469
|
C | T | 2 | a0001c0001t0002g0031a0001c0001t0002g0130 | 3 | HG04204.hp1 HG04228.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.-14-1502G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 1/13 | chr5 | 154036469 | ||||||
chr5:154036533
|
T | C | 1 | a0001c0001t0018g0030 | 2 | HG02615.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-14-1566A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 1/13 | chr5 | 154036533 | ||||||
chr5:154036572
|
G | A | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(152): Show | 214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.-14-1605C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 1/13 | chr5 | 154036572 | ||||||
chr5:154036668
|
G | GA | 8 | a0001c0001t0011g0009a0001c0001t0011g0243a0001c0001t0011g0244others(5): Show | 14 | HG01192.hp1 HG01884.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.-14-1702dupT | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 1/13 | chr5 | 154036668 | ||||||
chr5:154036806
|
G | A | 170 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(167): Show | 234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.-14-1839C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 1/13 | chr5 | 154036806 | ||||||
chr5:154036859
|
T | TA | 15 | a0001c0001t0011g0009a0001c0001t0011g0243a0001c0001t0011g0244others(12): Show | 20 | HG01192.hp1 HG01884.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.-14-1893dupT | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 1/13 | chr5 | 154036859 | ||||||
chr5:154037079
|
G | A | 1 | a0002c0002t0004g0058 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-15+1778C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 1/13 | chr5 | 154037079 | ||||||
chr5:154037248
|
A | G | 2 | a0001c0001t0020g0125a0001c0001t0020g0126 | 2 | HG02258.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.-15+1609T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 1/13 | chr5 | 154037248 | ||||||
chr5:154037428
|
T | C | 1 | a0001c0001t0015g0239 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.-15+1429A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 1/13 | chr5 | 154037428 | ||||||
chr5:154037448
|
C | T | 17 | a0001c0001t0006g0012a0001c0001t0006g0028a0001c0001t0006g0029others(14): Show | 22 | HG00438.hp2 HG02071.hp1 HG02132.hp2 others(19): Show |
intron_variant | MODIFIER | c.-15+1409G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 1/13 | chr5 | 154037448 | ||||||
chr5:154037617
|
C | A | 1 | a0002c0002t0007g0100 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-15+1240G>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 1/13 | chr5 | 154037617 | ||||||
chr5:154037742
|
C | T | 1 | a0001c0001t0001g0110 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-15+1115G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 1/13 | chr5 | 154037742 | ||||||
chr5:154037780
|
G | A | 1 | a0001c0001t0034g0240 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-15+1077C>T | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 1/13 | chr5 | 154037780 | ||||||
chr5:154037814
|
A | G | 1 | a0002c0002t0004g0059 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-15+1043T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 1/13 | chr5 | 154037814 | ||||||
chr5:154037868
|
C | T | 8 | a0001c0001t0011g0009a0001c0001t0011g0243a0001c0001t0011g0244others(5): Show | 13 | HG01192.hp1 HG01884.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.-15+989G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 1/13 | chr5 | 154037868 | ||||||
chr5:154038049
|
A | G | 20 | a0002c0002t0003g0004a0002c0002t0003g0007a0002c0002t0003g0010others(17): Show | 37 | HG00735.hp1 HG01257.hp2 HG01928.hp2 others(34): Show |
intron_variant | MODIFIER | c.-15+808T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 1/13 | chr5 | 154038049 | ||||||
chr5:154038085
|
A | G | 2 | a0002c0002t0003g0044a0002c0002t0029g0045 | 2 | NA18969.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.-15+772T>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 1/13 | chr5 | 154038085 | ||||||
chr5:154038161
|
T | C | 174 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(171): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.-15+696A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 1/13 | chr5 | 154038161 | ||||||
chr5:154038245
|
C | T | 1 | a0002c0002t0003g0010 | 4 | NA18946.hp2 NA18982.hp1 NA18987.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15+612G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 1/13 | chr5 | 154038245 | ||||||
chr5:154038255
|
T | C | 15 | a0001c0001t0011g0009a0001c0001t0011g0243a0001c0001t0011g0244others(12): Show | 20 | HG01192.hp1 HG01884.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.-15+602A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 1/13 | chr5 | 154038255 | ||||||
chr5:154038399
|
T | G | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(156): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.-15+458A>C | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 1/13 | chr5 | 154038399 | ||||||
chr5:154038546
|
T | C | 1 | a0001c0001t0001g0241 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-15+311A>G | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 1/13 | chr5 | 154038546 | ||||||
chr5:154038685
|
ATTCCTCA others(15): Show |
A | 1 | a0001c0001t0002g0242 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-15+150_-15+171del others(22): Show |
FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 1/13 | chr5 | 154038685 | ||||||
chr5:154038828
|
C | T | 2 | a0004c0005t0009g0042a0004c0005t0009g0043 | 2 | HG03098.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-15+29G>A | FAM114A2 | ENSG00000055147.19 | transcript | ENST00000351797.9 | protein_coding | 1/13 | chr5 | 154038828 |