geneid | 199870 |
---|---|
ensemblid | ENSG00000009780.16 |
hgncid | 28530 |
symbol | FAM76A |
name | family with sequence similarity 76 member A |
refseq_nuc | NM_152660.3 |
refseq_prot | NP_689873.1 |
ensembl_nuc | ENST00000373954.11 |
ensembl_prot | ENSP00000363065.5 |
mane_status | MANE Select |
chr | chr1 |
start | 27725961 |
end | 27763116 |
strand | + |
ver | v1.2 |
region | chr1:27725961-27763116 |
region5000 | chr1:27720961-27768116 |
regionname0 | FAM76A_chr1_27725961_27763116 |
regionname5000 | FAM76A_chr1_27720961_27768116 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 307 | 260 | 88 | 38 | 100 | 4 | 28 | 66 | FAM76A_chr1_27720961_27768116 | FAM76A | copy fasta | chr1 | 27720961 | 27768116 |
a0002 | 0/0 | 307 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAM76A_chr1_27720961_27768116 | FAM76A | copy fasta | chr1 | 27720961 | 27768116 |
a0003 | 0/0 | 307 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | copy fasta | chr1 | 27720961 | 27768116 |
a0004 | 0/0 | 307 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | copy fasta | chr1 | 27720961 | 27768116 |
a0005 | 0/0 | 307 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAM76A_chr1_27720961_27768116 | FAM76A | copy fasta | chr1 | 27720961 | 27768116 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 924 | 154 | 33 | 30 | 64 | 4 | 21 | FAM76A_chr1_27720961_27768116 | FAM76A | copy fasta | chr1 | 27720961 | 27768116 |
c0002 | 0/0 | 924 | 105 | 54 | 8 | 36 | 0 | 7 | FAM76A_chr1_27720961_27768116 | FAM76A | copy fasta | chr1 | 27720961 | 27768116 |
c0003 | 0/0 | 924 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | copy fasta | chr1 | 27720961 | 27768116 |
c0004 | 0/0 | 924 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | copy fasta | chr1 | 27720961 | 27768116 |
c0005 | 0/0 | 924 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | copy fasta | chr1 | 27720961 | 27768116 |
c0006 | 0/0 | 924 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | copy fasta | chr1 | 27720961 | 27768116 |
c0007 | 0/0 | 924 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | copy fasta | chr1 | 27720961 | 27768116 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 2655 | 118 | 25 | 26 | 50 | 2 | 14 | FAM76A_chr1_27720961_27768116 | FAM76A | copy fasta | chr1 | 27720961 | 27768116 |
t0002 | 0/0 | 2658 | 45 | 9 | 1 | 29 | 0 | 6 | FAM76A_chr1_27720961_27768116 | FAM76A | copy fasta | chr1 | 27720961 | 27768116 |
t0003 | 0/0 | 2656 | 12 | 10 | 2 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | copy fasta | chr1 | 27720961 | 27768116 |
t0004 | 0/0 | 2659 | 11 | 8 | 3 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | copy fasta | chr1 | 27720961 | 27768116 |
t0005 | 0/0 | 2656 | 9 | 4 | 1 | 4 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | copy fasta | chr1 | 27720961 | 27768116 |
t0006 | 0/0 | 2656 | 8 | 0 | 1 | 7 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | copy fasta | chr1 | 27720961 | 27768116 |
t0007 | 0/0 | 2654 | 6 | 1 | 0 | 1 | 2 | 2 | FAM76A_chr1_27720961_27768116 | FAM76A | copy fasta | chr1 | 27720961 | 27768116 |
t0008 | 0/0 | 2658 | 5 | 5 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | copy fasta | chr1 | 27720961 | 27768116 |
t0009 | 0/0 | 2657 | 4 | 3 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | copy fasta | chr1 | 27720961 | 27768116 |
t0010 | 0/0 | 2657 | 4 | 2 | 0 | 1 | 0 | 1 | FAM76A_chr1_27720961_27768116 | FAM76A | copy fasta | chr1 | 27720961 | 27768116 |
t0011 | 0/0 | 2655 | 3 | 0 | 0 | 0 | 0 | 3 | FAM76A_chr1_27720961_27768116 | FAM76A | copy fasta | chr1 | 27720961 | 27768116 |
t0012 | 0/0 | 2658 | 3 | 3 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | copy fasta | chr1 | 27720961 | 27768116 |
t0013 | 0/0 | 2659 | 3 | 1 | 0 | 2 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | copy fasta | chr1 | 27720961 | 27768116 |
t0014 | 0/0 | 2655 | 2 | 0 | 0 | 2 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | copy fasta | chr1 | 27720961 | 27768116 |
t0015 | 1/0 | 2656 | 2 | 0 | 1 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | copy fasta | chr1 | 27720961 | 27768116 |
t0016 | 0/0 | 2660 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | copy fasta | chr1 | 27720961 | 27768116 |
t0017 | 0/0 | 2657 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | copy fasta | chr1 | 27720961 | 27768116 |
t0018 | 0/0 | 2658 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | copy fasta | chr1 | 27720961 | 27768116 |
t0019 | 0/0 | 2657 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | copy fasta | chr1 | 27720961 | 27768116 |
t0020 | 0/0 | 2657 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | copy fasta | chr1 | 27720961 | 27768116 |
t0021 | 0/0 | 2658 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | copy fasta | chr1 | 27720961 | 27768116 |
t0022 | 0/0 | 2657 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | copy fasta | chr1 | 27720961 | 27768116 |
t0023 | 0/0 | 2657 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | copy fasta | chr1 | 27720961 | 27768116 |
t0024 | 0/0 | 2657 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | copy fasta | chr1 | 27720961 | 27768116 |
t0025 | 0/0 | 2655 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76A_chr1_27720961_27768116 | FAM76A | copy fasta | chr1 | 27720961 | 27768116 |
t0026 | 0/0 | 2659 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | copy fasta | chr1 | 27720961 | 27768116 |
t0027 | 0/0 | 2659 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | copy fasta | chr1 | 27720961 | 27768116 |
t0028 | 0/0 | 2656 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | copy fasta | chr1 | 27720961 | 27768116 |
t0029 | 0/0 | 2655 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76A_chr1_27720961_27768116 | FAM76A | copy fasta | chr1 | 27720961 | 27768116 |
t0030 | 0/0 | 2658 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | copy fasta | chr1 | 27720961 | 27768116 |
t0031 | 0/0 | 2658 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | copy fasta | chr1 | 27720961 | 27768116 |
t0032 | 0/0 | 2655 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | copy fasta | chr1 | 27720961 | 27768116 |
t0033 | 0/0 | 2655 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | copy fasta | chr1 | 27720961 | 27768116 |
t0034 | 0/0 | 2659 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | copy fasta | chr1 | 27720961 | 27768116 |
t0035 | 0/0 | 2658 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | copy fasta | chr1 | 27720961 | 27768116 |
t0036 | 0/0 | 2658 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | copy fasta | chr1 | 27720961 | 27768116 |
t0037 | 0/0 | 2656 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | copy fasta | chr1 | 27720961 | 27768116 |
t0038 | 0/0 | 2660 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | copy fasta | chr1 | 27720961 | 27768116 |
t0039 | 0/0 | 2659 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | copy fasta | chr1 | 27720961 | 27768116 |
t0040 | 0/0 | 2660 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | copy fasta | chr1 | 27720961 | 27768116 |
t0041 | 0/0 | 2656 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | copy fasta | chr1 | 27720961 | 27768116 |
t0042 | 0/0 | 2657 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | copy fasta | chr1 | 27720961 | 27768116 |
t0043 | 0/0 | 2658 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | copy fasta | chr1 | 27720961 | 27768116 |
t0044 | 0/0 | 2658 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | copy fasta | chr1 | 27720961 | 27768116 |
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 | 6 | 0 | 0 | 6 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0002 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0003 | 0/0 | 5 | 0 | 3 | 0 | 0 | 2 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0004 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0005 | 0/0 | 4 | 0 | 1 | 2 | 0 | 1 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0006 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0009 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0012 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0014 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0016 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0120 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0200 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 924 | 154 | 33 | 30 | 64 | 4 | 21 | FAM76A_chr1_27720961_27768116 | FAM76A | copy fasta | chr1 | 27720961 | 27768116 |
a0001c0002 | 0/0 | 924 | 105 | 54 | 8 | 36 | 0 | 7 | FAM76A_chr1_27720961_27768116 | FAM76A | copy fasta | chr1 | 27720961 | 27768116 |
a0001c0007 | 0/0 | 924 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | copy fasta | chr1 | 27720961 | 27768116 |
a0002c0005 | 0/0 | 924 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | copy fasta | chr1 | 27720961 | 27768116 |
a0003c0003 | 0/0 | 924 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | copy fasta | chr1 | 27720961 | 27768116 |
a0004c0004 | 0/0 | 924 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | copy fasta | chr1 | 27720961 | 27768116 |
a0005c0006 | 0/0 | 924 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | copy fasta | chr1 | 27720961 | 27768116 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 3578 | 116 | 25 | 26 | 48 | 2 | 14 | FAM76A_chr1_27720961_27768116 | FAM76A | copy fasta | chr1 | 27720961 | 27768116 |
a0001c0001t0005 | 0/0 | 3579 | 9 | 4 | 1 | 4 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | copy fasta | chr1 | 27720961 | 27768116 |
a0001c0001t0006 | 0/0 | 3579 | 8 | 0 | 1 | 7 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | copy fasta | chr1 | 27720961 | 27768116 |
a0001c0001t0007 | 0/0 | 3577 | 6 | 1 | 0 | 1 | 2 | 2 | FAM76A_chr1_27720961_27768116 | FAM76A | copy fasta | chr1 | 27720961 | 27768116 |
a0001c0001t0010 | 0/0 | 3580 | 3 | 1 | 0 | 1 | 0 | 1 | FAM76A_chr1_27720961_27768116 | FAM76A | copy fasta | chr1 | 27720961 | 27768116 |
a0001c0001t0011 | 0/0 | 3578 | 3 | 0 | 0 | 0 | 0 | 3 | FAM76A_chr1_27720961_27768116 | FAM76A | copy fasta | chr1 | 27720961 | 27768116 |
a0001c0001t0014 | 0/0 | 3578 | 2 | 0 | 0 | 2 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | copy fasta | chr1 | 27720961 | 27768116 |
a0001c0001t0015 | 1/0 | 3579 | 2 | 0 | 1 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | copy fasta | chr1 | 27720961 | 27768116 |
a0001c0001t0029 | 0/0 | 3578 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76A_chr1_27720961_27768116 | FAM76A | copy fasta | chr1 | 27720961 | 27768116 |
a0001c0001t0032 | 0/0 | 3578 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | copy fasta | chr1 | 27720961 | 27768116 |
a0001c0001t0033 | 0/0 | 3578 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | copy fasta | chr1 | 27720961 | 27768116 |
a0001c0001t0041 | 0/0 | 3579 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | copy fasta | chr1 | 27720961 | 27768116 |
a0001c0001t0042 | 0/0 | 3580 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | copy fasta | chr1 | 27720961 | 27768116 |
a0001c0002t0002 | 0/0 | 3581 | 45 | 9 | 1 | 29 | 0 | 6 | FAM76A_chr1_27720961_27768116 | FAM76A | copy fasta | chr1 | 27720961 | 27768116 |
a0001c0002t0003 | 0/0 | 3579 | 12 | 10 | 2 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | copy fasta | chr1 | 27720961 | 27768116 |
a0001c0002t0004 | 0/0 | 3582 | 11 | 8 | 3 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | copy fasta | chr1 | 27720961 | 27768116 |
a0001c0002t0008 | 0/0 | 3581 | 4 | 4 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | copy fasta | chr1 | 27720961 | 27768116 |
a0001c0002t0009 | 0/0 | 3580 | 4 | 3 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | copy fasta | chr1 | 27720961 | 27768116 |
a0001c0002t0012 | 0/0 | 3581 | 3 | 3 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | copy fasta | chr1 | 27720961 | 27768116 |
a0001c0002t0013 | 0/0 | 3582 | 3 | 1 | 0 | 2 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | copy fasta | chr1 | 27720961 | 27768116 |
a0001c0002t0016 | 0/0 | 3583 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | copy fasta | chr1 | 27720961 | 27768116 |
a0001c0002t0017 | 0/0 | 3580 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | copy fasta | chr1 | 27720961 | 27768116 |
a0001c0002t0018 | 0/0 | 3581 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | copy fasta | chr1 | 27720961 | 27768116 |
a0001c0002t0019 | 0/0 | 3580 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | copy fasta | chr1 | 27720961 | 27768116 |
a0001c0002t0020 | 0/0 | 3580 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | copy fasta | chr1 | 27720961 | 27768116 |
a0001c0002t0021 | 0/0 | 3581 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | copy fasta | chr1 | 27720961 | 27768116 |
a0001c0002t0022 | 0/0 | 3580 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | copy fasta | chr1 | 27720961 | 27768116 |
a0001c0002t0023 | 0/0 | 3580 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | copy fasta | chr1 | 27720961 | 27768116 |
a0001c0002t0024 | 0/0 | 3580 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | copy fasta | chr1 | 27720961 | 27768116 |
a0001c0002t0025 | 0/0 | 3578 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76A_chr1_27720961_27768116 | FAM76A | copy fasta | chr1 | 27720961 | 27768116 |
a0001c0002t0026 | 0/0 | 3582 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | copy fasta | chr1 | 27720961 | 27768116 |
a0001c0002t0027 | 0/0 | 3582 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | copy fasta | chr1 | 27720961 | 27768116 |
a0001c0002t0028 | 0/0 | 3579 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | copy fasta | chr1 | 27720961 | 27768116 |
a0001c0002t0030 | 0/0 | 3581 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | copy fasta | chr1 | 27720961 | 27768116 |
a0001c0002t0031 | 0/0 | 3581 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | copy fasta | chr1 | 27720961 | 27768116 |
a0001c0002t0034 | 0/0 | 3582 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | copy fasta | chr1 | 27720961 | 27768116 |
a0001c0002t0035 | 0/0 | 3581 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | copy fasta | chr1 | 27720961 | 27768116 |
a0001c0002t0037 | 0/0 | 3579 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | copy fasta | chr1 | 27720961 | 27768116 |
a0001c0002t0038 | 0/0 | 3583 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | copy fasta | chr1 | 27720961 | 27768116 |
a0001c0002t0039 | 0/0 | 3582 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | copy fasta | chr1 | 27720961 | 27768116 |
a0001c0002t0040 | 0/0 | 3583 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | copy fasta | chr1 | 27720961 | 27768116 |
a0001c0002t0043 | 0/0 | 3581 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | copy fasta | chr1 | 27720961 | 27768116 |
a0001c0002t0044 | 0/0 | 3581 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | copy fasta | chr1 | 27720961 | 27768116 |
a0001c0007t0008 | 0/0 | 3581 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | copy fasta | chr1 | 27720961 | 27768116 |
a0002c0005t0001 | 0/0 | 3578 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | copy fasta | chr1 | 27720961 | 27768116 |
a0003c0003t0010 | 0/0 | 3580 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | copy fasta | chr1 | 27720961 | 27768116 |
a0004c0004t0036 | 0/0 | 3581 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | copy fasta | chr1 | 27720961 | 27768116 |
a0005c0006t0001 | 0/0 | 3578 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | copy fasta | chr1 | 27720961 | 27768116 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 5 | 0 | 3 | 0 | 0 | 2 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0001g0005 | 0/0 | 4 | 0 | 1 | 2 | 0 | 1 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0001g0006 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0001g0120 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0005g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0005g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0005g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0005g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0005g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0005g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0005g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0005g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0005g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0006g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0006g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0006g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0006g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0006g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0006g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0006g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0006g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0007g0009 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0007g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0007g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0007g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0007g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0007g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0010g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0010g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0010g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0011g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0011g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0011g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0014g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0014g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0015g0200 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0015g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0029g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0032g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0033g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0041g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0001t0042g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0002t0002g0001 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0002t0002g0004 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0002t0002g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0002t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0002t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0002t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0002t0002g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0002t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0002t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0002t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0002t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0002t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0002t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0002t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0002t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0002t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0002t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0002t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0002t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0002t0003g0002 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0002t0003g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0002t0003g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0002t0003g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0002t0003g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0002t0003g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0002t0003g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0002t0003g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0002t0004g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0002t0004g0016 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0002t0004g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0002t0004g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0002t0004g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0002t0004g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0002t0004g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0002t0004g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0002t0004g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0002t0008g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0002t0008g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0002t0008g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0002t0008g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0002t0009g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0002t0009g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0002t0009g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0002t0012g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0002t0012g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0002t0012g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0002t0013g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0002t0013g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0002t0013g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0002t0016g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0002t0017g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0002t0018g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0002t0019g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0002t0020g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0002t0021g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0002t0022g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0002t0023g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0002t0024g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0002t0025g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0002t0026g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0002t0027g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0002t0028g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0002t0030g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0002t0031g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0002t0034g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0002t0035g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0002t0037g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0002t0038g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0002t0039g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0002t0040g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0002t0043g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0002t0044g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0001c0007t0008g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0002c0005t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0003c0003t0010g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0004c0004t0036g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
a0005c0006t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00408 | hp1 | a0001 | c0002 | t0002 | g0021 | EAS | CHS | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | CHS | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG00544 | hp1 | a0001 | c0002 | t0002 | g0058 | EAS | CHS | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | CHS | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG00597 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | CHS | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG00609 | hp2 | a0001 | c0001 | t0006 | g0111 | EAS | CHS | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG00621 | hp1 | a0001 | c0001 | t0006 | g0143 | EAS | CHS | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG00621 | hp2 | a0001 | c0002 | t0002 | g0022 | EAS | CHS | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG00639 | hp2 | a0001 | c0002 | t0003 | g0027 | AMR | PUR | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG00673 | hp1 | a0001 | c0002 | t0002 | g0050 | EAS | CHS | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | CHS | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG00741 | hp1 | a0001 | c0001 | t0042 | g0110 | AMR | PUR | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG00741 | hp2 | a0001 | c0001 | t0005 | g0185 | AMR | PUR | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG01069 | hp1 | a0001 | c0002 | t0002 | g0026 | AMR | PUR | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG01069 | hp2 | a0001 | c0002 | t0004 | g0015 | AMR | PUR | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG01071 | hp1 | a0001 | c0002 | t0004 | g0015 | AMR | PUR | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG01106 | hp1 | a0001 | c0002 | t0003 | g0071 | AMR | PUR | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG01175 | hp1 | a0001 | c0001 | t0006 | g0134 | AMR | PUR | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG01243 | hp1 | a0001 | c0002 | t0019 | g0074 | AMR | PUR | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG01243 | hp2 | a0001 | c0002 | t0004 | g0016 | AMR | PUR | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG01255 | hp1 | a0001 | c0001 | t0015 | g0201 | AMR | CLM | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG01255 | hp2 | a0001 | c0002 | t0026 | g0033 | AMR | CLM | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | CLM | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | CLM | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | CLM | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | CLM | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | CLM | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | CLM | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG01515 | hp1 | a0001 | c0001 | t0007 | g0009 | EUR | IBS | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG01515 | hp2 | a0001 | c0001 | t0007 | g0155 | EUR | IBS | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG01884 | hp1 | a0001 | c0002 | t0003 | g0002 | AFR | ACB | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG01884 | hp2 | a0001 | c0002 | t0002 | g0036 | AFR | ACB | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG01891 | hp1 | a0001 | c0002 | t0004 | g0213 | AFR | ACB | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | ACB | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PEL | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | PEL | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | PEL | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | PEL | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | PEL | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG02040 | hp2 | a0001 | c0002 | t0002 | g0007 | EAS | KHV | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG02055 | hp1 | a0001 | c0002 | t0021 | g0075 | AFR | ACB | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG02055 | hp2 | a0001 | c0002 | t0016 | g0208 | AFR | ACB | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | KHV | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG02056 | hp2 | a0001 | c0002 | t0002 | g0062 | EAS | KHV | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG02074 | hp1 | a0001 | c0001 | t0006 | g0184 | EAS | KHV | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | KHV | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | KHV | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG02080 | hp2 | a0001 | c0002 | t0002 | g0041 | EAS | KHV | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG02129 | hp1 | a0001 | c0002 | t0013 | g0004 | EAS | KHV | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | KHV | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG02145 | hp1 | a0001 | c0002 | t0002 | g0037 | AFR | ACB | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG02145 | hp2 | a0001 | c0002 | t0003 | g0073 | AFR | ACB | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | CDX | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG02155 | hp2 | a0001 | c0002 | t0002 | g0044 | EAS | CDX | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | CDX | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | CDX | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG02257 | hp1 | a0001 | c0002 | t0003 | g0076 | AFR | ACB | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG02257 | hp2 | a0001 | c0002 | t0004 | g0211 | AFR | ACB | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG02258 | hp1 | a0001 | c0002 | t0012 | g0024 | AFR | ACB | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG02258 | hp2 | a0001 | c0002 | t0027 | g0217 | AFR | ACB | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG02280 | hp1 | a0001 | c0001 | t0010 | g0084 | AFR | ACB | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | ACB | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG02451 | hp1 | a0001 | c0002 | t0037 | g0230 | AFR | ACB | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG02451 | hp2 | a0001 | c0002 | t0044 | g0038 | AFR | ACB | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG02523 | hp1 | a0001 | c0001 | t0005 | g0160 | EAS | KHV | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG02523 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | KHV | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG02572 | hp1 | a0001 | c0002 | t0008 | g0215 | AFR | GWD | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG02572 | hp2 | a0001 | c0002 | t0013 | g0032 | AFR | GWD | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG02615 | hp1 | a0001 | c0002 | t0020 | g0018 | AFR | GWD | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG02615 | hp2 | a0001 | c0001 | t0032 | g0129 | AFR | GWD | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | GWD | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG02622 | hp2 | a0001 | c0002 | t0004 | g0206 | AFR | GWD | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG02630 | hp1 | a0001 | c0002 | t0002 | g0067 | AFR | GWD | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | GWD | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG02647 | hp1 | a0001 | c0002 | t0002 | g0034 | AFR | GWD | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG02647 | hp2 | a0001 | c0002 | t0030 | g0212 | AFR | GWD | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG02683 | hp1 | a0001 | c0002 | t0002 | g0064 | SAS | PJL | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG02698 | hp1 | a0001 | c0001 | t0011 | g0197 | SAS | PJL | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG02698 | hp2 | a0001 | c0001 | t0007 | g0106 | SAS | PJL | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG02717 | hp1 | a0001 | c0002 | t0003 | g0070 | AFR | GWD | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG02723 | hp1 | a0001 | c0002 | t0003 | g0002 | AFR | GWD | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG02723 | hp2 | a0001 | c0002 | t0004 | g0205 | AFR | GWD | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG02738 | hp2 | a0001 | c0001 | t0010 | g0098 | SAS | PJL | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG02809 | hp1 | a0001 | c0002 | t0009 | g0069 | AFR | GWD | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG02809 | hp2 | a0001 | c0002 | t0009 | g0008 | AFR | GWD | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | GWD | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG02818 | hp2 | a0001 | c0002 | t0003 | g0002 | AFR | GWD | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG02886 | hp1 | a0001 | c0002 | t0038 | g0042 | AFR | GWD | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | GWD | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG02895 | hp2 | a0001 | c0002 | t0002 | g0043 | AFR | GWD | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG02896 | hp1 | a0001 | c0002 | t0012 | g0081 | AFR | GWD | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | GWD | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | GWD | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG02897 | hp2 | a0001 | c0002 | t0012 | g0025 | AFR | GWD | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG02965 | hp1 | a0001 | c0002 | t0002 | g0056 | AFR | ESN | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG02965 | hp2 | a0001 | c0002 | t0003 | g0002 | AFR | ESN | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | ESN | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG02970 | hp2 | a0001 | c0002 | t0008 | g0216 | AFR | ESN | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG02976 | hp1 | a0001 | c0002 | t0002 | g0031 | AFR | ESN | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | ESN | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG03017 | hp1 | a0001 | c0002 | t0002 | g0061 | SAS | PJL | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0227 | AFR | GWD | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | GWD | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG03098 | hp1 | a0004 | c0004 | t0036 | g0096 | AFR | MSL | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG03098 | hp2 | a0001 | c0002 | t0040 | g0209 | AFR | MSL | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | ESN | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG03130 | hp2 | a0001 | c0002 | t0018 | g0051 | AFR | ESN | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG03139 | hp1 | a0001 | c0002 | t0008 | g0219 | AFR | ESN | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG03139 | hp2 | a0001 | c0001 | t0005 | g0193 | AFR | ESN | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG03195 | hp1 | a0001 | c0002 | t0004 | g0204 | AFR | ESN | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG03195 | hp2 | a0001 | c0002 | t0031 | g0019 | AFR | ESN | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | MSL | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG03209 | hp2 | a0001 | c0002 | t0017 | g0066 | AFR | MSL | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG03225 | hp1 | a0001 | c0001 | t0005 | g0214 | AFR | MSL | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | MSL | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG03239 | hp1 | a0001 | c0002 | t0002 | g0045 | SAS | PJL | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG03239 | hp2 | a0001 | c0002 | t0002 | g0004 | SAS | PJL | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | MSL | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG03453 | hp2 | a0001 | c0002 | t0034 | g0035 | AFR | MSL | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG03486 | hp1 | a0001 | c0001 | t0005 | g0223 | AFR | MSL | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG03486 | hp2 | a0001 | c0002 | t0002 | g0029 | AFR | MSL | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG03669 | hp1 | a0001 | c0002 | t0002 | g0048 | SAS | PJL | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG03669 | hp2 | a0001 | c0001 | t0029 | g0174 | SAS | PJL | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG03704 | hp2 | a0001 | c0001 | t0011 | g0180 | SAS | PJL | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0190 | SAS | BEB | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG03831 | hp2 | a0001 | c0001 | t0007 | g0113 | SAS | BEB | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG03834 | hp1 | a0001 | c0002 | t0025 | g0057 | SAS | BEB | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0085 | SAS | BEB | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG03942 | hp1 | a0001 | c0001 | t0011 | g0179 | SAS | BEB | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0118 | SAS | BEB | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0191 | SAS | STU | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0183 | SAS | STU | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | STU | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | STU | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0090 | SAS | STU | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG04228 | hp2 | a0001 | c0002 | t0002 | g0046 | SAS | STU | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | YRI | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
NA18522 | hp2 | a0001 | c0002 | t0022 | g0020 | AFR | YRI | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | CHB | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
NA18612 | hp2 | a0001 | c0002 | t0002 | g0080 | EAS | CHB | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | CHB | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
NA18747 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | CHB | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
NA18906 | hp1 | a0001 | c0001 | t0007 | g0203 | AFR | YRI | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
NA18906 | hp2 | a0001 | c0002 | t0003 | g0002 | AFR | YRI | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
NA18939 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
NA18943 | hp2 | a0001 | c0002 | t0002 | g0047 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
NA18944 | hp2 | a0001 | c0001 | t0014 | g0232 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
NA18945 | hp2 | a0002 | c0005 | t0001 | g0014 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
NA18946 | hp1 | a0001 | c0002 | t0009 | g0039 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
NA18946 | hp2 | a0001 | c0001 | t0007 | g0167 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
NA18950 | hp1 | a0001 | c0001 | t0006 | g0153 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
NA18950 | hp2 | a0001 | c0001 | t0006 | g0138 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
NA18952 | hp2 | a0001 | c0002 | t0043 | g0007 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
NA18956 | hp1 | a0001 | c0001 | t0041 | g0233 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
NA18960 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
NA18961 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
NA18964 | hp2 | a0001 | c0002 | t0002 | g0040 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
NA18971 | hp1 | a0001 | c0002 | t0002 | g0059 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
NA18977 | hp1 | a0001 | c0002 | t0002 | g0023 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
NA18977 | hp2 | a0001 | c0001 | t0005 | g0123 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
NA18978 | hp2 | a0001 | c0002 | t0039 | g0079 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
NA18979 | hp1 | a0001 | c0002 | t0002 | g0068 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
NA18990 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
NA18993 | hp1 | a0001 | c0001 | t0005 | g0169 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
NA18993 | hp2 | a0001 | c0002 | t0002 | g0055 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
NA18995 | hp1 | a0001 | c0002 | t0002 | g0049 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
NA18995 | hp2 | a0001 | c0001 | t0006 | g0175 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
NA18999 | hp2 | a0005 | c0006 | t0001 | g0186 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
NA19000 | hp1 | a0001 | c0002 | t0028 | g0221 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
NA19000 | hp2 | a0001 | c0001 | t0006 | g0151 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
NA19002 | hp2 | a0001 | c0002 | t0002 | g0065 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
NA19030 | hp1 | a0001 | c0002 | t0004 | g0207 | AFR | LWK | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
NA19030 | hp2 | a0001 | c0001 | t0005 | g0130 | AFR | LWK | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | LWK | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
NA19043 | hp2 | a0001 | c0002 | t0035 | g0077 | AFR | LWK | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
NA19054 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
NA19054 | hp2 | a0001 | c0001 | t0005 | g0092 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
NA19058 | hp1 | a0001 | c0002 | t0002 | g0060 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
NA19060 | hp1 | a0001 | c0002 | t0002 | g0063 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
NA19076 | hp1 | a0001 | c0002 | t0024 | g0054 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
NA19076 | hp2 | a0001 | c0001 | t0010 | g0152 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
NA19078 | hp2 | a0001 | c0002 | t0013 | g0078 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
NA19081 | hp2 | a0001 | c0002 | t0002 | g0052 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
NA19090 | hp1 | a0001 | c0002 | t0002 | g0222 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
NA19091 | hp1 | a0001 | c0001 | t0014 | g0231 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | YRI | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | YRI | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
NA20129 | hp1 | a0001 | c0002 | t0023 | g0053 | AFR | ASW | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
NA20129 | hp2 | a0001 | c0002 | t0003 | g0072 | AFR | ASW | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0158 | EUR | TSI | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0121 | EUR | TSI | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG02109 | hp1 | a0001 | c0002 | t0004 | g0016 | AFR | ACB | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG02109 | hp2 | a0003 | c0003 | t0010 | g0097 | AFR | ACB | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | ACB | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG02486 | hp2 | a0001 | c0007 | t0008 | g0220 | AFR | ACB | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG02559 | hp1 | a0001 | c0002 | t0009 | g0008 | AFR | ACB | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG02559 | hp2 | a0001 | c0001 | t0033 | g0105 | AFR | ACB | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG03471 | hp2 | a0001 | c0002 | t0008 | g0218 | AFR | MSL | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG06807 | hp1 | a0001 | c0002 | t0003 | g0028 | AFR | USA | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
HG06807 | hp2 | a0001 | c0002 | t0004 | g0210 | AFR | USA | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | LWK | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
NA21309 | hp2 | a0001 | c0002 | t0002 | g0030 | AFR | LWK | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0120 | REF | REF | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0015 | g0200 | REF | REF | FAM76A_chr1_27720961_27768116 | FAM76A | chr1 | 27720961 | 27768116 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:27744718
|
A | G | 1 | a0005 | 1 | NA18999.hp2 | missense_variant | MODERATE | c.419A>G | p.Lys140Arg | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 5/9 | 539/3579 | 419/924 | 140/307 | chr1 | 27744718 | ||
chr1:27744774
|
C | G | 1 | a0002 | 1 | NA18945.hp2 | missense_variant | MODERATE | c.475C>G | p.Gln159Glu | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 5/9 | 595/3579 | 475/924 | 159/307 | chr1 | 27744774 | ||
chr1:27755244
|
A | G | 1 | a0004 | 1 | HG03098.hp1 | missense_variant | MODERATE | c.649A>G | p.Ile217Val | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 7/9 | 769/3579 | 649/924 | 217/307 | chr1 | 27755244 | ||
chr1:27760541
|
G | T | 1 | a0003 | 1 | HG02109.hp2 | missense_variant | MODERATE | c.884G>T | p.Ser295Ile | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 9/9 | 1004/3579 | 884/924 | 295/307 | chr1 | 27760541 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:27734063
|
A | G | 2 | a0001c0002a0001c0007 | 106 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(103): Show |
synonymous_variant | LOW | c.234A>G | p.Ala78Ala | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/9 | 354/3579 | 234/924 | 78/307 | chr1 | 27734063 | ||
chr1:27734174
|
T | C | 1 | a0001c0007 | 1 | HG02486.hp2 | synonymous_variant | LOW | c.345T>C | p.Asp115Asp | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/9 | 465/3579 | 345/924 | 115/307 | chr1 | 27734174 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:27725981
|
C | T | 1 | a0001c0002t0044 | 1 | HG02451.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-100C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 1/9 | chr1 | 27725981 | ||||||
chr1:27760715
|
G | A | 1 | a0001c0002t0016 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*134G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 9/9 | 134 | chr1 | 27760715 | |||||
chr1:27760774
|
T | C | 2 | a0001c0002t0017a0001c0002t0018 | 2 | HG03130.hp2 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*193T>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 9/9 | 193 | chr1 | 27760774 | |||||
chr1:27760778
|
T | C | 1 | a0001c0001t0011 | 3 | HG02698.hp1 HG03704.hp2 HG03942.hp1 |
3_prime_UTR_variant | MODIFIER | c.*197T>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 9/9 | 197 | chr1 | 27760778 | |||||
chr1:27760806
|
C | T | 1 | a0001c0002t0043 | 1 | NA18952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*225C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 9/9 | 225 | chr1 | 27760806 | |||||
chr1:27760877
|
C | CT | 6 | a0001c0001t0005a0001c0001t0041a0001c0001t0042others(3): Show | 24 | HG00741.hp1 HG00741.hp2 HG01069.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*319dupT | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 9/9 | 320 | INFO_REALIGN_3_PRIME | chr1 | 27760877 | ||||
chr1:27760877
|
CT | C | 13 | a0001c0001t0007a0001c0002t0002a0001c0002t0012others(10): Show | 64 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*319delT | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 9/9 | 319 | INFO_REALIGN_3_PRIME | chr1 | 27760877 | ||||
chr1:27760877
|
CTT | C | 6 | a0001c0002t0008a0001c0002t0009a0001c0002t0017others(3): Show | 12 | HG02055.hp1 HG02486.hp2 HG02559.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*318_*319delTT | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 9/9 | 318 | INFO_REALIGN_3_PRIME | chr1 | 27760877 | ||||
chr1:27760877
|
CTTT | C | 2 | a0001c0002t0003a0001c0002t0019 | 13 | HG00639.hp2 HG01106.hp1 HG01243.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*317_*319delTTT | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 9/9 | 317 | INFO_REALIGN_3_PRIME | chr1 | 27760877 | ||||
chr1:27760946
|
G | GT | 18 | a0001c0001t0006a0001c0001t0042a0001c0002t0002others(15): Show | 87 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*382dupT | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 9/9 | 383 | INFO_REALIGN_3_PRIME | chr1 | 27760946 | ||||
chr1:27760946
|
G | GTT | 9 | a0001c0002t0008a0001c0002t0019a0001c0002t0021others(6): Show | 12 | HG01243.hp1 HG01255.hp2 HG02055.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*381_*382dupTT | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 9/9 | 383 | INFO_REALIGN_3_PRIME | chr1 | 27760946 | ||||
chr1:27760952
|
T | G | 1 | a0001c0001t0029 | 1 | HG03669.hp2 | 3_prime_UTR_variant | MODIFIER | c.*371T>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 9/9 | 371 | chr1 | 27760952 | |||||
chr1:27760952
|
T | TG | 5 | a0001c0002t0004a0001c0002t0016a0001c0002t0020others(2): Show | 15 | HG01069.hp2 HG01071.hp1 HG01243.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*371_*372insG | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 9/9 | 372 | chr1 | 27760952 | |||||
chr1:27761124
|
G | A | 2 | a0001c0001t0014a0001c0001t0041 | 3 | NA18944.hp2 NA18956.hp1 NA19091.hp1 |
3_prime_UTR_variant | MODIFIER | c.*543G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 9/9 | 543 | chr1 | 27761124 | |||||
chr1:27761261
|
GA | G | 47 | a0001c0001t0001a0001c0001t0005a0001c0001t0006others(44): Show | 262 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(259): Show |
3_prime_UTR_variant | MODIFIER | c.*689delA | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 9/9 | 689 | INFO_REALIGN_3_PRIME | chr1 | 27761261 | ||||
chr1:27761450
|
T | G | 1 | a0001c0002t0012 | 3 | HG02258.hp1 HG02896.hp1 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*869T>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 9/9 | 869 | chr1 | 27761450 | |||||
chr1:27761640
|
T | C | 1 | a0001c0002t0023 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1059T>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 9/9 | 1059 | chr1 | 27761640 | |||||
chr1:27761809
|
C | T | 1 | a0001c0001t0029 | 1 | HG03669.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1228C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 9/9 | 1228 | chr1 | 27761809 | |||||
chr1:27761907
|
A | G | 4 | a0001c0002t0004a0001c0002t0016a0001c0002t0030others(1): Show | 14 | HG01069.hp2 HG01071.hp1 HG01243.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1326A>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 9/9 | 1326 | chr1 | 27761907 | |||||
chr1:27761964
|
C | CAA | 9 | a0001c0001t0010a0001c0002t0004a0001c0002t0023others(6): Show | 21 | HG01069.hp2 HG01071.hp1 HG01243.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*1398_*1399dupAA | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 9/9 | 1400 | INFO_REALIGN_3_PRIME | chr1 | 27761964 | ||||
chr1:27761964
|
C | CAAA | 22 | a0001c0002t0002a0001c0002t0003a0001c0002t0008others(19): Show | 87 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*1397_*1399dupAAA | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 9/9 | 1400 | INFO_REALIGN_3_PRIME | chr1 | 27761964 | ||||
chr1:27762072
|
C | A | 31 | a0001c0002t0002a0001c0002t0003a0001c0002t0004others(28): Show | 106 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(103): Show |
3_prime_UTR_variant | MODIFIER | c.*1491C>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 9/9 | 1491 | chr1 | 27762072 | |||||
chr1:27762084
|
T | G | 1 | a0001c0001t0032 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1503T>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 9/9 | 1503 | chr1 | 27762084 | |||||
chr1:27762157
|
A | G | 31 | a0001c0002t0002a0001c0002t0003a0001c0002t0004others(28): Show | 106 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(103): Show |
3_prime_UTR_variant | MODIFIER | c.*1576A>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 9/9 | 1576 | chr1 | 27762157 | |||||
chr1:27762482
|
T | C | 1 | a0001c0001t0033 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1901T>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 9/9 | 1901 | chr1 | 27762482 | |||||
chr1:27762524
|
G | C | 4 | a0001c0002t0004a0001c0002t0016a0001c0002t0030others(1): Show | 14 | HG01069.hp2 HG01071.hp1 HG01243.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1943G>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 9/9 | 1943 | chr1 | 27762524 | |||||
chr1:27762556
|
A | G | 3 | a0001c0002t0008a0001c0002t0027a0001c0007t0008 | 6 | HG02258.hp2 HG02486.hp2 HG02572.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1975A>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 9/9 | 1975 | chr1 | 27762556 | |||||
chr1:27762740
|
T | C | 1 | a0001c0002t0034 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2159T>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 9/9 | 2159 | chr1 | 27762740 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:27726165
|
C | G | 3 | a0001c0001t0014g0231a0001c0001t0014g0232a0001c0001t0041g0233 | 3 | NA18944.hp2 NA18956.hp1 NA19091.hp1 |
splice_region_variant&intron_variant | LOW | c.81+4C>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 1/8 | chr1 | 27726165 | ||||||
chr1:27726186
|
G | C | 1 | a0001c0001t0001g0017 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.81+25G>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 1/8 | chr1 | 27726186 | ||||||
chr1:27726329
|
G | A | 1 | a0001c0002t0020g0018 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.81+168G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 1/8 | chr1 | 27726329 | ||||||
chr1:27726381
|
C | T | 1 | a0001c0002t0037g0230 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.81+220C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 1/8 | chr1 | 27726381 | ||||||
chr1:27726509
|
C | T | 3 | a0001c0001t0001g0227a0001c0001t0001g0228a0001c0001t0001g0229 | 3 | HG02818.hp1 HG03041.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.81+348C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 1/8 | chr1 | 27726509 | ||||||
chr1:27726628
|
A | AT | 6 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0001g0226others(3): Show | 6 | HG02056.hp1 HG03225.hp2 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.81+483dupT | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 27726628 | |||||
chr1:27726629
|
T | A | 2 | a0001c0002t0022g0020a0001c0002t0031g0019 | 2 | HG03195.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.81+468T>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 1/8 | chr1 | 27726629 | ||||||
chr1:27726694
|
A | C | 6 | a0001c0002t0008g0215a0001c0002t0008g0216a0001c0002t0008g0218others(3): Show | 6 | HG02258.hp2 HG02486.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.81+533A>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 1/8 | chr1 | 27726694 | ||||||
chr1:27726752
|
C | T | 1 | a0001c0001t0005g0214 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.81+591C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 1/8 | chr1 | 27726752 | ||||||
chr1:27726800
|
G | A | 80 | a0001c0002t0002g0001a0001c0002t0002g0004a0001c0002t0002g0007others(77): Show | 92 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(89): Show |
intron_variant | MODIFIER | c.81+639G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 1/8 | chr1 | 27726800 | ||||||
chr1:27726966
|
C | T | 12 | a0001c0002t0004g0015a0001c0002t0004g0016a0001c0002t0004g0204others(9): Show | 14 | HG01069.hp2 HG01071.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.82-506C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 1/8 | chr1 | 27726966 | ||||||
chr1:27727083
|
T | C | 1 | a0001c0002t0002g0021 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.82-389T>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 1/8 | chr1 | 27727083 | ||||||
chr1:27727136
|
T | C | 1 | a0001c0002t0002g0022 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.82-336T>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 1/8 | chr1 | 27727136 | ||||||
chr1:27727615
|
A | G | 1 | a0001c0001t0007g0203 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.146+79A>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | chr1 | 27727615 | ||||||
chr1:27727800
|
AT | A | 116 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(113): Show | 129 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(126): Show |
intron_variant | MODIFIER | c.146+289delT | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 27727800 | |||||
chr1:27727800
|
ATT | A | 22 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0085others(19): Show | 22 | HG02080.hp1 HG02109.hp2 HG02280.hp1 others(19): Show |
intron_variant | MODIFIER | c.146+288_146+289del others(2): Show |
FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 27727800 | |||||
chr1:27727800
|
ATTT | A | 17 | a0001c0002t0002g0080a0001c0002t0004g0015a0001c0002t0004g0016others(14): Show | 19 | HG01069.hp2 HG01071.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.146+287_146+289del others(3): Show |
FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 27727800 | |||||
chr1:27727800
|
ATTTT | A | 68 | a0001c0002t0002g0001a0001c0002t0002g0004a0001c0002t0002g0007others(65): Show | 80 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(77): Show |
intron_variant | MODIFIER | c.146+286_146+289del others(4): Show |
FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 27727800 | |||||
chr1:27727800
|
ATTTTT | A | 5 | a0001c0002t0002g0026a0001c0002t0003g0027a0001c0002t0003g0028others(2): Show | 5 | HG00639.hp2 HG01069.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.146+285_146+289del others(5): Show |
FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 27727800 | |||||
chr1:27727822
|
T | G | 2 | a0001c0002t0002g0023a0001c0002t0028g0221 | 2 | NA18977.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.146+286T>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | chr1 | 27727822 | ||||||
chr1:27727883
|
C | G | 12 | a0001c0002t0003g0002a0001c0002t0003g0027a0001c0002t0003g0028others(9): Show | 17 | HG00639.hp2 HG01106.hp1 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.146+347C>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | chr1 | 27727883 | ||||||
chr1:27727916
|
T | G | 1 | a0001c0001t0001g0082 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.146+380T>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | chr1 | 27727916 | ||||||
chr1:27728084
|
G | A | 80 | a0001c0002t0002g0001a0001c0002t0002g0004a0001c0002t0002g0007others(77): Show | 92 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(89): Show |
intron_variant | MODIFIER | c.146+548G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | chr1 | 27728084 | ||||||
chr1:27728198
|
T | G | 2 | a0001c0002t0022g0020a0001c0002t0031g0019 | 2 | HG03195.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.146+662T>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | chr1 | 27728198 | ||||||
chr1:27728303
|
C | T | 77 | a0001c0002t0002g0001a0001c0002t0002g0004a0001c0002t0002g0007others(74): Show | 89 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.146+767C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | chr1 | 27728303 | ||||||
chr1:27728359
|
CT | C | 7 | a0001c0001t0001g0083a0001c0001t0001g0102a0001c0001t0001g0103others(4): Show | 7 | HG00639.hp1 HG02559.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.146+830delT | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 27728359 | |||||
chr1:27728445
|
C | T | 3 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0011g0197 | 3 | HG01192.hp2 HG01258.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.146+909C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | chr1 | 27728445 | ||||||
chr1:27728509
|
C | T | 1 | a0001c0001t0001g0194 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.146+973C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | chr1 | 27728509 | ||||||
chr1:27728510
|
G | A | 1 | a0001c0001t0010g0084 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.146+974G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | chr1 | 27728510 | ||||||
chr1:27728551
|
C | T | 1 | a0001c0001t0005g0193 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.146+1015C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | chr1 | 27728551 | ||||||
chr1:27728656
|
T | G | 1 | a0001c0002t0008g0215 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.146+1120T>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | chr1 | 27728656 | ||||||
chr1:27728690
|
G | A | 27 | a0001c0002t0002g0029a0001c0002t0002g0030a0001c0002t0002g0031others(24): Show | 32 | HG00639.hp2 HG01106.hp1 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.146+1154G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | chr1 | 27728690 | ||||||
chr1:27728708
|
A | T | 92 | a0001c0002t0002g0001a0001c0002t0002g0004a0001c0002t0002g0007others(89): Show | 106 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(103): Show |
intron_variant | MODIFIER | c.146+1172A>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | chr1 | 27728708 | ||||||
chr1:27728774
|
T | C | 1 | a0001c0001t0001g0085 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.146+1238T>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | chr1 | 27728774 | ||||||
chr1:27728846
|
C | A | 77 | a0001c0002t0002g0001a0001c0002t0002g0004a0001c0002t0002g0007others(74): Show | 89 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.146+1310C>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | chr1 | 27728846 | ||||||
chr1:27728905
|
G | C | 1 | a0001c0001t0007g0106 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.146+1369G>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | chr1 | 27728905 | ||||||
chr1:27728959
|
G | C | 6 | a0001c0002t0004g0015a0001c0002t0004g0204a0001c0002t0004g0205others(3): Show | 7 | HG01069.hp2 HG01071.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.146+1423G>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | chr1 | 27728959 | ||||||
chr1:27728990
|
G | A | 80 | a0001c0002t0002g0001a0001c0002t0002g0004a0001c0002t0002g0007others(77): Show | 92 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(89): Show |
intron_variant | MODIFIER | c.146+1454G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | chr1 | 27728990 | ||||||
chr1:27729040
|
A | AT | 29 | a0001c0001t0001g0202a0001c0002t0002g0029a0001c0002t0002g0030others(26): Show | 34 | HG00639.hp2 HG01106.hp1 HG01243.hp1 others(31): Show |
intron_variant | MODIFIER | c.146+1513dupT | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 27729040 | |||||
chr1:27729113
|
G | A | 2 | a0001c0002t0022g0020a0001c0002t0031g0019 | 2 | HG03195.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.146+1577G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | chr1 | 27729113 | ||||||
chr1:27729395
|
G | A | 80 | a0001c0002t0002g0001a0001c0002t0002g0004a0001c0002t0002g0007others(77): Show | 92 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(89): Show |
intron_variant | MODIFIER | c.146+1859G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | chr1 | 27729395 | ||||||
chr1:27729495
|
C | T | 1 | a0001c0001t0001g0192 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.146+1959C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | chr1 | 27729495 | ||||||
chr1:27729529
|
C | CA | 92 | a0001c0002t0002g0001a0001c0002t0002g0004a0001c0002t0002g0007others(89): Show | 106 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(103): Show |
intron_variant | MODIFIER | c.146+2003dupA | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 27729529 | |||||
chr1:27729635
|
C | A | 80 | a0001c0002t0002g0001a0001c0002t0002g0004a0001c0002t0002g0007others(77): Show | 92 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(89): Show |
intron_variant | MODIFIER | c.146+2099C>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | chr1 | 27729635 | ||||||
chr1:27729831
|
A | G | 198 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0010others(195): Show | 221 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(218): Show |
intron_variant | MODIFIER | c.146+2295A>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | chr1 | 27729831 | ||||||
chr1:27730135
|
A | G | 80 | a0001c0002t0002g0001a0001c0002t0002g0004a0001c0002t0002g0007others(77): Show | 92 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(89): Show |
intron_variant | MODIFIER | c.147-2468A>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | chr1 | 27730135 | ||||||
chr1:27730181
|
C | CT | 74 | a0001c0002t0002g0001a0001c0002t0002g0004a0001c0002t0002g0007others(71): Show | 86 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(83): Show |
intron_variant | MODIFIER | c.147-2412dupT | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 27730181 | |||||
chr1:27730255
|
C | T | 1 | a0001c0001t0001g0191 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.147-2348C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | chr1 | 27730255 | ||||||
chr1:27730256
|
G | A | 3 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109 | 3 | HG01169.hp2 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.147-2347G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | chr1 | 27730256 | ||||||
chr1:27730280
|
A | C | 1 | a0001c0002t0003g0076 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.147-2323A>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | chr1 | 27730280 | ||||||
chr1:27730318
|
C | T | 1 | a0001c0001t0001g0190 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.147-2285C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | chr1 | 27730318 | ||||||
chr1:27730373
|
A | G | 44 | a0001c0002t0002g0001a0001c0002t0002g0004a0001c0002t0002g0007others(41): Show | 51 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.147-2230A>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | chr1 | 27730373 | ||||||
chr1:27730454
|
G | A | 2 | a0001c0001t0001g0131a0001c0001t0001g0132 | 2 | HG03209.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.147-2149G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | chr1 | 27730454 | ||||||
chr1:27730767
|
CT | C | 4 | a0001c0002t0012g0024a0001c0002t0012g0025a0001c0002t0012g0081others(1): Show | 4 | HG02258.hp1 HG02451.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.147-1833delT | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 27730767 | |||||
chr1:27730822
|
T | C | 2 | a0001c0001t0001g0133a0001c0001t0006g0134 | 2 | HG01175.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.147-1781T>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | chr1 | 27730822 | ||||||
chr1:27730822
|
T | G | 1 | a0001c0001t0001g0228 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.147-1781T>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | chr1 | 27730822 | ||||||
chr1:27730824
|
G | T | 80 | a0001c0002t0002g0001a0001c0002t0002g0004a0001c0002t0002g0007others(77): Show | 92 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(89): Show |
intron_variant | MODIFIER | c.147-1779G>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | chr1 | 27730824 | ||||||
chr1:27730914
|
G | A | 1 | a0001c0001t0001g0135 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.147-1689G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | chr1 | 27730914 | ||||||
chr1:27731058
|
G | A | 3 | a0001c0002t0002g0040a0001c0002t0002g0041a0001c0002t0009g0039 | 3 | HG02080.hp2 NA18946.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.147-1545G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | chr1 | 27731058 | ||||||
chr1:27731079
|
A | T | 2 | a0001c0002t0035g0077a0001c0002t0037g0230 | 2 | HG02451.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.147-1524A>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | chr1 | 27731079 | ||||||
chr1:27731198
|
A | AT | 5 | a0001c0001t0001g0101a0001c0001t0001g0187a0001c0001t0001g0188others(2): Show | 5 | HG01433.hp1 HG02486.hp1 NA18954.hp2 others(2): Show |
intron_variant | MODIFIER | c.147-1381dupT | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 27731198 | |||||
chr1:27731198
|
AT | A | 24 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0088others(21): Show | 26 | HG01069.hp2 HG01071.hp1 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.147-1381delT | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 27731198 | |||||
chr1:27731198
|
ATT | A | 61 | a0001c0002t0002g0001a0001c0002t0002g0004a0001c0002t0002g0007others(58): Show | 73 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.147-1382_147-1381d others(4): Show |
FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 27731198 | |||||
chr1:27731198
|
ATTT | A | 11 | a0001c0002t0002g0026a0001c0002t0002g0043a0001c0002t0002g0044others(8): Show | 11 | HG01069.hp1 HG02155.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.147-1383_147-1381d others(5): Show |
FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr1 | 27731198 | |||||
chr1:27731200
|
T | A | 5 | a0001c0002t0002g0036a0001c0002t0002g0037a0001c0002t0002g0067others(2): Show | 5 | HG01884.hp2 HG02145.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.147-1403T>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | chr1 | 27731200 | ||||||
chr1:27731201
|
T | A | 61 | a0001c0002t0002g0001a0001c0002t0002g0004a0001c0002t0002g0007others(58): Show | 73 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.147-1402T>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | chr1 | 27731201 | ||||||
chr1:27731202
|
T | A | 11 | a0001c0002t0002g0026a0001c0002t0002g0043a0001c0002t0002g0044others(8): Show | 11 | HG01069.hp1 HG02155.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.147-1401T>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | chr1 | 27731202 | ||||||
chr1:27731222
|
T | C | 2 | a0001c0002t0022g0020a0001c0002t0031g0019 | 2 | HG03195.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.147-1381T>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | chr1 | 27731222 | ||||||
chr1:27731227
|
A | G | 12 | a0001c0002t0003g0002a0001c0002t0003g0027a0001c0002t0003g0028others(9): Show | 17 | HG00639.hp2 HG01106.hp1 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.147-1376A>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | chr1 | 27731227 | ||||||
chr1:27731268
|
A | G | 1 | a0005c0006t0001g0186 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.147-1335A>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | chr1 | 27731268 | ||||||
chr1:27731352
|
C | T | 1 | a0001c0002t0002g0045 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.147-1251C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | chr1 | 27731352 | ||||||
chr1:27731907
|
C | T | 1 | a0001c0001t0001g0198 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.147-696C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | chr1 | 27731907 | ||||||
chr1:27731915
|
G | A | 1 | a0001c0001t0042g0110 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.147-688G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | chr1 | 27731915 | ||||||
chr1:27731970
|
C | T | 1 | a0001c0001t0005g0185 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.147-633C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | chr1 | 27731970 | ||||||
chr1:27732423
|
G | A | 77 | a0001c0002t0002g0001a0001c0002t0002g0004a0001c0002t0002g0007others(74): Show | 89 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.147-180G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | chr1 | 27732423 | ||||||
chr1:27732479
|
G | T | 77 | a0001c0002t0002g0001a0001c0002t0002g0004a0001c0002t0002g0007others(74): Show | 89 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.147-124G>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 2/8 | chr1 | 27732479 | ||||||
chr1:27732940
|
G | GT | 5 | a0001c0001t0001g0100a0001c0001t0001g0183a0001c0001t0001g0224others(2): Show | 5 | HG02074.hp1 HG03225.hp2 HG04115.hp2 others(2): Show |
intron_variant | MODIFIER | c.201+296dupT | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 27732940 | |||||
chr1:27732946
|
T | G | 1 | a0001c0001t0006g0138 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.201+289T>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 3/8 | chr1 | 27732946 | ||||||
chr1:27732986
|
A | T | 6 | a0001c0002t0008g0215a0001c0002t0008g0216a0001c0002t0008g0218others(3): Show | 6 | HG02258.hp2 HG02486.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.201+329A>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 3/8 | chr1 | 27732986 | ||||||
chr1:27732998
|
G | A | 77 | a0001c0002t0002g0001a0001c0002t0002g0004a0001c0002t0002g0007others(74): Show | 89 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.201+341G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 3/8 | chr1 | 27732998 | ||||||
chr1:27733212
|
G | A | 1 | a0001c0001t0006g0111 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.201+555G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 3/8 | chr1 | 27733212 | ||||||
chr1:27733225
|
C | T | 77 | a0001c0002t0002g0001a0001c0002t0002g0004a0001c0002t0002g0007others(74): Show | 89 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.201+568C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 3/8 | chr1 | 27733225 | ||||||
chr1:27733228
|
G | A | 2 | a0001c0002t0022g0020a0001c0002t0031g0019 | 2 | HG03195.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.201+571G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 3/8 | chr1 | 27733228 | ||||||
chr1:27733231
|
A | G | 1 | a0001c0002t0017g0066 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.201+574A>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 3/8 | chr1 | 27733231 | ||||||
chr1:27733447
|
C | G | 77 | a0001c0002t0002g0001a0001c0002t0002g0004a0001c0002t0002g0007others(74): Show | 89 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.202-584C>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 3/8 | chr1 | 27733447 | ||||||
chr1:27733569
|
C | T | 1 | a0001c0001t0032g0129 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.202-462C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 3/8 | chr1 | 27733569 | ||||||
chr1:27733726
|
G | C | 1 | a0001c0001t0001g0139 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.202-305G>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 3/8 | chr1 | 27733726 | ||||||
chr1:27734352
|
C | T | 1 | a0001c0002t0002g0041 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.354+169C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27734352 | ||||||
chr1:27734375
|
G | A | 1 | a0001c0002t0012g0024 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.354+192G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27734375 | ||||||
chr1:27734419
|
C | T | 1 | a0001c0001t0001g0101 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.354+236C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27734419 | ||||||
chr1:27735008
|
A | G | 1 | a0001c0001t0001g0182 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.354+825A>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27735008 | ||||||
chr1:27735492
|
G | A | 1 | a0001c0001t0001g0140 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.354+1309G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27735492 | ||||||
chr1:27735545
|
A | G | 1 | a0001c0001t0001g0202 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.354+1362A>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27735545 | ||||||
chr1:27735564
|
T | C | 92 | a0001c0002t0002g0001a0001c0002t0002g0004a0001c0002t0002g0007others(89): Show | 106 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(103): Show |
intron_variant | MODIFIER | c.354+1381T>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27735564 | ||||||
chr1:27735596
|
G | C | 92 | a0001c0002t0002g0001a0001c0002t0002g0004a0001c0002t0002g0007others(89): Show | 106 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(103): Show |
intron_variant | MODIFIER | c.354+1413G>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27735596 | ||||||
chr1:27735668
|
C | T | 1 | a0001c0001t0001g0181 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.354+1485C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27735668 | ||||||
chr1:27735880
|
A | T | 92 | a0001c0002t0002g0001a0001c0002t0002g0004a0001c0002t0002g0007others(89): Show | 106 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(103): Show |
intron_variant | MODIFIER | c.354+1697A>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27735880 | ||||||
chr1:27736147
|
C | G | 1 | a0001c0002t0044g0038 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.354+1964C>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27736147 | ||||||
chr1:27736149
|
G | A | 1 | a0001c0001t0001g0141 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.354+1966G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27736149 | ||||||
chr1:27736179
|
G | A | 92 | a0001c0002t0002g0001a0001c0002t0002g0004a0001c0002t0002g0007others(89): Show | 106 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(103): Show |
intron_variant | MODIFIER | c.354+1996G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27736179 | ||||||
chr1:27736182
|
C | T | 3 | a0001c0001t0001g0099a0001c0001t0005g0193a0001c0001t0005g0214 | 3 | HG02896.hp2 HG03139.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.354+1999C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27736182 | ||||||
chr1:27736183
|
G | A | 1 | a0001c0001t0001g0190 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.354+2000G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27736183 | ||||||
chr1:27736511
|
C | T | 77 | a0001c0002t0002g0001a0001c0002t0002g0004a0001c0002t0002g0007others(74): Show | 89 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.354+2328C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27736511 | ||||||
chr1:27736719
|
C | G | 1 | a0001c0001t0001g0085 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.354+2536C>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27736719 | ||||||
chr1:27736832
|
C | T | 1 | a0001c0001t0006g0134 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.354+2649C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27736832 | ||||||
chr1:27736972
|
G | A | 1 | a0001c0001t0001g0010 | 2 | HG00609.hp1 HG02040.hp1 |
intron_variant | MODIFIER | c.354+2789G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27736972 | ||||||
chr1:27737239
|
G | A | 1 | a0001c0002t0020g0018 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.354+3056G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27737239 | ||||||
chr1:27737276
|
T | C | 1 | a0001c0001t0001g0142 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.354+3093T>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27737276 | ||||||
chr1:27737277
|
A | G | 2 | a0001c0001t0001g0131a0001c0001t0001g0132 | 2 | HG03209.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.354+3094A>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27737277 | ||||||
chr1:27737455
|
C | A | 12 | a0001c0002t0004g0015a0001c0002t0004g0016a0001c0002t0004g0204others(9): Show | 14 | HG01069.hp2 HG01071.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.354+3272C>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27737455 | ||||||
chr1:27737543
|
T | G | 4 | a0001c0001t0001g0011a0001c0001t0001g0086a0001c0001t0001g0144others(1): Show | 5 | HG00558.hp2 HG00621.hp1 HG02165.hp2 others(2): Show |
intron_variant | MODIFIER | c.354+3360T>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27737543 | ||||||
chr1:27737589
|
C | T | 1 | a0001c0002t0020g0018 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.354+3406C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27737589 | ||||||
chr1:27737694
|
A | T | 1 | a0001c0001t0001g0144 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.354+3511A>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27737694 | ||||||
chr1:27737719
|
A | G | 92 | a0001c0002t0002g0001a0001c0002t0002g0004a0001c0002t0002g0007others(89): Show | 106 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(103): Show |
intron_variant | MODIFIER | c.354+3536A>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27737719 | ||||||
chr1:27737853
|
AAAC | A | 27 | a0001c0002t0002g0001a0001c0002t0002g0004a0001c0002t0002g0007others(24): Show | 34 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.354+3685_354+3687d others(5): Show |
FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 27737853 | |||||
chr1:27737866
|
AAC | A | 12 | a0001c0002t0002g0022a0001c0002t0002g0023a0001c0002t0002g0047others(9): Show | 12 | HG00621.hp2 HG00673.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.354+3685_354+3686d others(4): Show |
FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 27737866 | |||||
chr1:27737867
|
AC | A | 4 | a0001c0002t0002g0026a0001c0002t0002g0043a0001c0002t0002g0046others(1): Show | 4 | HG01069.hp1 HG02895.hp2 HG04228.hp2 others(1): Show |
intron_variant | MODIFIER | c.354+3685delC | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27737867 | ||||||
chr1:27737868
|
C | A | 3 | a0001c0001t0001g0112a0001c0002t0002g0045a0001c0002t0038g0042 | 3 | HG01928.hp2 HG02886.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.354+3685C>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27737868 | ||||||
chr1:27737868
|
C | CA | 40 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0083others(37): Show | 42 | HG00408.hp2 HG00609.hp1 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.354+3709dupA | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 27737868 | |||||
chr1:27737868
|
C | CAA | 5 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(2): Show | 5 | HG02280.hp2 HG02622.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.354+3708_354+3709d others(4): Show |
FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 27737868 | |||||
chr1:27737868
|
CAA | C | 16 | a0001c0002t0002g0029a0001c0002t0002g0030a0001c0002t0002g0031others(13): Show | 17 | HG01255.hp2 HG01884.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.354+3708_354+3709d others(4): Show |
FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 27737868 | |||||
chr1:27737868
|
CAAA | C | 28 | a0001c0001t0006g0111a0001c0002t0003g0002a0001c0002t0003g0027others(25): Show | 34 | HG00609.hp2 HG00639.hp2 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.354+3707_354+3709d others(5): Show |
FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 27737868 | |||||
chr1:27737868
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0005g0185 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.354+3699_354+3709d others(13): Show |
FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 27737868 | |||||
chr1:27737870
|
A | AC | 4 | a0001c0001t0001g0095a0001c0001t0001g0178a0001c0001t0010g0084others(1): Show | 4 | HG02080.hp1 HG02280.hp1 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.354+3687_354+3688i others(3): Show |
FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27737870 | ||||||
chr1:27737871
|
A | C | 9 | a0001c0001t0001g0101a0001c0001t0001g0132a0001c0001t0010g0098others(6): Show | 9 | HG02109.hp2 HG02698.hp1 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.354+3688A>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27737871 | ||||||
chr1:27737874
|
A | C | 13 | a0001c0002t0004g0015a0001c0002t0004g0016a0001c0002t0004g0204others(10): Show | 15 | HG01069.hp2 HG01071.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.354+3691A>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27737874 | ||||||
chr1:27737877
|
A | C | 13 | a0001c0002t0004g0015a0001c0002t0004g0016a0001c0002t0004g0204others(10): Show | 15 | HG01069.hp2 HG01071.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.354+3694A>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27737877 | ||||||
chr1:27737880
|
A | C | 12 | a0001c0002t0004g0015a0001c0002t0004g0016a0001c0002t0004g0204others(9): Show | 14 | HG01069.hp2 HG01071.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.354+3697A>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27737880 | ||||||
chr1:27737883
|
A | C | 12 | a0001c0002t0004g0015a0001c0002t0004g0016a0001c0002t0004g0204others(9): Show | 14 | HG01069.hp2 HG01071.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.354+3700A>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27737883 | ||||||
chr1:27737886
|
A | C | 6 | a0001c0002t0012g0024a0001c0002t0012g0025a0001c0002t0012g0081others(3): Show | 6 | HG02258.hp1 HG02451.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.354+3703A>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27737886 | ||||||
chr1:27737916
|
G | A | 1 | a0001c0001t0001g0090 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.354+3733G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27737916 | ||||||
chr1:27737937
|
C | T | 1 | a0001c0002t0034g0035 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.354+3754C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27737937 | ||||||
chr1:27737978
|
A | G | 1 | a0001c0002t0020g0018 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.354+3795A>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27737978 | ||||||
chr1:27738218
|
G | A | 1 | a0001c0002t0020g0018 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.354+4035G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27738218 | ||||||
chr1:27738476
|
C | CA | 12 | a0001c0002t0003g0002a0001c0002t0003g0027a0001c0002t0003g0028others(9): Show | 17 | HG00639.hp2 HG01106.hp1 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.354+4303dupA | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 27738476 | |||||
chr1:27738484
|
A | T | 1 | a0001c0002t0008g0218 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.354+4301A>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27738484 | ||||||
chr1:27738487
|
T | A | 60 | a0001c0001t0001g0158a0001c0001t0001g0198a0001c0002t0002g0001others(57): Show | 72 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.354+4304T>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27738487 | ||||||
chr1:27738693
|
C | T | 1 | a0001c0001t0005g0130 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.354+4510C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27738693 | ||||||
chr1:27739028
|
A | C | 1 | a0001c0001t0001g0104 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.354+4845A>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27739028 | ||||||
chr1:27739218
|
T | C | 2 | a0001c0001t0001g0107a0001c0001t0001g0108 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.354+5035T>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27739218 | ||||||
chr1:27739411
|
T | C | 1 | a0001c0002t0002g0045 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.354+5228T>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27739411 | ||||||
chr1:27739434
|
G | T | 1 | a0001c0001t0001g0140 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.355-5220G>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27739434 | ||||||
chr1:27739809
|
A | G | 1 | a0001c0002t0020g0018 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.355-4845A>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27739809 | ||||||
chr1:27739820
|
C | CAATA | 92 | a0001c0002t0002g0001a0001c0002t0002g0004a0001c0002t0002g0007others(89): Show | 106 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(103): Show |
intron_variant | MODIFIER | c.355-4826_355-4823d others(6): Show |
FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 27739820 | |||||
chr1:27739840
|
T | TA | 90 | a0001c0002t0002g0001a0001c0002t0002g0004a0001c0002t0002g0007others(87): Show | 104 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(101): Show |
intron_variant | MODIFIER | c.355-4806dupA | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 27739840 | |||||
chr1:27739964
|
G | A | 1 | a0001c0001t0005g0193 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.355-4690G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27739964 | ||||||
chr1:27739970
|
A | T | 1 | a0001c0001t0001g0128 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.355-4684A>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27739970 | ||||||
chr1:27739991
|
A | G | 6 | a0001c0002t0008g0215a0001c0002t0008g0216a0001c0002t0008g0218others(3): Show | 6 | HG02258.hp2 HG02486.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.355-4663A>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27739991 | ||||||
chr1:27740062
|
A | T | 1 | a0001c0002t0038g0042 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.355-4592A>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27740062 | ||||||
chr1:27740151
|
C | G | 44 | a0001c0002t0002g0001a0001c0002t0002g0004a0001c0002t0002g0007others(41): Show | 51 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.355-4503C>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27740151 | ||||||
chr1:27740249
|
G | A | 1 | a0001c0001t0001g0117 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.355-4405G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27740249 | ||||||
chr1:27740443
|
T | G | 12 | a0001c0002t0004g0015a0001c0002t0004g0016a0001c0002t0004g0204others(9): Show | 14 | HG01069.hp2 HG01071.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.355-4211T>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27740443 | ||||||
chr1:27740665
|
C | T | 1 | a0001c0001t0005g0223 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.355-3989C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27740665 | ||||||
chr1:27740669
|
T | A | 1 | a0001c0001t0001g0159 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.355-3985T>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27740669 | ||||||
chr1:27740787
|
G | A | 1 | a0001c0001t0005g0160 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.355-3867G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27740787 | ||||||
chr1:27741027
|
G | A | 92 | a0001c0002t0002g0001a0001c0002t0002g0004a0001c0002t0002g0007others(89): Show | 106 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(103): Show |
intron_variant | MODIFIER | c.355-3627G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27741027 | ||||||
chr1:27741089
|
G | A | 1 | a0001c0002t0003g0070 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.355-3565G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27741089 | ||||||
chr1:27741132
|
C | CA | 7 | a0001c0001t0001g0013a0001c0001t0001g0148a0001c0001t0001g0149others(4): Show | 8 | HG01109.hp1 HG01891.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.355-3510dupA | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 27741132 | |||||
chr1:27741193
|
A | AT | 69 | a0001c0001t0001g0017a0001c0001t0001g0087a0001c0001t0001g0088others(66): Show | 77 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.355-3439dupT | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 27741193 | |||||
chr1:27741193
|
A | ATT | 37 | a0001c0001t0007g0106a0001c0001t0011g0197a0001c0002t0002g0022others(34): Show | 43 | HG00621.hp2 HG00639.hp2 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.355-3440_355-3439d others(4): Show |
FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 27741193 | |||||
chr1:27741193
|
A | ATTT | 9 | a0001c0002t0002g0034a0001c0002t0002g0065a0001c0002t0003g0076others(6): Show | 9 | HG02055.hp1 HG02257.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.355-3441_355-3439d others(5): Show |
FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 27741193 | |||||
chr1:27741199
|
T | C | 1 | a0001c0002t0020g0018 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.355-3455T>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27741199 | ||||||
chr1:27741298
|
A | G | 3 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0156 | 3 | HG02622.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.355-3356A>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27741298 | ||||||
chr1:27741370
|
G | A | 2 | a0001c0001t0001g0009a0001c0001t0007g0009 | 2 | HG01515.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.355-3284G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27741370 | ||||||
chr1:27741394
|
A | C | 2 | a0001c0002t0022g0020a0001c0002t0031g0019 | 2 | HG03195.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.355-3260A>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27741394 | ||||||
chr1:27741557
|
A | T | 2 | a0001c0002t0002g0061a0001c0002t0002g0064 | 2 | HG02683.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.355-3097A>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27741557 | ||||||
chr1:27741558
|
A | T | 93 | a0001c0001t0006g0138a0001c0002t0002g0001a0001c0002t0002g0004others(90): Show | 107 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(104): Show |
intron_variant | MODIFIER | c.355-3096A>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27741558 | ||||||
chr1:27741756
|
G | A | 1 | a0001c0002t0022g0020 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.355-2898G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27741756 | ||||||
chr1:27741867
|
AGT | A | 12 | a0001c0002t0004g0015a0001c0002t0004g0016a0001c0002t0004g0204others(9): Show | 14 | HG01069.hp2 HG01071.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.355-2785_355-2784d others(4): Show |
FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 27741867 | |||||
chr1:27741879
|
T | C | 1 | a0001c0001t0006g0111 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.355-2775T>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27741879 | ||||||
chr1:27741896
|
AG | A | 87 | a0001c0002t0002g0001a0001c0002t0002g0004a0001c0002t0002g0007others(84): Show | 101 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(98): Show |
intron_variant | MODIFIER | c.355-2757delG | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27741896 | ||||||
chr1:27741897
|
G | A | 3 | a0001c0002t0002g0062a0001c0002t0022g0020a0001c0002t0031g0019 | 3 | HG02056.hp2 HG03195.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.355-2757G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27741897 | ||||||
chr1:27742063
|
C | T | 1 | a0001c0002t0022g0020 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.355-2591C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27742063 | ||||||
chr1:27742233
|
A | C | 1 | a0001c0001t0001g0093 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.355-2421A>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27742233 | ||||||
chr1:27742313
|
G | T | 1 | a0001c0002t0031g0019 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.355-2341G>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27742313 | ||||||
chr1:27742556
|
T | C | 1 | a0001c0001t0001g0228 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.355-2098T>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27742556 | ||||||
chr1:27742637
|
T | C | 1 | a0001c0002t0020g0018 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.355-2017T>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27742637 | ||||||
chr1:27742782
|
G | A | 77 | a0001c0002t0002g0001a0001c0002t0002g0004a0001c0002t0002g0007others(74): Show | 89 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.355-1872G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27742782 | ||||||
chr1:27742794
|
C | T | 1 | a0001c0002t0022g0020 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.355-1860C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27742794 | ||||||
chr1:27742935
|
C | T | 1 | a0001c0001t0001g0149 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.355-1719C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27742935 | ||||||
chr1:27742936
|
G | A | 2 | a0001c0002t0035g0077a0001c0002t0037g0230 | 2 | HG02451.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.355-1718G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27742936 | ||||||
chr1:27743018
|
G | C | 1 | a0001c0001t0001g0114 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.355-1636G>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27743018 | ||||||
chr1:27743257
|
T | C | 1 | a0001c0002t0002g0045 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.355-1397T>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27743257 | ||||||
chr1:27743382
|
G | C | 1 | a0001c0001t0001g0118 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.355-1272G>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27743382 | ||||||
chr1:27743488
|
G | A | 1 | a0001c0002t0020g0018 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.355-1166G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27743488 | ||||||
chr1:27743767
|
GA | G | 11 | a0001c0002t0004g0015a0001c0002t0004g0016a0001c0002t0004g0204others(8): Show | 13 | HG01069.hp2 HG01071.hp1 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.355-874delA | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 27743767 | |||||
chr1:27743781
|
C | T | 75 | a0001c0002t0002g0001a0001c0002t0002g0004a0001c0002t0002g0007others(72): Show | 87 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.355-873C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27743781 | ||||||
chr1:27743961
|
T | C | 1 | a0001c0002t0002g0052 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.355-693T>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27743961 | ||||||
chr1:27743962
|
G | A | 1 | a0001c0002t0002g0052 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.355-692G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27743962 | ||||||
chr1:27744355
|
C | T | 12 | a0001c0002t0004g0015a0001c0002t0004g0016a0001c0002t0004g0204others(9): Show | 14 | HG01069.hp2 HG01071.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.355-299C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27744355 | ||||||
chr1:27744428
|
G | A | 1 | a0001c0002t0035g0077 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.355-226G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27744428 | ||||||
chr1:27744460
|
G | A | 1 | a0001c0002t0003g0076 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.355-194G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27744460 | ||||||
chr1:27744548
|
A | C | 1 | a0001c0001t0007g0155 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.355-106A>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27744548 | ||||||
chr1:27744596
|
C | T | 1 | a0001c0001t0010g0084 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.355-58C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 4/8 | chr1 | 27744596 | ||||||
chr1:27745175
|
G | C | 3 | a0001c0002t0020g0018a0001c0002t0022g0020a0001c0002t0031g0019 | 3 | HG02615.hp1 HG03195.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.512+364G>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 5/8 | chr1 | 27745175 | ||||||
chr1:27745258
|
C | T | 1 | a0001c0001t0001g0177 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.512+447C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 5/8 | chr1 | 27745258 | ||||||
chr1:27745302
|
C | T | 1 | a0001c0001t0001g0190 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.512+491C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 5/8 | chr1 | 27745302 | ||||||
chr1:27745325
|
C | T | 89 | a0001c0002t0002g0001a0001c0002t0002g0004a0001c0002t0002g0007others(86): Show | 103 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(100): Show |
intron_variant | MODIFIER | c.512+514C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 5/8 | chr1 | 27745325 | ||||||
chr1:27745728
|
G | C | 92 | a0001c0002t0002g0001a0001c0002t0002g0004a0001c0002t0002g0007others(89): Show | 106 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(103): Show |
intron_variant | MODIFIER | c.512+917G>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 5/8 | chr1 | 27745728 | ||||||
chr1:27746048
|
A | G | 89 | a0001c0002t0002g0001a0001c0002t0002g0004a0001c0002t0002g0007others(86): Show | 103 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(100): Show |
intron_variant | MODIFIER | c.512+1237A>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 5/8 | chr1 | 27746048 | ||||||
chr1:27746083
|
TA | T | 36 | a0001c0002t0002g0001a0001c0002t0002g0004a0001c0002t0002g0007others(33): Show | 43 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.512+1275delA | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr1 | 27746083 | |||||
chr1:27746197
|
T | G | 92 | a0001c0002t0002g0001a0001c0002t0002g0004a0001c0002t0002g0007others(89): Show | 106 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(103): Show |
intron_variant | MODIFIER | c.512+1386T>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 5/8 | chr1 | 27746197 | ||||||
chr1:27746451
|
G | A | 3 | a0001c0002t0012g0024a0001c0002t0012g0025a0001c0002t0012g0081 | 3 | HG02258.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.512+1640G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 5/8 | chr1 | 27746451 | ||||||
chr1:27746595
|
TG | T | 6 | a0001c0002t0004g0015a0001c0002t0004g0204a0001c0002t0004g0205others(3): Show | 7 | HG01069.hp2 HG01071.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.512+1785delG | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 5/8 | chr1 | 27746595 | ||||||
chr1:27746663
|
G | T | 2 | a0001c0002t0022g0020a0001c0002t0031g0019 | 2 | HG03195.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.512+1852G>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 5/8 | chr1 | 27746663 | ||||||
chr1:27746689
|
C | T | 4 | a0001c0002t0012g0024a0001c0002t0012g0025a0001c0002t0012g0081others(1): Show | 4 | HG02258.hp1 HG02451.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.512+1878C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 5/8 | chr1 | 27746689 | ||||||
chr1:27746723
|
T | C | 2 | a0001c0001t0001g0140a0001c0001t0001g0145 | 2 | HG02280.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.512+1912T>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 5/8 | chr1 | 27746723 | ||||||
chr1:27746903
|
C | T | 3 | a0001c0002t0012g0024a0001c0002t0012g0025a0001c0002t0012g0081 | 3 | HG02258.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.512+2092C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 5/8 | chr1 | 27746903 | ||||||
chr1:27747009
|
A | C | 1 | a0001c0001t0001g0154 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.513-2059A>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 5/8 | chr1 | 27747009 | ||||||
chr1:27747138
|
T | C | 1 | a0001c0001t0001g0164 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.513-1930T>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 5/8 | chr1 | 27747138 | ||||||
chr1:27747146
|
A | G | 1 | a0001c0001t0001g0017 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.513-1922A>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 5/8 | chr1 | 27747146 | ||||||
chr1:27747155
|
G | T | 89 | a0001c0002t0002g0001a0001c0002t0002g0004a0001c0002t0002g0007others(86): Show | 103 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(100): Show |
intron_variant | MODIFIER | c.513-1913G>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 5/8 | chr1 | 27747155 | ||||||
chr1:27747253
|
A | C | 2 | a0001c0002t0022g0020a0001c0002t0031g0019 | 2 | HG03195.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.513-1815A>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 5/8 | chr1 | 27747253 | ||||||
chr1:27747379
|
C | T | 19 | a0001c0001t0001g0006a0001c0001t0001g0082a0001c0001t0001g0087others(16): Show | 21 | HG00558.hp1 HG00673.hp2 HG01928.hp1 others(18): Show |
intron_variant | MODIFIER | c.513-1689C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 5/8 | chr1 | 27747379 | ||||||
chr1:27747520
|
T | C | 75 | a0001c0002t0002g0001a0001c0002t0002g0004a0001c0002t0002g0007others(72): Show | 87 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.513-1548T>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 5/8 | chr1 | 27747520 | ||||||
chr1:27747609
|
C | G | 1 | a0001c0001t0001g0126 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.513-1459C>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 5/8 | chr1 | 27747609 | ||||||
chr1:27747745
|
G | A | 2 | a0001c0002t0022g0020a0001c0002t0031g0019 | 2 | HG03195.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.513-1323G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 5/8 | chr1 | 27747745 | ||||||
chr1:27747813
|
G | A | 1 | a0001c0002t0020g0018 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.513-1255G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 5/8 | chr1 | 27747813 | ||||||
chr1:27747944
|
C | G | 1 | a0001c0001t0029g0174 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.513-1124C>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 5/8 | chr1 | 27747944 | ||||||
chr1:27747956
|
T | C | 2 | a0001c0002t0022g0020a0001c0002t0031g0019 | 2 | HG03195.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.513-1112T>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 5/8 | chr1 | 27747956 | ||||||
chr1:27748074
|
C | T | 1 | a0001c0002t0002g0052 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.513-994C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 5/8 | chr1 | 27748074 | ||||||
chr1:27748120
|
G | GT | 64 | a0001c0001t0001g0082a0001c0001t0001g0114a0001c0001t0001g0125others(61): Show | 76 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(73): Show |
intron_variant | MODIFIER | c.513-925dupT | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr1 | 27748120 | |||||
chr1:27748120
|
G | GTT | 25 | a0001c0002t0002g0007a0001c0002t0002g0022a0001c0002t0002g0030others(22): Show | 25 | HG00621.hp2 HG00673.hp1 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.513-926_513-925dup others(2): Show |
FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr1 | 27748120 | |||||
chr1:27748126
|
T | G | 1 | a0001c0001t0001g0196 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.513-942T>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 5/8 | chr1 | 27748126 | ||||||
chr1:27748130
|
T | G | 6 | a0001c0001t0001g0140a0001c0001t0001g0145a0001c0001t0001g0146others(3): Show | 6 | HG02280.hp2 HG02622.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.513-938T>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 5/8 | chr1 | 27748130 | ||||||
chr1:27748148
|
C | T | 12 | a0001c0002t0004g0015a0001c0002t0004g0016a0001c0002t0004g0204others(9): Show | 14 | HG01069.hp2 HG01071.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.513-920C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 5/8 | chr1 | 27748148 | ||||||
chr1:27748226
|
C | T | 2 | a0001c0002t0002g0026a0001c0002t0002g0043 | 2 | HG01069.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.513-842C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 5/8 | chr1 | 27748226 | ||||||
chr1:27748375
|
C | T | 1 | a0001c0001t0001g0168 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.513-693C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 5/8 | chr1 | 27748375 | ||||||
chr1:27748426
|
A | G | 75 | a0001c0002t0002g0001a0001c0002t0002g0004a0001c0002t0002g0007others(72): Show | 87 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.513-642A>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 5/8 | chr1 | 27748426 | ||||||
chr1:27748469
|
G | GT | 8 | a0001c0001t0001g0104a0001c0001t0001g0154a0001c0001t0001g0188others(5): Show | 8 | HG02055.hp1 HG02055.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.513-579dupT | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr1 | 27748469 | |||||
chr1:27748469
|
GT | G | 45 | a0001c0002t0002g0001a0001c0002t0002g0004a0001c0002t0002g0007others(42): Show | 52 | HG00544.hp1 HG00597.hp1 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.513-579delT | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr1 | 27748469 | |||||
chr1:27748469
|
GTT | G | 6 | a0001c0002t0017g0066a0001c0002t0020g0018a0001c0002t0022g0020others(3): Show | 6 | HG02451.hp2 HG02615.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.513-580_513-579del others(2): Show |
FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr1 | 27748469 | |||||
chr1:27748568
|
G | GC | 236 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(233): Show | 263 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(260): Show |
intron_variant | MODIFIER | c.513-495dupC | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr1 | 27748568 | |||||
chr1:27748608
|
C | T | 3 | a0001c0002t0020g0018a0001c0002t0022g0020a0001c0002t0031g0019 | 3 | HG02615.hp1 HG03195.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.513-460C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 5/8 | chr1 | 27748608 | ||||||
chr1:27748622
|
C | T | 1 | a0001c0002t0002g0068 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.513-446C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 5/8 | chr1 | 27748622 | ||||||
chr1:27748748
|
C | T | 89 | a0001c0002t0002g0001a0001c0002t0002g0004a0001c0002t0002g0007others(86): Show | 103 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(100): Show |
intron_variant | MODIFIER | c.513-320C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 5/8 | chr1 | 27748748 | ||||||
chr1:27748770
|
C | T | 2 | a0001c0001t0001g0124a0001c0001t0001g0127 | 2 | NA18945.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.513-298C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 5/8 | chr1 | 27748770 | ||||||
chr1:27748856
|
G | T | 1 | a0001c0002t0022g0020 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.513-212G>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 5/8 | chr1 | 27748856 | ||||||
chr1:27748895
|
C | G | 1 | a0001c0002t0009g0069 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.513-173C>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 5/8 | chr1 | 27748895 | ||||||
chr1:27748946
|
A | G | 1 | a0001c0002t0004g0015 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.513-122A>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 5/8 | chr1 | 27748946 | ||||||
chr1:27748963
|
A | G | 1 | a0001c0001t0001g0142 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.513-105A>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 5/8 | chr1 | 27748963 | ||||||
chr1:27748991
|
A | G | 1 | a0001c0002t0003g0070 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.513-77A>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 5/8 | chr1 | 27748991 | ||||||
chr1:27749179
|
G | A | 3 | a0001c0001t0001g0099a0001c0001t0005g0193a0001c0001t0005g0214 | 3 | HG02896.hp2 HG03139.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.599+25G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 6/8 | chr1 | 27749179 | ||||||
chr1:27749463
|
G | A | 77 | a0001c0002t0002g0001a0001c0002t0002g0004a0001c0002t0002g0007others(74): Show | 89 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.599+309G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 6/8 | chr1 | 27749463 | ||||||
chr1:27749466
|
C | G | 3 | a0001c0001t0001g0135a0001c0001t0001g0166a0001c0001t0007g0167 | 3 | HG01934.hp1 HG02004.hp2 NA18946.hp2 |
intron_variant | MODIFIER | c.599+312C>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 6/8 | chr1 | 27749466 | ||||||
chr1:27749484
|
C | T | 1 | a0001c0002t0031g0019 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.599+330C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 6/8 | chr1 | 27749484 | ||||||
chr1:27749651
|
C | T | 2 | a0001c0002t0035g0077a0001c0002t0037g0230 | 2 | HG02451.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.599+497C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 6/8 | chr1 | 27749651 | ||||||
chr1:27749795
|
G | A | 2 | a0001c0001t0001g0099a0001c0001t0005g0193 | 2 | HG02896.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.599+641G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 6/8 | chr1 | 27749795 | ||||||
chr1:27749875
|
G | A | 92 | a0001c0002t0002g0001a0001c0002t0002g0004a0001c0002t0002g0007others(89): Show | 106 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(103): Show |
intron_variant | MODIFIER | c.599+721G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 6/8 | chr1 | 27749875 | ||||||
chr1:27749952
|
C | T | 77 | a0001c0002t0002g0001a0001c0002t0002g0004a0001c0002t0002g0007others(74): Show | 89 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.599+798C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 6/8 | chr1 | 27749952 | ||||||
chr1:27750024
|
A | G | 2 | a0001c0002t0022g0020a0001c0002t0031g0019 | 2 | HG03195.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.599+870A>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 6/8 | chr1 | 27750024 | ||||||
chr1:27750149
|
C | A | 4 | a0001c0002t0012g0024a0001c0002t0012g0025a0001c0002t0012g0081others(1): Show | 4 | HG02258.hp1 HG02451.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.599+995C>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 6/8 | chr1 | 27750149 | ||||||
chr1:27750314
|
A | G | 1 | a0001c0002t0020g0018 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.599+1160A>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 6/8 | chr1 | 27750314 | ||||||
chr1:27750677
|
C | A | 1 | a0001c0002t0020g0018 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.599+1523C>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 6/8 | chr1 | 27750677 | ||||||
chr1:27750901
|
G | A | 1 | a0001c0001t0001g0199 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.599+1747G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 6/8 | chr1 | 27750901 | ||||||
chr1:27751099
|
G | C | 12 | a0001c0002t0004g0015a0001c0002t0004g0016a0001c0002t0004g0204others(9): Show | 14 | HG01069.hp2 HG01071.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.599+1945G>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 6/8 | chr1 | 27751099 | ||||||
chr1:27751147
|
C | CA | 28 | a0001c0002t0002g0029a0001c0002t0002g0030a0001c0002t0002g0031others(25): Show | 33 | HG00639.hp2 HG01106.hp1 HG01243.hp1 others(30): Show |
intron_variant | MODIFIER | c.599+2002dupA | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr1 | 27751147 | |||||
chr1:27751498
|
CT | C | 38 | a0001c0002t0002g0029a0001c0002t0002g0030a0001c0002t0002g0031others(35): Show | 43 | HG00639.hp2 HG01106.hp1 HG01243.hp1 others(40): Show |
intron_variant | MODIFIER | c.599+2359delT | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr1 | 27751498 | |||||
chr1:27751994
|
G | A | 2 | a0001c0002t0035g0077a0001c0002t0037g0230 | 2 | HG02451.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.599+2840G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 6/8 | chr1 | 27751994 | ||||||
chr1:27752070
|
A | G | 1 | a0001c0002t0002g0045 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.599+2916A>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 6/8 | chr1 | 27752070 | ||||||
chr1:27752130
|
C | CG | 3 | a0001c0002t0012g0024a0001c0002t0012g0025a0001c0002t0012g0081 | 3 | HG02258.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.599+2976_599+2977i others(3): Show |
FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 6/8 | chr1 | 27752130 | ||||||
chr1:27752131
|
A | G | 1 | a0001c0002t0044g0038 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.599+2977A>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 6/8 | chr1 | 27752131 | ||||||
chr1:27752131
|
A | T | 3 | a0001c0002t0012g0024a0001c0002t0012g0025a0001c0002t0012g0081 | 3 | HG02258.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.599+2977A>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 6/8 | chr1 | 27752131 | ||||||
chr1:27752254
|
C | T | 36 | a0001c0002t0002g0001a0001c0002t0002g0004a0001c0002t0002g0007others(33): Show | 43 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.600-2941C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 6/8 | chr1 | 27752254 | ||||||
chr1:27752343
|
C | A | 92 | a0001c0002t0002g0001a0001c0002t0002g0004a0001c0002t0002g0007others(89): Show | 106 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(103): Show |
intron_variant | MODIFIER | c.600-2852C>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 6/8 | chr1 | 27752343 | ||||||
chr1:27752565
|
G | A | 2 | a0001c0002t0002g0036a0001c0002t0002g0037 | 2 | HG01884.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.600-2630G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 6/8 | chr1 | 27752565 | ||||||
chr1:27752589
|
G | A | 12 | a0001c0002t0004g0015a0001c0002t0004g0016a0001c0002t0004g0204others(9): Show | 14 | HG01069.hp2 HG01071.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.600-2606G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 6/8 | chr1 | 27752589 | ||||||
chr1:27752605
|
C | T | 1 | a0001c0002t0002g0068 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.600-2590C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 6/8 | chr1 | 27752605 | ||||||
chr1:27752743
|
A | G | 1 | a0001c0001t0005g0185 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.600-2452A>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 6/8 | chr1 | 27752743 | ||||||
chr1:27752954
|
G | T | 1 | a0001c0002t0034g0035 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.600-2241G>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 6/8 | chr1 | 27752954 | ||||||
chr1:27753032
|
C | T | 2 | a0001c0002t0035g0077a0001c0002t0037g0230 | 2 | HG02451.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.600-2163C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 6/8 | chr1 | 27753032 | ||||||
chr1:27753381
|
T | C | 8 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0094others(5): Show | 8 | NA18939.hp2 NA18944.hp1 NA18956.hp2 others(5): Show |
intron_variant | MODIFIER | c.600-1814T>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 6/8 | chr1 | 27753381 | ||||||
chr1:27753629
|
G | A | 1 | a0001c0001t0001g0086 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.600-1566G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 6/8 | chr1 | 27753629 | ||||||
chr1:27753850
|
T | C | 1 | a0001c0001t0001g0158 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.600-1345T>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 6/8 | chr1 | 27753850 | ||||||
chr1:27753894
|
A | G | 1 | a0001c0001t0007g0155 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.600-1301A>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 6/8 | chr1 | 27753894 | ||||||
chr1:27753916
|
A | C | 1 | a0001c0001t0001g0168 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.600-1279A>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 6/8 | chr1 | 27753916 | ||||||
chr1:27754014
|
T | G | 2 | a0001c0002t0002g0044a0001c0002t0002g0080 | 2 | HG02155.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.600-1181T>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 6/8 | chr1 | 27754014 | ||||||
chr1:27754099
|
C | CT | 8 | a0001c0001t0001g0162a0001c0001t0005g0123a0001c0001t0006g0151others(5): Show | 8 | HG01109.hp1 HG02886.hp1 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.600-1072dupT | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr1 | 27754099 | |||||
chr1:27754099
|
CT | C | 46 | a0001c0001t0001g0188a0001c0002t0002g0026a0001c0002t0002g0029others(43): Show | 52 | HG00639.hp2 HG01069.hp1 HG01069.hp2 others(49): Show |
intron_variant | MODIFIER | c.600-1072delT | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr1 | 27754099 | |||||
chr1:27754100
|
T | C | 2 | a0001c0001t0011g0179a0001c0001t0011g0197 | 2 | HG02698.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.600-1095T>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 6/8 | chr1 | 27754100 | ||||||
chr1:27754167
|
C | T | 6 | a0001c0002t0004g0015a0001c0002t0004g0204a0001c0002t0004g0205others(3): Show | 7 | HG01069.hp2 HG01071.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.600-1028C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 6/8 | chr1 | 27754167 | ||||||
chr1:27754249
|
G | T | 2 | a0001c0001t0001g0135a0001c0001t0007g0167 | 2 | HG01934.hp1 NA18946.hp2 |
intron_variant | MODIFIER | c.600-946G>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 6/8 | chr1 | 27754249 | ||||||
chr1:27754365
|
C | A | 75 | a0001c0002t0002g0001a0001c0002t0002g0004a0001c0002t0002g0007others(72): Show | 87 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.600-830C>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 6/8 | chr1 | 27754365 | ||||||
chr1:27754704
|
G | A | 1 | a0001c0001t0001g0183 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.600-491G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 6/8 | chr1 | 27754704 | ||||||
chr1:27755346
|
T | C | 2 | a0001c0002t0035g0077a0001c0002t0037g0230 | 2 | HG02451.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.735+16T>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 7/8 | chr1 | 27755346 | ||||||
chr1:27755478
|
A | G | 1 | a0001c0001t0001g0141 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.735+148A>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 7/8 | chr1 | 27755478 | ||||||
chr1:27755665
|
C | G | 1 | a0001c0002t0031g0019 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.735+335C>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 7/8 | chr1 | 27755665 | ||||||
chr1:27755829
|
C | T | 1 | a0001c0001t0001g0122 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.735+499C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 7/8 | chr1 | 27755829 | ||||||
chr1:27755918
|
A | T | 3 | a0001c0001t0001g0014a0001c0001t0001g0170a0002c0005t0001g0014 | 3 | HG01099.hp2 HG01106.hp2 NA18945.hp2 |
intron_variant | MODIFIER | c.735+588A>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 7/8 | chr1 | 27755918 | ||||||
chr1:27755951
|
G | A | 1 | a0001c0001t0001g0171 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.735+621G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 7/8 | chr1 | 27755951 | ||||||
chr1:27756096
|
A | G | 1 | a0001c0001t0001g0176 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.735+766A>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 7/8 | chr1 | 27756096 | ||||||
chr1:27756346
|
G | A | 1 | a0001c0002t0018g0051 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.735+1016G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 7/8 | chr1 | 27756346 | ||||||
chr1:27756409
|
A | G | 3 | a0001c0001t0014g0231a0001c0001t0014g0232a0001c0001t0041g0233 | 3 | NA18944.hp2 NA18956.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.735+1079A>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 7/8 | chr1 | 27756409 | ||||||
chr1:27756458
|
T | C | 1 | a0001c0001t0001g0192 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.735+1128T>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 7/8 | chr1 | 27756458 | ||||||
chr1:27756510
|
C | T | 1 | a0001c0001t0001g0117 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.735+1180C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 7/8 | chr1 | 27756510 | ||||||
chr1:27756654
|
A | G | 12 | a0001c0002t0004g0015a0001c0002t0004g0016a0001c0002t0004g0204others(9): Show | 14 | HG01069.hp2 HG01071.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.735+1324A>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 7/8 | chr1 | 27756654 | ||||||
chr1:27756722
|
T | C | 39 | a0001c0002t0002g0001a0001c0002t0002g0004a0001c0002t0002g0007others(36): Show | 46 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.735+1392T>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 7/8 | chr1 | 27756722 | ||||||
chr1:27757188
|
C | CT | 72 | a0001c0001t0001g0088a0001c0001t0001g0090a0001c0001t0001g0100others(69): Show | 84 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.735+1883dupT | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr1 | 27757188 | |||||
chr1:27757188
|
C | CTT | 18 | a0001c0001t0001g0198a0001c0002t0002g0022a0001c0002t0002g0037others(15): Show | 18 | HG00621.hp2 HG00639.hp2 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.735+1882_735+1883d others(4): Show |
FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr1 | 27757188 | |||||
chr1:27757188
|
CT | C | 8 | a0001c0001t0001g0099a0001c0001t0001g0119a0001c0001t0001g0150others(5): Show | 8 | HG00408.hp2 HG02615.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.735+1883delT | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr1 | 27757188 | |||||
chr1:27757342
|
G | A | 8 | a0001c0002t0002g0029a0001c0002t0002g0030a0001c0002t0002g0031others(5): Show | 8 | HG01255.hp2 HG01884.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.735+2012G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 7/8 | chr1 | 27757342 | ||||||
chr1:27757611
|
C | T | 1 | a0001c0001t0010g0152 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.736-1915C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 7/8 | chr1 | 27757611 | ||||||
chr1:27757684
|
A | T | 89 | a0001c0002t0002g0001a0001c0002t0002g0004a0001c0002t0002g0007others(86): Show | 103 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(100): Show |
intron_variant | MODIFIER | c.736-1842A>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 7/8 | chr1 | 27757684 | ||||||
chr1:27757688
|
C | T | 2 | a0001c0001t0001g0107a0001c0001t0001g0108 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.736-1838C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 7/8 | chr1 | 27757688 | ||||||
chr1:27757698
|
C | T | 1 | a0001c0002t0002g0063 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.736-1828C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 7/8 | chr1 | 27757698 | ||||||
chr1:27757714
|
T | C | 6 | a0001c0001t0001g0010a0001c0001t0001g0083a0001c0001t0001g0089others(3): Show | 7 | HG00609.hp1 HG00639.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.736-1812T>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 7/8 | chr1 | 27757714 | ||||||
chr1:27757728
|
C | G | 89 | a0001c0002t0002g0001a0001c0002t0002g0004a0001c0002t0002g0007others(86): Show | 103 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(100): Show |
intron_variant | MODIFIER | c.736-1798C>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 7/8 | chr1 | 27757728 | ||||||
chr1:27757803
|
T | C | 3 | a0001c0001t0001g0083a0001c0001t0001g0102a0001c0001t0006g0184 | 3 | HG00639.hp1 HG02074.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.736-1723T>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 7/8 | chr1 | 27757803 | ||||||
chr1:27757833
|
T | C | 84 | a0001c0002t0002g0001a0001c0002t0002g0004a0001c0002t0002g0007others(81): Show | 98 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.736-1693T>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 7/8 | chr1 | 27757833 | ||||||
chr1:27757850
|
G | A | 1 | a0001c0002t0002g0056 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.736-1676G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 7/8 | chr1 | 27757850 | ||||||
chr1:27757894
|
G | A | 12 | a0001c0002t0004g0015a0001c0002t0004g0016a0001c0002t0004g0204others(9): Show | 14 | HG01069.hp2 HG01071.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.736-1632G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 7/8 | chr1 | 27757894 | ||||||
chr1:27757896
|
G | A | 6 | a0001c0002t0004g0015a0001c0002t0004g0204a0001c0002t0004g0205others(3): Show | 7 | HG01069.hp2 HG01071.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.736-1630G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 7/8 | chr1 | 27757896 | ||||||
chr1:27757933
|
T | C | 92 | a0001c0002t0002g0001a0001c0002t0002g0004a0001c0002t0002g0007others(89): Show | 106 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(103): Show |
intron_variant | MODIFIER | c.736-1593T>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 7/8 | chr1 | 27757933 | ||||||
chr1:27757976
|
CA | C | 93 | a0001c0001t0001g0101a0001c0002t0002g0001a0001c0002t0002g0004others(90): Show | 107 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(104): Show |
intron_variant | MODIFIER | c.736-1536delA | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr1 | 27757976 | |||||
chr1:27758038
|
C | T | 1 | a0001c0001t0001g0202 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.736-1488C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 7/8 | chr1 | 27758038 | ||||||
chr1:27758056
|
T | C | 1 | a0001c0001t0001g0158 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.736-1470T>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 7/8 | chr1 | 27758056 | ||||||
chr1:27758060
|
G | A | 89 | a0001c0002t0002g0001a0001c0002t0002g0004a0001c0002t0002g0007others(86): Show | 103 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(100): Show |
intron_variant | MODIFIER | c.736-1466G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 7/8 | chr1 | 27758060 | ||||||
chr1:27758224
|
C | T | 89 | a0001c0002t0002g0001a0001c0002t0002g0004a0001c0002t0002g0007others(86): Show | 103 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(100): Show |
intron_variant | MODIFIER | c.736-1302C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 7/8 | chr1 | 27758224 | ||||||
chr1:27758262
|
G | A | 3 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109 | 3 | HG01169.hp2 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.736-1264G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 7/8 | chr1 | 27758262 | ||||||
chr1:27758272
|
T | A | 89 | a0001c0002t0002g0001a0001c0002t0002g0004a0001c0002t0002g0007others(86): Show | 103 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(100): Show |
intron_variant | MODIFIER | c.736-1254T>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 7/8 | chr1 | 27758272 | ||||||
chr1:27758329
|
C | A | 2 | a0001c0002t0002g0030a0001c0002t0026g0033 | 2 | HG01255.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.736-1197C>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 7/8 | chr1 | 27758329 | ||||||
chr1:27758514
|
T | A | 1 | a0001c0002t0008g0216 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.736-1012T>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 7/8 | chr1 | 27758514 | ||||||
chr1:27758590
|
C | T | 2 | a0001c0001t0005g0169a0001c0001t0006g0151 | 2 | NA18993.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.736-936C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 7/8 | chr1 | 27758590 | ||||||
chr1:27758647
|
G | A | 1 | a0001c0002t0020g0018 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.736-879G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 7/8 | chr1 | 27758647 | ||||||
chr1:27758679
|
G | GT | 39 | a0001c0001t0001g0083a0001c0001t0001g0100a0001c0001t0001g0102others(36): Show | 39 | HG00621.hp1 HG00639.hp1 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.736-827dupT | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr1 | 27758679 | |||||
chr1:27758689
|
T | G | 86 | a0001c0002t0002g0001a0001c0002t0002g0004a0001c0002t0002g0007others(83): Show | 100 | HG00408.hp1 HG00597.hp1 HG00621.hp2 others(97): Show |
intron_variant | MODIFIER | c.736-837T>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 7/8 | chr1 | 27758689 | ||||||
chr1:27758699
|
T | G | 1 | a0001c0002t0020g0018 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.736-827T>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 7/8 | chr1 | 27758699 | ||||||
chr1:27758788
|
G | T | 1 | a0001c0001t0001g0133 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.736-738G>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 7/8 | chr1 | 27758788 | ||||||
chr1:27758876
|
T | G | 1 | a0001c0001t0001g0158 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.736-650T>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 7/8 | chr1 | 27758876 | ||||||
chr1:27759201
|
G | A | 1 | a0001c0002t0020g0018 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.736-325G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 7/8 | chr1 | 27759201 | ||||||
chr1:27759248
|
T | C | 1 | a0001c0001t0015g0201 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.736-278T>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 7/8 | chr1 | 27759248 | ||||||
chr1:27759765
|
G | GGTTTTTT others(5): Show |
1 | a0001c0002t0027g0217 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.837+139_837+150dup others(12): Show |
FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr1 | 27759765 | |||||
chr1:27759765
|
G | GGTTTTTT others(6): Show |
3 | a0001c0002t0020g0018a0001c0002t0022g0020a0001c0002t0031g0019 | 3 | HG02615.hp1 HG03195.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.837+150_837+162dup others(13): Show |
FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr1 | 27759765 | |||||
chr1:27759776
|
T | TTTTGTTT others(7): Show |
1 | a0001c0002t0002g0045 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.837+151_837+152ins others(14): Show |
FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr1 | 27759776 | |||||
chr1:27759776
|
T | TTTTGTTT others(7): Show |
3 | a0001c0002t0002g0026a0001c0002t0002g0043a0001c0002t0038g0042 | 3 | HG01069.hp1 HG02886.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.837+151_837+152ins others(14): Show |
FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr1 | 27759776 | |||||
chr1:27759779
|
G | GTTTTTTG others(6): Show |
3 | a0001c0002t0002g0061a0001c0002t0002g0064a0001c0002t0025g0057 | 3 | HG02683.hp1 HG03017.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.837+158_837+159ins others(13): Show |
FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr1 | 27759779 | |||||
chr1:27759779
|
G | GTTTTTTT others(6): Show |
1 | a0001c0002t0044g0038 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.837+159_837+160ins others(13): Show |
FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr1 | 27759779 | |||||
chr1:27759779
|
G | GTTTTTTT others(5): Show |
1 | a0001c0002t0023g0053 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.837+162_837+163ins others(12): Show |
FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr1 | 27759779 | |||||
chr1:27759779
|
G | GTTTTTTT others(6): Show |
40 | a0001c0002t0002g0004a0001c0002t0002g0023a0001c0002t0002g0030others(37): Show | 47 | HG00597.hp1 HG00639.hp2 HG01243.hp1 others(44): Show |
intron_variant | MODIFIER | c.837+162_837+163ins others(13): Show |
FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr1 | 27759779 | |||||
chr1:27759779
|
G | GTTTTTTT others(7): Show |
11 | a0001c0002t0002g0021a0001c0002t0002g0029a0001c0002t0002g0034others(8): Show | 11 | HG00408.hp1 HG01106.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.837+162_837+163ins others(14): Show |
FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr1 | 27759779 | |||||
chr1:27759779
|
G | T | 5 | a0001c0002t0002g0026a0001c0002t0002g0043a0001c0002t0002g0045others(2): Show | 5 | HG01069.hp1 HG02258.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.837+152G>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 8/8 | chr1 | 27759779 | ||||||
chr1:27759780
|
T | TTTTTTTT others(6): Show |
4 | a0001c0002t0009g0069a0001c0002t0012g0024a0001c0002t0012g0025others(1): Show | 4 | HG02258.hp1 HG02809.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.837+162_837+163ins others(13): Show |
FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr1 | 27759780 | |||||
chr1:27759781
|
T | TTTTTTGT others(6): Show |
12 | a0001c0002t0004g0015a0001c0002t0004g0016a0001c0002t0004g0204others(9): Show | 14 | HG01069.hp2 HG01071.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.837+159_837+160ins others(13): Show |
FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr1 | 27759781 | |||||
chr1:27759875
|
C | T | 77 | a0001c0002t0002g0001a0001c0002t0002g0004a0001c0002t0002g0007others(74): Show | 89 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.837+248C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 8/8 | chr1 | 27759875 | ||||||
chr1:27759938
|
A | C | 2 | a0001c0001t0001g0150a0001c0001t0001g0165 | 2 | HG00408.hp2 NA18974.hp2 |
intron_variant | MODIFIER | c.837+311A>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 8/8 | chr1 | 27759938 | ||||||
chr1:27759973
|
A | G | 1 | a0001c0001t0001g0017 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.837+346A>G | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 8/8 | chr1 | 27759973 | ||||||
chr1:27760017
|
C | T | 3 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109 | 3 | HG01169.hp2 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.837+390C>T | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 8/8 | chr1 | 27760017 | ||||||
chr1:27760090
|
G | A | 1 | a0001c0002t0023g0053 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.838-405G>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 8/8 | chr1 | 27760090 | ||||||
chr1:27760283
|
T | C | 12 | a0001c0002t0004g0015a0001c0002t0004g0016a0001c0002t0004g0204others(9): Show | 14 | HG01069.hp2 HG01071.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.838-212T>C | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 8/8 | chr1 | 27760283 | ||||||
chr1:27760444
|
C | A | 234 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(231): Show | 261 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(258): Show |
intron_variant | MODIFIER | c.838-51C>A | FAM76A | ENSG00000009780.16 | transcript | ENST00000373954.11 | protein_coding | 8/8 | chr1 | 27760444 |