geneid | 83648 |
---|---|
ensemblid | ENSG00000154319.16 |
hgncid | 15549 |
symbol | FAM167A |
name | family with sequence similarity 167 member A |
refseq_nuc | NM_053279.3 |
refseq_prot | NP_444509.2 |
ensembl_nuc | ENST00000284486.9 |
ensembl_prot | ENSP00000284486.4 |
mane_status | MANE Select |
chr | chr8 |
start | 11421476 |
end | 11466753 |
strand | - |
ver | v1.2 |
region | chr8:11421476-11466753 |
region5000 | chr8:11416476-11471753 |
regionname0 | FAM167A_chr8_11421476_11466753 |
regionname5000 | FAM167A_chr8_11416476_11471753 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 214 | 338 | 88 | 59 | 135 | 10 | 45 | 98 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0002 | 0/0 | 214 | 25 | 5 | 14 | 0 | 4 | 2 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0003 | 0/0 | 214 | 4 | 0 | 1 | 2 | 0 | 1 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0004 | 0/0 | 214 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0005 | 0/0 | 214 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0006 | 1/0 | 214 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0007 | 0/0 | 214 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0008 | 0/0 | 214 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 645 | 334 | 86 | 58 | 134 | 10 | 45 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
c0002 | 0/0 | 645 | 25 | 5 | 14 | 0 | 4 | 2 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
c0003 | 0/0 | 645 | 4 | 0 | 1 | 2 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
c0004 | 0/0 | 645 | 2 | 2 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
c0005 | 0/0 | 645 | 2 | 0 | 1 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
c0006 | 0/0 | 645 | 2 | 0 | 0 | 2 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
c0007 | 0/0 | 645 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
c0008 | 0/0 | 645 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
c0009 | 0/0 | 645 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
c0010 | 1/0 | 645 | 1 | 0 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
c0011 | 0/0 | 645 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 3423 | 103 | 3 | 22 | 63 | 4 | 11 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
t0002 | 1/0 | 3423 | 62 | 4 | 9 | 43 | 0 | 5 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
t0003 | 0/0 | 3419 | 14 | 13 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
t0004 | 0/0 | 3425 | 8 | 0 | 2 | 6 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
t0005 | 0/0 | 3419 | 7 | 0 | 4 | 0 | 1 | 2 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
t0006 | 0/0 | 3423 | 6 | 0 | 0 | 6 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
t0007 | 0/0 | 3427 | 6 | 0 | 0 | 5 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
t0008 | 0/0 | 3423 | 5 | 3 | 2 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
t0009 | 0/0 | 3419 | 5 | 5 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
t0010 | 0/0 | 3419 | 5 | 1 | 1 | 1 | 0 | 2 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
t0011 | 0/0 | 3421 | 5 | 2 | 1 | 2 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
t0012 | 0/0 | 3419 | 5 | 4 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
t0013 | 0/0 | 3434 | 4 | 0 | 2 | 0 | 2 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
t0014 | 0/0 | 3424 | 4 | 0 | 2 | 0 | 2 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
t0015 | 0/0 | 3423 | 4 | 4 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
t0016 | 0/0 | 3423 | 3 | 0 | 0 | 0 | 0 | 3 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
t0017 | 0/0 | 3415 | 3 | 3 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
t0018 | 0/0 | 3438 | 3 | 0 | 3 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
t0019 | 0/0 | 3421 | 3 | 0 | 3 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
t0020 | 0/0 | 3421 | 3 | 3 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
t0021 | 0/0 | 3419 | 3 | 3 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
t0022 | 0/0 | 3419 | 3 | 3 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
t0023 | 0/0 | 3419 | 3 | 0 | 0 | 0 | 0 | 3 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
t0024 | 0/0 | 3415 | 3 | 3 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
t0025 | 0/0 | 3419 | 3 | 3 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
t0026 | 0/0 | 3423 | 3 | 0 | 1 | 2 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
t0027 | 0/0 | 3419 | 2 | 0 | 2 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
t0028 | 0/0 | 3423 | 2 | 2 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
t0029 | 0/0 | 3419 | 2 | 2 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
t0030 | 0/0 | 3413 | 2 | 2 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
t0031 | 0/0 | 3414 | 2 | 2 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
t0032 | 0/0 | 3414 | 2 | 0 | 2 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
t0033 | 0/0 | 3429 | 2 | 0 | 0 | 2 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
t0034 | 0/0 | 3423 | 2 | 0 | 1 | 0 | 1 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
t0035 | 0/0 | 3440 | 2 | 0 | 0 | 0 | 0 | 2 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
t0036 | 0/0 | 3438 | 2 | 0 | 0 | 0 | 0 | 2 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
t0037 | 0/1 | 3434 | 2 | 0 | 0 | 0 | 1 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
t0038 | 0/0 | 3423 | 2 | 0 | 2 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
t0039 | 0/0 | 3423 | 2 | 0 | 2 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
t0040 | 0/0 | 3419 | 2 | 0 | 0 | 0 | 0 | 2 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
t0041 | 0/0 | 3429 | 2 | 0 | 0 | 2 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
t0042 | 0/0 | 3419 | 2 | 0 | 0 | 1 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
t0043 | 0/0 | 3419 | 2 | 2 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
t0044 | 0/0 | 3419 | 2 | 2 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
t0045 | 0/0 | 3414 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
t0046 | 0/0 | 3421 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
t0047 | 0/0 | 3423 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
t0048 | 0/0 | 3438 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
t0049 | 0/0 | 3434 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
t0050 | 0/0 | 3421 | 1 | 0 | 0 | 0 | 1 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
t0051 | 0/0 | 3423 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
t0052 | 0/0 | 3419 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
t0053 | 0/0 | 3421 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
t0054 | 0/0 | 3423 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
t0055 | 0/0 | 3405 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
t0056 | 0/0 | 3440 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
t0057 | 0/0 | 3421 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
t0058 | 0/0 | 3423 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
t0059 | 0/0 | 3423 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
t0060 | 0/0 | 3438 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
t0061 | 0/0 | 3438 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
t0062 | 0/0 | 3415 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
t0063 | 0/0 | 3423 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
t0064 | 0/0 | 3419 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
t0065 | 0/0 | 3423 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
t0066 | 0/0 | 3421 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
t0067 | 0/0 | 3419 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
t0068 | 0/0 | 3423 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
t0069 | 0/0 | 3423 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
t0070 | 0/0 | 3427 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
t0071 | 0/0 | 3423 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
t0072 | 0/0 | 3423 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
t0073 | 0/0 | 3423 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
t0074 | 0/0 | 3421 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
t0075 | 0/0 | 3419 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
t0076 | 0/0 | 3405 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
t0077 | 0/0 | 3423 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
t0078 | 0/0 | 3421 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
t0079 | 0/0 | 3419 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
t0080 | 0/0 | 3419 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
t0081 | 0/0 | 3423 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
t0082 | 0/0 | 3421 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
t0083 | 0/0 | 3401 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
t0084 | 0/0 | 3419 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
t0085 | 0/0 | 3424 | 1 | 0 | 0 | 0 | 1 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
t0086 | 0/0 | 3423 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
t0087 | 0/0 | 3421 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
t0088 | 0/0 | 3413 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
t0089 | 0/0 | 3405 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
t0090 | 0/0 | 3414 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
t0091 | 0/0 | 3442 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
t0092 | 0/0 | 3421 | 1 | 0 | 0 | 0 | 1 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
t0093 | 0/0 | 3414 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
t0094 | 0/0 | 3425 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
t0095 | 0/0 | 3423 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
t0096 | 0/0 | 3421 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
t0097 | 0/0 | 3419 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
t0098 | 0/0 | 3419 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
t0099 | 0/0 | 3419 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
t0100 | 0/0 | 3423 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
t0101 | 0/0 | 3421 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
t0102 | 0/0 | 3423 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
t0103 | 0/0 | 3419 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
t0104 | 0/0 | 3421 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
t0105 | 0/0 | 3414 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
t0106 | 0/0 | 3419 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 10 | 0 | 0 | 10 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0002 | 0/0 | 9 | 0 | 2 | 6 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0003 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0006 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0017 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0019 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0023 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0085 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0293 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0301 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0302 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0314 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0320 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 645 | 334 | 86 | 58 | 134 | 10 | 45 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0001c0005 | 0/0 | 645 | 2 | 0 | 1 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0001c0008 | 0/0 | 645 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0001c0009 | 0/0 | 645 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0002c0002 | 0/0 | 645 | 25 | 5 | 14 | 0 | 4 | 2 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0003c0003 | 0/0 | 645 | 4 | 0 | 1 | 2 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0004c0006 | 0/0 | 645 | 2 | 0 | 0 | 2 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0005c0004 | 0/0 | 645 | 2 | 2 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0006c0010 | 1/0 | 645 | 1 | 0 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0007c0011 | 0/0 | 645 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0008c0007 | 0/0 | 645 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 4067 | 98 | 3 | 20 | 62 | 3 | 10 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0001c0001t0002 | 0/0 | 4067 | 59 | 4 | 9 | 41 | 0 | 5 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0001c0001t0003 | 0/0 | 4063 | 12 | 11 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0001c0001t0004 | 0/0 | 4069 | 8 | 0 | 2 | 6 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0001c0001t0005 | 0/0 | 4063 | 7 | 0 | 4 | 0 | 1 | 2 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0001c0001t0006 | 0/0 | 4067 | 5 | 0 | 0 | 5 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0001c0001t0007 | 0/0 | 4071 | 6 | 0 | 0 | 5 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0001c0001t0008 | 0/0 | 4067 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0001c0001t0009 | 0/0 | 4063 | 4 | 4 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0001c0001t0010 | 0/0 | 4063 | 5 | 1 | 1 | 1 | 0 | 2 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0001c0001t0011 | 0/0 | 4065 | 5 | 2 | 1 | 2 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0001c0001t0012 | 0/0 | 4063 | 5 | 4 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0001c0001t0013 | 0/0 | 4078 | 4 | 0 | 2 | 0 | 2 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0001c0001t0015 | 0/0 | 4067 | 4 | 4 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0001c0001t0016 | 0/0 | 4067 | 3 | 0 | 0 | 0 | 0 | 3 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0001c0001t0017 | 0/0 | 4059 | 3 | 3 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0001c0001t0020 | 0/0 | 4065 | 3 | 3 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0001c0001t0021 | 0/0 | 4063 | 3 | 3 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0001c0001t0022 | 0/0 | 4063 | 3 | 3 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0001c0001t0023 | 0/0 | 4063 | 3 | 0 | 0 | 0 | 0 | 3 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0001c0001t0024 | 0/0 | 4059 | 3 | 3 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0001c0001t0025 | 0/0 | 4063 | 3 | 3 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0001c0001t0026 | 0/0 | 4067 | 3 | 0 | 1 | 2 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0001c0001t0028 | 0/0 | 4067 | 2 | 2 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0001c0001t0029 | 0/0 | 4063 | 2 | 2 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0001c0001t0030 | 0/0 | 4057 | 2 | 2 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0001c0001t0031 | 0/0 | 4058 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0001c0001t0032 | 0/0 | 4058 | 2 | 0 | 2 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0001c0001t0033 | 0/0 | 4073 | 2 | 0 | 0 | 2 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0001c0001t0034 | 0/0 | 4067 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0001c0001t0035 | 0/0 | 4084 | 2 | 0 | 0 | 0 | 0 | 2 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0001c0001t0036 | 0/0 | 4082 | 2 | 0 | 0 | 0 | 0 | 2 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0001c0001t0037 | 0/1 | 4078 | 2 | 0 | 0 | 0 | 1 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0001c0001t0038 | 0/0 | 4067 | 2 | 0 | 2 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0001c0001t0039 | 0/0 | 4067 | 2 | 0 | 2 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0001c0001t0040 | 0/0 | 4063 | 2 | 0 | 0 | 0 | 0 | 2 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0001c0001t0041 | 0/0 | 4073 | 2 | 0 | 0 | 2 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0001c0001t0042 | 0/0 | 4063 | 2 | 0 | 0 | 1 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0001c0001t0043 | 0/0 | 4063 | 2 | 2 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0001c0001t0044 | 0/0 | 4063 | 2 | 2 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0001c0001t0045 | 0/0 | 4058 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0001c0001t0046 | 0/0 | 4065 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0001c0001t0047 | 0/0 | 4067 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0001c0001t0048 | 0/0 | 4082 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0001c0001t0049 | 0/0 | 4078 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0001c0001t0050 | 0/0 | 4065 | 1 | 0 | 0 | 0 | 1 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0001c0001t0051 | 0/0 | 4067 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0001c0001t0052 | 0/0 | 4063 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0001c0001t0053 | 0/0 | 4065 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0001c0001t0055 | 0/0 | 4049 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0001c0001t0057 | 0/0 | 4065 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0001c0001t0058 | 0/0 | 4067 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0001c0001t0062 | 0/0 | 4059 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0001c0001t0063 | 0/0 | 4067 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0001c0001t0064 | 0/0 | 4063 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0001c0001t0065 | 0/0 | 4067 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0001c0001t0066 | 0/0 | 4065 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0001c0001t0067 | 0/0 | 4063 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0001c0001t0068 | 0/0 | 4067 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0001c0001t0071 | 0/0 | 4067 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0001c0001t0072 | 0/0 | 4067 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0001c0001t0074 | 0/0 | 4065 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0001c0001t0075 | 0/0 | 4063 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0001c0001t0076 | 0/0 | 4049 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0001c0001t0079 | 0/0 | 4063 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0001c0001t0080 | 0/0 | 4063 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0001c0001t0081 | 0/0 | 4067 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0001c0001t0082 | 0/0 | 4065 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0001c0001t0083 | 0/0 | 4045 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0001c0001t0084 | 0/0 | 4063 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0001c0001t0085 | 0/0 | 4068 | 1 | 0 | 0 | 0 | 1 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0001c0001t0086 | 0/0 | 4067 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0001c0001t0087 | 0/0 | 4065 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0001c0001t0088 | 0/0 | 4057 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0001c0001t0089 | 0/0 | 4049 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0001c0001t0090 | 0/0 | 4058 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0001c0001t0091 | 0/0 | 4086 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0001c0001t0092 | 0/0 | 4065 | 1 | 0 | 0 | 0 | 1 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0001c0001t0093 | 0/0 | 4058 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0001c0001t0094 | 0/0 | 4069 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0001c0001t0095 | 0/0 | 4067 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0001c0001t0096 | 0/0 | 4065 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0001c0001t0097 | 0/0 | 4063 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0001c0001t0098 | 0/0 | 4063 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0001c0001t0099 | 0/0 | 4063 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0001c0001t0100 | 0/0 | 4067 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0001c0001t0101 | 0/0 | 4065 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0001c0001t0102 | 0/0 | 4067 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0001c0001t0103 | 0/0 | 4063 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0001c0001t0104 | 0/0 | 4065 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0001c0001t0105 | 0/0 | 4058 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0001c0001t0106 | 0/0 | 4063 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0001c0005t0002 | 0/0 | 4067 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0001c0005t0073 | 0/0 | 4067 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0001c0008t0077 | 0/0 | 4067 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0001c0009t0009 | 0/0 | 4063 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0002c0002t0001 | 0/0 | 4067 | 2 | 0 | 1 | 0 | 1 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0002c0002t0008 | 0/0 | 4067 | 4 | 3 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0002c0002t0014 | 0/0 | 4068 | 4 | 0 | 2 | 0 | 2 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0002c0002t0018 | 0/0 | 4082 | 3 | 0 | 3 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0002c0002t0019 | 0/0 | 4065 | 3 | 0 | 3 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0002c0002t0027 | 0/0 | 4063 | 2 | 0 | 2 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0002c0002t0031 | 0/0 | 4058 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0002c0002t0034 | 0/0 | 4067 | 1 | 0 | 0 | 0 | 1 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0002c0002t0056 | 0/0 | 4084 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0002c0002t0059 | 0/0 | 4067 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0002c0002t0060 | 0/0 | 4082 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0002c0002t0061 | 0/0 | 4082 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0002c0002t0078 | 0/0 | 4065 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0003c0003t0001 | 0/0 | 4067 | 3 | 0 | 1 | 1 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0003c0003t0070 | 0/0 | 4071 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0004c0006t0006 | 0/0 | 4067 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0004c0006t0069 | 0/0 | 4067 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0005c0004t0003 | 0/0 | 4063 | 2 | 2 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0006c0010t0002 | 1/0 | 4067 | 1 | 0 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0007c0011t0054 | 0/0 | 4067 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
a0008c0007t0002 | 0/0 | 4067 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | copy fasta | chr8 | 11416476 | 11471753 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 9 | 0 | 2 | 6 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0003 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0006 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0002g0001 | 0/0 | 10 | 0 | 0 | 10 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0002g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0002g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0002g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0002g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0002g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0002g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0003g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0003g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0003g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0003g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0003g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0003g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0003g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0003g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0003g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0003g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0004g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0004g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0004g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0004g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0004g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0004g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0004g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0004g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0005g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0005g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0005g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0005g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0005g0320 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0005g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0006g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0006g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0006g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0006g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0007g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0007g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0007g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0007g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0007g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0007g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0008g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0009g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0009g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0009g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0009g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0010g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0010g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0010g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0010g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0010g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0011g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0011g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0011g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0011g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0011g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0012g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0012g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0012g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0012g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0012g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0013g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0013g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0013g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0013g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0015g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0015g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0016g0023 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0016g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0017g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0017g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0017g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0020g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0020g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0021g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0021g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0021g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0022g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0022g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0022g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0023g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0023g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0023g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0024g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0024g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0024g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0025g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0025g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0025g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0026g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0026g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0026g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0028g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0028g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0029g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0029g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0030g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0030g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0031g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0032g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0032g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0033g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0033g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0034g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0035g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0035g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0036g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0036g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0037g0293 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0037g0302 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0038g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0039g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0039g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0040g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0040g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0041g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0041g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0042g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0042g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0043g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0043g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0044g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0044g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0045g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0046g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0047g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0048g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0049g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0050g0314 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0051g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0052g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0053g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0055g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0057g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0058g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0062g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0063g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0064g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0065g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0066g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0067g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0068g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0071g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0072g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0074g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0075g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0076g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0079g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0080g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0081g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0082g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0083g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0084g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0085g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0086g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0087g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0088g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0089g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0090g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0091g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0092g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0093g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0094g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0095g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0096g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0097g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0098g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0099g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0100g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0101g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0102g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0103g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0104g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0105g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0106g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0005t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0005t0073g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0008t0077g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0009t0009g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0002c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0002c0002t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0002c0002t0008g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0002c0002t0008g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0002c0002t0008g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0002c0002t0008g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0002c0002t0014g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0002c0002t0014g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0002c0002t0014g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0002c0002t0014g0301 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0002c0002t0018g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0002c0002t0018g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0002c0002t0018g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0002c0002t0019g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0002c0002t0019g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0002c0002t0027g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0002c0002t0031g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0002c0002t0034g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0002c0002t0056g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0002c0002t0059g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0002c0002t0060g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0002c0002t0061g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0002c0002t0078g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0003c0003t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0003c0003t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0003c0003t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0003c0003t0070g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0004c0006t0006g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0004c0006t0069g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0005c0004t0003g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0006c0010t0002g0085 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0007c0011t0054g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0008c0007t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0002 | t0001 | g0146 | EUR | GBR | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG00099 | hp2 | a0001 | c0001 | t0092 | g0307 | EUR | GBR | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG00323 | hp1 | a0002 | c0002 | t0034 | g0150 | EUR | FIN | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG00323 | hp2 | a0002 | c0002 | t0014 | g0154 | EUR | FIN | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG00438 | hp1 | a0001 | c0001 | t0006 | g0160 | EAS | CHS | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | CHS | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG00544 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | CHS | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | CHS | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG00558 | hp1 | a0001 | c0001 | t0033 | g0216 | EAS | CHS | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | CHS | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG00597 | hp1 | a0001 | c0001 | t0042 | g0035 | EAS | CHS | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | CHS | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG00609 | hp1 | a0001 | c0001 | t0026 | g0059 | EAS | CHS | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG00609 | hp2 | a0001 | c0001 | t0072 | g0193 | EAS | CHS | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG00621 | hp1 | a0001 | c0001 | t0026 | g0077 | EAS | CHS | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | CHS | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG00639 | hp1 | a0001 | c0001 | t0011 | g0299 | AMR | PUR | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0280 | AMR | PUR | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG00642 | hp1 | a0002 | c0002 | t0008 | g0138 | AMR | PUR | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG00642 | hp2 | a0001 | c0001 | t0038 | g0021 | AMR | PUR | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG00673 | hp1 | a0001 | c0001 | t0004 | g0204 | EAS | CHS | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | CHS | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG00733 | hp1 | a0002 | c0002 | t0018 | g0145 | AMR | PUR | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG00733 | hp2 | a0001 | c0001 | t0004 | g0207 | AMR | PUR | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG00735 | hp1 | a0001 | c0001 | t0038 | g0021 | AMR | PUR | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0217 | AMR | PUR | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0190 | AMR | PUR | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG00738 | hp2 | a0001 | c0001 | t0005 | g0022 | AMR | PUR | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG00741 | hp1 | a0001 | c0001 | t0010 | g0246 | AMR | PUR | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG00741 | hp2 | a0002 | c0002 | t0056 | g0144 | AMR | PUR | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01070 | hp1 | a0002 | c0002 | t0027 | g0014 | AMR | PUR | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01071 | hp1 | a0002 | c0002 | t0027 | g0014 | AMR | PUR | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01074 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | PUR | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | PUR | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01081 | hp1 | a0002 | c0002 | t0078 | g0148 | AMR | PUR | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01081 | hp2 | a0003 | c0003 | t0001 | g0287 | AMR | PUR | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01099 | hp1 | a0001 | c0001 | t0039 | g0073 | AMR | PUR | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0259 | AMR | PUR | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01106 | hp1 | a0002 | c0002 | t0001 | g0152 | AMR | PUR | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01106 | hp2 | a0001 | c0001 | t0026 | g0281 | AMR | PUR | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01109 | hp1 | a0001 | c0001 | t0083 | g0306 | AMR | PUR | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01109 | hp2 | a0001 | c0001 | t0039 | g0074 | AMR | PUR | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01167 | hp1 | a0001 | c0001 | t0032 | g0027 | AMR | PUR | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01167 | hp2 | a0001 | c0001 | t0034 | g0225 | AMR | PUR | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01168 | hp1 | a0001 | c0001 | t0013 | g0290 | AMR | PUR | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01169 | hp1 | a0001 | c0001 | t0013 | g0291 | AMR | PUR | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01169 | hp2 | a0001 | c0001 | t0032 | g0028 | AMR | PUR | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0294 | AMR | PUR | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01175 | hp2 | a0001 | c0001 | t0047 | g0312 | AMR | PUR | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | PUR | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | PUR | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01243 | hp1 | a0001 | c0001 | t0005 | g0318 | AMR | PUR | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01243 | hp2 | a0001 | c0001 | t0045 | g0292 | AMR | PUR | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0268 | AMR | CLM | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01255 | hp2 | a0001 | c0001 | t0049 | g0324 | AMR | CLM | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01256 | hp1 | a0002 | c0002 | t0018 | g0141 | AMR | CLM | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01256 | hp2 | a0002 | c0002 | t0019 | g0015 | AMR | CLM | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01257 | hp1 | a0002 | c0002 | t0018 | g0149 | AMR | CLM | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01258 | hp1 | a0002 | c0002 | t0019 | g0015 | AMR | CLM | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0069 | AMR | CLM | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01261 | hp2 | a0001 | c0001 | t0005 | g0313 | AMR | CLM | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | CLM | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01358 | hp1 | a0001 | c0001 | t0104 | g0091 | AMR | CLM | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01358 | hp2 | a0002 | c0002 | t0019 | g0147 | AMR | CLM | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01361 | hp1 | a0001 | c0005 | t0073 | g0226 | AMR | CLM | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01361 | hp2 | a0002 | c0002 | t0014 | g0153 | AMR | CLM | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01496 | hp1 | a0001 | c0001 | t0008 | g0267 | AMR | CLM | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01496 | hp2 | a0002 | c0002 | t0014 | g0151 | AMR | CLM | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0017 | EUR | IBS | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01515 | hp2 | a0001 | c0001 | t0085 | g0284 | EUR | IBS | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01516 | hp1 | a0001 | c0001 | t0005 | g0320 | EUR | IBS | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01516 | hp2 | a0001 | c0001 | t0013 | g0282 | EUR | IBS | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01517 | hp1 | a0001 | c0001 | t0013 | g0283 | EUR | IBS | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0019 | EUR | IBS | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01884 | hp1 | a0001 | c0001 | t0102 | g0116 | AFR | ACB | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01884 | hp2 | a0001 | c0001 | t0062 | g0132 | AFR | ACB | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01891 | hp1 | a0001 | c0001 | t0097 | g0120 | AFR | ACB | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01891 | hp2 | a0001 | c0001 | t0075 | g0096 | AFR | ACB | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PEL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01934 | hp2 | a0001 | c0001 | t0005 | g0022 | AMR | PEL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01978 | hp1 | a0001 | c0001 | t0093 | g0322 | AMR | PEL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0212 | AMR | PEL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01981 | hp1 | a0001 | c0001 | t0100 | g0189 | AMR | PEL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01993 | hp1 | a0001 | c0001 | t0046 | g0316 | AMR | PEL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | PEL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02004 | hp1 | a0001 | c0001 | t0003 | g0029 | AMR | PEL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | KHV | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | KHV | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02055 | hp1 | a0001 | c0001 | t0024 | g0295 | AFR | ACB | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02055 | hp2 | a0002 | c0002 | t0008 | g0114 | AFR | ACB | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | KHV | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02056 | hp2 | a0001 | c0001 | t0011 | g0062 | EAS | KHV | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02071 | hp1 | a0001 | c0001 | t0004 | g0241 | EAS | KHV | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02080 | hp2 | a0001 | c0001 | t0006 | g0016 | EAS | KHV | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02083 | hp1 | a0001 | c0001 | t0004 | g0214 | EAS | KHV | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02083 | hp2 | a0001 | c0001 | t0010 | g0236 | EAS | KHV | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | KHV | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | KHV | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | KHV | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02145 | hp1 | a0001 | c0001 | t0103 | g0260 | AFR | ACB | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02145 | hp2 | a0001 | c0001 | t0029 | g0156 | AFR | ACB | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | CDX | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02155 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CDX | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | CDX | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | CDX | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02257 | hp1 | a0001 | c0001 | t0031 | g0095 | AFR | ACB | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | ACB | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02258 | hp1 | a0001 | c0001 | t0002 | g0134 | AFR | ACB | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02258 | hp2 | a0001 | c0001 | t0011 | g0119 | AFR | ACB | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02273 | hp1 | a0001 | c0001 | t0002 | g0045 | AMR | PEL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02273 | hp2 | a0001 | c0001 | t0004 | g0230 | AMR | PEL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02280 | hp1 | a0001 | c0001 | t0105 | g0326 | AFR | ACB | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0063 | AFR | ACB | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0079 | AMR | PEL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | PEL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02451 | hp1 | a0001 | c0001 | t0099 | g0088 | AFR | ACB | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02451 | hp2 | a0001 | c0001 | t0029 | g0276 | AFR | ACB | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02523 | hp1 | a0003 | c0003 | t0001 | g0086 | EAS | KHV | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | KHV | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02572 | hp1 | a0001 | c0001 | t0020 | g0126 | AFR | GWD | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02572 | hp2 | a0001 | c0001 | t0024 | g0100 | AFR | GWD | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0237 | SAS | PJL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02602 | hp2 | a0001 | c0001 | t0065 | g0206 | SAS | PJL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02615 | hp1 | a0001 | c0001 | t0021 | g0277 | AFR | GWD | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02615 | hp2 | a0001 | c0001 | t0017 | g0264 | AFR | GWD | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02622 | hp1 | a0001 | c0001 | t0015 | g0110 | AFR | GWD | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02622 | hp2 | a0002 | c0002 | t0008 | g0137 | AFR | GWD | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02630 | hp1 | a0001 | c0001 | t0012 | g0089 | AFR | GWD | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02630 | hp2 | a0001 | c0001 | t0009 | g0257 | AFR | GWD | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02647 | hp1 | a0001 | c0001 | t0021 | g0157 | AFR | GWD | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02647 | hp2 | a0001 | c0001 | t0076 | g0266 | AFR | GWD | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02683 | hp1 | a0001 | c0001 | t0063 | g0068 | SAS | PJL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02683 | hp2 | a0001 | c0001 | t0081 | g0123 | SAS | PJL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02698 | hp1 | a0001 | c0001 | t0036 | g0135 | SAS | PJL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02698 | hp2 | a0001 | c0001 | t0042 | g0105 | SAS | PJL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02717 | hp1 | a0001 | c0001 | t0012 | g0090 | AFR | GWD | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02717 | hp2 | a0001 | c0001 | t0025 | g0270 | AFR | GWD | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02723 | hp1 | a0001 | c0001 | t0044 | g0117 | AFR | GWD | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02723 | hp2 | a0001 | c0001 | t0017 | g0262 | AFR | GWD | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0244 | SAS | PJL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02735 | hp2 | a0001 | c0001 | t0010 | g0286 | SAS | PJL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0102 | SAS | PJL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02738 | hp2 | a0001 | c0001 | t0005 | g0325 | SAS | PJL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02818 | hp1 | a0001 | c0001 | t0098 | g0106 | AFR | GWD | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02818 | hp2 | a0001 | c0001 | t0106 | g0113 | AFR | GWD | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02886 | hp1 | a0001 | c0001 | t0009 | g0256 | AFR | GWD | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02886 | hp2 | a0007 | c0011 | t0054 | g0131 | AFR | GWD | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | GWD | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02895 | hp2 | a0001 | c0001 | t0020 | g0013 | AFR | GWD | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02896 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | GWD | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02896 | hp2 | a0001 | c0001 | t0003 | g0219 | AFR | GWD | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | GWD | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02897 | hp2 | a0001 | c0001 | t0002 | g0012 | AFR | GWD | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02922 | hp1 | a0005 | c0004 | t0003 | g0020 | AFR | ESN | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02922 | hp2 | a0001 | c0001 | t0003 | g0007 | AFR | ESN | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02965 | hp1 | a0001 | c0001 | t0030 | g0125 | AFR | ESN | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02965 | hp2 | a0001 | c0001 | t0053 | g0327 | AFR | ESN | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02970 | hp1 | a0001 | c0001 | t0015 | g0004 | AFR | ESN | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02970 | hp2 | a0001 | c0001 | t0003 | g0220 | AFR | ESN | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02976 | hp1 | a0001 | c0001 | t0022 | g0094 | AFR | ESN | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02976 | hp2 | a0001 | c0001 | t0003 | g0122 | AFR | ESN | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0195 | SAS | PJL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0076 | SAS | PJL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG03041 | hp1 | a0001 | c0001 | t0015 | g0004 | AFR | GWD | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG03041 | hp2 | a0001 | c0001 | t0021 | g0321 | AFR | GWD | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG03098 | hp1 | a0001 | c0001 | t0015 | g0004 | AFR | MSL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG03098 | hp2 | a0001 | c0001 | t0012 | g0055 | AFR | MSL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG03130 | hp1 | a0001 | c0001 | t0090 | g0124 | AFR | ESN | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG03130 | hp2 | a0001 | c0001 | t0025 | g0328 | AFR | ESN | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG03139 | hp1 | a0001 | c0001 | t0057 | g0323 | AFR | ESN | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG03139 | hp2 | a0001 | c0001 | t0012 | g0329 | AFR | ESN | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG03195 | hp1 | a0001 | c0001 | t0024 | g0242 | AFR | ESN | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG03195 | hp2 | a0001 | c0001 | t0066 | g0133 | AFR | ESN | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG03209 | hp1 | a0001 | c0001 | t0080 | g0130 | AFR | MSL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG03209 | hp2 | a0001 | c0001 | t0003 | g0275 | AFR | MSL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG03225 | hp1 | a0001 | c0001 | t0009 | g0128 | AFR | MSL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG03225 | hp2 | a0001 | c0001 | t0043 | g0121 | AFR | MSL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0289 | SAS | PJL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG03239 | hp2 | a0001 | c0001 | t0012 | g0030 | SAS | PJL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG03453 | hp1 | a0005 | c0004 | t0003 | g0020 | AFR | MSL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG03453 | hp2 | a0001 | c0001 | t0003 | g0007 | AFR | MSL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG03486 | hp1 | a0001 | c0001 | t0028 | g0129 | AFR | MSL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG03486 | hp2 | a0001 | c0001 | t0088 | g0269 | AFR | MSL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG03490 | hp1 | a0002 | c0002 | t0060 | g0142 | SAS | PJL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG03490 | hp2 | a0001 | c0001 | t0016 | g0317 | SAS | PJL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0221 | SAS | PJL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG03491 | hp2 | a0001 | c0001 | t0023 | g0103 | SAS | PJL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG03492 | hp1 | a0001 | c0001 | t0016 | g0023 | SAS | PJL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG03492 | hp2 | a0001 | c0001 | t0023 | g0104 | SAS | PJL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG03516 | hp1 | a0001 | c0001 | t0064 | g0099 | AFR | ESN | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG03516 | hp2 | a0001 | c0001 | t0009 | g0255 | AFR | ESN | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG03540 | hp1 | a0001 | c0001 | t0074 | g0093 | AFR | GWD | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG03540 | hp2 | a0001 | c0001 | t0068 | g0273 | AFR | GWD | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG03579 | hp1 | a0001 | c0001 | t0011 | g0265 | AFR | MSL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG03579 | hp2 | a0001 | c0001 | t0055 | g0025 | AFR | MSL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0218 | SAS | PJL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0080 | SAS | PJL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG03669 | hp1 | a0001 | c0001 | t0016 | g0023 | SAS | PJL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG03669 | hp2 | a0003 | c0003 | t0001 | g0288 | SAS | PJL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG03688 | hp1 | a0001 | c0001 | t0087 | g0279 | SAS | STU | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG03688 | hp2 | a0001 | c0001 | t0040 | g0065 | SAS | STU | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG03704 | hp2 | a0001 | c0001 | t0035 | g0101 | SAS | PJL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG03710 | hp1 | a0001 | c0001 | t0036 | g0139 | SAS | PJL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG03710 | hp2 | a0001 | c0001 | t0040 | g0083 | SAS | PJL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG03831 | hp1 | a0001 | c0001 | t0071 | g0211 | SAS | BEB | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG03831 | hp2 | a0001 | c0001 | t0052 | g0319 | SAS | BEB | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG03834 | hp1 | a0001 | c0001 | t0005 | g0309 | SAS | BEB | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG03834 | hp2 | a0001 | c0001 | t0082 | g0303 | SAS | BEB | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG03927 | hp1 | a0002 | c0002 | t0061 | g0143 | SAS | BEB | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0194 | SAS | BEB | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG03942 | hp1 | a0001 | c0001 | t0086 | g0297 | SAS | BEB | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG03942 | hp2 | a0001 | c0001 | t0051 | g0308 | SAS | BEB | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG04115 | hp1 | a0001 | c0001 | t0035 | g0271 | SAS | STU | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0081 | SAS | STU | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0252 | SAS | BEB | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0166 | SAS | BEB | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG04204 | hp1 | a0001 | c0001 | t0010 | g0210 | SAS | STU | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG04204 | hp2 | a0001 | c0001 | t0091 | g0140 | SAS | STU | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG04228 | hp1 | a0001 | c0001 | t0023 | g0251 | SAS | STU | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | STU | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18522 | hp1 | a0001 | c0001 | t0020 | g0013 | AFR | YRI | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18522 | hp2 | a0001 | c0001 | t0022 | g0092 | AFR | YRI | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18612 | hp1 | a0001 | c0001 | t0011 | g0056 | EAS | CHB | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | CHB | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18747 | hp1 | a0001 | c0005 | t0002 | g0115 | EAS | CHB | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18747 | hp2 | a0001 | c0001 | t0004 | g0250 | EAS | CHB | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18939 | hp2 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18948 | hp1 | a0001 | c0001 | t0002 | g0300 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18953 | hp1 | a0008 | c0007 | t0002 | g0031 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18956 | hp1 | a0001 | c0001 | t0002 | g0298 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18956 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18961 | hp1 | a0001 | c0001 | t0004 | g0198 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18961 | hp2 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18962 | hp2 | a0001 | c0001 | t0004 | g0233 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18963 | hp1 | a0001 | c0001 | t0041 | g0058 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18964 | hp1 | a0001 | c0001 | t0006 | g0016 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18964 | hp2 | a0001 | c0001 | t0007 | g0040 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18966 | hp2 | a0001 | c0001 | t0094 | g0044 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18967 | hp1 | a0001 | c0001 | t0041 | g0041 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18967 | hp2 | a0003 | c0003 | t0070 | g0191 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18968 | hp2 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18969 | hp1 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18971 | hp2 | a0001 | c0001 | t0007 | g0042 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18973 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18977 | hp1 | a0001 | c0001 | t0033 | g0239 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18977 | hp2 | a0001 | c0001 | t0002 | g0285 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18980 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18983 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18988 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18991 | hp1 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18994 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18995 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18995 | hp2 | a0004 | c0006 | t0006 | g0179 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18997 | hp2 | a0001 | c0001 | t0095 | g0054 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA19004 | hp2 | a0001 | c0001 | t0007 | g0057 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA19005 | hp1 | a0001 | c0001 | t0006 | g0208 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA19005 | hp2 | a0001 | c0001 | t0096 | g0032 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA19009 | hp1 | a0004 | c0006 | t0069 | g0178 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA19009 | hp2 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA19012 | hp2 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA19030 | hp1 | a0001 | c0001 | t0010 | g0199 | AFR | LWK | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA19030 | hp2 | a0001 | c0009 | t0009 | g0245 | AFR | LWK | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA19043 | hp1 | a0001 | c0001 | t0003 | g0310 | AFR | LWK | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA19043 | hp2 | a0001 | c0001 | t0044 | g0026 | AFR | LWK | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA19054 | hp1 | a0001 | c0001 | t0067 | g0159 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA19054 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA19056 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA19060 | hp2 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA19062 | hp1 | a0001 | c0001 | t0007 | g0051 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA19063 | hp2 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA19065 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA19068 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA19070 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA19076 | hp2 | a0001 | c0001 | t0007 | g0039 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA19080 | hp2 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA19081 | hp2 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA19083 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA19084 | hp2 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA19087 | hp2 | a0001 | c0001 | t0006 | g0229 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA19088 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA19091 | hp1 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA19240 | hp1 | a0002 | c0002 | t0059 | g0278 | AFR | YRI | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA19240 | hp2 | a0001 | c0001 | t0022 | g0098 | AFR | YRI | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA20129 | hp1 | a0002 | c0002 | t0008 | g0136 | AFR | ASW | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA20129 | hp2 | a0001 | c0001 | t0089 | g0024 | AFR | ASW | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA20752 | hp1 | a0002 | c0002 | t0014 | g0301 | EUR | TSI | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA20752 | hp2 | a0001 | c0001 | t0037 | g0293 | EUR | TSI | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | TSI | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA20805 | hp2 | a0001 | c0001 | t0050 | g0314 | EUR | TSI | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA20905 | hp1 | a0001 | c0001 | t0101 | g0305 | SAS | GIH | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA20905 | hp2 | a0001 | c0001 | t0007 | g0197 | SAS | GIH | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0072 | AMR | CLM | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01123 | hp2 | a0001 | c0001 | t0048 | g0315 | AMR | CLM | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02109 | hp1 | a0001 | c0001 | t0028 | g0258 | AFR | ACB | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02109 | hp2 | a0001 | c0001 | t0003 | g0311 | AFR | ACB | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02486 | hp1 | a0002 | c0002 | t0031 | g0304 | AFR | ACB | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02486 | hp2 | a0001 | c0001 | t0003 | g0007 | AFR | ACB | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02559 | hp1 | a0001 | c0001 | t0043 | g0263 | AFR | ACB | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02559 | hp2 | a0001 | c0001 | t0003 | g0330 | AFR | ACB | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG03471 | hp1 | a0001 | c0008 | t0077 | g0108 | AFR | MSL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG03471 | hp2 | a0001 | c0001 | t0003 | g0274 | AFR | MSL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG06807 | hp1 | a0001 | c0001 | t0058 | g0127 | AFR | USA | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG06807 | hp2 | a0001 | c0001 | t0025 | g0118 | AFR | USA | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA20300 | hp1 | a0001 | c0001 | t0030 | g0097 | AFR | USA | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA20300 | hp2 | a0001 | c0001 | t0017 | g0261 | AFR | USA | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA21309 | hp1 | a0001 | c0001 | t0084 | g0272 | AFR | LWK | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA21309 | hp2 | a0001 | c0001 | t0079 | g0162 | AFR | LWK | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0037 | g0302 | REF | REF | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
homoSapiens_grch38 | hp1 | a0006 | c0010 | t0002 | g0085 | REF | REF | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:11444092
|
G | C | 1 | a0002 | 25 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(22): Show |
missense_variant | MODERATE | c.320C>G | p.Thr107Ser | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/3 | 845/4067 | 320/645 | 107/214 | chr8 | 11444092 | ||
chr8:11444116
|
C | G | 1 | a0005 | 2 | HG02922.hp1 HG03453.hp1 |
missense_variant | MODERATE | c.296G>C | p.Ser99Thr | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/3 | 821/4067 | 296/645 | 99/214 | chr8 | 11444116 | ||
chr8:11444126
|
T | C | 1 | a0004 | 2 | NA18995.hp2 NA19009.hp1 |
missense_variant | MODERATE | c.286A>G | p.Arg96Gly | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/3 | 811/4067 | 286/645 | 96/214 | chr8 | 11444126 | ||
chr8:11444224
|
G | A | 1 | a0003 | 4 | HG01081.hp2 HG02523.hp1 HG03669.hp2 others(1): Show |
missense_variant | MODERATE | c.188C>T | p.Pro63Leu | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/3 | 713/4067 | 188/645 | 63/214 | chr8 | 11444224 | ||
chr8:11444244
|
A | C | 7 | a0001a0002a0003others(4): Show | 373 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(370): Show |
missense_variant | MODERATE | c.168T>G | p.His56Gln | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/3 | 693/4067 | 168/645 | 56/214 | chr8 | 11444244 | ||
chr8:11444336
|
G | A | 1 | a0007 | 1 | HG02886.hp2 | missense_variant | MODERATE | c.76C>T | p.His26Tyr | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/3 | 601/4067 | 76/645 | 26/214 | chr8 | 11444336 | ||
chr8:11444356
|
G | T | 1 | a0008 | 1 | NA18953.hp1 | missense_variant | MODERATE | c.56C>A | p.Ala19Glu | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/3 | 581/4067 | 56/645 | 19/214 | chr8 | 11444356 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:11424511
|
G | A | 1 | a0001c0005 | 2 | HG01361.hp1 NA18747.hp1 |
synonymous_variant | LOW | c.507C>T | p.Tyr169Tyr | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 1032/4067 | 507/645 | 169/214 | chr8 | 11424511 | ||
chr8:11424565
|
C | G | 1 | a0001c0008 | 1 | HG03471.hp1 | synonymous_variant | LOW | c.453G>C | p.Leu151Leu | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 978/4067 | 453/645 | 151/214 | chr8 | 11424565 | ||
chr8:11444049
|
G | A | 1 | a0001c0009 | 1 | NA19030.hp2 | synonymous_variant | LOW | c.363C>T | p.Ala121Ala | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/3 | 888/4067 | 363/645 | 121/214 | chr8 | 11444049 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:11421630
|
T | A | 1 | a0001c0001t0072 | 1 | HG00609.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2743A>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 2743 | chr8 | 11421630 | |||||
chr8:11421655
|
C | G | 1 | a0001c0001t0038 | 2 | HG00642.hp2 HG00735.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2718G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 2718 | chr8 | 11421655 | |||||
chr8:11421712
|
C | T | 20 | a0001c0001t0008a0001c0001t0017a0001c0001t0021others(17): Show | 35 | HG00597.hp1 HG00642.hp1 HG01109.hp1 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*2661G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 2661 | chr8 | 11421712 | |||||
chr8:11421791
|
G | A | 5 | a0001c0001t0006a0001c0001t0072a0001c0001t0095others(2): Show | 9 | HG00438.hp1 HG00609.hp2 HG02080.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2582C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 2582 | chr8 | 11421791 | |||||
chr8:11421876
|
G | GA | 13 | a0001c0001t0013a0001c0001t0035a0001c0001t0036others(10): Show | 24 | HG00323.hp2 HG00733.hp1 HG00741.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*2496dupT | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 2496 | chr8 | 11421876 | |||||
chr8:11422157
|
C | T | 1 | a0001c0001t0099 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2216G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 2216 | chr8 | 11422157 | |||||
chr8:11422334
|
T | C | 2 | a0001c0001t0030a0001c0001t0088 | 3 | HG02965.hp1 HG03486.hp2 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2039A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 2039 | chr8 | 11422334 | |||||
chr8:11422355
|
CGT | C | 9 | a0001c0001t0046a0001c0001t0050a0001c0001t0053others(6): Show | 11 | HG01256.hp2 HG01258.hp1 HG01358.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2016_*2017delAC | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 2016 | chr8 | 11422355 | |||||
chr8:11422367
|
T | G | 1 | a0001c0001t0102 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2006A>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 2006 | chr8 | 11422367 | |||||
chr8:11422367
|
TGTGG | T | 2 | a0001c0001t0022a0001c0001t0097 | 4 | HG01891.hp1 HG02976.hp1 NA18522.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2002_*2005delCCAC | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 2002 | chr8 | 11422367 | |||||
chr8:11422369
|
T | G | 30 | a0001c0001t0005a0001c0001t0009a0001c0001t0015others(27): Show | 52 | HG00642.hp2 HG00735.hp1 HG00738.hp2 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*2004A>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 2004 | chr8 | 11422369 | |||||
chr8:11422371
|
G | T | 13 | a0001c0001t0013a0001c0001t0035a0001c0001t0036others(10): Show | 24 | HG00323.hp2 HG00733.hp1 HG00741.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*2002C>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 2002 | chr8 | 11422371 | |||||
chr8:11422371
|
GGGGTGTG others(15): Show |
G | 1 | a0001c0001t0083 | 1 | HG01109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1980_*2001delACAC others(18): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 1980 | chr8 | 11422371 | |||||
chr8:11422373
|
G | GGGGTGTG others(3): Show |
1 | a0001c0001t0037 | 2 | NA20752.hp2 homoSapiens_chm13v2.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1999_*2000insACAC others(6): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 1999 | chr8 | 11422373 | |||||
chr8:11422373
|
G | GGGGTGTG others(7): Show |
5 | a0001c0001t0036a0001c0001t0048a0002c0002t0018others(2): Show | 8 | HG00733.hp1 HG01123.hp2 HG01256.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1999_*2000insACAC others(10): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 1999 | chr8 | 11422373 | |||||
chr8:11422373
|
G | GGGGTGTG others(9): Show |
2 | a0001c0001t0035a0002c0002t0056 | 3 | HG00741.hp2 HG03704.hp2 HG04115.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1999_*2000insACAC others(12): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 1999 | chr8 | 11422373 | |||||
chr8:11422373
|
G | GGGGTGTG others(11): Show |
1 | a0001c0001t0091 | 1 | HG04204.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1999_*2000insACAC others(14): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 1999 | chr8 | 11422373 | |||||
chr8:11422373
|
G | GGT | 2 | a0001c0001t0004a0001c0001t0094 | 9 | HG00673.hp1 HG00733.hp2 HG02071.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1998_*1999dupAC | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 1999 | chr8 | 11422373 | |||||
chr8:11422373
|
G | GGTGT | 2 | a0001c0001t0007a0003c0003t0070 | 7 | NA18964.hp2 NA18967.hp2 NA18971.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1996_*1999dupACAC | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 1999 | chr8 | 11422373 | |||||
chr8:11422373
|
G | GGTGTGT | 2 | a0001c0001t0033a0001c0001t0041 | 4 | HG00558.hp1 NA18963.hp1 NA18967.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1994_*1999dupACAC others(2): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 1999 | chr8 | 11422373 | |||||
chr8:11422373
|
G | GGTGTGTG others(3): Show |
2 | a0001c0001t0013a0001c0001t0049 | 5 | HG01168.hp1 HG01169.hp1 HG01255.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1990_*1999dupACAC others(6): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 1999 | chr8 | 11422373 | |||||
chr8:11422373
|
G | T | 6 | a0001c0001t0015a0001c0001t0026a0001c0001t0028others(3): Show | 12 | HG00609.hp1 HG00621.hp1 HG01106.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2000C>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 2000 | chr8 | 11422373 | |||||
chr8:11422373
|
GGT | G | 7 | a0001c0001t0011a0001c0001t0020a0001c0001t0066others(4): Show | 13 | HG00099.hp2 HG00639.hp1 HG01081.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1998_*1999delAC | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 1998 | chr8 | 11422373 | |||||
chr8:11422373
|
GGTGT | G | 27 | a0001c0001t0003a0001c0001t0005a0001c0001t0009others(24): Show | 68 | HG00597.hp1 HG00738.hp2 HG00741.hp1 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*1996_*1999delACAC | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 1996 | chr8 | 11422373 | |||||
chr8:11422373
|
GGTGTGTG others(1): Show |
G | 3 | a0001c0001t0017a0001c0001t0024a0001c0001t0062 | 7 | HG01884.hp2 HG02055.hp1 HG02572.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1992_*1999delACAC others(4): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 1992 | chr8 | 11422373 | |||||
chr8:11422373
|
GGTGTGTG others(3): Show |
G | 2 | a0001c0001t0030a0001c0001t0088 | 3 | HG02965.hp1 HG03486.hp2 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1990_*1999delACAC others(6): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 1990 | chr8 | 11422373 | |||||
chr8:11422373
|
GGTGTGTG others(11): Show |
G | 3 | a0001c0001t0055a0001c0001t0076a0001c0001t0089 | 3 | HG02647.hp2 HG03579.hp2 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1982_*1999delACAC others(14): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 1982 | chr8 | 11422373 | |||||
chr8:11422374
|
GTGTGTGT others(2): Show |
G | 7 | a0001c0001t0031a0001c0001t0032a0001c0001t0045others(4): Show | 8 | HG01167.hp1 HG01169.hp2 HG01243.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1990_*1998delACAC others(5): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 1990 | chr8 | 11422374 | |||||
chr8:11422375
|
T | G | 6 | a0001c0001t0016a0001c0001t0022a0001c0001t0046others(3): Show | 10 | HG01891.hp1 HG01993.hp1 HG02976.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1998A>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 1998 | chr8 | 11422375 | |||||
chr8:11422377
|
T | G | 1 | a0001c0001t0046 | 1 | HG01993.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1996A>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 1996 | chr8 | 11422377 | |||||
chr8:11422379
|
T | G | 12 | a0001c0001t0005a0001c0001t0010a0001c0001t0012others(9): Show | 31 | HG00738.hp2 HG00741.hp1 HG01070.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*1994A>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 1994 | chr8 | 11422379 | |||||
chr8:11422381
|
T | G | 2 | a0001c0001t0029a0001c0001t0103 | 3 | HG02145.hp1 HG02145.hp2 HG02451.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1992A>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 1992 | chr8 | 11422381 | |||||
chr8:11422383
|
T | G | 1 | a0001c0001t0102 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1990A>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 1990 | chr8 | 11422383 | |||||
chr8:11422385
|
T | G | 1 | a0001c0001t0102 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1988A>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 1988 | chr8 | 11422385 | |||||
chr8:11422445
|
T | C | 6 | a0001c0001t0031a0001c0001t0038a0001c0001t0058others(3): Show | 7 | HG00642.hp2 HG00735.hp1 HG02257.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1928A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 1928 | chr8 | 11422445 | |||||
chr8:11422499
|
A | T | 1 | a0004c0006t0069 | 1 | NA19009.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1874T>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 1874 | chr8 | 11422499 | |||||
chr8:11422571
|
G | T | 1 | a0001c0001t0055 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1802C>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 1802 | chr8 | 11422571 | |||||
chr8:11422583
|
C | T | 1 | a0001c0001t0068 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1790G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 1790 | chr8 | 11422583 | |||||
chr8:11422676
|
G | A | 1 | a0002c0002t0060 | 1 | HG03490.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1697C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 1697 | chr8 | 11422676 | |||||
chr8:11422732
|
C | T | 1 | a0001c0001t0067 | 1 | NA19054.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1641G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 1641 | chr8 | 11422732 | |||||
chr8:11422749
|
C | T | 4 | a0001c0001t0021a0001c0001t0025a0001c0001t0066others(1): Show | 8 | HG02615.hp1 HG02647.hp1 HG02717.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1624G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 1624 | chr8 | 11422749 | |||||
chr8:11422809
|
C | T | 1 | a0001c0001t0084 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1564G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 1564 | chr8 | 11422809 | |||||
chr8:11422810
|
G | A | 1 | a0002c0002t0061 | 1 | HG03927.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1563C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 1563 | chr8 | 11422810 | |||||
chr8:11422892
|
G | T | 1 | a0001c0001t0083 | 1 | HG01109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1481C>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 1481 | chr8 | 11422892 | |||||
chr8:11422894
|
A | G | 1 | a0001c0001t0065 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1479T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 1479 | chr8 | 11422894 | |||||
chr8:11422933
|
G | C | 1 | a0001c0001t0100 | 1 | HG01981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1440C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 1440 | chr8 | 11422933 | |||||
chr8:11422960
|
G | C | 1 | a0001c0001t0102 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1413C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 1413 | chr8 | 11422960 | |||||
chr8:11423040
|
A | C | 1 | a0001c0001t0064 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1333T>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 1333 | chr8 | 11423040 | |||||
chr8:11423131
|
A | T | 1 | a0001c0001t0040 | 2 | HG03688.hp2 HG03710.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1242T>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 1242 | chr8 | 11423131 | |||||
chr8:11423134
|
A | T | 1 | a0001c0001t0040 | 2 | HG03688.hp2 HG03710.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1239T>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 1239 | chr8 | 11423134 | |||||
chr8:11423135
|
C | G | 1 | a0001c0001t0040 | 2 | HG03688.hp2 HG03710.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1238G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 1238 | chr8 | 11423135 | |||||
chr8:11423138
|
G | A | 1 | a0001c0001t0040 | 2 | HG03688.hp2 HG03710.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1235C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 1235 | chr8 | 11423138 | |||||
chr8:11423139
|
A | T | 1 | a0001c0001t0040 | 2 | HG03688.hp2 HG03710.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1234T>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 1234 | chr8 | 11423139 | |||||
chr8:11423144
|
A | T | 1 | a0001c0001t0040 | 2 | HG03688.hp2 HG03710.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1229T>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 1229 | chr8 | 11423144 | |||||
chr8:11423145
|
T | C | 1 | a0001c0001t0040 | 2 | HG03688.hp2 HG03710.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1228A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 1228 | chr8 | 11423145 | |||||
chr8:11423148
|
C | G | 1 | a0001c0001t0040 | 2 | HG03688.hp2 HG03710.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1225G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 1225 | chr8 | 11423148 | |||||
chr8:11423149
|
A | T | 1 | a0001c0001t0040 | 2 | HG03688.hp2 HG03710.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1224T>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 1224 | chr8 | 11423149 | |||||
chr8:11423152
|
A | T | 1 | a0001c0001t0040 | 2 | HG03688.hp2 HG03710.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1221T>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 1221 | chr8 | 11423152 | |||||
chr8:11423167
|
T | G | 1 | a0001c0001t0091 | 1 | HG04204.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1206A>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 1206 | chr8 | 11423167 | |||||
chr8:11423195
|
C | T | 1 | a0001c0001t0039 | 2 | HG01099.hp1 HG01109.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1178G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 1178 | chr8 | 11423195 | |||||
chr8:11423215
|
C | G | 7 | a0001c0001t0032a0001c0001t0045a0001c0001t0063others(4): Show | 8 | HG00099.hp2 HG01167.hp1 HG01169.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1158G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 1158 | chr8 | 11423215 | |||||
chr8:11423228
|
A | G | 11 | a0001c0001t0017a0001c0001t0024a0001c0001t0032others(8): Show | 16 | HG00099.hp2 HG01167.hp1 HG01169.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1145T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 1145 | chr8 | 11423228 | |||||
chr8:11423376
|
A | G | 8 | a0001c0001t0005a0001c0001t0016a0001c0001t0023others(5): Show | 19 | HG00738.hp2 HG01070.hp1 HG01071.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*997T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 997 | chr8 | 11423376 | |||||
chr8:11423574
|
C | A | 1 | a0001c0008t0077 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*799G>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 799 | chr8 | 11423574 | |||||
chr8:11423653
|
C | A | 1 | a0001c0001t0062 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*720G>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 720 | chr8 | 11423653 | |||||
chr8:11423764
|
A | G | 56 | a0001c0001t0005a0001c0001t0008a0001c0001t0011others(53): Show | 100 | HG00323.hp1 HG00323.hp2 HG00639.hp1 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*609T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 609 | chr8 | 11423764 | |||||
chr8:11423839
|
T | G | 4 | a0001c0001t0034a0001c0001t0101a0002c0002t0034others(1): Show | 4 | HG00323.hp1 HG01081.hp1 HG01167.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*534A>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 534 | chr8 | 11423839 | |||||
chr8:11423929
|
G | A | 1 | a0001c0001t0102 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*444C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 444 | chr8 | 11423929 | |||||
chr8:11423932
|
C | T | 8 | a0001c0001t0005a0001c0001t0016a0001c0001t0023others(5): Show | 19 | HG00738.hp2 HG01070.hp1 HG01071.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*441G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 441 | chr8 | 11423932 | |||||
chr8:11424061
|
G | A | 1 | a0001c0001t0053 | 1 | HG02965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*312C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 312 | chr8 | 11424061 | |||||
chr8:11424110
|
C | A | 1 | a0001c0001t0079 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*263G>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 263 | chr8 | 11424110 | |||||
chr8:11424277
|
C | G | 1 | a0001c0001t0102 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*96G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 96 | chr8 | 11424277 | |||||
chr8:11444535
|
G | T | 10 | a0001c0001t0005a0001c0001t0016a0001c0001t0046others(7): Show | 18 | HG00738.hp2 HG01123.hp2 HG01175.hp2 others(15): Show |
5_prime_UTR_variant | MODIFIER | c.-124C>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/3 | 124 | chr8 | 11444535 | |||||
chr8:11444545
|
C | T | 1 | a0001c0001t0080 | 1 | HG03209.hp1 | 5_prime_UTR_variant | MODIFIER | c.-134G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/3 | 134 | chr8 | 11444545 | |||||
chr8:11444552
|
A | G | 71 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(68): Show | 233 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(230): Show |
5_prime_UTR_variant | MODIFIER | c.-141T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/3 | 141 | chr8 | 11444552 | |||||
chr8:11444586
|
C | T | 2 | a0001c0001t0013a0001c0001t0045 | 5 | HG01168.hp1 HG01169.hp1 HG01243.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-175G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/3 | 175 | chr8 | 11444586 | |||||
chr8:11444704
|
C | A | 5 | a0001c0001t0102a0001c0001t0103a0001c0001t0104others(2): Show | 5 | HG01358.hp1 HG01884.hp1 HG02145.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-293G>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/3 | 293 | chr8 | 11444704 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:11424757
|
T | C | 3 | a0001c0001t0011g0119a0001c0001t0020g0013a0001c0001t0020g0126 | 4 | HG02258.hp2 HG02572.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.382-121A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11424757 | ||||||
chr8:11424776
|
G | C | 1 | a0007c0011t0054g0131 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.382-140C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11424776 | ||||||
chr8:11424779
|
A | C | 1 | a0007c0011t0054g0131 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.382-143T>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11424779 | ||||||
chr8:11424876
|
G | C | 2 | a0001c0001t0038g0021a0002c0002t0059g0278 | 3 | HG00642.hp2 HG00735.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.382-240C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11424876 | ||||||
chr8:11424888
|
G | A | 5 | a0001c0001t0002g0134a0001c0001t0031g0095a0001c0001t0058g0127others(2): Show | 5 | HG02257.hp1 HG02258.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.382-252C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11424888 | ||||||
chr8:11425056
|
A | T | 1 | a0001c0008t0077g0108 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.382-420T>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11425056 | ||||||
chr8:11425120
|
C | T | 1 | a0001c0008t0077g0108 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.382-484G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11425120 | ||||||
chr8:11425121
|
G | A | 1 | a0001c0008t0077g0108 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.382-485C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11425121 | ||||||
chr8:11425125
|
T | C | 1 | a0001c0008t0077g0108 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.382-489A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11425125 | ||||||
chr8:11425128
|
A | G | 1 | a0001c0008t0077g0108 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.382-492T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11425128 | ||||||
chr8:11425129
|
A | C | 1 | a0001c0008t0077g0108 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.382-493T>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11425129 | ||||||
chr8:11425130
|
T | A | 1 | a0001c0008t0077g0108 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.382-494A>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11425130 | ||||||
chr8:11425131
|
G | T | 1 | a0001c0008t0077g0108 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.382-495C>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11425131 | ||||||
chr8:11425132
|
C | T | 1 | a0001c0008t0077g0108 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.382-496G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11425132 | ||||||
chr8:11425135
|
G | A | 1 | a0001c0008t0077g0108 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.382-499C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11425135 | ||||||
chr8:11425139
|
T | C | 1 | a0001c0008t0077g0108 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.382-503A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11425139 | ||||||
chr8:11425140
|
A | G | 1 | a0001c0008t0077g0108 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.382-504T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11425140 | ||||||
chr8:11425243
|
A | G | 2 | a0001c0001t0009g0255a0001c0001t0055g0025 | 2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.382-607T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11425243 | ||||||
chr8:11425266
|
G | A | 7 | a0001c0001t0017g0261a0001c0001t0017g0262a0001c0001t0017g0264others(4): Show | 7 | HG01884.hp2 HG02055.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.382-630C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11425266 | ||||||
chr8:11425304
|
G | C | 1 | a0001c0001t0004g0214 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.382-668C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11425304 | ||||||
chr8:11425307
|
G | A | 5 | a0001c0001t0050g0314a0001c0001t0083g0306a0001c0001t0087g0279others(2): Show | 6 | HG01109.hp1 HG01256.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.382-671C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11425307 | ||||||
chr8:11425327
|
G | A | 3 | a0001c0001t0001g0209a0001c0001t0001g0212a0001c0001t0001g0231 | 3 | HG01346.hp1 HG01978.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.382-691C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11425327 | ||||||
chr8:11425384
|
C | T | 24 | a0001c0001t0013g0282a0001c0001t0013g0283a0001c0001t0013g0290others(21): Show | 24 | HG00323.hp2 HG00733.hp1 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.382-748G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11425384 | ||||||
chr8:11425398
|
C | G | 11 | a0001c0001t0015g0004a0001c0001t0015g0110a0001c0001t0028g0129others(8): Show | 14 | HG01109.hp1 HG01256.hp2 HG01258.hp1 others(11): Show |
intron_variant | MODIFIER | c.382-762G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11425398 | ||||||
chr8:11425405
|
C | T | 1 | a0001c0001t0001g0173 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.382-769G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11425405 | ||||||
chr8:11425444
|
G | A | 1 | a0001c0001t0009g0255 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.382-808C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11425444 | ||||||
chr8:11425511
|
G | C | 1 | a0001c0001t0034g0225 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.382-875C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11425511 | ||||||
chr8:11425668
|
A | AC | 37 | a0001c0001t0001g0161a0001c0001t0008g0267a0001c0001t0011g0056others(34): Show | 42 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.382-1033dupG | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11425668 | ||||||
chr8:11425671
|
C | G | 3 | a0001c0001t0030g0097a0001c0001t0030g0125a0001c0001t0088g0269 | 3 | HG02965.hp1 HG03486.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.382-1035G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11425671 | ||||||
chr8:11425673
|
C | G | 1 | a0001c0001t0001g0254 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.382-1037G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11425673 | ||||||
chr8:11425674
|
C | G | 1 | a0001c0001t0079g0162 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.382-1038G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11425674 | ||||||
chr8:11425726
|
A | C | 37 | a0001c0001t0001g0161a0001c0001t0001g0200a0001c0001t0008g0267others(34): Show | 38 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.382-1090T>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11425726 | ||||||
chr8:11425759
|
G | A | 1 | a0001c0001t0093g0322 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.382-1123C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11425759 | ||||||
chr8:11425782
|
TGGTATAG others(12): Show |
T | 20 | a0001c0001t0005g0022a0001c0001t0005g0309a0001c0001t0005g0313others(17): Show | 23 | HG00738.hp2 HG01070.hp1 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.382-1165_382-1147d others(21): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11425782 | ||||||
chr8:11425823
|
T | G | 1 | a0001c0001t0082g0303 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.382-1187A>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11425823 | ||||||
chr8:11425830
|
A | C | 2 | a0001c0001t0024g0100a0001c0001t0024g0295 | 2 | HG02055.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.382-1194T>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11425830 | ||||||
chr8:11425875
|
T | C | 5 | a0001c0001t0001g0201a0001c0001t0002g0049a0001c0001t0002g0053others(2): Show | 5 | NA18969.hp1 NA18994.hp2 NA19060.hp2 others(2): Show |
intron_variant | MODIFIER | c.382-1239A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11425875 | ||||||
chr8:11425905
|
C | G | 1 | a0001c0001t0002g0253 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.382-1269G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11425905 | ||||||
chr8:11425929
|
G | A | 1 | a0001c0001t0076g0266 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.382-1293C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11425929 | ||||||
chr8:11425947
|
T | G | 2 | a0001c0001t0038g0021a0002c0002t0059g0278 | 3 | HG00642.hp2 HG00735.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.382-1311A>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11425947 | ||||||
chr8:11425954
|
C | A | 1 | a0001c0001t0025g0270 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.382-1318G>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11425954 | ||||||
chr8:11425967
|
A | C | 1 | a0001c0001t0029g0276 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.382-1331T>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11425967 | ||||||
chr8:11426026
|
A | G | 24 | a0001c0001t0001g0161a0001c0001t0008g0267a0001c0001t0011g0056others(21): Show | 25 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.382-1390T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11426026 | ||||||
chr8:11426450
|
G | C | 6 | a0001c0001t0005g0022a0001c0001t0005g0313a0001c0001t0005g0318others(3): Show | 8 | HG00738.hp2 HG01070.hp1 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.382-1814C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11426450 | ||||||
chr8:11426601
|
T | G | 1 | a0001c0001t0015g0110 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.382-1965A>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11426601 | ||||||
chr8:11426647
|
G | A | 16 | a0001c0001t0005g0022a0001c0001t0005g0309a0001c0001t0005g0313others(13): Show | 19 | HG00738.hp2 HG01070.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.382-2011C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11426647 | ||||||
chr8:11426690
|
G | A | 4 | a0002c0002t0008g0114a0002c0002t0008g0136a0002c0002t0008g0137others(1): Show | 4 | HG00642.hp1 HG02055.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.382-2054C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11426690 | ||||||
chr8:11426705
|
A | G | 1 | a0001c0001t0079g0162 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.382-2069T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11426705 | ||||||
chr8:11426907
|
C | T | 1 | a0001c0001t0004g0241 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.382-2271G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11426907 | ||||||
chr8:11427044
|
T | C | 22 | a0001c0001t0013g0282a0001c0001t0013g0283a0001c0001t0013g0290others(19): Show | 22 | HG00323.hp2 HG00733.hp1 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.382-2408A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11427044 | ||||||
chr8:11427052
|
T | C | 2 | a0001c0001t0025g0118a0001c0001t0055g0025 | 2 | HG03579.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.382-2416A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11427052 | ||||||
chr8:11427167
|
G | T | 17 | a0001c0001t0005g0022a0001c0001t0005g0309a0001c0001t0005g0313others(14): Show | 20 | HG00738.hp2 HG01070.hp1 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.382-2531C>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11427167 | ||||||
chr8:11427248
|
C | A | 1 | a0001c0001t0053g0327 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.382-2612G>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11427248 | ||||||
chr8:11427373
|
G | A | 2 | a0001c0001t0002g0009a0001c0001t0085g0284 | 3 | HG01074.hp1 HG01192.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.382-2737C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11427373 | ||||||
chr8:11427448
|
G | C | 2 | a0001c0001t0043g0121a0001c0001t0097g0120 | 2 | HG01891.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.382-2812C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11427448 | ||||||
chr8:11427516
|
T | C | 18 | a0001c0001t0001g0196a0001c0001t0002g0134a0001c0001t0011g0062others(15): Show | 18 | HG00642.hp1 HG02015.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.382-2880A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11427516 | ||||||
chr8:11427540
|
C | G | 2 | a0001c0001t0013g0282a0001c0001t0013g0283 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.382-2904G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11427540 | ||||||
chr8:11427591
|
A | G | 4 | a0001c0001t0012g0329a0001c0001t0055g0025a0001c0001t0102g0116others(1): Show | 4 | HG01884.hp1 HG02818.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.382-2955T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11427591 | ||||||
chr8:11427626
|
G | C | 23 | a0001c0001t0008g0267a0001c0001t0011g0119a0001c0001t0013g0282others(20): Show | 24 | HG00099.hp2 HG00642.hp2 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.382-2990C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11427626 | ||||||
chr8:11427669
|
G | A | 3 | a0001c0001t0012g0089a0001c0001t0034g0225a0001c0001t0099g0088 | 3 | HG01167.hp2 HG02451.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.382-3033C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11427669 | ||||||
chr8:11427677
|
T | C | 62 | a0001c0001t0001g0161a0001c0001t0002g0102a0001c0001t0002g0285others(59): Show | 66 | HG00099.hp2 HG00639.hp1 HG00642.hp1 others(63): Show |
intron_variant | MODIFIER | c.382-3041A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11427677 | ||||||
chr8:11427710
|
A | C | 115 | a0001c0001t0001g0158a0001c0001t0001g0172a0001c0001t0001g0183others(112): Show | 124 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.382-3074T>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11427710 | ||||||
chr8:11427729
|
A | C | 1 | a0001c0001t0007g0057 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.382-3093T>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11427729 | ||||||
chr8:11427859
|
A | G | 67 | a0001c0001t0001g0107a0001c0001t0001g0109a0001c0001t0001g0217others(64): Show | 73 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.382-3223T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11427859 | ||||||
chr8:11427868
|
C | G | 1 | a0001c0001t0004g0241 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.382-3232G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11427868 | ||||||
chr8:11427872
|
T | G | 5 | a0001c0001t0009g0128a0001c0001t0020g0126a0001c0001t0024g0242others(2): Show | 5 | HG01884.hp1 HG02572.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.382-3236A>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11427872 | ||||||
chr8:11427875
|
C | T | 257 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(254): Show | 289 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(286): Show |
intron_variant | MODIFIER | c.382-3239G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11427875 | ||||||
chr8:11427901
|
A | C | 3 | a0001c0001t0022g0094a0001c0001t0022g0098a0001c0001t0030g0097 | 3 | HG02976.hp1 NA19240.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.382-3265T>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11427901 | ||||||
chr8:11427954
|
G | A | 1 | a0002c0002t0014g0301 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.382-3318C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11427954 | ||||||
chr8:11427971
|
A | T | 1 | a0001c0001t0004g0198 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.382-3335T>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11427971 | ||||||
chr8:11427993
|
G | C | 5 | a0001c0001t0009g0255a0001c0001t0009g0256a0001c0001t0009g0257others(2): Show | 5 | HG02630.hp2 HG02886.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.382-3357C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11427993 | ||||||
chr8:11428014
|
T | C | 1 | a0001c0001t0010g0210 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.382-3378A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11428014 | ||||||
chr8:11428028
|
C | G | 9 | a0001c0001t0003g0029a0001c0001t0009g0255a0001c0001t0009g0256others(6): Show | 9 | HG01167.hp1 HG01169.hp2 HG02004.hp1 others(6): Show |
intron_variant | MODIFIER | c.382-3392G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11428028 | ||||||
chr8:11428072
|
C | G | 153 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(150): Show | 177 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(174): Show |
intron_variant | MODIFIER | c.382-3436G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11428072 | ||||||
chr8:11428100
|
A | C | 33 | a0001c0001t0001g0107a0001c0001t0001g0109a0001c0001t0002g0012others(30): Show | 36 | HG00738.hp2 HG01123.hp2 HG01175.hp2 others(33): Show |
intron_variant | MODIFIER | c.382-3464T>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11428100 | ||||||
chr8:11428120
|
TA | T | 90 | a0001c0001t0001g0107a0001c0001t0001g0109a0001c0001t0002g0012others(87): Show | 98 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.382-3485delT | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11428120 | ||||||
chr8:11428224
|
C | T | 19 | a0001c0001t0036g0139a0001c0001t0091g0140a0002c0002t0001g0146others(16): Show | 21 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(18): Show |
intron_variant | MODIFIER | c.382-3588G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11428224 | ||||||
chr8:11428296
|
T | G | 1 | a0001c0001t0071g0211 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.382-3660A>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11428296 | ||||||
chr8:11428398
|
G | C | 2 | a0001c0001t0012g0089a0001c0001t0099g0088 | 2 | HG02451.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.382-3762C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11428398 | ||||||
chr8:11428420
|
C | T | 1 | a0001c0001t0002g0061 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.382-3784G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11428420 | ||||||
chr8:11428440
|
A | G | 1 | a0001c0001t0066g0133 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.382-3804T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11428440 | ||||||
chr8:11428526
|
C | T | 3 | a0001c0001t0022g0094a0001c0001t0022g0098a0001c0001t0030g0097 | 3 | HG02976.hp1 NA19240.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.382-3890G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11428526 | ||||||
chr8:11428560
|
T | C | 53 | a0001c0001t0002g0102a0001c0001t0003g0007a0001c0001t0003g0122others(50): Show | 56 | HG00099.hp2 HG00642.hp1 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.382-3924A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11428560 | ||||||
chr8:11428594
|
A | G | 3 | a0001c0001t0009g0128a0001c0001t0020g0126a0001c0001t0058g0127 | 3 | HG02572.hp1 HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.382-3958T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11428594 | ||||||
chr8:11428637
|
C | A | 89 | a0001c0001t0001g0107a0001c0001t0001g0109a0001c0001t0003g0007others(86): Show | 98 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.382-4001G>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11428637 | ||||||
chr8:11428639
|
C | G | 1 | a0001c0001t0066g0133 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.382-4003G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11428639 | ||||||
chr8:11428713
|
G | T | 1 | a0001c0001t0104g0091 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.382-4077C>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11428713 | ||||||
chr8:11428729
|
C | T | 1 | a0001c0001t0067g0159 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.382-4093G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11428729 | ||||||
chr8:11428873
|
A | G | 1 | a0001c0001t0001g0268 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.382-4237T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11428873 | ||||||
chr8:11428888
|
G | A | 1 | a0001c0001t0089g0024 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.382-4252C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11428888 | ||||||
chr8:11429088
|
A | C | 2 | a0001c0001t0028g0258a0001c0001t0062g0132 | 2 | HG01884.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.382-4452T>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11429088 | ||||||
chr8:11429126
|
C | G | 1 | a0001c0001t0052g0319 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.382-4490G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11429126 | ||||||
chr8:11429136
|
A | G | 2 | a0001c0001t0025g0118a0001c0001t0044g0117 | 2 | HG02723.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.382-4500T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11429136 | ||||||
chr8:11429231
|
C | G | 1 | a0001c0001t0024g0242 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.382-4595G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11429231 | ||||||
chr8:11429572
|
G | C | 113 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(110): Show | 133 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(130): Show |
intron_variant | MODIFIER | c.382-4936C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11429572 | ||||||
chr8:11429613
|
G | T | 253 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(250): Show | 283 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(280): Show |
intron_variant | MODIFIER | c.382-4977C>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11429613 | ||||||
chr8:11429639
|
T | C | 27 | a0001c0001t0001g0107a0001c0001t0001g0109a0001c0001t0003g0310others(24): Show | 29 | HG00738.hp2 HG01123.hp2 HG01175.hp2 others(26): Show |
intron_variant | MODIFIER | c.382-5003A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11429639 | ||||||
chr8:11429709
|
C | T | 3 | a0001c0001t0003g0029a0001c0001t0032g0027a0001c0001t0032g0028 | 3 | HG01167.hp1 HG01169.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.382-5073G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11429709 | ||||||
chr8:11429736
|
G | T | 10 | a0001c0001t0003g0029a0001c0001t0009g0255a0001c0001t0009g0256others(7): Show | 10 | HG01167.hp1 HG01169.hp2 HG02004.hp1 others(7): Show |
intron_variant | MODIFIER | c.382-5100C>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11429736 | ||||||
chr8:11429862
|
T | C | 27 | a0001c0001t0001g0107a0001c0001t0001g0109a0001c0001t0003g0310others(24): Show | 29 | HG00738.hp2 HG01123.hp2 HG01175.hp2 others(26): Show |
intron_variant | MODIFIER | c.382-5226A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11429862 | ||||||
chr8:11429865
|
C | T | 1 | a0001c0001t0020g0126 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.382-5229G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11429865 | ||||||
chr8:11429906
|
T | C | 23 | a0001c0001t0003g0007a0001c0001t0003g0122a0001c0001t0003g0274others(20): Show | 25 | HG01358.hp1 HG01884.hp1 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.382-5270A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11429906 | ||||||
chr8:11429955
|
G | A | 1 | a0001c0001t0089g0024 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.382-5319C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11429955 | ||||||
chr8:11429958
|
C | G | 6 | a0001c0001t0017g0261a0001c0001t0017g0262a0001c0001t0017g0264others(3): Show | 6 | HG02145.hp1 HG02615.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.382-5322G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11429958 | ||||||
chr8:11430041
|
A | G | 19 | a0001c0001t0036g0139a0001c0001t0091g0140a0002c0002t0001g0146others(16): Show | 21 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(18): Show |
intron_variant | MODIFIER | c.382-5405T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11430041 | ||||||
chr8:11430057
|
C | G | 2 | a0001c0001t0015g0004a0001c0001t0088g0269 | 4 | HG02970.hp1 HG03041.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.382-5421G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11430057 | ||||||
chr8:11430109
|
C | T | 1 | a0001c0001t0063g0068 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.382-5473G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11430109 | ||||||
chr8:11430125
|
C | T | 1 | a0001c0001t0001g0203 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.382-5489G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11430125 | ||||||
chr8:11430244
|
G | T | 1 | a0001c0001t0026g0077 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.382-5608C>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11430244 | ||||||
chr8:11430245
|
T | A | 29 | a0001c0001t0001g0107a0001c0001t0001g0109a0001c0001t0002g0134others(26): Show | 31 | HG00738.hp2 HG01123.hp2 HG01175.hp2 others(28): Show |
intron_variant | MODIFIER | c.382-5609A>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11430245 | ||||||
chr8:11430267
|
G | A | 1 | a0001c0001t0035g0101 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.382-5631C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11430267 | ||||||
chr8:11430305
|
C | T | 7 | a0001c0001t0003g0007a0001c0001t0003g0122a0001c0001t0003g0274others(4): Show | 9 | HG02451.hp2 HG02486.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.382-5669G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11430305 | ||||||
chr8:11430372
|
G | T | 2 | a0001c0001t0021g0157a0001c0001t0029g0156 | 2 | HG02145.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.382-5736C>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11430372 | ||||||
chr8:11430381
|
T | C | 1 | a0001c0001t0100g0189 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.382-5745A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11430381 | ||||||
chr8:11430399
|
T | G | 1 | a0001c0001t0002g0253 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.382-5763A>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11430399 | ||||||
chr8:11430420
|
G | A | 1 | a0001c0001t0071g0211 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.382-5784C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11430420 | ||||||
chr8:11430531
|
A | C | 35 | a0001c0001t0002g0102a0001c0001t0013g0282a0001c0001t0013g0283others(32): Show | 38 | HG00099.hp2 HG00642.hp1 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.382-5895T>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11430531 | ||||||
chr8:11430575
|
A | T | 3 | a0001c0001t0025g0270a0001c0001t0043g0263a0001c0001t0080g0130 | 3 | HG02559.hp1 HG02717.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.382-5939T>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11430575 | ||||||
chr8:11430633
|
T | C | 1 | a0002c0002t0027g0014 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.382-5997A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11430633 | ||||||
chr8:11430738
|
C | G | 1 | a0001c0001t0058g0127 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.382-6102G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11430738 | ||||||
chr8:11430753
|
G | T | 1 | a0001c0001t0009g0255 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.382-6117C>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11430753 | ||||||
chr8:11430778
|
G | A | 1 | a0001c0001t0001g0224 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.382-6142C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11430778 | ||||||
chr8:11430786
|
C | T | 9 | a0001c0001t0017g0261a0001c0001t0017g0262a0001c0001t0017g0264others(6): Show | 9 | HG01358.hp2 HG01884.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.382-6150G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11430786 | ||||||
chr8:11430787
|
G | A | 2 | a0001c0001t0102g0116a0001c0001t0106g0113 | 2 | HG01884.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.382-6151C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11430787 | ||||||
chr8:11430887
|
T | TG | 8 | a0001c0001t0017g0261a0001c0001t0017g0262a0001c0001t0017g0264others(5): Show | 8 | HG01884.hp2 HG02109.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.382-6252dupC | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11430887 | ||||||
chr8:11430972
|
A | C | 12 | a0001c0001t0003g0029a0001c0001t0009g0255a0001c0001t0009g0256others(9): Show | 12 | HG01167.hp1 HG01169.hp2 HG02004.hp1 others(9): Show |
intron_variant | MODIFIER | c.382-6336T>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11430972 | ||||||
chr8:11430976
|
T | G | 19 | a0001c0001t0036g0139a0001c0001t0091g0140a0002c0002t0001g0146others(16): Show | 21 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(18): Show |
intron_variant | MODIFIER | c.382-6340A>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11430976 | ||||||
chr8:11431036
|
G | A | 1 | a0002c0002t0078g0148 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.382-6400C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11431036 | ||||||
chr8:11431084
|
A | T | 1 | a0001c0001t0020g0126 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.382-6448T>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11431084 | ||||||
chr8:11431097
|
G | C | 1 | a0008c0007t0002g0031 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.382-6461C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11431097 | ||||||
chr8:11431135
|
A | G | 1 | a0001c0001t0001g0217 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.382-6499T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11431135 | ||||||
chr8:11431291
|
T | G | 1 | a0001c0001t0001g0212 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.382-6655A>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11431291 | ||||||
chr8:11431298
|
C | T | 1 | a0001c0001t0024g0242 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.382-6662G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11431298 | ||||||
chr8:11431327
|
G | T | 1 | a0001c0001t0081g0123 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.382-6691C>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11431327 | ||||||
chr8:11431368
|
A | T | 1 | a0001c0001t0083g0306 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.382-6732T>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11431368 | ||||||
chr8:11431514
|
A | G | 1 | a0001c0001t0064g0099 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.382-6878T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11431514 | ||||||
chr8:11431515
|
T | C | 124 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(121): Show | 145 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(142): Show |
intron_variant | MODIFIER | c.382-6879A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11431515 | ||||||
chr8:11431522
|
T | C | 44 | a0001c0001t0003g0029a0001c0001t0003g0219a0001c0001t0003g0220others(41): Show | 47 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(44): Show |
intron_variant | MODIFIER | c.382-6886A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11431522 | ||||||
chr8:11431544
|
T | C | 236 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(233): Show | 267 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(264): Show |
intron_variant | MODIFIER | c.382-6908A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11431544 | ||||||
chr8:11431560
|
A | G | 1 | a0001c0001t0002g0038 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.382-6924T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11431560 | ||||||
chr8:11431637
|
A | C | 237 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(234): Show | 268 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(265): Show |
intron_variant | MODIFIER | c.382-7001T>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11431637 | ||||||
chr8:11431674
|
G | A | 1 | a0001c0001t0024g0242 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.382-7038C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11431674 | ||||||
chr8:11431789
|
C | G | 1 | a0001c0001t0002g0134 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.382-7153G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11431789 | ||||||
chr8:11431851
|
C | A | 3 | a0001c0001t0001g0107a0001c0001t0001g0109a0001c0008t0077g0108 | 3 | HG02895.hp1 HG02897.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.382-7215G>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11431851 | ||||||
chr8:11431885
|
C | G | 6 | a0001c0001t0024g0100a0001c0001t0025g0328a0001c0001t0090g0124others(3): Show | 6 | HG01884.hp1 HG02280.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.382-7249G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11431885 | ||||||
chr8:11431893
|
C | CA | 9 | a0001c0001t0002g0011a0001c0001t0002g0034a0001c0001t0002g0050others(6): Show | 10 | HG02056.hp2 HG03098.hp2 HG04115.hp2 others(7): Show |
intron_variant | MODIFIER | c.382-7258dupT | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11431893 | ||||||
chr8:11431893
|
CAAAAAAA others(3): Show |
C | 4 | a0001c0001t0003g0219a0001c0001t0003g0220a0001c0001t0098g0106others(1): Show | 5 | HG02818.hp1 HG02896.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.382-7267_382-7258d others(12): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11431893 | ||||||
chr8:11431893
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0010g0246 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.382-7268_382-7258d others(13): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11431893 | ||||||
chr8:11431917
|
A | AAAAAAG | 21 | a0001c0001t0002g0134a0001c0001t0036g0139a0001c0001t0091g0140others(18): Show | 23 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(20): Show |
intron_variant | MODIFIER | c.382-7282_382-7281i others(8): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11431917 | ||||||
chr8:11431917
|
A | AAAAAG | 8 | a0001c0001t0002g0102a0001c0001t0009g0128a0001c0001t0020g0126others(5): Show | 8 | HG02145.hp2 HG02559.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.382-7282_382-7281i others(7): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11431917 | ||||||
chr8:11431917
|
A | AAAAG | 56 | a0001c0001t0001g0107a0001c0001t0001g0109a0001c0001t0002g0285others(53): Show | 58 | HG00639.hp1 HG00738.hp2 HG01123.hp2 others(55): Show |
intron_variant | MODIFIER | c.382-7282_382-7281i others(6): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11431917 | ||||||
chr8:11431917
|
A | AAAG | 32 | a0001c0001t0001g0161a0001c0001t0003g0007a0001c0001t0003g0275others(29): Show | 35 | HG00099.hp2 HG00642.hp2 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.382-7284_382-7282d others(5): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11431917 | ||||||
chr8:11431917
|
A | AAG | 29 | a0001c0001t0001g0019a0001c0001t0001g0215a0001c0001t0001g0231others(26): Show | 32 | HG00558.hp2 HG01167.hp1 HG01169.hp2 others(29): Show |
intron_variant | MODIFIER | c.382-7282_382-7281i others(4): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11431917 | ||||||
chr8:11431917
|
A | AG | 101 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(98): Show | 120 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(117): Show |
intron_variant | MODIFIER | c.382-7282_382-7281i others(3): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11431917 | ||||||
chr8:11431917
|
A | G | 14 | a0001c0001t0001g0018a0001c0001t0001g0087a0001c0001t0001g0202others(11): Show | 16 | HG00597.hp2 HG00673.hp1 HG00673.hp2 others(13): Show |
intron_variant | MODIFIER | c.382-7281T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11431917 | ||||||
chr8:11431941
|
G | T | 2 | a0001c0001t0024g0242a0001c0001t0081g0123 | 2 | HG02683.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.382-7305C>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11431941 | ||||||
chr8:11431956
|
C | T | 1 | a0001c0001t0001g0249 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.382-7320G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11431956 | ||||||
chr8:11431966
|
C | G | 1 | a0001c0001t0009g0255 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.382-7330G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11431966 | ||||||
chr8:11432176
|
A | G | 30 | a0001c0001t0011g0119a0001c0001t0025g0270a0001c0001t0036g0139others(27): Show | 32 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(29): Show |
intron_variant | MODIFIER | c.382-7540T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11432176 | ||||||
chr8:11432188
|
A | G | 117 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(114): Show | 138 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(135): Show |
intron_variant | MODIFIER | c.382-7552T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11432188 | ||||||
chr8:11432195
|
G | A | 5 | a0001c0001t0003g0219a0001c0001t0003g0220a0001c0001t0010g0246others(2): Show | 6 | HG00741.hp1 HG02818.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.382-7559C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11432195 | ||||||
chr8:11432220
|
G | A | 1 | a0001c0001t0104g0091 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.382-7584C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11432220 | ||||||
chr8:11432260
|
T | G | 121 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(118): Show | 142 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(139): Show |
intron_variant | MODIFIER | c.382-7624A>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11432260 | ||||||
chr8:11432288
|
C | G | 1 | a0007c0011t0054g0131 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.382-7652G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11432288 | ||||||
chr8:11432306
|
T | A | 1 | a0001c0001t0007g0039 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.382-7670A>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11432306 | ||||||
chr8:11432469
|
ACTC | A | 1 | a0001c0001t0015g0004 | 3 | HG02970.hp1 HG03041.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.382-7836_382-7834d others(5): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11432469 | ||||||
chr8:11432550
|
T | C | 24 | a0001c0001t0036g0139a0001c0001t0091g0140a0002c0002t0001g0146others(21): Show | 26 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(23): Show |
intron_variant | MODIFIER | c.382-7914A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11432550 | ||||||
chr8:11432654
|
G | A | 1 | a0001c0001t0005g0325 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.382-8018C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11432654 | ||||||
chr8:11432667
|
G | A | 1 | a0001c0001t0102g0116 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.382-8031C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11432667 | ||||||
chr8:11432809
|
A | G | 1 | a0001c0001t0022g0092 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.382-8173T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11432809 | ||||||
chr8:11432858
|
A | G | 4 | a0001c0001t0024g0100a0001c0001t0025g0328a0001c0001t0090g0124others(1): Show | 4 | HG02280.hp1 HG02572.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.382-8222T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11432858 | ||||||
chr8:11433020
|
C | T | 7 | a0001c0001t0024g0100a0001c0001t0025g0328a0001c0001t0090g0124others(4): Show | 7 | HG01358.hp1 HG01884.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.382-8384G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11433020 | ||||||
chr8:11433053
|
C | T | 3 | a0001c0001t0003g0219a0001c0001t0003g0220a0001c0001t0098g0106 | 3 | HG02818.hp1 HG02896.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.382-8417G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11433053 | ||||||
chr8:11433111
|
G | A | 11 | a0001c0001t0002g0102a0001c0001t0002g0285a0001c0001t0002g0300others(8): Show | 11 | HG00639.hp1 HG02723.hp1 HG02738.hp1 others(8): Show |
intron_variant | MODIFIER | c.382-8475C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11433111 | ||||||
chr8:11433173
|
C | G | 24 | a0001c0001t0036g0139a0001c0001t0091g0140a0002c0002t0001g0146others(21): Show | 26 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(23): Show |
intron_variant | MODIFIER | c.382-8537G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11433173 | ||||||
chr8:11433204
|
T | TA | 39 | a0001c0001t0003g0029a0001c0001t0003g0219a0001c0001t0003g0220others(36): Show | 42 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.382-8569dupT | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11433204 | ||||||
chr8:11433204
|
T | TAAA | 6 | a0001c0001t0011g0119a0001c0001t0025g0270a0001c0001t0043g0121others(3): Show | 6 | HG01891.hp1 HG02258.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.382-8571_382-8569d others(5): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11433204 | ||||||
chr8:11433214
|
T | A | 1 | a0001c0001t0088g0269 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.382-8578A>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11433214 | ||||||
chr8:11433244
|
G | A | 7 | a0001c0001t0011g0119a0001c0001t0025g0270a0001c0001t0043g0121others(4): Show | 7 | HG01891.hp1 HG02258.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.382-8608C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11433244 | ||||||
chr8:11433293
|
T | C | 232 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(229): Show | 260 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(257): Show |
intron_variant | MODIFIER | c.382-8657A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11433293 | ||||||
chr8:11433311
|
C | T | 9 | a0001c0001t0003g0029a0001c0001t0009g0255a0001c0001t0009g0256others(6): Show | 9 | HG01167.hp1 HG01169.hp2 HG02004.hp1 others(6): Show |
intron_variant | MODIFIER | c.382-8675G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11433311 | ||||||
chr8:11433374
|
C | A | 1 | a0001c0001t0001g0235 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.382-8738G>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11433374 | ||||||
chr8:11433375
|
G | A | 4 | a0001c0001t0003g0007a0001c0001t0003g0122a0001c0001t0003g0330others(1): Show | 6 | HG02451.hp2 HG02486.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.382-8739C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11433375 | ||||||
chr8:11433405
|
A | G | 3 | a0001c0001t0024g0242a0001c0001t0028g0258a0001c0001t0062g0132 | 3 | HG01884.hp2 HG02109.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.382-8769T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11433405 | ||||||
chr8:11433430
|
G | C | 14 | a0001c0001t0003g0029a0001c0001t0003g0219a0001c0001t0003g0220others(11): Show | 15 | HG00741.hp1 HG01167.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.382-8794C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11433430 | ||||||
chr8:11433446
|
A | G | 265 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(262): Show | 296 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(293): Show |
intron_variant | MODIFIER | c.382-8810T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11433446 | ||||||
chr8:11433457
|
C | T | 260 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(257): Show | 291 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(288): Show |
intron_variant | MODIFIER | c.382-8821G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11433457 | ||||||
chr8:11433593
|
A | G | 1 | a0001c0001t0001g0202 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.382-8957T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11433593 | ||||||
chr8:11433608
|
C | T | 1 | a0001c0001t0006g0229 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.382-8972G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11433608 | ||||||
chr8:11433784
|
G | A | 21 | a0001c0001t0003g0029a0001c0001t0003g0219a0001c0001t0003g0220others(18): Show | 22 | HG00741.hp1 HG01167.hp1 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.382-9148C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11433784 | ||||||
chr8:11433801
|
G | A | 1 | a0001c0001t0022g0092 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.382-9165C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11433801 | ||||||
chr8:11433832
|
G | C | 260 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(257): Show | 291 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(288): Show |
intron_variant | MODIFIER | c.382-9196C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11433832 | ||||||
chr8:11433938
|
G | A | 1 | a0001c0001t0005g0313 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.382-9302C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11433938 | ||||||
chr8:11433990
|
A | G | 8 | a0001c0001t0011g0119a0001c0001t0025g0270a0001c0001t0043g0121others(5): Show | 8 | HG01891.hp1 HG02258.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.382-9354T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11433990 | ||||||
chr8:11434066
|
C | T | 1 | a0001c0001t0042g0105 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.382-9430G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11434066 | ||||||
chr8:11434088
|
G | A | 21 | a0001c0001t0003g0029a0001c0001t0003g0219a0001c0001t0003g0220others(18): Show | 22 | HG00741.hp1 HG01167.hp1 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.382-9452C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11434088 | ||||||
chr8:11434095
|
G | C | 1 | a0001c0001t0106g0113 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.382-9459C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11434095 | ||||||
chr8:11434114
|
C | G | 1 | a0001c0001t0017g0261 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.382-9478G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11434114 | ||||||
chr8:11434114
|
C | T | 3 | a0001c0001t0002g0134a0001c0001t0012g0329a0001c0001t0055g0025 | 3 | HG02258.hp1 HG03139.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.382-9478G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11434114 | ||||||
chr8:11434123
|
C | T | 1 | a0001c0001t0001g0201 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.382-9487G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11434123 | ||||||
chr8:11434151
|
T | C | 8 | a0001c0001t0022g0092a0001c0001t0022g0094a0001c0001t0022g0098others(5): Show | 8 | HG01891.hp2 HG02257.hp1 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.382-9515A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11434151 | ||||||
chr8:11434177
|
C | A | 1 | a0001c0001t0066g0133 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.382-9541G>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11434177 | ||||||
chr8:11434200
|
G | A | 1 | a0001c0001t0106g0113 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.382-9564C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11434200 | ||||||
chr8:11434213
|
C | T | 1 | a0001c0001t0104g0091 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.382-9577G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11434213 | ||||||
chr8:11434221
|
G | C | 1 | a0001c0001t0068g0273 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.382-9585C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11434221 | ||||||
chr8:11434264
|
C | G | 29 | a0001c0001t0002g0102a0001c0001t0002g0280a0001c0001t0002g0294others(26): Show | 32 | HG00099.hp2 HG00639.hp2 HG00642.hp2 others(29): Show |
intron_variant | MODIFIER | c.382-9628G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11434264 | ||||||
chr8:11434271
|
C | T | 3 | a0001c0001t0024g0100a0001c0001t0025g0328a0001c0001t0090g0124 | 3 | HG02572.hp2 HG03130.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.382-9635G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11434271 | ||||||
chr8:11434283
|
T | G | 1 | a0001c0001t0030g0125 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.382-9647A>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11434283 | ||||||
chr8:11434291
|
G | A | 1 | a0001c0001t0081g0123 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.382-9655C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11434291 | ||||||
chr8:11434361
|
G | A | 18 | a0001c0001t0002g0285a0001c0001t0002g0300a0001c0001t0011g0265others(15): Show | 18 | HG00639.hp1 HG01891.hp2 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.381+9670C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11434361 | ||||||
chr8:11434363
|
C | A | 4 | a0001c0001t0025g0270a0001c0001t0043g0263a0001c0001t0080g0130others(1): Show | 4 | HG02559.hp1 HG02717.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.381+9668G>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11434363 | ||||||
chr8:11434418
|
G | T | 1 | a0001c0001t0015g0004 | 3 | HG02970.hp1 HG03041.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.381+9613C>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11434418 | ||||||
chr8:11434433
|
G | A | 1 | a0001c0001t0104g0091 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.381+9598C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11434433 | ||||||
chr8:11434511
|
G | C | 1 | a0001c0001t0104g0091 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.381+9520C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11434511 | ||||||
chr8:11434535
|
G | C | 4 | a0001c0001t0025g0270a0001c0001t0043g0263a0001c0001t0080g0130others(1): Show | 4 | HG02559.hp1 HG02717.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.381+9496C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11434535 | ||||||
chr8:11434559
|
G | A | 23 | a0001c0001t0001g0107a0001c0001t0001g0109a0001c0001t0003g0310others(20): Show | 25 | HG00738.hp2 HG01123.hp2 HG01175.hp2 others(22): Show |
intron_variant | MODIFIER | c.381+9472C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11434559 | ||||||
chr8:11434699
|
C | G | 1 | a0001c0001t0001g0244 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.381+9332G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11434699 | ||||||
chr8:11434726
|
G | C | 1 | a0001c0001t0104g0091 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.381+9305C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11434726 | ||||||
chr8:11434738
|
A | G | 22 | a0001c0001t0003g0029a0001c0001t0003g0219a0001c0001t0003g0220others(19): Show | 23 | HG00741.hp1 HG01167.hp1 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.381+9293T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11434738 | ||||||
chr8:11434745
|
C | G | 1 | a0001c0001t0066g0133 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.381+9286G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11434745 | ||||||
chr8:11434748
|
C | T | 3 | a0001c0001t0002g0134a0001c0001t0012g0329a0001c0001t0055g0025 | 3 | HG02258.hp1 HG03139.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.381+9283G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11434748 | ||||||
chr8:11434860
|
A | G | 1 | a0001c0001t0001g0200 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.381+9171T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11434860 | ||||||
chr8:11434891
|
G | A | 1 | a0001c0001t0002g0134 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.381+9140C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11434891 | ||||||
chr8:11434988
|
C | T | 1 | a0001c0001t0015g0110 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.381+9043G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11434988 | ||||||
chr8:11434995
|
G | C | 6 | a0001c0001t0003g0007a0001c0001t0003g0122a0001c0001t0003g0274others(3): Show | 8 | HG02451.hp2 HG02486.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.381+9036C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11434995 | ||||||
chr8:11435020
|
T | C | 1 | a0001c0001t0002g0080 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.381+9011A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11435020 | ||||||
chr8:11435033
|
C | G | 2 | a0001c0001t0039g0073a0001c0001t0039g0074 | 2 | HG01099.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.381+8998G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11435033 | ||||||
chr8:11435033
|
C | T | 183 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(180): Show | 209 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(206): Show |
intron_variant | MODIFIER | c.381+8998G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11435033 | ||||||
chr8:11435085
|
T | G | 1 | a0001c0001t0102g0116 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.381+8946A>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11435085 | ||||||
chr8:11435099
|
A | G | 7 | a0001c0001t0017g0261a0001c0001t0017g0262a0001c0001t0017g0264others(4): Show | 7 | HG01884.hp2 HG02109.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.381+8932T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11435099 | ||||||
chr8:11435144
|
C | T | 1 | a0001c0001t0021g0321 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.381+8887G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11435144 | ||||||
chr8:11435231
|
C | T | 2 | a0001c0001t0001g0006a0001c0001t0034g0225 | 4 | HG01071.hp2 HG01167.hp2 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.381+8800G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11435231 | ||||||
chr8:11435323
|
A | G | 5 | a0001c0001t0003g0219a0001c0001t0003g0220a0001c0001t0010g0246others(2): Show | 6 | HG00741.hp1 HG02818.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.381+8708T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11435323 | ||||||
chr8:11435336
|
C | T | 1 | a0001c0001t0104g0091 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.381+8695G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11435336 | ||||||
chr8:11435337
|
G | A | 7 | a0001c0001t0011g0119a0001c0001t0025g0270a0001c0001t0043g0121others(4): Show | 7 | HG01891.hp1 HG02258.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.381+8694C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11435337 | ||||||
chr8:11435381
|
A | G | 7 | a0001c0001t0011g0119a0001c0001t0025g0270a0001c0001t0043g0121others(4): Show | 7 | HG01891.hp1 HG02258.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.381+8650T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11435381 | ||||||
chr8:11435483
|
G | A | 1 | a0001c0001t0095g0054 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.381+8548C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11435483 | ||||||
chr8:11435526
|
A | C | 262 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(259): Show | 293 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(290): Show |
intron_variant | MODIFIER | c.381+8505T>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11435526 | ||||||
chr8:11435617
|
C | T | 1 | a0001c0001t0002g0102 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.381+8414G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11435617 | ||||||
chr8:11435626
|
C | G | 4 | a0001c0001t0003g0029a0001c0001t0032g0027a0001c0001t0032g0028others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG02004.hp1 others(1): Show |
intron_variant | MODIFIER | c.381+8405G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11435626 | ||||||
chr8:11435711
|
C | T | 1 | a0002c0002t0014g0301 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.381+8320G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11435711 | ||||||
chr8:11435782
|
C | G | 1 | a0001c0001t0105g0326 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.381+8249G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11435782 | ||||||
chr8:11435881
|
C | T | 56 | a0001c0001t0002g0102a0001c0001t0002g0134a0001c0001t0002g0280others(53): Show | 59 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.381+8150G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11435881 | ||||||
chr8:11435889
|
G | A | 34 | a0001c0001t0003g0007a0001c0001t0003g0029a0001c0001t0003g0122others(31): Show | 37 | HG00741.hp1 HG01167.hp1 HG01169.hp2 others(34): Show |
intron_variant | MODIFIER | c.381+8142C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11435889 | ||||||
chr8:11435920
|
A | G | 25 | a0001c0001t0036g0139a0001c0001t0091g0140a0002c0002t0001g0146others(22): Show | 27 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(24): Show |
intron_variant | MODIFIER | c.381+8111T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11435920 | ||||||
chr8:11435949
|
G | A | 140 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(137): Show | 164 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(161): Show |
intron_variant | MODIFIER | c.381+8082C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11435949 | ||||||
chr8:11435993
|
T | G | 25 | a0001c0001t0036g0139a0001c0001t0091g0140a0002c0002t0001g0146others(22): Show | 27 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(24): Show |
intron_variant | MODIFIER | c.381+8038A>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11435993 | ||||||
chr8:11435996
|
C | T | 1 | a0001c0001t0002g0078 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.381+8035G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11435996 | ||||||
chr8:11436172
|
A | C | 3 | a0001c0001t0024g0100a0001c0001t0025g0328a0001c0001t0090g0124 | 3 | HG02572.hp2 HG03130.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.381+7859T>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11436172 | ||||||
chr8:11436250
|
G | T | 1 | a0001c0001t0002g0102 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.381+7781C>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11436250 | ||||||
chr8:11436320
|
C | T | 2 | a0001c0001t0025g0118a0001c0001t0044g0117 | 2 | HG02723.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.381+7711G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11436320 | ||||||
chr8:11436406
|
C | T | 1 | a0001c0001t0030g0125 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.381+7625G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11436406 | ||||||
chr8:11436420
|
T | C | 65 | a0001c0001t0002g0102a0001c0001t0002g0280a0001c0001t0002g0294others(62): Show | 71 | HG00099.hp2 HG00639.hp2 HG00642.hp2 others(68): Show |
intron_variant | MODIFIER | c.381+7611A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11436420 | ||||||
chr8:11436675
|
A | G | 25 | a0001c0001t0036g0139a0001c0001t0091g0140a0002c0002t0001g0146others(22): Show | 27 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(24): Show |
intron_variant | MODIFIER | c.381+7356T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11436675 | ||||||
chr8:11436711
|
G | C | 1 | a0001c0001t0053g0327 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.381+7320C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11436711 | ||||||
chr8:11436736
|
C | G | 36 | a0001c0001t0001g0107a0001c0001t0001g0109a0001c0001t0003g0310others(33): Show | 38 | HG00738.hp2 HG01123.hp2 HG01175.hp2 others(35): Show |
intron_variant | MODIFIER | c.381+7295G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11436736 | ||||||
chr8:11436845
|
C | G | 5 | a0001c0001t0003g0219a0001c0001t0003g0220a0001c0001t0010g0246others(2): Show | 6 | HG00741.hp1 HG02818.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.381+7186G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11436845 | ||||||
chr8:11436911
|
G | A | 1 | a0001c0001t0012g0329 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.381+7120C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11436911 | ||||||
chr8:11436956
|
G | T | 1 | a0001c0001t0010g0199 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.381+7075C>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11436956 | ||||||
chr8:11437028
|
A | G | 2 | a0001c0001t0015g0004a0001c0001t0015g0110 | 4 | HG02622.hp1 HG02970.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.381+7003T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11437028 | ||||||
chr8:11437066
|
C | T | 5 | a0001c0001t0003g0219a0001c0001t0003g0220a0001c0001t0010g0246others(2): Show | 6 | HG00741.hp1 HG02818.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.381+6965G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11437066 | ||||||
chr8:11437079
|
G | A | 1 | a0001c0001t0001g0222 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.381+6952C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11437079 | ||||||
chr8:11437127
|
G | T | 1 | a0001c0001t0048g0315 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.381+6904C>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11437127 | ||||||
chr8:11437132
|
A | C | 7 | a0001c0001t0017g0261a0001c0001t0017g0262a0001c0001t0017g0264others(4): Show | 7 | HG01884.hp2 HG02109.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.381+6899T>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11437132 | ||||||
chr8:11437134
|
A | C | 1 | a0001c0001t0001g0217 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.381+6897T>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11437134 | ||||||
chr8:11437228
|
T | C | 1 | a0001c0001t0001g0213 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.381+6803A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11437228 | ||||||
chr8:11437291
|
G | A | 22 | a0001c0001t0003g0007a0001c0001t0003g0029a0001c0001t0003g0122others(19): Show | 25 | HG00741.hp1 HG01167.hp1 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.381+6740C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11437291 | ||||||
chr8:11437301
|
C | T | 19 | a0001c0001t0036g0139a0001c0001t0091g0140a0002c0002t0001g0146others(16): Show | 21 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(18): Show |
intron_variant | MODIFIER | c.381+6730G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11437301 | ||||||
chr8:11437333
|
T | A | 1 | a0001c0001t0002g0037 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.381+6698A>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11437333 | ||||||
chr8:11437341
|
C | T | 1 | a0001c0001t0001g0171 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.381+6690G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11437341 | ||||||
chr8:11437345
|
A | G | 1 | a0001c0001t0104g0091 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.381+6686T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11437345 | ||||||
chr8:11437425
|
C | T | 104 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(101): Show | 125 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(122): Show |
intron_variant | MODIFIER | c.381+6606G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11437425 | ||||||
chr8:11437429
|
G | T | 1 | a0002c0002t0078g0148 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.381+6602C>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11437429 | ||||||
chr8:11437430
|
C | T | 18 | a0001c0001t0002g0285a0001c0001t0002g0298a0001c0001t0002g0300others(15): Show | 18 | HG00639.hp1 HG01891.hp2 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.381+6601G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11437430 | ||||||
chr8:11437511
|
T | C | 8 | a0001c0001t0017g0261a0001c0001t0017g0262a0001c0001t0017g0264others(5): Show | 8 | HG01884.hp2 HG02109.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.381+6520A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11437511 | ||||||
chr8:11437575
|
T | C | 25 | a0001c0001t0036g0139a0001c0001t0091g0140a0002c0002t0001g0146others(22): Show | 27 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(24): Show |
intron_variant | MODIFIER | c.381+6456A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11437575 | ||||||
chr8:11437638
|
T | C | 7 | a0001c0001t0017g0261a0001c0001t0017g0262a0001c0001t0017g0264others(4): Show | 7 | HG01884.hp2 HG02109.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.381+6393A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11437638 | ||||||
chr8:11437648
|
T | A | 1 | a0001c0001t0020g0126 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.381+6383A>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11437648 | ||||||
chr8:11437676
|
G | A | 1 | a0001c0001t0053g0327 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.381+6355C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11437676 | ||||||
chr8:11437682
|
G | A | 1 | a0001c0001t0002g0037 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.381+6349C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11437682 | ||||||
chr8:11437698
|
A | AAACGCTC others(109): Show |
6 | a0001c0001t0011g0119a0001c0001t0025g0270a0001c0001t0043g0121others(3): Show | 6 | HG01891.hp1 HG02258.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.381+6332_381+6333i others(118): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11437698 | ||||||
chr8:11437742
|
C | CGTGTGCT others(109): Show |
1 | a0001c0001t0088g0269 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.381+6288_381+6289i others(118): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11437742 | ||||||
chr8:11437742
|
C | G | 224 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(221): Show | 252 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(249): Show |
intron_variant | MODIFIER | c.381+6289G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11437742 | ||||||
chr8:11437805
|
C | T | 1 | a0001c0001t0011g0056 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.381+6226G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11437805 | ||||||
chr8:11437812
|
G | A | 5 | a0001c0001t0003g0219a0001c0001t0003g0220a0001c0001t0010g0246others(2): Show | 6 | HG00741.hp1 HG02818.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.381+6219C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11437812 | ||||||
chr8:11438001
|
C | T | 1 | a0001c0001t0005g0313 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.381+6030G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11438001 | ||||||
chr8:11438002
|
A | G | 233 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(230): Show | 261 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(258): Show |
intron_variant | MODIFIER | c.381+6029T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11438002 | ||||||
chr8:11438088
|
C | T | 3 | a0001c0001t0001g0161a0001c0001t0001g0215a0001c0001t0001g0289 | 3 | HG01070.hp2 HG01192.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.381+5943G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11438088 | ||||||
chr8:11438127
|
G | A | 1 | a0001c0001t0089g0024 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.381+5904C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11438127 | ||||||
chr8:11438155
|
G | A | 12 | a0001c0001t0011g0119a0001c0001t0024g0100a0001c0001t0025g0270others(9): Show | 12 | HG01358.hp1 HG01884.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.381+5876C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11438155 | ||||||
chr8:11438170
|
T | C | 1 | a0001c0001t0104g0091 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.381+5861A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11438170 | ||||||
chr8:11438186
|
G | A | 2 | a0001c0001t0004g0214a0001c0001t0072g0193 | 2 | HG00609.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.381+5845C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11438186 | ||||||
chr8:11438238
|
A | G | 16 | a0001c0001t0005g0022a0001c0001t0005g0309a0001c0001t0005g0313others(13): Show | 18 | HG00738.hp2 HG01123.hp2 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.381+5793T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11438238 | ||||||
chr8:11438254
|
C | T | 6 | a0002c0002t0008g0114a0002c0002t0008g0136a0002c0002t0008g0137others(3): Show | 6 | HG00642.hp1 HG02055.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.381+5777G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11438254 | ||||||
chr8:11438277
|
G | C | 1 | a0001c0001t0104g0091 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.381+5754C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11438277 | ||||||
chr8:11438297
|
G | A | 1 | a0001c0005t0073g0226 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.381+5734C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11438297 | ||||||
chr8:11438316
|
T | G | 7 | a0001c0001t0017g0261a0001c0001t0017g0262a0001c0001t0017g0264others(4): Show | 7 | HG01884.hp2 HG02109.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.381+5715A>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11438316 | ||||||
chr8:11438359
|
GGAATGTT others(27): Show |
G | 1 | a0001c0001t0053g0327 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.381+5638_381+5671d others(36): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11438359 | ||||||
chr8:11438416
|
T | C | 25 | a0001c0001t0036g0139a0001c0001t0091g0140a0002c0002t0001g0146others(22): Show | 27 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(24): Show |
intron_variant | MODIFIER | c.381+5615A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11438416 | ||||||
chr8:11438540
|
T | A | 25 | a0001c0001t0036g0139a0001c0001t0091g0140a0002c0002t0001g0146others(22): Show | 27 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(24): Show |
intron_variant | MODIFIER | c.381+5491A>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11438540 | ||||||
chr8:11438582
|
G | A | 220 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(217): Show | 248 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(245): Show |
intron_variant | MODIFIER | c.381+5449C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11438582 | ||||||
chr8:11438666
|
T | G | 2 | a0001c0001t0036g0139a0001c0001t0091g0140 | 2 | HG03710.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.381+5365A>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11438666 | ||||||
chr8:11438680
|
T | C | 47 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0296others(44): Show | 58 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.381+5351A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11438680 | ||||||
chr8:11438784
|
G | A | 1 | a0001c0001t0020g0013 | 2 | HG02895.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.381+5247C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11438784 | ||||||
chr8:11438827
|
C | T | 3 | a0001c0001t0001g0112a0001c0001t0015g0004a0001c0001t0015g0110 | 5 | HG02622.hp1 HG02970.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.381+5204G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11438827 | ||||||
chr8:11438828
|
G | T | 30 | a0001c0001t0003g0007a0001c0001t0003g0029a0001c0001t0003g0122others(27): Show | 32 | HG01167.hp1 HG01169.hp2 HG01358.hp1 others(29): Show |
intron_variant | MODIFIER | c.381+5203C>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11438828 | ||||||
chr8:11438855
|
C | A | 1 | a0001c0001t0053g0327 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.381+5176G>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11438855 | ||||||
chr8:11438907
|
G | T | 1 | a0001c0001t0053g0327 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.381+5124C>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11438907 | ||||||
chr8:11438990
|
C | T | 2 | a0001c0001t0012g0089a0001c0001t0099g0088 | 2 | HG02451.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.381+5041G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11438990 | ||||||
chr8:11439037
|
T | C | 4 | a0001c0001t0016g0023a0001c0001t0016g0317a0001c0001t0046g0316others(1): Show | 5 | HG01123.hp2 HG01993.hp1 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.381+4994A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11439037 | ||||||
chr8:11439091
|
T | C | 160 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(157): Show | 183 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(180): Show |
intron_variant | MODIFIER | c.381+4940A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11439091 | ||||||
chr8:11439131
|
A | G | 7 | a0001c0001t0022g0092a0001c0001t0022g0094a0001c0001t0022g0098others(4): Show | 7 | HG01891.hp2 HG02976.hp1 HG03516.hp1 others(4): Show |
intron_variant | MODIFIER | c.381+4900T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11439131 | ||||||
chr8:11439308
|
C | G | 1 | a0001c0001t0001g0183 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.381+4723G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11439308 | ||||||
chr8:11439329
|
A | G | 1 | a0001c0001t0007g0040 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.381+4702T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11439329 | ||||||
chr8:11439334
|
C | T | 9 | a0001c0001t0003g0029a0001c0001t0009g0255a0001c0001t0009g0256others(6): Show | 9 | HG01167.hp1 HG01169.hp2 HG02004.hp1 others(6): Show |
intron_variant | MODIFIER | c.381+4697G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11439334 | ||||||
chr8:11439415
|
C | G | 1 | a0001c0001t0001g0112 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.381+4616G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11439415 | ||||||
chr8:11439472
|
G | A | 1 | a0001c0001t0001g0215 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.381+4559C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11439472 | ||||||
chr8:11439562
|
GTTCTC | G | 116 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(113): Show | 138 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(135): Show |
intron_variant | MODIFIER | c.381+4464_381+4468d others(7): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11439562 | ||||||
chr8:11439672
|
G | GA | 121 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(118): Show | 144 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(141): Show |
intron_variant | MODIFIER | c.381+4358dupT | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11439672 | ||||||
chr8:11439768
|
T | C | 228 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(225): Show | 256 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(253): Show |
intron_variant | MODIFIER | c.381+4263A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11439768 | ||||||
chr8:11439769
|
G | A | 1 | a0001c0001t0001g0175 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.381+4262C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11439769 | ||||||
chr8:11439818
|
C | T | 25 | a0001c0001t0036g0139a0001c0001t0091g0140a0002c0002t0001g0146others(22): Show | 27 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(24): Show |
intron_variant | MODIFIER | c.381+4213G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11439818 | ||||||
chr8:11439851
|
G | C | 7 | a0001c0001t0017g0261a0001c0001t0017g0262a0001c0001t0017g0264others(4): Show | 7 | HG01884.hp2 HG02109.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.381+4180C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11439851 | ||||||
chr8:11439878
|
T | C | 208 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(205): Show | 234 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(231): Show |
intron_variant | MODIFIER | c.381+4153A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11439878 | ||||||
chr8:11439922
|
C | T | 12 | a0001c0001t0011g0119a0001c0001t0025g0270a0001c0001t0043g0121others(9): Show | 12 | HG01358.hp1 HG01884.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.381+4109G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11439922 | ||||||
chr8:11439955
|
G | A | 1 | a0001c0001t0001g0176 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.381+4076C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11439955 | ||||||
chr8:11439995
|
A | T | 12 | a0001c0001t0011g0119a0001c0001t0025g0270a0001c0001t0043g0121others(9): Show | 12 | HG01358.hp1 HG01884.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.381+4036T>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11439995 | ||||||
chr8:11440040
|
C | G | 25 | a0001c0001t0036g0139a0001c0001t0091g0140a0002c0002t0001g0146others(22): Show | 27 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(24): Show |
intron_variant | MODIFIER | c.381+3991G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11440040 | ||||||
chr8:11440059
|
C | T | 1 | a0001c0001t0043g0263 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.381+3972G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11440059 | ||||||
chr8:11440086
|
G | A | 5 | a0001c0001t0003g0219a0001c0001t0003g0220a0001c0001t0010g0246others(2): Show | 6 | HG00741.hp1 HG02818.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.381+3945C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11440086 | ||||||
chr8:11440089
|
G | C | 3 | a0001c0001t0102g0116a0001c0001t0105g0326a0001c0001t0106g0113 | 3 | HG01884.hp1 HG02280.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.381+3942C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11440089 | ||||||
chr8:11440102
|
G | A | 21 | a0001c0001t0001g0107a0001c0001t0001g0109a0001c0001t0003g0310others(18): Show | 22 | HG01123.hp2 HG01993.hp1 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.381+3929C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11440102 | ||||||
chr8:11440186
|
G | A | 9 | a0001c0001t0003g0029a0001c0001t0009g0255a0001c0001t0009g0256others(6): Show | 9 | HG01167.hp1 HG01169.hp2 HG02004.hp1 others(6): Show |
intron_variant | MODIFIER | c.381+3845C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11440186 | ||||||
chr8:11440198
|
T | C | 28 | a0001c0001t0002g0280a0001c0001t0002g0294a0001c0001t0008g0267others(25): Show | 31 | HG00099.hp2 HG00639.hp2 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.381+3833A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11440198 | ||||||
chr8:11440230
|
C | A | 1 | a0001c0001t0042g0105 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.381+3801G>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11440230 | ||||||
chr8:11440243
|
G | T | 1 | a0001c0001t0095g0054 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.381+3788C>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11440243 | ||||||
chr8:11440482
|
A | G | 262 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(259): Show | 293 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(290): Show |
intron_variant | MODIFIER | c.381+3549T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11440482 | ||||||
chr8:11440501
|
G | C | 5 | a0001c0001t0003g0219a0001c0001t0003g0220a0001c0001t0010g0246others(2): Show | 6 | HG00741.hp1 HG02818.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.381+3530C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11440501 | ||||||
chr8:11440510
|
G | A | 8 | a0001c0001t0001g0107a0001c0001t0001g0109a0001c0001t0003g0310others(5): Show | 8 | HG02109.hp2 HG02895.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.381+3521C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11440510 | ||||||
chr8:11440515
|
C | T | 1 | a0001c0001t0011g0299 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.381+3516G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11440515 | ||||||
chr8:11440639
|
C | T | 1 | a0001c0001t0004g0198 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.381+3392G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11440639 | ||||||
chr8:11440640
|
T | G | 14 | a0001c0001t0003g0029a0001c0001t0003g0219a0001c0001t0003g0220others(11): Show | 15 | HG00741.hp1 HG01167.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.381+3391A>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11440640 | ||||||
chr8:11440747
|
C | G | 2 | a0001c0001t0001g0006a0001c0001t0034g0225 | 4 | HG01071.hp2 HG01167.hp2 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.381+3284G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11440747 | ||||||
chr8:11440857
|
T | C | 2 | a0001c0001t0012g0329a0001c0001t0055g0025 | 2 | HG03139.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.381+3174A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11440857 | ||||||
chr8:11440859
|
G | A | 2 | a0001c0001t0015g0004a0001c0001t0015g0110 | 4 | HG02622.hp1 HG02970.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.381+3172C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11440859 | ||||||
chr8:11440876
|
A | G | 215 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(212): Show | 243 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(240): Show |
intron_variant | MODIFIER | c.381+3155T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11440876 | ||||||
chr8:11440895
|
G | A | 1 | a0001c0001t0009g0257 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.381+3136C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11440895 | ||||||
chr8:11440982
|
T | A | 14 | a0001c0001t0003g0029a0001c0001t0003g0219a0001c0001t0003g0220others(11): Show | 15 | HG00741.hp1 HG01167.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.381+3049A>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11440982 | ||||||
chr8:11441007
|
GT | G | 14 | a0001c0001t0003g0029a0001c0001t0003g0219a0001c0001t0003g0220others(11): Show | 15 | HG00741.hp1 HG01167.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.381+3023delA | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11441007 | ||||||
chr8:11441052
|
C | T | 1 | a0001c0001t0001g0163 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.381+2979G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11441052 | ||||||
chr8:11441097
|
A | G | 257 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(254): Show | 288 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(285): Show |
intron_variant | MODIFIER | c.381+2934T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11441097 | ||||||
chr8:11441194
|
A | G | 19 | a0001c0001t0002g0102a0001c0001t0002g0285a0001c0001t0002g0300others(16): Show | 19 | HG00639.hp1 HG01891.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.381+2837T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11441194 | ||||||
chr8:11441212
|
T | C | 2 | a0001c0001t0012g0089a0001c0001t0099g0088 | 2 | HG02451.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.381+2819A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11441212 | ||||||
chr8:11441240
|
G | C | 2 | a0001c0001t0015g0004a0001c0001t0015g0110 | 4 | HG02622.hp1 HG02970.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.381+2791C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11441240 | ||||||
chr8:11441248
|
G | A | 11 | a0001c0001t0002g0102a0001c0001t0002g0285a0001c0001t0002g0300others(8): Show | 11 | HG00639.hp1 HG02723.hp1 HG02738.hp1 others(8): Show |
intron_variant | MODIFIER | c.381+2783C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11441248 | ||||||
chr8:11441263
|
G | C | 1 | a0001c0001t0005g0313 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.381+2768C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11441263 | ||||||
chr8:11441308
|
G | A | 1 | a0001c0001t0002g0064 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.381+2723C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11441308 | ||||||
chr8:11441310
|
C | T | 9 | a0001c0001t0003g0029a0001c0001t0009g0255a0001c0001t0009g0256others(6): Show | 9 | HG01167.hp1 HG01169.hp2 HG02004.hp1 others(6): Show |
intron_variant | MODIFIER | c.381+2721G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11441310 | ||||||
chr8:11441442
|
G | A | 1 | a0001c0001t0001g0217 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.381+2589C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11441442 | ||||||
chr8:11441453
|
A | T | 5 | a0001c0001t0003g0219a0001c0001t0003g0220a0001c0001t0010g0246others(2): Show | 6 | HG00741.hp1 HG02818.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.381+2578T>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11441453 | ||||||
chr8:11441567
|
G | A | 14 | a0001c0001t0003g0029a0001c0001t0003g0219a0001c0001t0003g0220others(11): Show | 15 | HG00741.hp1 HG01167.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.381+2464C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11441567 | ||||||
chr8:11441625
|
G | C | 1 | a0001c0001t0038g0021 | 2 | HG00642.hp2 HG00735.hp1 |
intron_variant | MODIFIER | c.381+2406C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11441625 | ||||||
chr8:11441674
|
A | G | 7 | a0001c0001t0017g0261a0001c0001t0017g0262a0001c0001t0017g0264others(4): Show | 7 | HG01884.hp2 HG02109.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.381+2357T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11441674 | ||||||
chr8:11441747
|
C | G | 9 | a0001c0001t0011g0119a0001c0001t0025g0270a0001c0001t0043g0121others(6): Show | 9 | HG01358.hp1 HG01884.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.381+2284G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11441747 | ||||||
chr8:11441755
|
T | C | 1 | a0001c0001t0106g0113 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.381+2276A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11441755 | ||||||
chr8:11441833
|
C | T | 1 | a0001c0001t0001g0237 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.381+2198G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11441833 | ||||||
chr8:11441936
|
G | C | 29 | a0001c0001t0002g0280a0001c0001t0002g0294a0001c0001t0008g0267others(26): Show | 32 | HG00099.hp2 HG00639.hp2 HG00642.hp2 others(29): Show |
intron_variant | MODIFIER | c.381+2095C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11441936 | ||||||
chr8:11442100
|
T | C | 11 | a0001c0001t0002g0102a0001c0001t0002g0285a0001c0001t0002g0298others(8): Show | 11 | HG00639.hp1 HG02523.hp1 HG02738.hp1 others(8): Show |
intron_variant | MODIFIER | c.381+1931A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11442100 | ||||||
chr8:11442343
|
G | A | 5 | a0001c0001t0017g0261a0001c0001t0017g0262a0001c0001t0017g0264others(2): Show | 5 | HG02145.hp1 HG02615.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.381+1688C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11442343 | ||||||
chr8:11442396
|
C | T | 1 | a0001c0001t0001g0111 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.381+1635G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11442396 | ||||||
chr8:11442402
|
A | G | 1 | a0001c0001t0089g0024 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.381+1629T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11442402 | ||||||
chr8:11442403
|
C | G | 10 | a0001c0001t0012g0329a0001c0001t0017g0261a0001c0001t0017g0262others(7): Show | 10 | HG01884.hp2 HG02109.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.381+1628G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11442403 | ||||||
chr8:11442433
|
G | A | 1 | a0001c0001t0001g0248 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.381+1598C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11442433 | ||||||
chr8:11442442
|
A | G | 2 | a0001c0001t0002g0010a0001c0001t0002g0047 | 3 | NA18942.hp1 NA18980.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.381+1589T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11442442 | ||||||
chr8:11442475
|
C | G | 2 | a0001c0001t0013g0290a0001c0001t0013g0291 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.381+1556G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11442475 | ||||||
chr8:11442538
|
C | G | 19 | a0001c0001t0002g0280a0001c0001t0002g0294a0001c0001t0008g0267others(16): Show | 20 | HG00099.hp2 HG00639.hp2 HG00642.hp2 others(17): Show |
intron_variant | MODIFIER | c.381+1493G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11442538 | ||||||
chr8:11442552
|
A | T | 23 | a0001c0001t0003g0007a0001c0001t0003g0029a0001c0001t0003g0122others(20): Show | 26 | HG00741.hp1 HG01167.hp1 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.381+1479T>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11442552 | ||||||
chr8:11442694
|
C | T | 3 | a0001c0001t0012g0329a0001c0001t0055g0025a0001c0001t0105g0326 | 3 | HG02280.hp1 HG03139.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.381+1337G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11442694 | ||||||
chr8:11442748
|
C | T | 1 | a0001c0001t0004g0241 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.381+1283G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11442748 | ||||||
chr8:11442754
|
G | A | 3 | a0001c0001t0012g0329a0001c0001t0055g0025a0001c0001t0105g0326 | 3 | HG02280.hp1 HG03139.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.381+1277C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11442754 | ||||||
chr8:11442784
|
A | G | 20 | a0002c0002t0001g0146a0002c0002t0001g0152a0002c0002t0008g0114others(17): Show | 22 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(19): Show |
intron_variant | MODIFIER | c.381+1247T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11442784 | ||||||
chr8:11442862
|
C | T | 1 | a0001c0001t0002g0078 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.381+1169G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11442862 | ||||||
chr8:11443017
|
C | A | 5 | a0001c0001t0017g0261a0001c0001t0017g0262a0001c0001t0017g0264others(2): Show | 5 | HG02145.hp1 HG02615.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.381+1014G>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11443017 | ||||||
chr8:11443134
|
G | C | 21 | a0001c0001t0002g0102a0001c0001t0002g0285a0001c0001t0002g0298others(18): Show | 21 | HG00639.hp1 HG01891.hp2 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.381+897C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11443134 | ||||||
chr8:11443209
|
G | A | 1 | a0001c0001t0104g0091 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.381+822C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11443209 | ||||||
chr8:11443219
|
C | T | 1 | a0001c0001t0044g0117 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.381+812G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11443219 | ||||||
chr8:11443225
|
G | C | 1 | a0001c0001t0043g0263 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.381+806C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11443225 | ||||||
chr8:11443226
|
G | T | 8 | a0001c0001t0017g0261a0001c0001t0017g0262a0001c0001t0017g0264others(5): Show | 8 | HG01884.hp2 HG02109.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.381+805C>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11443226 | ||||||
chr8:11443258
|
C | T | 1 | a0001c0001t0051g0308 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.381+773G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11443258 | ||||||
chr8:11443264
|
C | A | 1 | a0001c0001t0001g0008 | 2 | NA18939.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.381+767G>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11443264 | ||||||
chr8:11443294
|
C | T | 1 | a0001c0001t0105g0326 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.381+737G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11443294 | ||||||
chr8:11443382
|
C | G | 187 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(184): Show | 213 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(210): Show |
intron_variant | MODIFIER | c.381+649G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11443382 | ||||||
chr8:11443469
|
C | G | 7 | a0001c0001t0017g0261a0001c0001t0017g0262a0001c0001t0017g0264others(4): Show | 7 | HG01884.hp2 HG02109.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.381+562G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11443469 | ||||||
chr8:11443502
|
T | TC | 5 | a0001c0001t0017g0261a0001c0001t0017g0262a0001c0001t0017g0264others(2): Show | 5 | HG02145.hp1 HG02615.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.381+528dupG | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11443502 | ||||||
chr8:11443575
|
A | G | 6 | a0002c0002t0001g0152a0002c0002t0014g0151a0002c0002t0014g0153others(3): Show | 6 | HG00323.hp1 HG00323.hp2 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.381+456T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11443575 | ||||||
chr8:11443736
|
C | T | 1 | a0001c0001t0090g0124 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.381+295G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11443736 | ||||||
chr8:11443782
|
G | C | 1 | a0003c0003t0001g0287 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.381+249C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11443782 | ||||||
chr8:11443830
|
T | C | 4 | a0001c0001t0102g0116a0001c0001t0104g0091a0001c0001t0105g0326others(1): Show | 4 | HG01358.hp1 HG01884.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.381+201A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11443830 | ||||||
chr8:11443838
|
G | A | 1 | a0001c0001t0066g0133 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.381+193C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11443838 | ||||||
chr8:11444921
|
G | A | 1 | a0001c0001t0072g0193 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-397-113C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11444921 | ||||||
chr8:11444936
|
T | C | 113 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(110): Show | 135 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(132): Show |
intron_variant | MODIFIER | c.-397-128A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11444936 | ||||||
chr8:11444955
|
C | CATTTTAA others(12): Show |
1 | a0001c0001t0001g0187 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.-397-148_-397-147i others(21): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11444955 | ||||||
chr8:11444972
|
T | G | 145 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(142): Show | 168 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(165): Show |
intron_variant | MODIFIER | c.-397-164A>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11444972 | ||||||
chr8:11444992
|
A | G | 22 | a0002c0002t0001g0146a0002c0002t0001g0152a0002c0002t0008g0136others(19): Show | 24 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(21): Show |
intron_variant | MODIFIER | c.-397-184T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11444992 | ||||||
chr8:11445005
|
T | C | 7 | a0001c0001t0011g0119a0001c0001t0025g0270a0001c0001t0043g0121others(4): Show | 7 | HG01891.hp1 HG02258.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.-397-197A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11445005 | ||||||
chr8:11445055
|
T | C | 8 | a0001c0001t0001g0107a0001c0001t0001g0109a0001c0001t0003g0310others(5): Show | 8 | HG02109.hp2 HG02895.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.-397-247A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11445055 | ||||||
chr8:11445111
|
G | A | 1 | a0002c0002t0019g0147 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-397-303C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11445111 | ||||||
chr8:11445121
|
C | A | 29 | a0001c0001t0002g0280a0001c0001t0002g0294a0001c0001t0008g0267others(26): Show | 32 | HG00099.hp2 HG00639.hp2 HG00642.hp2 others(29): Show |
intron_variant | MODIFIER | c.-397-313G>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11445121 | ||||||
chr8:11445133
|
G | T | 4 | a0001c0001t0017g0261a0001c0001t0017g0262a0001c0001t0017g0264others(1): Show | 4 | HG02615.hp2 HG02723.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-397-325C>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11445133 | ||||||
chr8:11445200
|
G | A | 27 | a0001c0001t0102g0116a0001c0001t0103g0260a0001c0001t0104g0091others(24): Show | 29 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(26): Show |
intron_variant | MODIFIER | c.-397-392C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11445200 | ||||||
chr8:11445212
|
T | C | 190 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(187): Show | 217 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(214): Show |
intron_variant | MODIFIER | c.-397-404A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11445212 | ||||||
chr8:11445324
|
C | A | 135 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(132): Show | 159 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(156): Show |
intron_variant | MODIFIER | c.-397-516G>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11445324 | ||||||
chr8:11445348
|
C | T | 1 | a0001c0001t0087g0279 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-397-540G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11445348 | ||||||
chr8:11445358
|
C | T | 2 | a0001c0001t0001g0008a0001c0001t0035g0101 | 3 | HG03704.hp2 NA18939.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.-397-550G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11445358 | ||||||
chr8:11445487
|
G | A | 27 | a0001c0001t0102g0116a0001c0001t0103g0260a0001c0001t0104g0091others(24): Show | 29 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(26): Show |
intron_variant | MODIFIER | c.-397-679C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11445487 | ||||||
chr8:11445502
|
A | G | 174 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(171): Show | 199 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(196): Show |
intron_variant | MODIFIER | c.-397-694T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11445502 | ||||||
chr8:11445531
|
G | A | 1 | a0001c0001t0040g0065 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-397-723C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11445531 | ||||||
chr8:11445572
|
T | G | 8 | a0001c0001t0001g0107a0001c0001t0001g0109a0001c0001t0003g0310others(5): Show | 8 | HG02109.hp2 HG02895.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.-397-764A>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11445572 | ||||||
chr8:11445628
|
G | C | 129 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(126): Show | 151 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(148): Show |
intron_variant | MODIFIER | c.-397-820C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11445628 | ||||||
chr8:11445711
|
A | G | 1 | a0001c0001t0001g0232 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-397-903T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11445711 | ||||||
chr8:11445724
|
C | T | 1 | a0001c0001t0043g0263 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-397-916G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11445724 | ||||||
chr8:11445740
|
G | A | 2 | a0001c0001t0028g0258a0001c0001t0062g0132 | 2 | HG01884.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.-397-932C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11445740 | ||||||
chr8:11445762
|
G | C | 2 | a0001c0001t0028g0258a0001c0001t0062g0132 | 2 | HG01884.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.-397-954C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11445762 | ||||||
chr8:11445821
|
T | TA | 124 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0010others(121): Show | 140 | HG00099.hp2 HG00544.hp1 HG00597.hp1 others(137): Show |
intron_variant | MODIFIER | c.-397-1014dupT | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11445821 | ||||||
chr8:11445827
|
A | G | 27 | a0001c0001t0102g0116a0001c0001t0103g0260a0001c0001t0104g0091others(24): Show | 29 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(26): Show |
intron_variant | MODIFIER | c.-397-1019T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11445827 | ||||||
chr8:11445864
|
G | C | 12 | a0001c0001t0003g0029a0001c0001t0003g0219a0001c0001t0003g0220others(9): Show | 13 | HG00741.hp1 HG01167.hp1 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.-397-1056C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11445864 | ||||||
chr8:11445936
|
G | A | 27 | a0001c0001t0102g0116a0001c0001t0103g0260a0001c0001t0104g0091others(24): Show | 29 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(26): Show |
intron_variant | MODIFIER | c.-397-1128C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11445936 | ||||||
chr8:11445968
|
A | G | 1 | a0001c0001t0002g0050 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-397-1160T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11445968 | ||||||
chr8:11446012
|
C | T | 5 | a0001c0001t0024g0100a0001c0001t0024g0242a0001c0001t0025g0328others(2): Show | 5 | HG02572.hp2 HG03130.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-397-1204G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11446012 | ||||||
chr8:11446016
|
C | CA | 47 | a0001c0001t0001g0166a0001c0001t0001g0169a0001c0001t0001g0170others(44): Show | 50 | HG00099.hp2 HG00639.hp2 HG00642.hp2 others(47): Show |
intron_variant | MODIFIER | c.-397-1209dupT | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11446016 | ||||||
chr8:11446016
|
C | CAA | 6 | a0001c0001t0017g0261a0001c0001t0017g0262a0001c0001t0017g0264others(3): Show | 6 | HG02615.hp2 HG02723.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-397-1210_-397-120 others(6): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11446016 | ||||||
chr8:11446016
|
CA | C | 20 | a0001c0001t0001g0017a0001c0001t0001g0107a0001c0001t0001g0183others(17): Show | 21 | HG01167.hp1 HG01167.hp2 HG01515.hp1 others(18): Show |
intron_variant | MODIFIER | c.-397-1209delT | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11446016 | ||||||
chr8:11446016
|
CAAAAA | C | 26 | a0001c0001t0102g0116a0001c0001t0103g0260a0001c0001t0104g0091others(23): Show | 28 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.-397-1213_-397-120 others(9): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11446016 | ||||||
chr8:11446119
|
G | T | 1 | a0001c0001t0002g0050 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-397-1311C>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11446119 | ||||||
chr8:11446169
|
G | A | 1 | a0001c0001t0001g0163 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-397-1361C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11446169 | ||||||
chr8:11446179
|
G | A | 7 | a0001c0001t0001g0107a0001c0001t0001g0109a0001c0001t0003g0311others(4): Show | 7 | HG02109.hp2 HG02895.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.-397-1371C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11446179 | ||||||
chr8:11446217
|
G | C | 27 | a0001c0001t0102g0116a0001c0001t0103g0260a0001c0001t0104g0091others(24): Show | 29 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(26): Show |
intron_variant | MODIFIER | c.-397-1409C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11446217 | ||||||
chr8:11446231
|
C | A | 12 | a0001c0001t0002g0134a0001c0001t0002g0285a0001c0001t0002g0298others(9): Show | 12 | HG00639.hp1 HG02258.hp1 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.-397-1423G>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11446231 | ||||||
chr8:11446254
|
C | A | 2 | a0001c0001t0025g0118a0001c0001t0044g0117 | 2 | HG02723.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-397-1446G>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11446254 | ||||||
chr8:11446277
|
A | C | 262 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(259): Show | 293 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(290): Show |
intron_variant | MODIFIER | c.-397-1469T>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11446277 | ||||||
chr8:11446279
|
G | A | 1 | a0001c0001t0053g0327 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-397-1471C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11446279 | ||||||
chr8:11446283
|
G | T | 1 | a0001c0001t0031g0095 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-397-1475C>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11446283 | ||||||
chr8:11446307
|
C | T | 1 | a0001c0001t0106g0113 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-397-1499G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11446307 | ||||||
chr8:11446319
|
C | T | 29 | a0001c0001t0001g0107a0001c0001t0001g0109a0001c0001t0003g0310others(26): Show | 31 | HG00738.hp2 HG01123.hp2 HG01175.hp2 others(28): Show |
intron_variant | MODIFIER | c.-397-1511G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11446319 | ||||||
chr8:11446376
|
CTGGTAAG others(77): Show |
C | 3 | a0001c0001t0024g0100a0001c0001t0025g0328a0001c0001t0090g0124 | 3 | HG02572.hp2 HG03130.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-397-1652_-397-156 others(88): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11446376 | ||||||
chr8:11446435
|
C | T | 1 | a0001c0001t0055g0025 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-397-1627G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11446435 | ||||||
chr8:11446479
|
T | C | 160 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(157): Show | 186 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(183): Show |
intron_variant | MODIFIER | c.-397-1671A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11446479 | ||||||
chr8:11446489
|
T | G | 1 | a0001c0001t0066g0133 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-397-1681A>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11446489 | ||||||
chr8:11446503
|
G | A | 160 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(157): Show | 186 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(183): Show |
intron_variant | MODIFIER | c.-397-1695C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11446503 | ||||||
chr8:11446504
|
A | G | 160 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(157): Show | 186 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(183): Show |
intron_variant | MODIFIER | c.-397-1696T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11446504 | ||||||
chr8:11446539
|
G | T | 2 | a0001c0001t0002g0010a0001c0001t0002g0047 | 3 | NA18942.hp1 NA18980.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.-397-1731C>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11446539 | ||||||
chr8:11446541
|
C | A | 27 | a0001c0001t0102g0116a0001c0001t0103g0260a0001c0001t0104g0091others(24): Show | 29 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(26): Show |
intron_variant | MODIFIER | c.-397-1733G>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11446541 | ||||||
chr8:11446607
|
T | C | 160 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(157): Show | 186 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(183): Show |
intron_variant | MODIFIER | c.-397-1799A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11446607 | ||||||
chr8:11446634
|
A | G | 160 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(157): Show | 186 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(183): Show |
intron_variant | MODIFIER | c.-397-1826T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11446634 | ||||||
chr8:11446655
|
A | G | 1 | a0001c0001t0062g0132 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-397-1847T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11446655 | ||||||
chr8:11446702
|
G | A | 1 | a0001c0001t0055g0025 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-397-1894C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11446702 | ||||||
chr8:11446721
|
G | A | 1 | a0001c0001t0053g0327 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-397-1913C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11446721 | ||||||
chr8:11446764
|
C | T | 11 | a0001c0001t0003g0007a0001c0001t0003g0122a0001c0001t0003g0274others(8): Show | 13 | HG02145.hp2 HG02451.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.-397-1956G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11446764 | ||||||
chr8:11446812
|
C | A | 119 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(116): Show | 141 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(138): Show |
intron_variant | MODIFIER | c.-397-2004G>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11446812 | ||||||
chr8:11446824
|
G | A | 4 | a0001c0001t0017g0261a0001c0001t0017g0262a0001c0001t0017g0264others(1): Show | 4 | HG02615.hp2 HG02723.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-397-2016C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11446824 | ||||||
chr8:11446827
|
G | A | 1 | a0001c0001t0017g0264 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-397-2019C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11446827 | ||||||
chr8:11446891
|
G | A | 1 | a0001c0001t0001g0180 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-397-2083C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11446891 | ||||||
chr8:11446952
|
T | C | 16 | a0001c0001t0002g0134a0001c0001t0002g0285a0001c0001t0002g0298others(13): Show | 16 | HG00639.hp1 HG02258.hp1 HG02572.hp2 others(13): Show |
intron_variant | MODIFIER | c.-397-2144A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11446952 | ||||||
chr8:11446977
|
C | A | 39 | a0001c0001t0001g0107a0001c0001t0001g0109a0001c0001t0003g0007others(36): Show | 43 | HG00738.hp2 HG01123.hp2 HG01175.hp2 others(40): Show |
intron_variant | MODIFIER | c.-397-2169G>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11446977 | ||||||
chr8:11446982
|
C | T | 1 | a0001c0001t0001g0196 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-397-2174G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11446982 | ||||||
chr8:11447135
|
G | A | 2 | a0001c0001t0102g0116a0001c0001t0106g0113 | 2 | HG01884.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.-397-2327C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11447135 | ||||||
chr8:11447183
|
C | CTTT | 4 | a0001c0001t0009g0128a0001c0001t0020g0126a0001c0001t0058g0127others(1): Show | 4 | HG02055.hp2 HG02572.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-397-2378_-397-237 others(7): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11447183 | ||||||
chr8:11447183
|
C | CTTTTCTT | 12 | a0001c0001t0001g0167a0001c0001t0001g0177a0001c0001t0003g0007others(9): Show | 14 | HG00544.hp2 HG02145.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.-397-2376_-397-237 others(11): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11447183 | ||||||
chr8:11447183
|
C | CTTTTCTT others(1): Show |
153 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(150): Show | 177 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(174): Show |
intron_variant | MODIFIER | c.-397-2376_-397-237 others(12): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11447183 | ||||||
chr8:11447183
|
C | CTTTTCTT others(2): Show |
4 | a0001c0001t0001g0166a0001c0001t0001g0187a0001c0001t0001g0195others(1): Show | 4 | HG02738.hp2 HG03017.hp1 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.-397-2376_-397-237 others(13): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11447183 | ||||||
chr8:11447189
|
C | CT | 5 | a0001c0001t0102g0116a0001c0001t0103g0260a0001c0001t0104g0091others(2): Show | 5 | HG01358.hp1 HG01884.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.-397-2382dupA | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11447189 | ||||||
chr8:11447189
|
C | T | 175 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(172): Show | 201 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(198): Show |
intron_variant | MODIFIER | c.-397-2381G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11447189 | ||||||
chr8:11447238
|
A | G | 3 | a0001c0001t0001g0268a0001c0001t0010g0286a0001c0001t0063g0068 | 3 | HG01255.hp1 HG02683.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.-397-2430T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11447238 | ||||||
chr8:11447284
|
C | T | 11 | a0001c0001t0003g0029a0001c0001t0011g0119a0001c0001t0025g0270others(8): Show | 11 | HG01167.hp1 HG01169.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.-397-2476G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11447284 | ||||||
chr8:11447332
|
C | T | 1 | a0001c0001t0001g0194 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-397-2524G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11447332 | ||||||
chr8:11447435
|
A | G | 30 | a0001c0001t0005g0318a0001c0001t0036g0139a0001c0001t0091g0140others(27): Show | 32 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(29): Show |
intron_variant | MODIFIER | c.-397-2627T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11447435 | ||||||
chr8:11447442
|
C | G | 27 | a0001c0001t0001g0107a0001c0001t0001g0109a0001c0001t0003g0310others(24): Show | 29 | HG00738.hp2 HG01123.hp2 HG01175.hp2 others(26): Show |
intron_variant | MODIFIER | c.-397-2634G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11447442 | ||||||
chr8:11447454
|
G | A | 15 | a0001c0001t0003g0029a0001c0001t0009g0255a0001c0001t0009g0256others(12): Show | 15 | HG01167.hp1 HG01169.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.-397-2646C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11447454 | ||||||
chr8:11447472
|
C | T | 1 | a0001c0001t0031g0095 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-397-2664G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11447472 | ||||||
chr8:11447506
|
G | C | 5 | a0001c0001t0102g0116a0001c0001t0103g0260a0001c0001t0104g0091others(2): Show | 5 | HG01358.hp1 HG01884.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.-397-2698C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11447506 | ||||||
chr8:11447539
|
A | C | 1 | a0001c0009t0009g0245 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-397-2731T>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11447539 | ||||||
chr8:11447548
|
A | G | 1 | a0001c0001t0005g0325 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-397-2740T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11447548 | ||||||
chr8:11447551
|
T | C | 1 | a0001c0001t0002g0066 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.-397-2743A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11447551 | ||||||
chr8:11447589
|
G | A | 3 | a0001c0001t0035g0271a0001c0001t0036g0135a0001c0001t0084g0272 | 3 | HG02698.hp1 HG04115.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-397-2781C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11447589 | ||||||
chr8:11447767
|
T | G | 6 | a0002c0002t0001g0152a0002c0002t0014g0151a0002c0002t0014g0153others(3): Show | 6 | HG00323.hp1 HG00323.hp2 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.-397-2959A>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11447767 | ||||||
chr8:11447795
|
C | A | 1 | a0002c0002t0034g0150 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-397-2987G>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11447795 | ||||||
chr8:11447813
|
C | T | 16 | a0001c0001t0005g0022a0001c0001t0005g0309a0001c0001t0005g0313others(13): Show | 18 | HG00738.hp2 HG01123.hp2 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.-397-3005G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11447813 | ||||||
chr8:11447827
|
T | C | 1 | a0001c0001t0055g0025 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-397-3019A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11447827 | ||||||
chr8:11447838
|
G | A | 4 | a0001c0001t0001g0003a0001c0001t0001g0231a0001c0001t0001g0238others(1): Show | 7 | HG01074.hp2 HG01346.hp1 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.-397-3030C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11447838 | ||||||
chr8:11447855
|
C | T | 1 | a0001c0001t0003g0274 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-397-3047G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11447855 | ||||||
chr8:11447856
|
A | G | 212 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(209): Show | 240 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(237): Show |
intron_variant | MODIFIER | c.-397-3048T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11447856 | ||||||
chr8:11447875
|
G | A | 16 | a0001c0001t0002g0134a0001c0001t0002g0285a0001c0001t0002g0298others(13): Show | 16 | HG00639.hp1 HG02258.hp1 HG02572.hp2 others(13): Show |
intron_variant | MODIFIER | c.-397-3067C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11447875 | ||||||
chr8:11447944
|
C | A | 10 | a0001c0001t0003g0007a0001c0001t0003g0122a0001c0001t0003g0274others(7): Show | 12 | HG02145.hp2 HG02451.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.-397-3136G>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11447944 | ||||||
chr8:11447961
|
C | T | 2 | a0001c0001t0102g0116a0001c0001t0106g0113 | 2 | HG01884.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.-397-3153G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11447961 | ||||||
chr8:11448055
|
G | A | 72 | a0001c0001t0001g0107a0001c0001t0001g0109a0001c0001t0003g0007others(69): Show | 78 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(75): Show |
intron_variant | MODIFIER | c.-397-3247C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11448055 | ||||||
chr8:11448076
|
C | G | 28 | a0001c0001t0001g0107a0001c0001t0001g0109a0001c0001t0003g0310others(25): Show | 30 | HG00738.hp2 HG01123.hp2 HG01175.hp2 others(27): Show |
intron_variant | MODIFIER | c.-397-3268G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11448076 | ||||||
chr8:11448077
|
C | T | 27 | a0001c0001t0001g0107a0001c0001t0001g0109a0001c0001t0003g0310others(24): Show | 29 | HG00738.hp2 HG01123.hp2 HG01175.hp2 others(26): Show |
intron_variant | MODIFIER | c.-397-3269G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11448077 | ||||||
chr8:11448126
|
A | G | 199 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(196): Show | 227 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(224): Show |
intron_variant | MODIFIER | c.-397-3318T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11448126 | ||||||
chr8:11448166
|
C | G | 1 | a0001c0001t0081g0123 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-397-3358G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11448166 | ||||||
chr8:11448172
|
C | T | 43 | a0001c0001t0001g0107a0001c0001t0001g0109a0001c0001t0003g0007others(40): Show | 47 | HG00738.hp2 HG01123.hp2 HG01175.hp2 others(44): Show |
intron_variant | MODIFIER | c.-397-3364G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11448172 | ||||||
chr8:11448193
|
TA | T | 42 | a0001c0001t0001g0187a0001c0001t0002g0009a0001c0001t0002g0036others(39): Show | 45 | HG00323.hp2 HG00639.hp1 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.-397-3386delT | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11448193 | ||||||
chr8:11448193
|
TAA | T | 129 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(126): Show | 151 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.-397-3387_-397-338 others(6): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11448193 | ||||||
chr8:11448194
|
A | T | 1 | a0001c0001t0002g0081 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-397-3386T>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11448194 | ||||||
chr8:11448226
|
C | CAAGACAG others(2): Show |
7 | a0001c0001t0001g0107a0001c0001t0001g0109a0001c0001t0003g0310others(4): Show | 7 | HG02109.hp2 HG02895.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.-397-3427_-397-341 others(13): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11448226 | ||||||
chr8:11448228
|
A | G | 1 | a0001c0001t0067g0159 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.-397-3420T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11448228 | ||||||
chr8:11448261
|
G | C | 3 | a0002c0002t0001g0146a0002c0002t0019g0015a0002c0002t0019g0147 | 4 | HG00099.hp1 HG01256.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.-397-3453C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11448261 | ||||||
chr8:11448298
|
C | T | 16 | a0001c0001t0005g0022a0001c0001t0005g0309a0001c0001t0005g0313others(13): Show | 18 | HG00738.hp2 HG01123.hp2 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.-397-3490G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11448298 | ||||||
chr8:11448320
|
C | A | 5 | a0001c0001t0102g0116a0001c0001t0103g0260a0001c0001t0104g0091others(2): Show | 5 | HG01358.hp1 HG01884.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.-397-3512G>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11448320 | ||||||
chr8:11448321
|
G | C | 1 | a0001c0001t0017g0264 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-397-3513C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11448321 | ||||||
chr8:11448334
|
AG | A | 29 | a0001c0001t0036g0139a0001c0001t0091g0140a0001c0001t0102g0116others(26): Show | 31 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(28): Show |
intron_variant | MODIFIER | c.-397-3527delC | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11448334 | ||||||
chr8:11448475
|
G | A | 9 | a0001c0001t0003g0007a0001c0001t0003g0122a0001c0001t0003g0274others(6): Show | 11 | HG02145.hp2 HG02451.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.-397-3667C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11448475 | ||||||
chr8:11448494
|
C | A | 29 | a0001c0001t0036g0139a0001c0001t0091g0140a0001c0001t0102g0116others(26): Show | 31 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(28): Show |
intron_variant | MODIFIER | c.-397-3686G>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11448494 | ||||||
chr8:11448515
|
A | T | 181 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(178): Show | 207 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(204): Show |
intron_variant | MODIFIER | c.-397-3707T>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11448515 | ||||||
chr8:11448643
|
T | C | 1 | a0001c0001t0001g0218 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-397-3835A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11448643 | ||||||
chr8:11448743
|
C | T | 1 | a0001c0001t0086g0297 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-397-3935G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11448743 | ||||||
chr8:11448749
|
C | T | 2 | a0001c0001t0002g0046a0001c0001t0081g0123 | 2 | HG02683.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.-397-3941G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11448749 | ||||||
chr8:11448763
|
G | T | 180 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(177): Show | 206 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(203): Show |
intron_variant | MODIFIER | c.-397-3955C>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11448763 | ||||||
chr8:11448857
|
C | A | 2 | a0001c0001t0009g0128a0002c0002t0008g0114 | 2 | HG02055.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-397-4049G>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11448857 | ||||||
chr8:11448857
|
C | T | 2 | a0001c0001t0032g0027a0001c0001t0032g0028 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-397-4049G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11448857 | ||||||
chr8:11448858
|
C | A | 2 | a0001c0001t0009g0128a0002c0002t0008g0114 | 2 | HG02055.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-397-4050G>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11448858 | ||||||
chr8:11448935
|
G | A | 176 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(173): Show | 202 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(199): Show |
intron_variant | MODIFIER | c.-397-4127C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11448935 | ||||||
chr8:11448951
|
G | A | 262 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(259): Show | 293 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(290): Show |
intron_variant | MODIFIER | c.-397-4143C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11448951 | ||||||
chr8:11449007
|
G | A | 182 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(179): Show | 208 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(205): Show |
intron_variant | MODIFIER | c.-397-4199C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11449007 | ||||||
chr8:11449106
|
T | C | 137 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(134): Show | 159 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(156): Show |
intron_variant | MODIFIER | c.-397-4298A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11449106 | ||||||
chr8:11449126
|
C | T | 4 | a0001c0001t0017g0261a0001c0001t0017g0262a0001c0001t0017g0264others(1): Show | 4 | HG02615.hp2 HG02723.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-397-4318G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11449126 | ||||||
chr8:11449159
|
C | A | 2 | a0001c0001t0001g0111a0001c0001t0001g0112 | 2 | HG02129.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.-397-4351G>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11449159 | ||||||
chr8:11449173
|
T | C | 182 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(179): Show | 208 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(205): Show |
intron_variant | MODIFIER | c.-397-4365A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11449173 | ||||||
chr8:11449199
|
C | T | 180 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(177): Show | 206 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(203): Show |
intron_variant | MODIFIER | c.-397-4391G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11449199 | ||||||
chr8:11449255
|
C | G | 181 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(178): Show | 207 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(204): Show |
intron_variant | MODIFIER | c.-397-4447G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11449255 | ||||||
chr8:11449296
|
A | G | 183 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(180): Show | 209 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(206): Show |
intron_variant | MODIFIER | c.-397-4488T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11449296 | ||||||
chr8:11449336
|
C | T | 2 | a0001c0001t0036g0139a0001c0001t0091g0140 | 2 | HG03710.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.-397-4528G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11449336 | ||||||
chr8:11449337
|
G | A | 151 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(148): Show | 175 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(172): Show |
intron_variant | MODIFIER | c.-397-4529C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11449337 | ||||||
chr8:11449455
|
T | A | 1 | a0001c0001t0044g0026 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-397-4647A>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11449455 | ||||||
chr8:11449465
|
G | C | 122 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(119): Show | 144 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(141): Show |
intron_variant | MODIFIER | c.-397-4657C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11449465 | ||||||
chr8:11449481
|
C | T | 3 | a0001c0001t0001g0107a0001c0001t0001g0109a0001c0008t0077g0108 | 3 | HG02895.hp1 HG02897.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-397-4673G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11449481 | ||||||
chr8:11449483
|
C | T | 1 | a0001c0001t0081g0123 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-397-4675G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11449483 | ||||||
chr8:11449609
|
C | A | 177 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(174): Show | 203 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(200): Show |
intron_variant | MODIFIER | c.-397-4801G>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11449609 | ||||||
chr8:11449643
|
G | A | 1 | a0001c0001t0089g0024 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-397-4835C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11449643 | ||||||
chr8:11449675
|
G | A | 1 | a0001c0001t0002g0034 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-397-4867C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11449675 | ||||||
chr8:11449694
|
C | T | 1 | a0001c0001t0002g0080 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-397-4886G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11449694 | ||||||
chr8:11449729
|
C | T | 15 | a0001c0001t0003g0029a0001c0001t0009g0255a0001c0001t0009g0256others(12): Show | 15 | HG01167.hp1 HG01169.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.-397-4921G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11449729 | ||||||
chr8:11449741
|
C | T | 1 | a0003c0003t0001g0086 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-397-4933G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11449741 | ||||||
chr8:11449802
|
G | A | 29 | a0001c0001t0036g0139a0001c0001t0091g0140a0001c0001t0102g0116others(26): Show | 31 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(28): Show |
intron_variant | MODIFIER | c.-397-4994C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11449802 | ||||||
chr8:11449915
|
G | A | 2 | a0001c0001t0011g0265a0001c0001t0012g0329 | 2 | HG03139.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-397-5107C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11449915 | ||||||
chr8:11449945
|
A | G | 182 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(179): Show | 208 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(205): Show |
intron_variant | MODIFIER | c.-397-5137T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11449945 | ||||||
chr8:11449960
|
G | A | 150 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(147): Show | 174 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(171): Show |
intron_variant | MODIFIER | c.-397-5152C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11449960 | ||||||
chr8:11449975
|
C | G | 1 | a0001c0001t0044g0026 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-397-5167G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11449975 | ||||||
chr8:11449997
|
C | G | 6 | a0001c0001t0005g0022a0001c0001t0005g0313a0001c0001t0005g0318others(3): Show | 7 | HG00738.hp2 HG01175.hp2 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.-397-5189G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11449997 | ||||||
chr8:11450063
|
A | G | 182 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(179): Show | 208 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(205): Show |
intron_variant | MODIFIER | c.-397-5255T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11450063 | ||||||
chr8:11450173
|
A | C | 182 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(179): Show | 208 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(205): Show |
intron_variant | MODIFIER | c.-397-5365T>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11450173 | ||||||
chr8:11450174
|
C | G | 182 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(179): Show | 208 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(205): Show |
intron_variant | MODIFIER | c.-397-5366G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11450174 | ||||||
chr8:11450282
|
A | C | 3 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170 | 3 | NA18994.hp1 NA19003.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.-397-5474T>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11450282 | ||||||
chr8:11450386
|
G | A | 1 | a0001c0001t0066g0133 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-397-5578C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11450386 | ||||||
chr8:11450644
|
T | G | 122 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(119): Show | 144 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(141): Show |
intron_variant | MODIFIER | c.-397-5836A>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11450644 | ||||||
chr8:11450711
|
A | C | 1 | a0001c0001t0088g0269 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-397-5903T>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11450711 | ||||||
chr8:11450718
|
T | C | 1 | a0001c0001t0066g0133 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-397-5910A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11450718 | ||||||
chr8:11450735
|
C | A | 3 | a0001c0001t0002g0072a0001c0001t0003g0219a0001c0001t0003g0220 | 3 | HG01123.hp1 HG02896.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.-397-5927G>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11450735 | ||||||
chr8:11450801
|
G | C | 1 | a0001c0001t0001g0166 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-397-5993C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11450801 | ||||||
chr8:11450985
|
G | T | 1 | a0001c0001t0002g0067 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-397-6177C>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11450985 | ||||||
chr8:11450987
|
C | A | 46 | a0001c0001t0003g0029a0001c0001t0009g0255a0001c0001t0009g0256others(43): Show | 48 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(45): Show |
intron_variant | MODIFIER | c.-397-6179G>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11450987 | ||||||
chr8:11450997
|
T | A | 219 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(216): Show | 246 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(243): Show |
intron_variant | MODIFIER | c.-397-6189A>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11450997 | ||||||
chr8:11451031
|
G | T | 1 | a0001c0001t0104g0091 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-397-6223C>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11451031 | ||||||
chr8:11451037
|
T | G | 158 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(155): Show | 183 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(180): Show |
intron_variant | MODIFIER | c.-397-6229A>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11451037 | ||||||
chr8:11451105
|
G | A | 43 | a0001c0001t0003g0029a0001c0001t0009g0255a0001c0001t0009g0256others(40): Show | 45 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(42): Show |
intron_variant | MODIFIER | c.-397-6297C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11451105 | ||||||
chr8:11451270
|
C | T | 72 | a0001c0001t0001g0161a0001c0001t0002g0102a0001c0001t0002g0280others(69): Show | 77 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.-397-6462G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11451270 | ||||||
chr8:11451284
|
C | G | 237 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(234): Show | 268 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(265): Show |
intron_variant | MODIFIER | c.-397-6476G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11451284 | ||||||
chr8:11451305
|
G | T | 1 | a0001c0001t0002g0285 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-397-6497C>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11451305 | ||||||
chr8:11451381
|
C | A | 1 | a0001c0001t0002g0067 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-397-6573G>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11451381 | ||||||
chr8:11451396
|
GA | G | 70 | a0001c0001t0002g0102a0001c0001t0002g0294a0001c0001t0003g0029others(67): Show | 75 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.-397-6589delT | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11451396 | ||||||
chr8:11451434
|
C | T | 1 | a0001c0001t0104g0091 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-397-6626G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11451434 | ||||||
chr8:11451611
|
C | T | 1 | a0001c0001t0089g0024 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-397-6803G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11451611 | ||||||
chr8:11451683
|
T | C | 104 | a0001c0001t0001g0107a0001c0001t0001g0109a0001c0001t0001g0221others(101): Show | 111 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.-397-6875A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11451683 | ||||||
chr8:11451768
|
A | G | 205 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(202): Show | 232 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(229): Show |
intron_variant | MODIFIER | c.-397-6960T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11451768 | ||||||
chr8:11451785
|
C | T | 60 | a0001c0001t0002g0102a0001c0001t0002g0280a0001c0001t0002g0294others(57): Show | 64 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.-397-6977G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11451785 | ||||||
chr8:11451790
|
G | A | 1 | a0002c0002t0014g0301 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-397-6982C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11451790 | ||||||
chr8:11451859
|
T | C | 1 | a0001c0001t0002g0134 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-397-7051A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11451859 | ||||||
chr8:11451860
|
G | T | 1 | a0001c0001t0089g0024 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-397-7052C>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11451860 | ||||||
chr8:11451891
|
C | T | 60 | a0001c0001t0002g0102a0001c0001t0002g0134a0001c0001t0002g0280others(57): Show | 64 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.-397-7083G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11451891 | ||||||
chr8:11451998
|
T | G | 268 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(265): Show | 300 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(297): Show |
intron_variant | MODIFIER | c.-397-7190A>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11451998 | ||||||
chr8:11452024
|
A | G | 62 | a0001c0001t0002g0102a0001c0001t0002g0134a0001c0001t0002g0280others(59): Show | 67 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.-397-7216T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11452024 | ||||||
chr8:11452057
|
G | C | 14 | a0001c0001t0001g0107a0001c0001t0001g0109a0001c0001t0003g0310others(11): Show | 14 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.-397-7249C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11452057 | ||||||
chr8:11452119
|
C | A | 1 | a0001c0001t0006g0160 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-397-7311G>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11452119 | ||||||
chr8:11452259
|
T | G | 5 | a0002c0002t0008g0136a0002c0002t0008g0137a0002c0002t0008g0138others(2): Show | 5 | HG00642.hp1 HG02486.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.-397-7451A>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11452259 | ||||||
chr8:11452271
|
G | A | 62 | a0001c0001t0002g0102a0001c0001t0002g0134a0001c0001t0002g0280others(59): Show | 66 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(63): Show |
intron_variant | MODIFIER | c.-397-7463C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11452271 | ||||||
chr8:11452306
|
C | T | 2 | a0001c0001t0001g0167a0001c0001t0089g0024 | 2 | HG00544.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-397-7498G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11452306 | ||||||
chr8:11452340
|
T | C | 209 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(206): Show | 238 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(235): Show |
intron_variant | MODIFIER | c.-397-7532A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11452340 | ||||||
chr8:11452384
|
A | G | 221 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(218): Show | 250 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(247): Show |
intron_variant | MODIFIER | c.-397-7576T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11452384 | ||||||
chr8:11452431
|
T | C | 2 | a0001c0001t0001g0180a0001c0001t0001g0222 | 2 | HG00438.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.-397-7623A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11452431 | ||||||
chr8:11452503
|
A | T | 65 | a0001c0001t0002g0102a0001c0001t0002g0134a0001c0001t0002g0280others(62): Show | 70 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.-397-7695T>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11452503 | ||||||
chr8:11452763
|
A | C | 1 | a0001c0001t0021g0277 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-397-7955T>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11452763 | ||||||
chr8:11452781
|
T | C | 255 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(252): Show | 286 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(283): Show |
intron_variant | MODIFIER | c.-397-7973A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11452781 | ||||||
chr8:11452786
|
G | A | 1 | a0001c0001t0042g0105 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-397-7978C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11452786 | ||||||
chr8:11452810
|
C | T | 44 | a0001c0001t0002g0102a0001c0001t0002g0134a0001c0001t0015g0004others(41): Show | 48 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(45): Show |
intron_variant | MODIFIER | c.-397-8002G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11452810 | ||||||
chr8:11452828
|
C | T | 1 | a0001c0001t0015g0110 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-397-8020G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11452828 | ||||||
chr8:11452853
|
C | T | 65 | a0001c0001t0002g0102a0001c0001t0002g0134a0001c0001t0002g0280others(62): Show | 70 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.-397-8045G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11452853 | ||||||
chr8:11452901
|
G | C | 1 | a0001c0001t0002g0190 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-397-8093C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11452901 | ||||||
chr8:11452909
|
G | A | 2 | a0001c0001t0002g0069a0001c0001t0063g0068 | 2 | HG01261.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.-397-8101C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11452909 | ||||||
chr8:11452933
|
G | A | 65 | a0001c0001t0002g0102a0001c0001t0002g0134a0001c0001t0002g0280others(62): Show | 70 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.-397-8125C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11452933 | ||||||
chr8:11452989
|
C | G | 189 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(186): Show | 216 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.-397-8181G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11452989 | ||||||
chr8:11452991
|
T | G | 1 | a0001c0001t0066g0133 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-397-8183A>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11452991 | ||||||
chr8:11453020
|
T | G | 65 | a0001c0001t0002g0102a0001c0001t0002g0134a0001c0001t0002g0280others(62): Show | 70 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.-397-8212A>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11453020 | ||||||
chr8:11453059
|
T | G | 65 | a0001c0001t0002g0102a0001c0001t0002g0134a0001c0001t0002g0280others(62): Show | 70 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.-397-8251A>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11453059 | ||||||
chr8:11453084
|
A | G | 65 | a0001c0001t0002g0102a0001c0001t0002g0134a0001c0001t0002g0280others(62): Show | 70 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.-397-8276T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11453084 | ||||||
chr8:11453146
|
T | G | 1 | a0001c0001t0001g0165 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-397-8338A>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11453146 | ||||||
chr8:11453275
|
C | G | 205 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(202): Show | 232 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(229): Show |
intron_variant | MODIFIER | c.-397-8467G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11453275 | ||||||
chr8:11453327
|
C | A | 1 | a0001c0001t0002g0084 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-397-8519G>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11453327 | ||||||
chr8:11453475
|
C | T | 2 | a0001c0001t0002g0036a0001c0001t0002g0037 | 2 | NA18988.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.-397-8667G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11453475 | ||||||
chr8:11453490
|
C | G | 23 | a0001c0001t0001g0107a0001c0001t0001g0109a0001c0001t0003g0310others(20): Show | 25 | HG00738.hp2 HG01123.hp2 HG01175.hp2 others(22): Show |
intron_variant | MODIFIER | c.-397-8682G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11453490 | ||||||
chr8:11453514
|
G | A | 190 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(187): Show | 216 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(213): Show |
intron_variant | MODIFIER | c.-397-8706C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11453514 | ||||||
chr8:11453637
|
G | A | 37 | a0001c0001t0002g0102a0001c0001t0002g0280a0001c0001t0002g0294others(34): Show | 40 | HG00099.hp2 HG00639.hp2 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.-397-8829C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11453637 | ||||||
chr8:11453640
|
C | T | 37 | a0001c0001t0002g0102a0001c0001t0002g0280a0001c0001t0002g0294others(34): Show | 40 | HG00099.hp2 HG00639.hp2 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.-397-8832G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11453640 | ||||||
chr8:11453672
|
C | T | 1 | a0001c0001t0104g0091 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-397-8864G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11453672 | ||||||
chr8:11453723
|
C | T | 1 | a0001c0001t0024g0242 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-397-8915G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11453723 | ||||||
chr8:11453757
|
C | T | 14 | a0001c0001t0002g0285a0001c0001t0002g0298a0001c0001t0002g0300others(11): Show | 14 | HG00639.hp1 HG01884.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.-397-8949G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11453757 | ||||||
chr8:11453765
|
G | A | 14 | a0001c0001t0002g0285a0001c0001t0002g0298a0001c0001t0002g0300others(11): Show | 14 | HG00639.hp1 HG01884.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.-397-8957C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11453765 | ||||||
chr8:11453811
|
C | T | 1 | a0001c0001t0001g0296 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-397-9003G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11453811 | ||||||
chr8:11453830
|
A | C | 64 | a0001c0001t0002g0102a0001c0001t0002g0134a0001c0001t0002g0280others(61): Show | 69 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.-397-9022T>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11453830 | ||||||
chr8:11453831
|
A | T | 64 | a0001c0001t0002g0102a0001c0001t0002g0134a0001c0001t0002g0280others(61): Show | 69 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.-397-9023T>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11453831 | ||||||
chr8:11453838
|
C | T | 9 | a0001c0001t0003g0007a0001c0001t0003g0122a0001c0001t0003g0274others(6): Show | 11 | HG02145.hp2 HG02451.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.-397-9030G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11453838 | ||||||
chr8:11453850
|
G | C | 5 | a0001c0001t0009g0128a0001c0001t0020g0126a0001c0001t0030g0125others(2): Show | 5 | HG02055.hp2 HG02572.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-397-9042C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11453850 | ||||||
chr8:11453877
|
C | A | 1 | a0001c0001t0001g0223 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-397-9069G>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11453877 | ||||||
chr8:11453952
|
C | G | 14 | a0001c0001t0002g0285a0001c0001t0002g0298a0001c0001t0002g0300others(11): Show | 14 | HG00639.hp1 HG01884.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.-397-9144G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11453952 | ||||||
chr8:11454150
|
G | A | 2 | a0001c0001t0028g0258a0001c0001t0062g0132 | 2 | HG01884.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.-397-9342C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11454150 | ||||||
chr8:11454157
|
C | T | 22 | a0001c0001t0036g0139a0001c0001t0091g0140a0002c0002t0001g0146others(19): Show | 24 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(21): Show |
intron_variant | MODIFIER | c.-397-9349G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11454157 | ||||||
chr8:11454175
|
C | T | 1 | a0001c0001t0042g0035 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-397-9367G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11454175 | ||||||
chr8:11454182
|
G | C | 1 | a0002c0002t0019g0015 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.-397-9374C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11454182 | ||||||
chr8:11454230
|
C | T | 22 | a0001c0001t0036g0139a0001c0001t0091g0140a0002c0002t0001g0146others(19): Show | 24 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(21): Show |
intron_variant | MODIFIER | c.-397-9422G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11454230 | ||||||
chr8:11454231
|
G | A | 1 | a0001c0001t0036g0135 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-397-9423C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11454231 | ||||||
chr8:11454241
|
G | A | 3 | a0001c0001t0008g0267a0001c0001t0021g0277a0001c0001t0076g0266 | 3 | HG01496.hp1 HG02615.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.-397-9433C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11454241 | ||||||
chr8:11454320
|
C | G | 57 | a0001c0001t0002g0102a0001c0001t0002g0134a0001c0001t0002g0280others(54): Show | 62 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.-397-9512G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11454320 | ||||||
chr8:11454323
|
G | A | 1 | a0001c0001t0005g0320 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-397-9515C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11454323 | ||||||
chr8:11454329
|
T | C | 123 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(120): Show | 145 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(142): Show |
intron_variant | MODIFIER | c.-397-9521A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11454329 | ||||||
chr8:11454377
|
G | A | 1 | a0001c0001t0001g0224 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-397-9569C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11454377 | ||||||
chr8:11454490
|
C | A | 2 | a0001c0001t0002g0070a0001c0001t0002g0071 | 2 | NA18970.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.-397-9682G>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11454490 | ||||||
chr8:11454666
|
C | G | 2 | a0001c0001t0024g0100a0001c0001t0090g0124 | 2 | HG02572.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-397-9858G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11454666 | ||||||
chr8:11454690
|
T | C | 226 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(223): Show | 255 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(252): Show |
intron_variant | MODIFIER | c.-397-9882A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11454690 | ||||||
chr8:11454741
|
G | T | 1 | a0001c0001t0081g0123 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-397-9933C>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11454741 | ||||||
chr8:11454755
|
C | G | 3 | a0002c0002t0008g0136a0002c0002t0008g0137a0002c0002t0008g0138 | 3 | HG00642.hp1 HG02622.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-397-9947G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11454755 | ||||||
chr8:11454828
|
T | C | 22 | a0001c0001t0036g0139a0001c0001t0091g0140a0002c0002t0001g0146others(19): Show | 24 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(21): Show |
intron_variant | MODIFIER | c.-397-10020A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11454828 | ||||||
chr8:11454874
|
C | A | 1 | a0001c0001t0066g0133 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-397-10066G>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11454874 | ||||||
chr8:11454969
|
G | A | 14 | a0001c0001t0003g0029a0001c0001t0009g0255a0001c0001t0009g0256others(11): Show | 14 | HG01167.hp1 HG01169.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.-397-10161C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11454969 | ||||||
chr8:11454970
|
C | A | 14 | a0001c0001t0003g0029a0001c0001t0009g0255a0001c0001t0009g0256others(11): Show | 14 | HG01167.hp1 HG01169.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.-397-10162G>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11454970 | ||||||
chr8:11455037
|
C | T | 1 | a0001c0001t0001g0228 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-397-10229G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11455037 | ||||||
chr8:11455139
|
C | CGT | 16 | a0001c0001t0002g0280a0001c0001t0002g0285a0001c0001t0002g0294others(13): Show | 17 | HG00099.hp2 HG00639.hp2 HG00642.hp2 others(14): Show |
intron_variant | MODIFIER | c.-397-10333_-397-10 others(8): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11455139 | ||||||
chr8:11455140
|
G | A | 1 | a0001c0001t0012g0329 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-397-10332C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11455140 | ||||||
chr8:11455169
|
G | C | 1 | a0001c0001t0100g0189 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-397-10361C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11455169 | ||||||
chr8:11455178
|
C | CTGTG | 183 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(180): Show | 206 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(203): Show |
intron_variant | MODIFIER | c.-397-10371_-397-10 others(10): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11455178 | ||||||
chr8:11455178
|
C | CTGTGTGA others(501): Show |
2 | a0001c0001t0001g0006a0001c0001t0034g0225 | 4 | HG01071.hp2 HG01167.hp2 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.-397-10371_-397-10 others(514): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11455178 | ||||||
chr8:11455317
|
G | C | 1 | a0001c0001t0021g0321 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-397-10509C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11455317 | ||||||
chr8:11455352
|
G | A | 135 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(132): Show | 157 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(154): Show |
intron_variant | MODIFIER | c.-397-10544C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11455352 | ||||||
chr8:11455373
|
T | C | 1 | a0001c0001t0066g0133 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-397-10565A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11455373 | ||||||
chr8:11455389
|
G | A | 1 | a0001c0001t0002g0072 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-397-10581C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11455389 | ||||||
chr8:11455395
|
TTGTGAGT others(28): Show |
T | 2 | a0001c0001t0028g0258a0001c0001t0062g0132 | 2 | HG01884.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.-397-10622_-397-10 others(41): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11455395 | ||||||
chr8:11455422
|
CTGGGTGT others(3): Show |
C | 1 | a0001c0001t0081g0123 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-397-10624_-397-10 others(16): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11455422 | ||||||
chr8:11455439
|
T | G | 1 | a0001c0001t0084g0272 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-397-10631A>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11455439 | ||||||
chr8:11455442
|
G | A | 1 | a0008c0007t0002g0031 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-397-10634C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11455442 | ||||||
chr8:11455475
|
G | C | 11 | a0001c0001t0002g0285a0001c0001t0002g0298a0001c0001t0002g0300others(8): Show | 11 | HG00639.hp1 HG02723.hp1 HG03688.hp1 others(8): Show |
intron_variant | MODIFIER | c.-397-10667C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11455475 | ||||||
chr8:11455510
|
G | C | 1 | a0002c0002t0014g0301 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-397-10702C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11455510 | ||||||
chr8:11455534
|
G | C | 10 | a0001c0001t0003g0007a0001c0001t0003g0122a0001c0001t0003g0274others(7): Show | 12 | HG02145.hp2 HG02451.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.-397-10726C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11455534 | ||||||
chr8:11455582
|
G | C | 2 | a0001c0001t0028g0258a0001c0001t0062g0132 | 2 | HG01884.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.-397-10774C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11455582 | ||||||
chr8:11455633
|
C | CCTCTGCT others(3): Show |
1 | a0001c0001t0001g0289 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-397-10826_-397-10 others(16): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11455633 | ||||||
chr8:11455636
|
G | GGTGT | 156 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(153): Show | 178 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(175): Show |
intron_variant | MODIFIER | c.-397-10832_-397-10 others(10): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11455636 | ||||||
chr8:11455636
|
G | T | 1 | a0001c0001t0001g0289 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-397-10828C>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11455636 | ||||||
chr8:11455637
|
G | T | 3 | a0001c0001t0024g0100a0001c0001t0079g0162a0001c0001t0090g0124 | 3 | HG02572.hp2 HG03130.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-397-10829C>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11455637 | ||||||
chr8:11455664
|
C | A | 1 | a0001c0001t0081g0123 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-397-10856G>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11455664 | ||||||
chr8:11455680
|
G | A | 3 | a0001c0001t0003g0029a0001c0001t0032g0027a0001c0001t0032g0028 | 3 | HG01167.hp1 HG01169.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.-397-10872C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11455680 | ||||||
chr8:11455699
|
T | C | 22 | a0001c0001t0036g0139a0001c0001t0091g0140a0002c0002t0001g0146others(19): Show | 24 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(21): Show |
intron_variant | MODIFIER | c.-397-10891A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11455699 | ||||||
chr8:11455717
|
G | A | 2 | a0001c0001t0001g0111a0001c0001t0001g0112 | 2 | HG02129.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.-398+10909C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11455717 | ||||||
chr8:11455719
|
G | GTGTGTGA others(67): Show |
1 | a0001c0001t0088g0269 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-398+10833_-398+10 others(80): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11455719 | ||||||
chr8:11455842
|
G | A | 1 | a0001c0001t0001g0181 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.-398+10784C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11455842 | ||||||
chr8:11455891
|
C | CTGAGTG | 10 | a0001c0001t0003g0029a0001c0001t0011g0119a0001c0001t0025g0270others(7): Show | 10 | HG01167.hp1 HG01169.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.-398+10734_-398+10 others(12): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11455891 | ||||||
chr8:11455891
|
C | CTGAGTGT others(11): Show |
4 | a0001c0001t0009g0255a0001c0001t0009g0256a0001c0001t0009g0257others(1): Show | 4 | HG02630.hp2 HG02886.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-398+10734_-398+10 others(24): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11455891 | ||||||
chr8:11455892
|
A | T | 258 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(255): Show | 289 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(286): Show |
intron_variant | MODIFIER | c.-398+10734T>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11455892 | ||||||
chr8:11455937
|
C | T | 7 | a0001c0001t0001g0003a0001c0001t0001g0228a0001c0001t0001g0231others(4): Show | 10 | HG01074.hp2 HG01346.hp1 HG01928.hp1 others(7): Show |
intron_variant | MODIFIER | c.-398+10689G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11455937 | ||||||
chr8:11455991
|
C | G | 258 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(255): Show | 289 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(286): Show |
intron_variant | MODIFIER | c.-398+10635G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11455991 | ||||||
chr8:11456004
|
G | T | 1 | a0001c0001t0088g0269 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-398+10622C>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456004 | ||||||
chr8:11456011
|
A | G | 1 | a0001c0001t0088g0269 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-398+10615T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456011 | ||||||
chr8:11456023
|
C | T | 1 | a0001c0001t0088g0269 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-398+10603G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456023 | ||||||
chr8:11456029
|
G | T | 2 | a0001c0001t0001g0289a0001c0001t0088g0269 | 2 | HG03239.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-398+10597C>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456029 | ||||||
chr8:11456032
|
A | G | 1 | a0001c0001t0088g0269 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-398+10594T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456032 | ||||||
chr8:11456039
|
T | C | 4 | a0001c0001t0009g0128a0001c0001t0020g0126a0001c0001t0058g0127others(1): Show | 4 | HG02055.hp2 HG02572.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-398+10587A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456039 | ||||||
chr8:11456044
|
G | A | 1 | a0002c0002t0008g0114 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-398+10582C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456044 | ||||||
chr8:11456070
|
A | T | 1 | a0001c0001t0088g0269 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-398+10556T>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456070 | ||||||
chr8:11456077
|
G | A | 1 | a0001c0001t0088g0269 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-398+10549C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456077 | ||||||
chr8:11456077
|
G | C | 1 | a0001c0001t0066g0133 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-398+10549C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456077 | ||||||
chr8:11456114
|
A | ATGTGGGG others(287): Show |
12 | a0001c0001t0002g0298a0001c0001t0002g0300a0001c0001t0011g0299others(9): Show | 12 | HG00639.hp1 HG01884.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.-398+10511_-398+10 others(300): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456114 | ||||||
chr8:11456117
|
T | TGGGGGGT others(326): Show |
1 | a0001c0001t0002g0285 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-398+10508_-398+10 others(339): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456117 | ||||||
chr8:11456121
|
A | G | 14 | a0001c0001t0002g0285a0001c0001t0002g0298a0001c0001t0002g0300others(11): Show | 14 | HG00639.hp1 HG01884.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.-398+10505T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456121 | ||||||
chr8:11456144
|
T | A | 13 | a0001c0001t0002g0285a0001c0001t0002g0298a0001c0001t0002g0300others(10): Show | 13 | HG00639.hp1 HG01884.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.-398+10482A>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456144 | ||||||
chr8:11456144
|
T | TGAATGTG others(320): Show |
1 | a0001c0001t0002g0134 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-398+10481_-398+10 others(333): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456144 | ||||||
chr8:11456144
|
T | TGTGTAAA others(324): Show |
1 | a0001c0001t0106g0113 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-398+10481_-398+10 others(337): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456144 | ||||||
chr8:11456144
|
T | TGTGTAAA others(324): Show |
1 | a0001c0001t0102g0116 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-398+10481_-398+10 others(337): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456144 | ||||||
chr8:11456146
|
T | A | 1 | a0001c0001t0088g0269 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-398+10480A>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456146 | ||||||
chr8:11456151
|
A | ATGTGGGG others(320): Show |
23 | a0001c0001t0036g0139a0001c0001t0066g0133a0001c0001t0091g0140others(20): Show | 25 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(22): Show |
intron_variant | MODIFIER | c.-398+10474_-398+10 others(333): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456151 | ||||||
chr8:11456151
|
A | ATGTGGGG others(324): Show |
122 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(119): Show | 144 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(141): Show |
intron_variant | MODIFIER | c.-398+10474_-398+10 others(337): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456151 | ||||||
chr8:11456151
|
A | ATGTGGGG others(861): Show |
1 | a0001c0001t0022g0092 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-398+10474_-398+10 others(874): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456151 | ||||||
chr8:11456151
|
A | ATGTGGGG others(312): Show |
3 | a0001c0001t0035g0271a0001c0001t0036g0135a0001c0001t0084g0272 | 3 | HG02698.hp1 HG04115.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-398+10474_-398+10 others(325): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456151 | ||||||
chr8:11456151
|
A | ATGTGGGG others(318): Show |
10 | a0001c0001t0008g0267a0001c0001t0015g0004a0001c0001t0015g0110others(7): Show | 12 | HG01496.hp1 HG02486.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.-398+10474_-398+10 others(331): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456151 | ||||||
chr8:11456151
|
A | ATGTGGGG others(318): Show |
20 | a0001c0001t0002g0102a0001c0001t0002g0280a0001c0001t0002g0294others(17): Show | 21 | HG00099.hp2 HG00639.hp2 HG00642.hp2 others(18): Show |
intron_variant | MODIFIER | c.-398+10474_-398+10 others(331): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456151 | ||||||
chr8:11456151
|
A | ATGTGGGG others(324): Show |
1 | a0001c0001t0010g0246 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-398+10474_-398+10 others(337): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456151 | ||||||
chr8:11456151
|
A | G | 16 | a0001c0001t0002g0134a0001c0001t0002g0298a0001c0001t0002g0300others(13): Show | 16 | HG00639.hp1 HG01884.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.-398+10475T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456151 | ||||||
chr8:11456172
|
C | CTG | 3 | a0001c0001t0012g0329a0001c0001t0025g0328a0001c0001t0044g0026 | 3 | HG03130.hp2 HG03139.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-398+10452_-398+10 others(8): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456172 | ||||||
chr8:11456175
|
T | G | 1 | a0001c0001t0088g0269 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-398+10451A>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456175 | ||||||
chr8:11456177
|
T | A | 1 | a0001c0001t0001g0240 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-398+10449A>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456177 | ||||||
chr8:11456177
|
T | TGA | 14 | a0001c0001t0003g0029a0001c0001t0009g0255a0001c0001t0009g0256others(11): Show | 14 | HG01167.hp1 HG01169.hp2 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.-398+10448_-398+10 others(8): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456177 | ||||||
chr8:11456178
|
G | A | 1 | a0001c0001t0088g0269 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-398+10448C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456178 | ||||||
chr8:11456180
|
G | C | 1 | a0001c0001t0088g0269 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-398+10446C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456180 | ||||||
chr8:11456181
|
T | A | 197 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(194): Show | 224 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(221): Show |
intron_variant | MODIFIER | c.-398+10445A>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456181 | ||||||
chr8:11456183
|
T | A | 15 | a0001c0001t0001g0240a0001c0001t0003g0029a0001c0001t0009g0255others(12): Show | 15 | HG01167.hp1 HG01169.hp2 HG01361.hp1 others(12): Show |
intron_variant | MODIFIER | c.-398+10443A>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456183 | ||||||
chr8:11456188
|
A | G | 16 | a0001c0001t0001g0240a0001c0001t0002g0285a0001c0001t0003g0029others(13): Show | 16 | HG01167.hp1 HG01169.hp2 HG01361.hp1 others(13): Show |
intron_variant | MODIFIER | c.-398+10438T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456188 | ||||||
chr8:11456193
|
G | T | 1 | a0001c0001t0088g0269 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-398+10433C>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456193 | ||||||
chr8:11456194
|
G | A | 1 | a0001c0001t0088g0269 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-398+10432C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456194 | ||||||
chr8:11456195
|
G | A | 1 | a0001c0001t0088g0269 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-398+10431C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456195 | ||||||
chr8:11456199
|
G | A | 1 | a0001c0001t0002g0285 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-398+10427C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456199 | ||||||
chr8:11456201
|
T | A | 1 | a0001c0001t0080g0130 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-398+10425A>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456201 | ||||||
chr8:11456206
|
T | C | 1 | a0001c0001t0088g0269 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-398+10420A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456206 | ||||||
chr8:11456208
|
G | GTGGGTAT | 15 | a0001c0001t0001g0240a0001c0001t0003g0029a0001c0001t0009g0255others(12): Show | 15 | HG01167.hp1 HG01169.hp2 HG01361.hp1 others(12): Show |
intron_variant | MODIFIER | c.-398+10417_-398+10 others(13): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456208 | ||||||
chr8:11456209
|
C | CTG | 196 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(193): Show | 223 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.-398+10415_-398+10 others(8): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456209 | ||||||
chr8:11456210
|
T | A | 15 | a0001c0001t0001g0240a0001c0001t0003g0029a0001c0001t0009g0255others(12): Show | 15 | HG01167.hp1 HG01169.hp2 HG01361.hp1 others(12): Show |
intron_variant | MODIFIER | c.-398+10416A>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456210 | ||||||
chr8:11456216
|
A | T | 1 | a0001c0001t0088g0269 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-398+10410T>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456216 | ||||||
chr8:11456217
|
G | A | 1 | a0001c0001t0088g0269 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-398+10409C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456217 | ||||||
chr8:11456220
|
T | G | 1 | a0001c0001t0088g0269 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-398+10406A>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456220 | ||||||
chr8:11456220
|
T | TAAGGTGG others(22): Show |
13 | a0001c0001t0003g0029a0001c0001t0009g0255a0001c0001t0009g0256others(10): Show | 13 | HG01167.hp1 HG01169.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.-398+10405_-398+10 others(35): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456220 | ||||||
chr8:11456221
|
G | A | 2 | a0001c0001t0001g0240a0001c0005t0073g0226 | 2 | HG01361.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.-398+10405C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456221 | ||||||
chr8:11456222
|
A | AGGTGGTT others(484): Show |
1 | a0001c0005t0073g0226 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-398+10403_-398+10 others(497): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456222 | ||||||
chr8:11456222
|
A | AGGTGGTT others(484): Show |
1 | a0001c0001t0001g0240 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-398+10403_-398+10 others(497): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456222 | ||||||
chr8:11456222
|
A | AGTGAGTG others(531): Show |
1 | a0001c0001t0001g0296 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-398+10403_-398+10 others(544): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456222 | ||||||
chr8:11456222
|
A | AGTGAGTG others(530): Show |
69 | a0001c0001t0001g0082a0001c0001t0001g0188a0001c0001t0001g0247others(66): Show | 82 | HG00544.hp1 HG00597.hp1 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.-398+10403_-398+10 others(543): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456222 | ||||||
chr8:11456222
|
A | AGTGAGTG others(526): Show |
1 | a0001c0001t0104g0091 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-398+10403_-398+10 others(539): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456222 | ||||||
chr8:11456222
|
A | AGTGAGTG others(530): Show |
2 | a0001c0001t0055g0025a0001c0001t0089g0024 | 2 | HG03579.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-398+10403_-398+10 others(543): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456222 | ||||||
chr8:11456222
|
A | AGTGAGTG others(530): Show |
43 | a0001c0001t0001g0107a0001c0001t0001g0109a0001c0001t0001g0164others(40): Show | 47 | HG00738.hp2 HG01123.hp2 HG01175.hp2 others(44): Show |
intron_variant | MODIFIER | c.-398+10403_-398+10 others(543): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456222 | ||||||
chr8:11456222
|
A | AGTGTGGG others(124): Show |
1 | a0001c0001t0002g0285 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-398+10403_-398+10 others(137): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456222 | ||||||
chr8:11456222
|
A | AGTGTGGG others(123): Show |
4 | a0001c0001t0022g0092a0001c0001t0024g0100a0001c0001t0079g0162others(1): Show | 4 | HG02572.hp2 HG03130.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.-398+10403_-398+10 others(136): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456222 | ||||||
chr8:11456222
|
A | AGTGTGGG others(161): Show |
1 | a0001c0001t0001g0187 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.-398+10403_-398+10 others(174): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456222 | ||||||
chr8:11456222
|
A | AGTGTGGG others(160): Show |
190 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(187): Show | 217 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.-398+10403_-398+10 others(173): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456222 | ||||||
chr8:11456222
|
A | T | 14 | a0001c0001t0003g0029a0001c0001t0009g0255a0001c0001t0009g0256others(11): Show | 14 | HG01167.hp1 HG01169.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.-398+10404T>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456222 | ||||||
chr8:11456232
|
G | A | 1 | a0001c0001t0001g0227 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-398+10394C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456232 | ||||||
chr8:11456239
|
G | GTTGCCTT others(68): Show |
1 | a0001c0001t0029g0156 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-398+10386_-398+10 others(81): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456239 | ||||||
chr8:11456239
|
G | T | 14 | a0001c0001t0003g0029a0001c0001t0009g0255a0001c0001t0009g0256others(11): Show | 14 | HG01167.hp1 HG01169.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.-398+10387C>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456239 | ||||||
chr8:11456253
|
T | A | 15 | a0001c0001t0003g0029a0001c0001t0009g0255a0001c0001t0009g0256others(12): Show | 15 | HG01167.hp1 HG01169.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.-398+10373A>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456253 | ||||||
chr8:11456254
|
G | A | 1 | a0001c0001t0002g0134 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-398+10372C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456254 | ||||||
chr8:11456264
|
A | G | 15 | a0001c0001t0003g0029a0001c0001t0009g0255a0001c0001t0009g0256others(12): Show | 15 | HG01167.hp1 HG01169.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.-398+10362T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456264 | ||||||
chr8:11456315
|
C | T | 2 | a0001c0001t0028g0258a0001c0001t0062g0132 | 2 | HG01884.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.-398+10311G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456315 | ||||||
chr8:11456345
|
G | C | 3 | a0001c0001t0015g0004a0001c0001t0015g0110a0001c0001t0098g0106 | 5 | HG02622.hp1 HG02818.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.-398+10281C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456345 | ||||||
chr8:11456361
|
T | C | 15 | a0001c0001t0003g0029a0001c0001t0009g0255a0001c0001t0009g0256others(12): Show | 15 | HG01167.hp1 HG01169.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.-398+10265A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456361 | ||||||
chr8:11456379
|
C | T | 15 | a0001c0001t0003g0029a0001c0001t0009g0255a0001c0001t0009g0256others(12): Show | 15 | HG01167.hp1 HG01169.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.-398+10247G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456379 | ||||||
chr8:11456392
|
T | TGAGTGTG others(1): Show |
207 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(204): Show | 236 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(233): Show |
intron_variant | MODIFIER | c.-398+10233_-398+10 others(14): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456392 | ||||||
chr8:11456392
|
T | TGAGTGTG others(326): Show |
14 | a0001c0001t0003g0029a0001c0001t0009g0255a0001c0001t0009g0256others(11): Show | 14 | HG01167.hp1 HG01169.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.-398+10233_-398+10 others(339): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456392 | ||||||
chr8:11456392
|
T | TGAGTGTG others(330): Show |
1 | a0001c0001t0029g0156 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-398+10233_-398+10 others(343): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456392 | ||||||
chr8:11456392
|
T | TGTGA | 33 | a0001c0001t0001g0107a0001c0001t0001g0109a0001c0001t0003g0310others(30): Show | 35 | HG00738.hp2 HG01123.hp2 HG01175.hp2 others(32): Show |
intron_variant | MODIFIER | c.-398+10233_-398+10 others(10): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456392 | ||||||
chr8:11456396
|
T | A | 1 | a0001c0001t0010g0236 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-398+10230A>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456396 | ||||||
chr8:11456404
|
G | A | 2 | a0001c0001t0055g0025a0001c0001t0089g0024 | 2 | HG03579.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-398+10222C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456404 | ||||||
chr8:11456426
|
G | A | 2 | a0001c0001t0013g0282a0001c0001t0013g0283 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.-398+10200C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456426 | ||||||
chr8:11456439
|
A | T | 1 | a0001c0001t0066g0133 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-398+10187T>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456439 | ||||||
chr8:11456448
|
A | G | 22 | a0001c0001t0036g0139a0001c0001t0091g0140a0002c0002t0001g0146others(19): Show | 24 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(21): Show |
intron_variant | MODIFIER | c.-398+10178T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456448 | ||||||
chr8:11456449
|
C | G | 201 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(198): Show | 228 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(225): Show |
intron_variant | MODIFIER | c.-398+10177G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456449 | ||||||
chr8:11456509
|
G | A | 2 | a0001c0001t0002g0012a0001c0001t0012g0090 | 3 | HG02717.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-398+10117C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456509 | ||||||
chr8:11456538
|
G | A | 1 | a0001c0001t0066g0133 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-398+10088C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456538 | ||||||
chr8:11456690
|
A | T | 9 | a0001c0001t0002g0134a0001c0001t0017g0261a0001c0001t0017g0262others(6): Show | 9 | HG01884.hp1 HG02258.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.-398+9936T>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456690 | ||||||
chr8:11456768
|
T | C | 22 | a0001c0001t0036g0139a0001c0001t0091g0140a0002c0002t0001g0146others(19): Show | 24 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(21): Show |
intron_variant | MODIFIER | c.-398+9858A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456768 | ||||||
chr8:11456835
|
G | T | 107 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(104): Show | 126 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(123): Show |
intron_variant | MODIFIER | c.-398+9791C>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456835 | ||||||
chr8:11456840
|
G | A | 1 | a0001c0001t0001g0289 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-398+9786C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456840 | ||||||
chr8:11456884
|
G | A | 1 | a0001c0001t0001g0182 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-398+9742C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456884 | ||||||
chr8:11456894
|
TGGG | T | 29 | a0001c0001t0001g0107a0001c0001t0001g0109a0001c0001t0002g0190others(26): Show | 31 | HG00738.hp1 HG00738.hp2 HG01123.hp2 others(28): Show |
intron_variant | MODIFIER | c.-398+9729_-398+973 others(7): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456894 | ||||||
chr8:11456905
|
G | T | 5 | a0001c0001t0008g0267a0001c0001t0021g0277a0001c0001t0076g0266others(2): Show | 5 | HG01496.hp1 HG02486.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-398+9721C>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456905 | ||||||
chr8:11456909
|
C | CGGGAAGT others(39): Show |
2 | a0001c0001t0102g0116a0001c0001t0106g0113 | 2 | HG01884.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.-398+9671_-398+971 others(50): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456909 | ||||||
chr8:11456966
|
CGGGGCTG others(16): Show |
C | 178 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(175): Show | 204 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(201): Show |
intron_variant | MODIFIER | c.-398+9637_-398+965 others(27): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456966 | ||||||
chr8:11456978
|
AGGGATGT others(17): Show |
A | 1 | a0001c0001t0001g0289 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-398+9624_-398+964 others(28): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456978 | ||||||
chr8:11456979
|
GGGATGTA others(62): Show |
G | 1 | a0001c0001t0001g0237 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-398+9578_-398+964 others(73): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456979 | ||||||
chr8:11457013
|
G | T | 1 | a0001c0001t0002g0034 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-398+9613C>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11457013 | ||||||
chr8:11457023
|
TA | T | 4 | a0001c0001t0017g0261a0001c0001t0017g0262a0001c0001t0017g0264others(1): Show | 4 | HG02559.hp1 HG02615.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.-398+9602delT | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11457023 | ||||||
chr8:11457028
|
G | A | 3 | a0001c0001t0025g0118a0001c0001t0044g0117a0001c0001t0066g0133 | 3 | HG02723.hp1 HG03195.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-398+9598C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11457028 | ||||||
chr8:11457029
|
T | A | 1 | a0001c0001t0066g0133 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-398+9597A>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11457029 | ||||||
chr8:11457030
|
A | G | 3 | a0001c0001t0025g0118a0001c0001t0044g0117a0001c0001t0066g0133 | 3 | HG02723.hp1 HG03195.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-398+9596T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11457030 | ||||||
chr8:11457032
|
G | A | 2 | a0001c0001t0025g0118a0001c0001t0044g0117 | 2 | HG02723.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-398+9594C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11457032 | ||||||
chr8:11457035
|
C | T | 2 | a0001c0001t0025g0118a0001c0001t0044g0117 | 2 | HG02723.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-398+9591G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11457035 | ||||||
chr8:11457047
|
A | G | 9 | a0001c0001t0002g0134a0001c0001t0017g0261a0001c0001t0017g0262others(6): Show | 9 | HG01884.hp1 HG02258.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.-398+9579T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11457047 | ||||||
chr8:11457048
|
A | G | 11 | a0001c0001t0002g0134a0001c0001t0017g0261a0001c0001t0017g0262others(8): Show | 11 | HG01884.hp1 HG02258.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.-398+9578T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11457048 | ||||||
chr8:11457048
|
AGGAAGTG others(16): Show |
A | 1 | a0001c0001t0001g0238 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-398+9555_-398+957 others(27): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11457048 | ||||||
chr8:11457058
|
T | C | 14 | a0001c0001t0001g0237a0001c0001t0002g0102a0001c0001t0015g0004others(11): Show | 16 | HG02602.hp1 HG02622.hp1 HG02698.hp1 others(13): Show |
intron_variant | MODIFIER | c.-398+9568A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11457058 | ||||||
chr8:11457058
|
T | TGGGGCTG others(16): Show |
2 | a0001c0001t0039g0073a0001c0001t0039g0074 | 2 | HG01099.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.-398+9545_-398+956 others(27): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11457058 | ||||||
chr8:11457070
|
G | A | 2 | a0001c0001t0025g0118a0001c0001t0044g0117 | 2 | HG02723.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-398+9556C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11457070 | ||||||
chr8:11457071
|
G | GGGGTATG others(16): Show |
2 | a0001c0001t0025g0118a0001c0001t0044g0117 | 2 | HG02723.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-398+9554_-398+955 others(27): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11457071 | ||||||
chr8:11457076
|
GTGGGCGG others(16): Show |
G | 46 | a0001c0001t0001g0166a0001c0001t0001g0296a0001c0001t0002g0033others(43): Show | 47 | HG00099.hp2 HG00544.hp1 HG00639.hp1 others(44): Show |
intron_variant | MODIFIER | c.-398+9527_-398+954 others(27): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11457076 | ||||||
chr8:11457081
|
C | T | 2 | a0001c0001t0025g0118a0001c0001t0044g0117 | 2 | HG02723.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-398+9545G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11457081 | ||||||
chr8:11457099
|
A | G | 283 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(280): Show | 326 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(323): Show |
intron_variant | MODIFIER | c.-398+9527T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11457099 | ||||||
chr8:11457218
|
G | A | 2 | a0001c0001t0001g0240a0001c0001t0033g0239 | 2 | NA18953.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.-398+9408C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11457218 | ||||||
chr8:11457232
|
T | C | 2 | a0001c0001t0028g0258a0001c0001t0062g0132 | 2 | HG01884.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.-398+9394A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11457232 | ||||||
chr8:11457276
|
T | G | 23 | a0001c0001t0001g0107a0001c0001t0001g0109a0001c0001t0003g0310others(20): Show | 25 | HG00738.hp2 HG01123.hp2 HG01175.hp2 others(22): Show |
intron_variant | MODIFIER | c.-398+9350A>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11457276 | ||||||
chr8:11457352
|
A | C | 1 | a0001c0001t0051g0308 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-398+9274T>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11457352 | ||||||
chr8:11457411
|
G | C | 11 | a0001c0001t0002g0134a0001c0001t0011g0265a0001c0001t0012g0329others(8): Show | 11 | HG01884.hp1 HG02258.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.-398+9215C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11457411 | ||||||
chr8:11457482
|
C | T | 256 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(253): Show | 286 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(283): Show |
intron_variant | MODIFIER | c.-398+9144G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11457482 | ||||||
chr8:11457539
|
G | A | 256 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(253): Show | 286 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(283): Show |
intron_variant | MODIFIER | c.-398+9087C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11457539 | ||||||
chr8:11457542
|
G | A | 2 | a0001c0001t0037g0302a0001c0001t0085g0284 | 2 | HG01515.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-398+9084C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11457542 | ||||||
chr8:11457613
|
G | A | 1 | a0001c0001t0002g0075 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-398+9013C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11457613 | ||||||
chr8:11457960
|
T | G | 2 | a0001c0001t0021g0157a0001c0001t0029g0156 | 2 | HG02145.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-398+8666A>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11457960 | ||||||
chr8:11458022
|
G | C | 12 | a0001c0001t0002g0134a0001c0001t0011g0265a0001c0001t0012g0329others(9): Show | 12 | HG01884.hp1 HG02258.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.-398+8604C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11458022 | ||||||
chr8:11458083
|
C | CAGA | 257 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(254): Show | 288 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(285): Show |
intron_variant | MODIFIER | c.-398+8540_-398+854 others(7): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11458083 | ||||||
chr8:11458210
|
C | G | 6 | a0001c0001t0001g0163a0001c0001t0001g0183a0001c0001t0001g0184others(3): Show | 6 | NA18951.hp1 NA18988.hp2 NA18991.hp2 others(3): Show |
intron_variant | MODIFIER | c.-398+8416G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11458210 | ||||||
chr8:11458536
|
C | G | 2 | a0001c0001t0013g0290a0001c0001t0013g0291 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-398+8090G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11458536 | ||||||
chr8:11458553
|
C | T | 28 | a0001c0001t0001g0107a0001c0001t0001g0109a0001c0001t0003g0310others(25): Show | 30 | HG00738.hp2 HG01123.hp2 HG01175.hp2 others(27): Show |
intron_variant | MODIFIER | c.-398+8073G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11458553 | ||||||
chr8:11458785
|
G | GAA | 10 | a0001c0001t0003g0007a0001c0001t0003g0122a0001c0001t0003g0274others(7): Show | 12 | HG02451.hp2 HG02486.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.-398+7839_-398+784 others(6): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11458785 | ||||||
chr8:11458799
|
A | G | 13 | a0001c0001t0003g0007a0001c0001t0003g0122a0001c0001t0003g0274others(10): Show | 15 | HG02451.hp2 HG02486.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.-398+7827T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11458799 | ||||||
chr8:11458941
|
C | G | 10 | a0001c0001t0003g0007a0001c0001t0003g0122a0001c0001t0003g0274others(7): Show | 12 | HG02451.hp2 HG02486.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.-398+7685G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11458941 | ||||||
chr8:11459053
|
G | A | 10 | a0001c0001t0002g0134a0001c0001t0017g0261a0001c0001t0017g0262others(7): Show | 10 | HG01884.hp1 HG01884.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.-398+7573C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11459053 | ||||||
chr8:11459079
|
C | T | 1 | a0001c0001t0038g0021 | 2 | HG00642.hp2 HG00735.hp1 |
intron_variant | MODIFIER | c.-398+7547G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11459079 | ||||||
chr8:11459182
|
C | G | 10 | a0001c0001t0003g0007a0001c0001t0003g0122a0001c0001t0003g0274others(7): Show | 12 | HG02451.hp2 HG02486.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.-398+7444G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11459182 | ||||||
chr8:11459183
|
T | C | 17 | a0001c0001t0001g0268a0001c0001t0002g0134a0001c0001t0010g0286others(14): Show | 18 | HG01255.hp1 HG01884.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.-398+7443A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11459183 | ||||||
chr8:11459357
|
G | A | 1 | a0001c0001t0012g0329 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-398+7269C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11459357 | ||||||
chr8:11459395
|
C | T | 1 | a0001c0001t0011g0265 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-398+7231G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11459395 | ||||||
chr8:11459563
|
G | A | 1 | a0001c0001t0024g0100 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-398+7063C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11459563 | ||||||
chr8:11459590
|
T | G | 8 | a0001c0001t0003g0007a0001c0001t0003g0122a0001c0001t0003g0274others(5): Show | 10 | HG02451.hp2 HG02486.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.-398+7036A>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11459590 | ||||||
chr8:11459732
|
G | C | 10 | a0001c0001t0003g0007a0001c0001t0003g0122a0001c0001t0003g0274others(7): Show | 12 | HG02451.hp2 HG02486.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.-398+6894C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11459732 | ||||||
chr8:11460017
|
C | T | 1 | a0002c0002t0078g0148 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-398+6609G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11460017 | ||||||
chr8:11460132
|
T | C | 1 | a0001c0001t0002g0076 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-398+6494A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11460132 | ||||||
chr8:11460162
|
G | T | 2 | a0001c0001t0021g0157a0001c0001t0029g0156 | 2 | HG02145.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-398+6464C>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11460162 | ||||||
chr8:11460175
|
G | A | 1 | a0001c0001t0102g0116 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-398+6451C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11460175 | ||||||
chr8:11460214
|
G | A | 2 | a0001c0001t0004g0241a0001c0001t0057g0323 | 2 | HG02071.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-398+6412C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11460214 | ||||||
chr8:11460318
|
G | C | 1 | a0001c0001t0026g0077 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-398+6308C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11460318 | ||||||
chr8:11460340
|
A | C | 17 | a0001c0001t0001g0107a0001c0001t0001g0109a0001c0001t0002g0134others(14): Show | 17 | HG01358.hp1 HG01884.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-398+6286T>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11460340 | ||||||
chr8:11460370
|
G | A | 2 | a0001c0001t0023g0251a0001c0001t0082g0303 | 2 | HG03834.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.-398+6256C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11460370 | ||||||
chr8:11460429
|
A | G | 1 | a0001c0001t0066g0133 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-398+6197T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11460429 | ||||||
chr8:11460494
|
G | A | 1 | a0001c0001t0001g0244 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-398+6132C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11460494 | ||||||
chr8:11460537
|
G | A | 1 | a0001c0001t0038g0021 | 2 | HG00642.hp2 HG00735.hp1 |
intron_variant | MODIFIER | c.-398+6089C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11460537 | ||||||
chr8:11460553
|
T | C | 44 | a0001c0001t0001g0296a0001c0001t0002g0102a0001c0001t0002g0280others(41): Show | 45 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.-398+6073A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11460553 | ||||||
chr8:11460554
|
G | A | 1 | a0001c0001t0001g0243 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.-398+6072C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11460554 | ||||||
chr8:11460623
|
A | G | 32 | a0001c0001t0001g0107a0001c0001t0001g0109a0001c0001t0001g0268others(29): Show | 36 | HG01167.hp1 HG01169.hp2 HG01255.hp1 others(33): Show |
intron_variant | MODIFIER | c.-398+6003T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11460623 | ||||||
chr8:11460738
|
G | A | 1 | a0001c0001t0002g0078 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-398+5888C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11460738 | ||||||
chr8:11460748
|
C | T | 3 | a0001c0001t0044g0026a0001c0001t0055g0025a0001c0001t0089g0024 | 3 | HG03579.hp2 NA19043.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-398+5878G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11460748 | ||||||
chr8:11460775
|
C | G | 167 | a0001c0001t0001g0107a0001c0001t0001g0109a0001c0001t0001g0268others(164): Show | 189 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(186): Show |
intron_variant | MODIFIER | c.-398+5851G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11460775 | ||||||
chr8:11460813
|
T | C | 1 | a0001c0001t0001g0244 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-398+5813A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11460813 | ||||||
chr8:11460870
|
A | T | 21 | a0001c0001t0001g0005a0001c0001t0001g0164a0001c0001t0001g0165others(18): Show | 24 | HG00438.hp2 HG00544.hp2 HG01928.hp2 others(21): Show |
intron_variant | MODIFIER | c.-398+5756T>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11460870 | ||||||
chr8:11460873
|
A | G | 17 | a0001c0001t0009g0255a0001c0001t0009g0256a0001c0001t0009g0257others(14): Show | 17 | HG01891.hp2 HG02257.hp1 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.-398+5753T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11460873 | ||||||
chr8:11460942
|
T | C | 3 | a0001c0001t0010g0246a0001c0009t0009g0245a0005c0004t0003g0020 | 4 | HG00741.hp1 HG02922.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-398+5684A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11460942 | ||||||
chr8:11460987
|
G | C | 2 | a0001c0001t0002g0134a0001c0001t0066g0133 | 2 | HG02258.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-398+5639C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11460987 | ||||||
chr8:11461086
|
G | C | 1 | a0001c0001t0024g0100 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-398+5540C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11461086 | ||||||
chr8:11461128
|
C | T | 3 | a0001c0001t0011g0265a0001c0001t0012g0329a0001c0001t0025g0328 | 3 | HG03130.hp2 HG03139.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-398+5498G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11461128 | ||||||
chr8:11461130
|
C | G | 1 | a0001c0001t0096g0032 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-398+5496G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11461130 | ||||||
chr8:11461139
|
G | A | 1 | a0001c0001t0001g0247 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-398+5487C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11461139 | ||||||
chr8:11461170
|
G | C | 24 | a0001c0001t0003g0122a0001c0001t0009g0128a0001c0001t0011g0119others(21): Show | 25 | HG01884.hp2 HG01891.hp1 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.-398+5456C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11461170 | ||||||
chr8:11461175
|
T | A | 1 | a0001c0001t0104g0091 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-398+5451A>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11461175 | ||||||
chr8:11461184
|
G | A | 1 | a0007c0011t0054g0131 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-398+5442C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11461184 | ||||||
chr8:11461253
|
G | A | 1 | a0001c0001t0002g0134 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-398+5373C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11461253 | ||||||
chr8:11461307
|
T | C | 1 | a0001c0001t0038g0021 | 2 | HG00642.hp2 HG00735.hp1 |
intron_variant | MODIFIER | c.-398+5319A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11461307 | ||||||
chr8:11461347
|
C | T | 1 | a0001c0001t0002g0285 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-398+5279G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11461347 | ||||||
chr8:11461366
|
G | A | 14 | a0001c0001t0001g0268a0001c0001t0003g0007a0001c0001t0003g0029others(11): Show | 16 | HG01167.hp1 HG01169.hp2 HG01255.hp1 others(13): Show |
intron_variant | MODIFIER | c.-398+5260C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11461366 | ||||||
chr8:11461377
|
C | G | 2 | a0001c0001t0012g0329a0001c0001t0025g0328 | 2 | HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-398+5249G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11461377 | ||||||
chr8:11461406
|
C | T | 1 | a0001c0001t0105g0326 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-398+5220G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11461406 | ||||||
chr8:11461705
|
T | A | 5 | a0002c0002t0001g0152a0002c0002t0014g0151a0002c0002t0014g0153others(2): Show | 5 | HG00323.hp1 HG00323.hp2 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.-398+4921A>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11461705 | ||||||
chr8:11461801
|
A | G | 3 | a0001c0001t0002g0134a0001c0001t0062g0132a0001c0001t0066g0133 | 3 | HG01884.hp2 HG02258.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-398+4825T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11461801 | ||||||
chr8:11461848
|
T | A | 6 | a0001c0001t0003g0330a0001c0001t0008g0267a0001c0001t0011g0265others(3): Show | 6 | HG01496.hp1 HG02486.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.-398+4778A>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11461848 | ||||||
chr8:11461968
|
G | A | 1 | a0001c0001t0001g0248 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-398+4658C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11461968 | ||||||
chr8:11461969
|
C | T | 1 | a0001c0001t0085g0284 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-398+4657G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11461969 | ||||||
chr8:11462041
|
C | T | 1 | a0001c0001t0001g0163 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-398+4585G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11462041 | ||||||
chr8:11462262
|
C | T | 1 | a0001c0001t0001g0249 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-398+4364G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11462262 | ||||||
chr8:11462410
|
G | C | 1 | a0001c0001t0104g0091 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-398+4216C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11462410 | ||||||
chr8:11462442
|
C | G | 16 | a0001c0001t0009g0255a0001c0001t0009g0256a0001c0001t0009g0257others(13): Show | 16 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.-398+4184G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11462442 | ||||||
chr8:11462455
|
C | T | 1 | a0001c0001t0001g0155 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.-398+4171G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11462455 | ||||||
chr8:11462503
|
G | A | 1 | a0001c0001t0104g0091 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-398+4123C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11462503 | ||||||
chr8:11462578
|
G | GCACAAGC others(10): Show |
16 | a0001c0001t0009g0255a0001c0001t0009g0256a0001c0001t0009g0257others(13): Show | 16 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.-398+4047_-398+404 others(21): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11462578 | ||||||
chr8:11462607
|
C | T | 1 | a0001c0001t0001g0158 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-398+4019G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11462607 | ||||||
chr8:11462643
|
T | C | 45 | a0001c0001t0001g0268a0001c0001t0001g0289a0001c0001t0001g0296others(42): Show | 48 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.-398+3983A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11462643 | ||||||
chr8:11462659
|
G | C | 2 | a0001c0001t0002g0134a0001c0001t0066g0133 | 2 | HG02258.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-398+3967C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11462659 | ||||||
chr8:11462691
|
G | C | 1 | a0001c0001t0001g0249 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-398+3935C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11462691 | ||||||
chr8:11462760
|
C | G | 44 | a0001c0001t0001g0268a0001c0001t0001g0289a0001c0001t0001g0296others(41): Show | 46 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.-398+3866G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11462760 | ||||||
chr8:11462776
|
C | CTCG | 16 | a0001c0001t0009g0255a0001c0001t0009g0256a0001c0001t0009g0257others(13): Show | 16 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.-398+3847_-398+384 others(7): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11462776 | ||||||
chr8:11462855
|
T | C | 1 | a0001c0001t0004g0250 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-398+3771A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11462855 | ||||||
chr8:11462978
|
G | C | 1 | a0001c0001t0104g0091 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-398+3648C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11462978 | ||||||
chr8:11462986
|
G | A | 1 | a0001c0001t0012g0090 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-398+3640C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11462986 | ||||||
chr8:11463041
|
C | T | 4 | a0001c0001t0001g0268a0001c0001t0003g0029a0001c0001t0032g0027others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.-398+3585G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11463041 | ||||||
chr8:11463242
|
T | C | 16 | a0001c0001t0009g0255a0001c0001t0009g0256a0001c0001t0009g0257others(13): Show | 16 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.-398+3384A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11463242 | ||||||
chr8:11463255
|
T | C | 1 | a0001c0001t0001g0259 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-398+3371A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11463255 | ||||||
chr8:11463259
|
G | A | 1 | a0001c0001t0083g0306 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-398+3367C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11463259 | ||||||
chr8:11463341
|
G | C | 3 | a0001c0001t0002g0134a0001c0001t0062g0132a0001c0001t0066g0133 | 3 | HG01884.hp2 HG02258.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-398+3285C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11463341 | ||||||
chr8:11463341
|
G | T | 1 | a0001c0001t0001g0259 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-398+3285C>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11463341 | ||||||
chr8:11463406
|
C | T | 1 | a0001c0001t0001g0161 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.-398+3220G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11463406 | ||||||
chr8:11463465
|
T | G | 3 | a0001c0001t0002g0134a0001c0001t0062g0132a0001c0001t0066g0133 | 3 | HG01884.hp2 HG02258.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-398+3161A>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11463465 | ||||||
chr8:11463555
|
A | G | 16 | a0001c0001t0009g0255a0001c0001t0009g0256a0001c0001t0009g0257others(13): Show | 16 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.-398+3071T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11463555 | ||||||
chr8:11463783
|
A | G | 161 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(158): Show | 186 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.-398+2843T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11463783 | ||||||
chr8:11463882
|
G | GTGGGGGA others(3): Show |
3 | a0001c0001t0002g0134a0001c0001t0062g0132a0001c0001t0066g0133 | 3 | HG01884.hp2 HG02258.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-398+2734_-398+274 others(14): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11463882 | ||||||
chr8:11463987
|
G | A | 1 | a0001c0001t0017g0264 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-398+2639C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11463987 | ||||||
chr8:11464025
|
C | T | 3 | a0001c0001t0001g0158a0001c0001t0006g0160a0001c0001t0067g0159 | 3 | HG00438.hp1 NA18612.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.-398+2601G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11464025 | ||||||
chr8:11464044
|
A | C | 2 | a0001c0001t0013g0282a0001c0001t0013g0283 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.-398+2582T>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11464044 | ||||||
chr8:11464052
|
A | G | 24 | a0001c0001t0003g0122a0001c0001t0009g0128a0001c0001t0011g0119others(21): Show | 25 | HG01358.hp1 HG01891.hp1 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.-398+2574T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11464052 | ||||||
chr8:11464162
|
G | GC | 23 | a0001c0001t0036g0135a0001c0001t0036g0139a0001c0001t0049g0324others(20): Show | 25 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(22): Show |
intron_variant | MODIFIER | c.-398+2463dupG | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11464162 | ||||||
chr8:11464198
|
A | G | 1 | a0003c0003t0001g0086 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-398+2428T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11464198 | ||||||
chr8:11464285
|
C | T | 2 | a0001c0001t0021g0157a0001c0001t0029g0156 | 2 | HG02145.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-398+2341G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11464285 | ||||||
chr8:11464318
|
C | G | 3 | a0001c0001t0008g0267a0001c0001t0011g0265a0001c0001t0076g0266 | 3 | HG01496.hp1 HG02647.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-398+2308G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11464318 | ||||||
chr8:11464318
|
C | T | 1 | a0008c0007t0002g0031 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-398+2308G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11464318 | ||||||
chr8:11464324
|
T | G | 1 | a0001c0001t0003g0330 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-398+2302A>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11464324 | ||||||
chr8:11464343
|
G | A | 1 | a0001c0001t0001g0254 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-398+2283C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11464343 | ||||||
chr8:11464343
|
G | C | 1 | a0001c0001t0003g0330 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-398+2283C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11464343 | ||||||
chr8:11464402
|
C | T | 2 | a0001c0001t0002g0280a0001c0001t0026g0281 | 2 | HG00639.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.-398+2224G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11464402 | ||||||
chr8:11464568
|
C | G | 11 | a0001c0001t0022g0092a0001c0001t0022g0094a0001c0001t0022g0098others(8): Show | 11 | HG01358.hp1 HG01884.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.-398+2058G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11464568 | ||||||
chr8:11464591
|
G | A | 1 | a0001c0001t0101g0305 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-398+2035C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11464591 | ||||||
chr8:11464763
|
C | T | 1 | a0001c0001t0001g0155 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.-398+1863G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11464763 | ||||||
chr8:11464870
|
G | C | 17 | a0001c0001t0009g0255a0001c0001t0009g0256a0001c0001t0009g0257others(14): Show | 17 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.-398+1756C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11464870 | ||||||
chr8:11464904
|
G | C | 1 | a0001c0001t0083g0306 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-398+1722C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11464904 | ||||||
chr8:11464982
|
G | C | 1 | a0001c0001t0001g0259 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-398+1644C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11464982 | ||||||
chr8:11464987
|
G | C | 2 | a0001c0001t0012g0329a0001c0001t0025g0328 | 2 | HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-398+1639C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11464987 | ||||||
chr8:11465068
|
C | A | 1 | a0001c0001t0003g0330 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-398+1558G>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11465068 | ||||||
chr8:11465246
|
G | C | 1 | a0001c0001t0092g0307 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-398+1380C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11465246 | ||||||
chr8:11465268
|
G | A | 18 | a0001c0001t0001g0268a0001c0001t0003g0007a0001c0001t0003g0029others(15): Show | 20 | HG01167.hp1 HG01169.hp2 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.-398+1358C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11465268 | ||||||
chr8:11465324
|
G | A | 11 | a0001c0001t0001g0107a0001c0001t0001g0109a0001c0001t0002g0102others(8): Show | 13 | HG02622.hp1 HG02698.hp2 HG02738.hp1 others(10): Show |
intron_variant | MODIFIER | c.-398+1302C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11465324 | ||||||
chr8:11465403
|
C | T | 1 | a0001c0001t0104g0091 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-398+1223G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11465403 | ||||||
chr8:11465516
|
G | A | 119 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(116): Show | 140 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(137): Show |
intron_variant | MODIFIER | c.-398+1110C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11465516 | ||||||
chr8:11465639
|
T | C | 1 | a0001c0001t0005g0325 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-398+987A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11465639 | ||||||
chr8:11465692
|
G | A | 1 | a0001c0001t0105g0326 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-398+934C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11465692 | ||||||
chr8:11465745
|
C | T | 13 | a0001c0001t0022g0092a0001c0001t0022g0094a0001c0001t0022g0098others(10): Show | 13 | HG01884.hp1 HG01891.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.-398+881G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11465745 | ||||||
chr8:11465772
|
G | C | 267 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(264): Show | 298 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(295): Show |
intron_variant | MODIFIER | c.-398+854C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11465772 | ||||||
chr8:11465803
|
G | C | 141 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(138): Show | 164 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(161): Show |
intron_variant | MODIFIER | c.-398+823C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11465803 | ||||||
chr8:11465853
|
C | A | 34 | a0001c0001t0001g0107a0001c0001t0001g0109a0001c0001t0001g0268others(31): Show | 38 | HG01167.hp1 HG01169.hp2 HG01255.hp1 others(35): Show |
intron_variant | MODIFIER | c.-398+773G>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11465853 | ||||||
chr8:11465853
|
C | T | 1 | a0002c0002t0008g0114 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-398+773G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11465853 | ||||||
chr8:11465940
|
G | A | 1 | a0001c0001t0053g0327 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-398+686C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11465940 | ||||||
chr8:11465970
|
G | A | 6 | a0001c0001t0001g0107a0001c0001t0001g0109a0001c0001t0015g0004others(3): Show | 8 | HG02622.hp1 HG02818.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.-398+656C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11465970 | ||||||
chr8:11466016
|
C | T | 1 | a0001c0001t0087g0279 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-398+610G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11466016 | ||||||
chr8:11466023
|
C | G | 30 | a0001c0001t0001g0289a0001c0001t0001g0296a0001c0001t0002g0280others(27): Show | 30 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.-398+603G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11466023 | ||||||
chr8:11466320
|
G | T | 1 | a0001c0001t0106g0113 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-398+306C>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11466320 | ||||||
chr8:11466369
|
G | A | 51 | a0001c0001t0001g0289a0001c0001t0001g0296a0001c0001t0002g0280others(48): Show | 53 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.-398+257C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11466369 | ||||||
chr8:11466423
|
CGAACCCG others(54): Show |
C | 11 | a0001c0001t0001g0107a0001c0001t0001g0109a0001c0001t0002g0102others(8): Show | 13 | HG02622.hp1 HG02698.hp2 HG02738.hp1 others(10): Show |
intron_variant | MODIFIER | c.-398+142_-398+202d others(63): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11466423 | ||||||
chr8:11466455
|
C | T | 2 | a0001c0001t0001g0111a0001c0001t0001g0112 | 2 | HG02129.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.-398+171G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11466455 | ||||||
chr8:11466484
|
A | G | 12 | a0001c0001t0022g0092a0001c0001t0022g0094a0001c0001t0022g0098others(9): Show | 12 | HG01891.hp2 HG02257.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.-398+142T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11466484 | ||||||
chr8:11466488
|
C | A | 51 | a0001c0001t0001g0289a0001c0001t0001g0296a0001c0001t0002g0280others(48): Show | 53 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.-398+138G>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11466488 | ||||||
chr8:11466503
|
C | G | 1 | a0001c0001t0104g0091 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-398+123G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11466503 | ||||||
chr8:11466516
|
G | C | 261 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(258): Show | 291 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(288): Show |
intron_variant | MODIFIER | c.-398+110C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11466516 | ||||||
chr8:11466539
|
C | T | 3 | a0001c0001t0003g0029a0001c0001t0032g0027a0001c0001t0032g0028 | 3 | HG01167.hp1 HG01169.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.-398+87G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11466539 | ||||||
chr8:11466587
|
C | T | 3 | a0001c0001t0044g0026a0001c0001t0055g0025a0001c0001t0089g0024 | 3 | HG03579.hp2 NA19043.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-398+39G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11466587 | ||||||
chr8:11466589
|
G | C | 3 | a0001c0001t0003g0330a0001c0001t0012g0329a0001c0001t0025g0328 | 3 | HG02559.hp2 HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-398+37C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11466589 | ||||||
chr8:11466592
|
C | T | 3 | a0001c0001t0044g0026a0001c0001t0055g0025a0001c0001t0089g0024 | 3 | HG03579.hp2 NA19043.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-398+34G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11466592 |