geneid | 375190 |
---|---|
ensemblid | ENSG00000219626.9 |
hgncid | 24736 |
symbol | FAM228B |
name | family with sequence similarity 228 member B |
refseq_nuc | NM_001145710.2 |
refseq_prot | NP_001139182.1 |
ensembl_nuc | ENST00000615575.5 |
ensembl_prot | ENSP00000482482.1 |
mane_status | MANE Select |
chr | chr2 |
start | 24123469 |
end | 24169638 |
strand | + |
ver | v1.2 |
region | chr2:24123469-24169638 |
region5000 | chr2:24118469-24174638 |
regionname0 | FAM228B_chr2_24123469_24169638 |
regionname5000 | FAM228B_chr2_24118469_24174638 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 324 | 242 | 68 | 49 | 93 | 7 | 24 | 72 | FAM228B_chr2_24118469_24174638 | FAM228B | copy fasta | chr2 | 24118469 | 24174638 |
a0002 | 0/1 | 324 | 27 | 8 | 5 | 6 | 2 | 5 | 4 | FAM228B_chr2_24118469_24174638 | FAM228B | copy fasta | chr2 | 24118469 | 24174638 |
a0003 | 0/0 | 319 | 20 | 2 | 3 | 11 | 3 | 1 | 8 | FAM228B_chr2_24118469_24174638 | FAM228B | copy fasta | chr2 | 24118469 | 24174638 |
a0004 | 0/0 | 324 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | copy fasta | chr2 | 24118469 | 24174638 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 975 | 141 | 21 | 36 | 67 | 4 | 13 | FAM228B_chr2_24118469_24174638 | FAM228B | copy fasta | chr2 | 24118469 | 24174638 |
c0002 | 0/0 | 975 | 47 | 12 | 8 | 18 | 1 | 8 | FAM228B_chr2_24118469_24174638 | FAM228B | copy fasta | chr2 | 24118469 | 24174638 |
c0003 | 1/0 | 975 | 33 | 27 | 3 | 1 | 1 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | copy fasta | chr2 | 24118469 | 24174638 |
c0004 | 0/0 | 974 | 19 | 2 | 3 | 10 | 3 | 1 | FAM228B_chr2_24118469_24174638 | FAM228B | copy fasta | chr2 | 24118469 | 24174638 |
c0005 | 0/1 | 975 | 16 | 8 | 0 | 5 | 1 | 1 | FAM228B_chr2_24118469_24174638 | FAM228B | copy fasta | chr2 | 24118469 | 24174638 |
c0006 | 0/0 | 975 | 15 | 4 | 2 | 6 | 0 | 3 | FAM228B_chr2_24118469_24174638 | FAM228B | copy fasta | chr2 | 24118469 | 24174638 |
c0007 | 0/0 | 975 | 9 | 0 | 4 | 1 | 1 | 3 | FAM228B_chr2_24118469_24174638 | FAM228B | copy fasta | chr2 | 24118469 | 24174638 |
c0008 | 0/0 | 975 | 3 | 3 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | copy fasta | chr2 | 24118469 | 24174638 |
c0009 | 0/0 | 975 | 2 | 0 | 1 | 0 | 0 | 1 | FAM228B_chr2_24118469_24174638 | FAM228B | copy fasta | chr2 | 24118469 | 24174638 |
c0010 | 0/0 | 975 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | copy fasta | chr2 | 24118469 | 24174638 |
c0011 | 0/0 | 975 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | copy fasta | chr2 | 24118469 | 24174638 |
c0012 | 0/0 | 975 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | copy fasta | chr2 | 24118469 | 24174638 |
c0013 | 0/0 | 974 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | copy fasta | chr2 | 24118469 | 24174638 |
c0014 | 0/0 | 975 | 1 | 0 | 0 | 0 | 1 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | copy fasta | chr2 | 24118469 | 24174638 |
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 | 1/1 | 395 | 286 | 77 | 58 | 108 | 12 | 29 | FAM228B_chr2_24118469_24174638 | FAM228B | copy fasta | chr2 | 24118469 | 24174638 |
t0002 | 0/0 | 395 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | copy fasta | chr2 | 24118469 | 24174638 |
t0003 | 0/0 | 395 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | copy fasta | chr2 | 24118469 | 24174638 |
t0004 | 0/0 | 395 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | copy fasta | chr2 | 24118469 | 24174638 |
t0005 | 0/0 | 405 | 1 | 0 | 0 | 0 | 0 | 1 | FAM228B_chr2_24118469_24174638 | FAM228B | copy fasta | chr2 | 24118469 | 24174638 |
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 | 3 | 0 | 0 | 3 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0003 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0006 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0008 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0021 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0094 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 975 | 141 | 21 | 36 | 67 | 4 | 13 | FAM228B_chr2_24118469_24174638 | FAM228B | copy fasta | chr2 | 24118469 | 24174638 |
a0001c0002 | 0/0 | 975 | 47 | 12 | 8 | 18 | 1 | 8 | FAM228B_chr2_24118469_24174638 | FAM228B | copy fasta | chr2 | 24118469 | 24174638 |
a0001c0003 | 1/0 | 975 | 33 | 27 | 3 | 1 | 1 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | copy fasta | chr2 | 24118469 | 24174638 |
a0001c0006 | 0/0 | 975 | 15 | 4 | 2 | 6 | 0 | 3 | FAM228B_chr2_24118469_24174638 | FAM228B | copy fasta | chr2 | 24118469 | 24174638 |
a0001c0008 | 0/0 | 975 | 3 | 3 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | copy fasta | chr2 | 24118469 | 24174638 |
a0001c0010 | 0/0 | 975 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | copy fasta | chr2 | 24118469 | 24174638 |
a0001c0011 | 0/0 | 975 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | copy fasta | chr2 | 24118469 | 24174638 |
a0001c0014 | 0/0 | 975 | 1 | 0 | 0 | 0 | 1 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | copy fasta | chr2 | 24118469 | 24174638 |
a0002c0005 | 0/1 | 975 | 16 | 8 | 0 | 5 | 1 | 1 | FAM228B_chr2_24118469_24174638 | FAM228B | copy fasta | chr2 | 24118469 | 24174638 |
a0002c0007 | 0/0 | 975 | 9 | 0 | 4 | 1 | 1 | 3 | FAM228B_chr2_24118469_24174638 | FAM228B | copy fasta | chr2 | 24118469 | 24174638 |
a0002c0009 | 0/0 | 975 | 2 | 0 | 1 | 0 | 0 | 1 | FAM228B_chr2_24118469_24174638 | FAM228B | copy fasta | chr2 | 24118469 | 24174638 |
a0003c0004 | 0/0 | 974 | 19 | 2 | 3 | 10 | 3 | 1 | FAM228B_chr2_24118469_24174638 | FAM228B | copy fasta | chr2 | 24118469 | 24174638 |
a0003c0013 | 0/0 | 974 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | copy fasta | chr2 | 24118469 | 24174638 |
a0004c0012 | 0/0 | 975 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | copy fasta | chr2 | 24118469 | 24174638 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 1369 | 139 | 21 | 36 | 66 | 4 | 12 | FAM228B_chr2_24118469_24174638 | FAM228B | copy fasta | chr2 | 24118469 | 24174638 |
a0001c0001t0004 | 0/0 | 1369 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | copy fasta | chr2 | 24118469 | 24174638 |
a0001c0001t0005 | 0/0 | 1379 | 1 | 0 | 0 | 0 | 0 | 1 | FAM228B_chr2_24118469_24174638 | FAM228B | copy fasta | chr2 | 24118469 | 24174638 |
a0001c0002t0001 | 0/0 | 1369 | 47 | 12 | 8 | 18 | 1 | 8 | FAM228B_chr2_24118469_24174638 | FAM228B | copy fasta | chr2 | 24118469 | 24174638 |
a0001c0003t0001 | 1/0 | 1369 | 33 | 27 | 3 | 1 | 1 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | copy fasta | chr2 | 24118469 | 24174638 |
a0001c0006t0001 | 0/0 | 1369 | 14 | 3 | 2 | 6 | 0 | 3 | FAM228B_chr2_24118469_24174638 | FAM228B | copy fasta | chr2 | 24118469 | 24174638 |
a0001c0006t0003 | 0/0 | 1369 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | copy fasta | chr2 | 24118469 | 24174638 |
a0001c0008t0001 | 0/0 | 1369 | 3 | 3 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | copy fasta | chr2 | 24118469 | 24174638 |
a0001c0010t0001 | 0/0 | 1369 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | copy fasta | chr2 | 24118469 | 24174638 |
a0001c0011t0001 | 0/0 | 1369 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | copy fasta | chr2 | 24118469 | 24174638 |
a0001c0014t0001 | 0/0 | 1369 | 1 | 0 | 0 | 0 | 1 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | copy fasta | chr2 | 24118469 | 24174638 |
a0002c0005t0001 | 0/1 | 1369 | 16 | 8 | 0 | 5 | 1 | 1 | FAM228B_chr2_24118469_24174638 | FAM228B | copy fasta | chr2 | 24118469 | 24174638 |
a0002c0007t0001 | 0/0 | 1369 | 9 | 0 | 4 | 1 | 1 | 3 | FAM228B_chr2_24118469_24174638 | FAM228B | copy fasta | chr2 | 24118469 | 24174638 |
a0002c0009t0001 | 0/0 | 1369 | 2 | 0 | 1 | 0 | 0 | 1 | FAM228B_chr2_24118469_24174638 | FAM228B | copy fasta | chr2 | 24118469 | 24174638 |
a0003c0004t0001 | 0/0 | 1368 | 19 | 2 | 3 | 10 | 3 | 1 | FAM228B_chr2_24118469_24174638 | FAM228B | copy fasta | chr2 | 24118469 | 24174638 |
a0003c0013t0002 | 0/0 | 1368 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | copy fasta | chr2 | 24118469 | 24174638 |
a0004c0012t0001 | 0/0 | 1369 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | copy fasta | chr2 | 24118469 | 24174638 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0003 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0006 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0008 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0004g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0001t0005g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0002t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0002t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0002t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0002t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0002t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0002t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0002t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0002t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0002t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0002t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0002t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0002t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0002t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0002t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0002t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0002t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0002t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0002t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0002t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0002t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0002t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0003t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0003t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0003t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0003t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0003t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0003t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0003t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0003t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0003t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0003t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0003t0001g0094 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0003t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0003t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0003t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0003t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0003t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0003t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0003t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0003t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0003t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0003t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0003t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0003t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0003t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0003t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0003t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0003t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0003t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0003t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0003t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0003t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0003t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0003t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0006t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0006t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0006t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0006t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0006t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0006t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0006t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0006t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0006t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0006t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0006t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0006t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0006t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0006t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0006t0003g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0008t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0008t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0008t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0010t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0011t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0001c0014t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0002c0005t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0002c0005t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0002c0005t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0002c0005t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0002c0005t0001g0021 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0002c0005t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0002c0005t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0002c0005t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0002c0005t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0002c0005t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0002c0005t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0002c0005t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0002c0005t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0002c0005t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0002c0005t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0002c0005t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0002c0007t0001g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0002c0007t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0002c0007t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0002c0007t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0002c0007t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0002c0007t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0002c0007t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0002c0007t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0002c0007t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0002c0009t0001g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0002c0009t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0003c0004t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0003c0004t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0003c0004t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0003c0004t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0003c0004t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0003c0004t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0003c0004t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0003c0004t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0003c0004t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0003c0004t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0003c0004t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0003c0004t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0003c0004t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0003c0004t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0003c0004t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0003c0004t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0003c0004t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0003c0004t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0003c0004t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0003c0013t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
a0004c0012t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0234 | EUR | GBR | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG00099 | hp2 | a0002 | c0005 | t0001 | g0025 | EUR | GBR | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG00140 | hp1 | a0003 | c0004 | t0001 | g0104 | EUR | GBR | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | GBR | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0186 | EUR | FIN | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG00323 | hp2 | a0003 | c0004 | t0001 | g0109 | EUR | FIN | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | CHS | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | CHS | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | CHS | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | CHS | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG00642 | hp1 | a0003 | c0004 | t0001 | g0107 | AMR | PUR | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0259 | AMR | PUR | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG00735 | hp2 | a0001 | c0002 | t0001 | g0050 | AMR | PUR | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG00741 | hp2 | a0001 | c0002 | t0001 | g0062 | AMR | PUR | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG01069 | hp1 | a0003 | c0004 | t0001 | g0105 | AMR | PUR | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG01069 | hp2 | a0002 | c0007 | t0001 | g0019 | AMR | PUR | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG01071 | hp1 | a0002 | c0007 | t0001 | g0018 | AMR | PUR | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG01074 | hp1 | a0001 | c0002 | t0001 | g0052 | AMR | PUR | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG01074 | hp2 | a0002 | c0009 | t0001 | g0037 | AMR | PUR | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0221 | AMR | PUR | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG01081 | hp2 | a0003 | c0004 | t0001 | g0106 | AMR | PUR | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG01099 | hp2 | a0001 | c0002 | t0001 | g0253 | AMR | PUR | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0235 | AMR | PUR | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG01109 | hp1 | a0001 | c0002 | t0001 | g0241 | AMR | PUR | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG01168 | hp1 | a0001 | c0002 | t0001 | g0064 | AMR | PUR | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0247 | AMR | PUR | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0200 | AMR | PUR | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG01175 | hp2 | a0004 | c0012 | t0001 | g0203 | AMR | PUR | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG01243 | hp2 | a0001 | c0003 | t0001 | g0231 | AMR | PUR | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | CLM | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG01255 | hp2 | a0001 | c0006 | t0001 | g0277 | AMR | CLM | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG01256 | hp2 | a0002 | c0007 | t0001 | g0020 | AMR | CLM | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | CLM | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG01257 | hp2 | a0001 | c0002 | t0001 | g0057 | AMR | CLM | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | CLM | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | CLM | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | CLM | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | CLM | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG01358 | hp1 | a0001 | c0003 | t0001 | g0212 | AMR | CLM | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | CLM | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG01361 | hp1 | a0001 | c0006 | t0001 | g0272 | AMR | CLM | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | CLM | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG01433 | hp1 | a0001 | c0002 | t0001 | g0051 | AMR | CLM | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | CLM | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0263 | AMR | CLM | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG01496 | hp2 | a0002 | c0007 | t0001 | g0017 | AMR | CLM | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0280 | EUR | IBS | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG01516 | hp2 | a0001 | c0014 | t0001 | g0274 | EUR | IBS | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | ACB | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG01891 | hp1 | a0001 | c0006 | t0001 | g0264 | AFR | ACB | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG01891 | hp2 | a0001 | c0003 | t0001 | g0092 | AFR | ACB | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | PEL | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG01934 | hp2 | a0001 | c0003 | t0001 | g0090 | AMR | PEL | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PEL | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0219 | AMR | PEL | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | PEL | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PEL | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG02015 | hp1 | a0003 | c0004 | t0001 | g0124 | EAS | KHV | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | KHV | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG02040 | hp1 | a0001 | c0002 | t0001 | g0080 | EAS | KHV | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG02040 | hp2 | a0002 | c0005 | t0001 | g0013 | EAS | KHV | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG02055 | hp1 | a0001 | c0003 | t0001 | g0244 | AFR | ACB | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG02055 | hp2 | a0001 | c0003 | t0001 | g0230 | AFR | ACB | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG02056 | hp1 | a0001 | c0002 | t0001 | g0073 | EAS | KHV | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | KHV | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG02071 | hp1 | a0002 | c0005 | t0001 | g0014 | EAS | KHV | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG02071 | hp2 | a0003 | c0004 | t0001 | g0112 | EAS | KHV | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | KHV | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | KHV | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG02080 | hp1 | a0003 | c0013 | t0002 | g0063 | EAS | KHV | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | KHV | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | KHV | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | KHV | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | KHV | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG02135 | hp1 | a0001 | c0002 | t0001 | g0074 | EAS | KHV | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG02135 | hp2 | a0001 | c0001 | t0004 | g0196 | EAS | KHV | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG02145 | hp1 | a0001 | c0002 | t0001 | g0242 | AFR | ACB | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | ACB | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PEL | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | PEL | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG02165 | hp2 | a0001 | c0002 | t0001 | g0061 | EAS | CDX | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG02257 | hp1 | a0001 | c0002 | t0001 | g0240 | AFR | ACB | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG02257 | hp2 | a0001 | c0003 | t0001 | g0133 | AFR | ACB | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0257 | AFR | ACB | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG02258 | hp2 | a0002 | c0005 | t0001 | g0024 | AFR | ACB | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG02280 | hp1 | a0001 | c0003 | t0001 | g0010 | AFR | ACB | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | ACB | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG02572 | hp1 | a0001 | c0002 | t0001 | g0117 | AFR | GWD | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0251 | AFR | GWD | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG02602 | hp2 | a0001 | c0006 | t0001 | g0218 | SAS | PJL | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG02615 | hp1 | a0002 | c0005 | t0001 | g0033 | AFR | GWD | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG02615 | hp2 | a0001 | c0003 | t0001 | g0162 | AFR | GWD | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | GWD | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG02622 | hp2 | a0001 | c0003 | t0001 | g0237 | AFR | GWD | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG02630 | hp1 | a0001 | c0003 | t0001 | g0211 | AFR | GWD | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG02630 | hp2 | a0003 | c0004 | t0001 | g0116 | AFR | GWD | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | GWD | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG02647 | hp2 | a0001 | c0003 | t0001 | g0163 | AFR | GWD | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG02698 | hp1 | a0001 | c0002 | t0001 | g0054 | SAS | PJL | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0181 | SAS | PJL | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG02717 | hp1 | a0001 | c0002 | t0001 | g0066 | AFR | GWD | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG02717 | hp2 | a0002 | c0005 | t0001 | g0023 | AFR | GWD | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG02723 | hp1 | a0001 | c0003 | t0001 | g0134 | AFR | GWD | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG02723 | hp2 | a0001 | c0002 | t0001 | g0070 | AFR | GWD | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG02886 | hp1 | a0001 | c0003 | t0001 | g0102 | AFR | GWD | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG02886 | hp2 | a0001 | c0002 | t0001 | g0056 | AFR | GWD | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG02897 | hp1 | a0001 | c0003 | t0001 | g0131 | AFR | GWD | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | GWD | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG02922 | hp1 | a0001 | c0003 | t0001 | g0086 | AFR | ESN | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG02922 | hp2 | a0002 | c0005 | t0001 | g0009 | AFR | ESN | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG02976 | hp1 | a0001 | c0002 | t0001 | g0239 | AFR | ESN | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG02976 | hp2 | a0001 | c0003 | t0001 | g0208 | AFR | ESN | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG03041 | hp1 | a0001 | c0008 | t0001 | g0160 | AFR | GWD | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG03041 | hp2 | a0002 | c0005 | t0001 | g0031 | AFR | GWD | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG03098 | hp1 | a0001 | c0003 | t0001 | g0256 | AFR | MSL | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0249 | AFR | MSL | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG03139 | hp1 | a0001 | c0003 | t0001 | g0210 | AFR | ESN | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG03139 | hp2 | a0001 | c0006 | t0001 | g0269 | AFR | ESN | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0250 | AFR | MSL | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG03209 | hp2 | a0001 | c0002 | t0001 | g0261 | AFR | MSL | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG03239 | hp1 | a0003 | c0004 | t0001 | g0099 | SAS | PJL | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0137 | SAS | PJL | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG03453 | hp1 | a0001 | c0003 | t0001 | g0087 | AFR | MSL | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG03453 | hp2 | a0001 | c0011 | t0001 | g0262 | AFR | MSL | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG03486 | hp1 | a0001 | c0002 | t0001 | g0069 | AFR | MSL | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG03486 | hp2 | a0002 | c0005 | t0001 | g0035 | AFR | MSL | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0143 | SAS | PJL | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG03490 | hp2 | a0001 | c0002 | t0001 | g0058 | SAS | PJL | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG03492 | hp1 | a0002 | c0007 | t0001 | g0012 | SAS | PJL | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG03492 | hp2 | a0001 | c0002 | t0001 | g0053 | SAS | PJL | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG03516 | hp1 | a0001 | c0006 | t0001 | g0265 | AFR | ESN | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG03516 | hp2 | a0001 | c0003 | t0001 | g0089 | AFR | ESN | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | GWD | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG03540 | hp2 | a0001 | c0003 | t0001 | g0209 | AFR | GWD | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | MSL | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG03579 | hp2 | a0002 | c0005 | t0001 | g0022 | AFR | MSL | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0205 | SAS | PJL | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG03669 | hp2 | a0002 | c0007 | t0001 | g0029 | SAS | PJL | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | STU | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG03688 | hp2 | a0001 | c0002 | t0001 | g0055 | SAS | STU | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG03710 | hp1 | a0001 | c0002 | t0001 | g0065 | SAS | PJL | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG03710 | hp2 | a0002 | c0007 | t0001 | g0016 | SAS | PJL | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG03831 | hp1 | a0001 | c0002 | t0001 | g0072 | SAS | BEB | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0202 | SAS | BEB | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG03834 | hp1 | a0001 | c0002 | t0001 | g0071 | SAS | BEB | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0199 | SAS | BEB | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG03927 | hp1 | a0002 | c0005 | t0001 | g0034 | SAS | BEB | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0245 | SAS | BEB | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG03942 | hp1 | a0002 | c0009 | t0001 | g0011 | SAS | BEB | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG03942 | hp2 | a0001 | c0006 | t0001 | g0268 | SAS | BEB | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0220 | SAS | STU | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG04204 | hp2 | a0001 | c0006 | t0001 | g0273 | SAS | STU | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0189 | SAS | STU | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG04228 | hp2 | a0001 | c0001 | t0005 | g0270 | SAS | STU | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | YRI | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
NA18522 | hp2 | a0001 | c0002 | t0001 | g0260 | AFR | YRI | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHB | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
NA18612 | hp2 | a0001 | c0002 | t0001 | g0049 | EAS | CHB | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | YRI | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
NA18906 | hp2 | a0001 | c0008 | t0001 | g0161 | AFR | YRI | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
NA18943 | hp2 | a0003 | c0004 | t0001 | g0111 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
NA18945 | hp1 | a0001 | c0002 | t0001 | g0041 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
NA18949 | hp1 | a0001 | c0006 | t0001 | g0275 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
NA18952 | hp1 | a0001 | c0003 | t0001 | g0190 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
NA18956 | hp1 | a0003 | c0004 | t0001 | g0114 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
NA18963 | hp2 | a0001 | c0006 | t0001 | g0276 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
NA18964 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
NA18967 | hp1 | a0001 | c0002 | t0001 | g0046 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
NA18968 | hp2 | a0001 | c0010 | t0001 | g0140 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
NA18969 | hp1 | a0001 | c0002 | t0001 | g0044 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
NA18972 | hp2 | a0003 | c0004 | t0001 | g0115 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
NA18980 | hp1 | a0001 | c0006 | t0001 | g0267 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
NA18981 | hp2 | a0001 | c0006 | t0001 | g0271 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
NA18985 | hp1 | a0001 | c0006 | t0001 | g0266 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
NA18989 | hp2 | a0001 | c0002 | t0001 | g0048 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
NA18993 | hp2 | a0003 | c0004 | t0001 | g0095 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
NA18995 | hp2 | a0002 | c0005 | t0001 | g0028 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
NA18999 | hp2 | a0002 | c0007 | t0001 | g0032 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
NA19001 | hp2 | a0003 | c0004 | t0001 | g0103 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
NA19002 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
NA19004 | hp2 | a0001 | c0006 | t0001 | g0278 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
NA19007 | hp1 | a0001 | c0002 | t0001 | g0042 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
NA19011 | hp2 | a0003 | c0004 | t0001 | g0098 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
NA19030 | hp1 | a0001 | c0003 | t0001 | g0159 | AFR | LWK | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | LWK | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
NA19043 | hp1 | a0003 | c0004 | t0001 | g0108 | AFR | LWK | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
NA19043 | hp2 | a0001 | c0006 | t0003 | g0075 | AFR | LWK | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
NA19057 | hp2 | a0003 | c0004 | t0001 | g0096 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
NA19064 | hp1 | a0001 | c0002 | t0001 | g0040 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
NA19066 | hp1 | a0001 | c0002 | t0001 | g0043 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
NA19072 | hp2 | a0001 | c0002 | t0001 | g0045 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
NA19074 | hp1 | a0002 | c0005 | t0001 | g0026 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
NA19075 | hp1 | a0001 | c0002 | t0001 | g0047 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
NA19077 | hp2 | a0001 | c0002 | t0001 | g0175 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
NA19079 | hp2 | a0003 | c0004 | t0001 | g0097 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
NA19083 | hp1 | a0002 | c0005 | t0001 | g0015 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
NA19083 | hp2 | a0001 | c0002 | t0001 | g0243 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
NA20129 | hp1 | a0001 | c0003 | t0001 | g0088 | AFR | ASW | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
NA20129 | hp2 | a0001 | c0002 | t0001 | g0281 | AFR | ASW | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
NA20752 | hp1 | a0001 | c0002 | t0001 | g0173 | EUR | TSI | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
NA20752 | hp2 | a0003 | c0004 | t0001 | g0093 | EUR | TSI | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
NA20805 | hp1 | a0001 | c0003 | t0001 | g0144 | EUR | TSI | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
NA20805 | hp2 | a0002 | c0007 | t0001 | g0027 | EUR | TSI | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
NA20905 | hp1 | a0001 | c0002 | t0001 | g0060 | SAS | GIH | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0184 | SAS | GIH | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG02109 | hp1 | a0001 | c0003 | t0001 | g0085 | AFR | ACB | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | ACB | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG02486 | hp1 | a0002 | c0005 | t0001 | g0036 | AFR | ACB | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG02486 | hp2 | a0001 | c0003 | t0001 | g0213 | AFR | ACB | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG02559 | hp1 | a0001 | c0008 | t0001 | g0238 | AFR | ACB | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG02559 | hp2 | a0001 | c0002 | t0001 | g0067 | AFR | ACB | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | MSL | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG03471 | hp2 | a0001 | c0003 | t0001 | g0091 | AFR | MSL | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG06807 | hp1 | a0001 | c0003 | t0001 | g0255 | AFR | USA | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0252 | AFR | USA | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
NA20300 | hp1 | a0001 | c0003 | t0001 | g0084 | AFR | USA | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | USA | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
NA21309 | hp1 | a0001 | c0003 | t0001 | g0158 | AFR | LWK | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | LWK | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
homoSapiens_chm13v2 | hp1 | a0002 | c0005 | t0001 | g0021 | REF | REF | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
homoSapiens_grch38 | hp1 | a0001 | c0003 | t0001 | g0094 | REF | REF | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:24135131
|
G | C | 1 | a0002 | 27 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(24): Show |
missense_variant | MODERATE | c.112G>C | p.Glu38Gln | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 3/11 | 209/1369 | 112/975 | 38/324 | chr2 | 24135131 | ||
chr2:24164308
|
GC | G | 1 | a0003 | 20 | HG00140.hp1 HG00323.hp2 HG00642.hp1 others(17): Show |
frameshift_variant | HIGH | c.907delC | p.Gln303fs | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/11 | 1004/1369 | 907/975 | 303/324 | INFO_REALIGN_3_PRIME | chr2 | 24164308 | |
chr2:24167638
|
C | T | 1 | a0004 | 1 | HG01175.hp2 | missense_variant | MODERATE | c.944C>T | p.Pro315Leu | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 10/11 | 1041/1369 | 944/975 | 315/324 | chr2 | 24167638 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:24137912
|
C | T | 1 | a0001c0014 | 1 | HG01516.hp2 | synonymous_variant | LOW | c.172C>T | p.Leu58Leu | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 4/11 | 269/1369 | 172/975 | 58/324 | chr2 | 24137912 | ||
chr2:24139381
|
T | C | 1 | a0001c0010 | 1 | NA18968.hp2 | synonymous_variant | LOW | c.372T>C | p.Phe124Phe | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/11 | 469/1369 | 372/975 | 124/324 | chr2 | 24139381 | ||
chr2:24146786
|
A | C | 1 | a0001c0008 | 3 | HG02559.hp1 HG03041.hp1 NA18906.hp2 |
synonymous_variant | LOW | c.480A>C | p.Ala160Ala | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 6/11 | 577/1369 | 480/975 | 160/324 | chr2 | 24146786 | ||
chr2:24146804
|
C | T | 10 | a0001c0001a0001c0002a0001c0006others(7): Show | 233 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(230): Show |
synonymous_variant | LOW | c.498C>T | p.Asn166Asn | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 6/11 | 595/1369 | 498/975 | 166/324 | chr2 | 24146804 | ||
chr2:24161512
|
G | A | 1 | a0001c0011 | 1 | HG03453.hp2 | synonymous_variant | LOW | c.693G>A | p.Lys231Lys | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 8/11 | 790/1369 | 693/975 | 231/324 | chr2 | 24161512 | ||
chr2:24161554
|
T | C | 7 | a0001c0001a0001c0002a0001c0010others(4): Show | 216 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(213): Show |
synonymous_variant | LOW | c.735T>C | p.Pro245Pro | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 8/11 | 832/1369 | 735/975 | 245/324 | chr2 | 24161554 | ||
chr2:24167648
|
G | A | 4 | a0001c0001a0001c0010a0002c0007others(1): Show | 152 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(149): Show |
synonymous_variant | LOW | c.954G>A | p.Gly318Gly | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 10/11 | 1051/1369 | 954/975 | 318/324 | chr2 | 24167648 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:24169375
|
A | G | 1 | a0001c0001t0005 | 1 | HG04228.hp2 | 3_prime_UTR_variant | MODIFIER | c.*34A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 11/11 | 1706 | chr2 | 24169375 | |||||
chr2:24169386
|
T | G | 1 | a0001c0001t0005 | 1 | HG04228.hp2 | 3_prime_UTR_variant | MODIFIER | c.*45T>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 11/11 | 1717 | chr2 | 24169386 | |||||
chr2:24169405
|
T | G | 1 | a0001c0001t0005 | 1 | HG04228.hp2 | 3_prime_UTR_variant | MODIFIER | c.*64T>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 11/11 | 1736 | chr2 | 24169405 | |||||
chr2:24169412
|
A | G | 1 | a0001c0001t0005 | 1 | HG04228.hp2 | 3_prime_UTR_variant | MODIFIER | c.*71A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 11/11 | 1743 | chr2 | 24169412 | |||||
chr2:24169416
|
A | T | 1 | a0001c0001t0005 | 1 | HG04228.hp2 | 3_prime_UTR_variant | MODIFIER | c.*75A>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 11/11 | 1747 | chr2 | 24169416 | |||||
chr2:24169418
|
G | C | 1 | a0001c0001t0005 | 1 | HG04228.hp2 | 3_prime_UTR_variant | MODIFIER | c.*77G>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 11/11 | 1749 | chr2 | 24169418 | |||||
chr2:24169419
|
C | T | 1 | a0001c0001t0005 | 1 | HG04228.hp2 | 3_prime_UTR_variant | MODIFIER | c.*78C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 11/11 | 1750 | chr2 | 24169419 | |||||
chr2:24169421
|
G | GTGGATTG others(3): Show |
1 | a0001c0001t0005 | 1 | HG04228.hp2 | 3_prime_UTR_variant | MODIFIER | c.*80_*81insTGGATTGG others(2): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 11/11 | 1753 | chr2 | 24169421 | |||||
chr2:24169437
|
T | C | 1 | a0003c0013t0002 | 1 | HG02080.hp1 | 3_prime_UTR_variant | MODIFIER | c.*96T>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 11/11 | 1768 | chr2 | 24169437 | |||||
chr2:24169442
|
T | G | 1 | a0001c0001t0005 | 1 | HG04228.hp2 | 3_prime_UTR_variant | MODIFIER | c.*101T>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 11/11 | 1773 | chr2 | 24169442 | |||||
chr2:24169516
|
G | A | 1 | a0001c0006t0003 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*175G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 11/11 | 1847 | chr2 | 24169516 | |||||
chr2:24169608
|
C | T | 1 | a0001c0001t0004 | 1 | HG02135.hp2 | 3_prime_UTR_variant | MODIFIER | c.*267C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 11/11 | 1939 | chr2 | 24169608 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:24123601
|
C | T | 1 | a0001c0002t0001g0281 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-33+68C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 1/10 | chr2 | 24123601 | ||||||
chr2:24123648
|
C | A | 29 | a0001c0001t0001g0030a0001c0003t0001g0010a0002c0005t0001g0009others(26): Show | 29 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.-33+115C>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 1/10 | chr2 | 24123648 | ||||||
chr2:24123824
|
A | G | 29 | a0001c0001t0001g0030a0001c0003t0001g0010a0002c0005t0001g0009others(26): Show | 29 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.-33+291A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 1/10 | chr2 | 24123824 | ||||||
chr2:24123842
|
C | G | 1 | a0001c0001t0001g0280 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-33+309C>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 1/10 | chr2 | 24123842 | ||||||
chr2:24123882
|
C | A | 1 | a0001c0001t0001g0038 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-33+349C>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 1/10 | chr2 | 24123882 | ||||||
chr2:24124055
|
C | T | 1 | a0001c0001t0001g0279 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-32-275C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 1/10 | chr2 | 24124055 | ||||||
chr2:24124093
|
C | A | 1 | a0001c0001t0001g0039 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-32-237C>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 1/10 | chr2 | 24124093 | ||||||
chr2:24124223
|
A | C | 45 | a0001c0001t0001g0030a0001c0001t0001g0263a0001c0001t0005g0270others(42): Show | 45 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(42): Show |
intron_variant | MODIFIER | c.-32-107A>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 1/10 | chr2 | 24124223 | ||||||
chr2:24125063
|
A | T | 3 | a0001c0002t0001g0260a0001c0002t0001g0261a0001c0011t0001g0262 | 3 | HG03209.hp2 HG03453.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.99+603A>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24125063 | ||||||
chr2:24125163
|
G | A | 16 | a0001c0001t0001g0263a0001c0001t0005g0270a0001c0006t0001g0264others(13): Show | 16 | HG01255.hp2 HG01361.hp1 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.99+703G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24125163 | ||||||
chr2:24125226
|
G | A | 87 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0059others(84): Show | 89 | HG00099.hp2 HG00140.hp2 HG00735.hp1 others(86): Show |
intron_variant | MODIFIER | c.99+766G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24125226 | ||||||
chr2:24125384
|
A | C | 1 | a0001c0006t0003g0075 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.99+924A>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24125384 | ||||||
chr2:24125439
|
A | G | 1 | a0001c0001t0001g0008 | 2 | HG00639.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.99+979A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24125439 | ||||||
chr2:24125494
|
G | A | 8 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(5): Show | 8 | HG01071.hp2 HG01192.hp1 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.99+1034G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24125494 | ||||||
chr2:24125512
|
C | T | 2 | a0001c0002t0001g0073a0001c0002t0001g0074 | 2 | HG02056.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.99+1052C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24125512 | ||||||
chr2:24125654
|
G | A | 1 | a0001c0002t0001g0260 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.99+1194G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24125654 | ||||||
chr2:24125921
|
A | C | 13 | a0001c0001t0005g0270a0001c0006t0001g0266a0001c0006t0001g0267others(10): Show | 13 | HG01255.hp2 HG01361.hp1 HG01516.hp2 others(10): Show |
intron_variant | MODIFIER | c.99+1461A>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24125921 | ||||||
chr2:24126046
|
A | G | 16 | a0001c0001t0001g0263a0001c0001t0005g0270a0001c0006t0001g0264others(13): Show | 16 | HG01255.hp2 HG01361.hp1 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.99+1586A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24126046 | ||||||
chr2:24126157
|
A | G | 16 | a0001c0001t0001g0263a0001c0001t0005g0270a0001c0006t0001g0264others(13): Show | 16 | HG01255.hp2 HG01361.hp1 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.99+1697A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24126157 | ||||||
chr2:24126348
|
G | T | 87 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0059others(84): Show | 89 | HG00099.hp2 HG00140.hp2 HG00735.hp1 others(86): Show |
intron_variant | MODIFIER | c.99+1888G>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24126348 | ||||||
chr2:24126592
|
A | C | 1 | a0001c0001t0001g0259 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.99+2132A>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24126592 | ||||||
chr2:24126612
|
C | CT | 13 | a0001c0001t0001g0247a0001c0001t0001g0248a0001c0001t0001g0249others(10): Show | 13 | HG01099.hp2 HG01169.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.99+2168dupT | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 24126612 | |||||
chr2:24126612
|
CT | C | 29 | a0001c0001t0001g0030a0001c0003t0001g0010a0002c0005t0001g0009others(26): Show | 29 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.99+2168delT | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 24126612 | |||||
chr2:24126663
|
C | T | 1 | a0002c0009t0001g0037 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.99+2203C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24126663 | ||||||
chr2:24126666
|
A | G | 1 | a0001c0002t0001g0071 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.99+2206A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24126666 | ||||||
chr2:24126726
|
T | C | 11 | a0001c0002t0001g0002a0001c0002t0001g0040a0001c0002t0001g0041others(8): Show | 12 | NA18612.hp2 NA18945.hp1 NA18964.hp1 others(9): Show |
intron_variant | MODIFIER | c.99+2266T>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24126726 | ||||||
chr2:24126809
|
TAGAG | T | 152 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(149): Show | 159 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(156): Show |
intron_variant | MODIFIER | c.99+2352_99+2355del others(4): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 24126809 | |||||
chr2:24126827
|
C | T | 3 | a0001c0001t0001g0068a0001c0002t0001g0069a0001c0002t0001g0070 | 3 | HG02622.hp1 HG02723.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.99+2367C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24126827 | ||||||
chr2:24126870
|
C | T | 16 | a0001c0001t0001g0263a0001c0001t0005g0270a0001c0006t0001g0264others(13): Show | 16 | HG01255.hp2 HG01361.hp1 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.99+2410C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24126870 | ||||||
chr2:24126975
|
A | T | 1 | a0001c0001t0001g0246 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.99+2515A>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24126975 | ||||||
chr2:24127699
|
A | G | 43 | a0001c0001t0001g0003a0001c0001t0001g0059a0001c0001t0001g0068others(40): Show | 45 | HG00140.hp2 HG00735.hp1 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.99+3239A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24127699 | ||||||
chr2:24127740
|
C | G | 1 | a0001c0001t0001g0245 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.99+3280C>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24127740 | ||||||
chr2:24127755
|
C | T | 1 | a0001c0003t0001g0244 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.99+3295C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24127755 | ||||||
chr2:24127854
|
G | A | 1 | a0001c0006t0003g0075 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.99+3394G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24127854 | ||||||
chr2:24127931
|
G | A | 1 | a0002c0005t0001g0009 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.99+3471G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24127931 | ||||||
chr2:24128037
|
A | G | 88 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0059others(85): Show | 90 | HG00099.hp2 HG00140.hp2 HG00735.hp1 others(87): Show |
intron_variant | MODIFIER | c.99+3577A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24128037 | ||||||
chr2:24128139
|
T | C | 28 | a0001c0001t0001g0030a0001c0003t0001g0010a0002c0005t0001g0009others(25): Show | 28 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.99+3679T>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24128139 | ||||||
chr2:24128210
|
G | A | 15 | a0001c0001t0001g0001a0001c0001t0001g0039a0001c0001t0001g0118others(12): Show | 17 | HG01192.hp2 HG01243.hp1 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.99+3750G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24128210 | ||||||
chr2:24128237
|
G | A | 34 | a0001c0001t0001g0003a0001c0001t0001g0059a0001c0001t0001g0280others(31): Show | 36 | HG00140.hp2 HG00735.hp1 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.99+3777G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24128237 | ||||||
chr2:24128271
|
T | G | 34 | a0001c0001t0001g0003a0001c0001t0001g0059a0001c0001t0001g0280others(31): Show | 36 | HG00140.hp2 HG00735.hp1 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.99+3811T>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24128271 | ||||||
chr2:24128456
|
A | C | 1 | a0002c0005t0001g0036 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.99+3996A>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24128456 | ||||||
chr2:24128614
|
G | A | 1 | a0001c0001t0001g0247 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.99+4154G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24128614 | ||||||
chr2:24128668
|
G | A | 16 | a0001c0001t0001g0263a0001c0001t0005g0270a0001c0006t0001g0264others(13): Show | 16 | HG01255.hp2 HG01361.hp1 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.99+4208G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24128668 | ||||||
chr2:24128700
|
C | CTT | 28 | a0001c0001t0001g0030a0001c0003t0001g0010a0002c0005t0001g0009others(25): Show | 28 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.99+4249_99+4250dup others(2): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 24128700 | |||||
chr2:24128722
|
C | T | 16 | a0001c0001t0001g0263a0001c0001t0005g0270a0001c0006t0001g0264others(13): Show | 16 | HG01255.hp2 HG01361.hp1 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.99+4262C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24128722 | ||||||
chr2:24128889
|
A | G | 1 | a0001c0006t0001g0265 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.99+4429A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24128889 | ||||||
chr2:24128921
|
AT | A | 34 | a0001c0001t0001g0030a0001c0002t0001g0260a0001c0002t0001g0261others(31): Show | 34 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.99+4474delT | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 24128921 | |||||
chr2:24128973
|
C | T | 1 | a0001c0002t0001g0243 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.99+4513C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24128973 | ||||||
chr2:24129085
|
G | A | 9 | a0001c0003t0001g0084a0001c0003t0001g0085a0001c0003t0001g0086others(6): Show | 9 | HG01891.hp2 HG01934.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.99+4625G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24129085 | ||||||
chr2:24129306
|
CT | C | 32 | a0001c0001t0001g0003a0001c0001t0001g0059a0001c0001t0001g0132others(29): Show | 34 | HG00140.hp2 HG00642.hp2 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.99+4862delT | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 24129306 | |||||
chr2:24129398
|
A | G | 16 | a0001c0001t0001g0263a0001c0001t0005g0270a0001c0006t0001g0264others(13): Show | 16 | HG01255.hp2 HG01361.hp1 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.99+4938A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24129398 | ||||||
chr2:24129474
|
G | A | 1 | a0001c0003t0001g0133 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.99+5014G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24129474 | ||||||
chr2:24129528
|
A | C | 87 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0059others(84): Show | 89 | HG00099.hp2 HG00140.hp2 HG00735.hp1 others(86): Show |
intron_variant | MODIFIER | c.99+5068A>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24129528 | ||||||
chr2:24129564
|
A | G | 279 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(276): Show | 288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.99+5104A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24129564 | ||||||
chr2:24129737
|
G | C | 1 | a0001c0003t0001g0084 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.99+5277G>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24129737 | ||||||
chr2:24129954
|
A | T | 87 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0059others(84): Show | 89 | HG00099.hp2 HG00140.hp2 HG00735.hp1 others(86): Show |
intron_variant | MODIFIER | c.100-5165A>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24129954 | ||||||
chr2:24129955
|
C | CT | 87 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0059others(84): Show | 89 | HG00099.hp2 HG00140.hp2 HG00735.hp1 others(86): Show |
intron_variant | MODIFIER | c.100-5164_100-5163i others(3): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24129955 | ||||||
chr2:24130040
|
G | C | 87 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0059others(84): Show | 89 | HG00099.hp2 HG00140.hp2 HG00735.hp1 others(86): Show |
intron_variant | MODIFIER | c.100-5079G>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24130040 | ||||||
chr2:24130124
|
C | G | 42 | a0001c0001t0001g0003a0001c0001t0001g0059a0001c0001t0001g0068others(39): Show | 44 | HG00140.hp2 HG00735.hp1 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.100-4995C>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24130124 | ||||||
chr2:24130193
|
C | G | 29 | a0001c0001t0001g0030a0001c0003t0001g0010a0002c0005t0001g0009others(26): Show | 29 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.100-4926C>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24130193 | ||||||
chr2:24130254
|
A | C | 5 | a0001c0002t0001g0239a0001c0002t0001g0240a0001c0002t0001g0241others(2): Show | 5 | HG01109.hp1 HG02145.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.100-4865A>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24130254 | ||||||
chr2:24130342
|
C | G | 87 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0059others(84): Show | 89 | HG00099.hp2 HG00140.hp2 HG00735.hp1 others(86): Show |
intron_variant | MODIFIER | c.100-4777C>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24130342 | ||||||
chr2:24130433
|
G | A | 1 | a0001c0003t0001g0134 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.100-4686G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24130433 | ||||||
chr2:24130436
|
A | T | 1 | a0001c0003t0001g0134 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.100-4683A>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24130436 | ||||||
chr2:24130627
|
C | G | 1 | a0001c0008t0001g0238 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.100-4492C>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24130627 | ||||||
chr2:24130675
|
T | C | 1 | a0003c0004t0001g0093 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.100-4444T>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24130675 | ||||||
chr2:24130818
|
C | T | 1 | a0001c0003t0001g0237 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.100-4301C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24130818 | ||||||
chr2:24130976
|
G | A | 16 | a0001c0001t0001g0263a0001c0001t0005g0270a0001c0006t0001g0264others(13): Show | 16 | HG01255.hp2 HG01361.hp1 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.100-4143G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24130976 | ||||||
chr2:24131120
|
C | T | 16 | a0001c0001t0001g0263a0001c0001t0005g0270a0001c0006t0001g0264others(13): Show | 16 | HG01255.hp2 HG01361.hp1 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.100-3999C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24131120 | ||||||
chr2:24131181
|
G | C | 1 | a0003c0004t0001g0095 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.100-3938G>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24131181 | ||||||
chr2:24131277
|
G | C | 29 | a0001c0001t0001g0030a0001c0003t0001g0010a0002c0005t0001g0009others(26): Show | 29 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.100-3842G>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24131277 | ||||||
chr2:24131351
|
C | G | 1 | a0001c0008t0001g0238 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.100-3768C>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24131351 | ||||||
chr2:24131359
|
A | G | 1 | a0002c0005t0001g0009 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.100-3760A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24131359 | ||||||
chr2:24131420
|
G | A | 2 | a0001c0001t0001g0135a0001c0001t0001g0136 | 2 | NA19007.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.100-3699G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24131420 | ||||||
chr2:24131426
|
C | T | 1 | a0001c0001t0001g0236 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.100-3693C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24131426 | ||||||
chr2:24131537
|
C | T | 2 | a0001c0001t0001g0234a0001c0001t0001g0235 | 2 | HG00099.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.100-3582C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24131537 | ||||||
chr2:24131558
|
A | G | 36 | a0001c0001t0001g0003a0001c0001t0001g0059a0001c0001t0001g0068others(33): Show | 38 | HG00140.hp2 HG00735.hp1 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.100-3561A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24131558 | ||||||
chr2:24131590
|
A | G | 1 | a0001c0003t0001g0244 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.100-3529A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24131590 | ||||||
chr2:24132166
|
C | T | 1 | a0001c0001t0001g0233 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.100-2953C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24132166 | ||||||
chr2:24132294
|
T | G | 1 | a0001c0001t0001g0137 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.100-2825T>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24132294 | ||||||
chr2:24132464
|
G | GT | 37 | a0001c0001t0001g0038a0001c0001t0001g0081a0001c0001t0001g0082others(34): Show | 37 | HG00438.hp1 HG00438.hp2 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.100-2629dupT | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 24132464 | |||||
chr2:24132464
|
G | GTT | 10 | a0001c0001t0001g0068a0001c0001t0001g0232a0001c0002t0001g0064others(7): Show | 10 | HG01168.hp1 HG01243.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.100-2630_100-2629d others(4): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 24132464 | |||||
chr2:24132464
|
G | GTTT | 29 | a0001c0001t0001g0003a0001c0001t0001g0059a0001c0001t0001g0280others(26): Show | 31 | HG00140.hp2 HG00735.hp1 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.100-2631_100-2629d others(5): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 24132464 | |||||
chr2:24132464
|
G | GTTTT | 9 | a0001c0002t0001g0047a0001c0002t0001g0048a0001c0002t0001g0061others(6): Show | 9 | HG00741.hp2 HG02080.hp1 HG02165.hp2 others(6): Show |
intron_variant | MODIFIER | c.100-2632_100-2629d others(6): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 24132464 | |||||
chr2:24132464
|
GT | G | 43 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(40): Show | 46 | HG00621.hp1 HG00639.hp1 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.100-2629delT | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 24132464 | |||||
chr2:24132464
|
GTTTTTTT others(7): Show |
G | 16 | a0001c0001t0001g0263a0001c0001t0005g0270a0001c0006t0001g0264others(13): Show | 16 | HG01255.hp2 HG01361.hp1 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.100-2642_100-2629d others(16): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 24132464 | |||||
chr2:24132492
|
G | A | 2 | a0001c0002t0001g0050a0001c0002t0001g0051 | 2 | HG00735.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.100-2627G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24132492 | ||||||
chr2:24132553
|
C | T | 1 | a0003c0013t0002g0063 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.100-2566C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24132553 | ||||||
chr2:24132658
|
T | A | 1 | a0001c0001t0001g0138 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.100-2461T>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24132658 | ||||||
chr2:24132699
|
A | G | 29 | a0001c0001t0001g0030a0001c0003t0001g0010a0002c0005t0001g0009others(26): Show | 29 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.100-2420A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24132699 | ||||||
chr2:24132875
|
G | C | 1 | a0003c0004t0001g0095 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.100-2244G>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24132875 | ||||||
chr2:24133096
|
A | G | 1 | a0003c0004t0001g0114 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.100-2023A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24133096 | ||||||
chr2:24133257
|
G | A | 3 | a0001c0001t0001g0263a0001c0006t0001g0264a0001c0006t0001g0265 | 3 | HG01496.hp1 HG01891.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.100-1862G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24133257 | ||||||
chr2:24133298
|
CT | C | 29 | a0001c0001t0001g0030a0001c0003t0001g0010a0002c0005t0001g0009others(26): Show | 29 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.100-1820delT | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24133298 | ||||||
chr2:24133586
|
T | G | 42 | a0001c0001t0001g0003a0001c0001t0001g0059a0001c0001t0001g0068others(39): Show | 44 | HG00140.hp2 HG00735.hp1 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.100-1533T>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24133586 | ||||||
chr2:24133606
|
C | T | 29 | a0001c0001t0001g0030a0001c0003t0001g0010a0002c0005t0001g0009others(26): Show | 29 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.100-1513C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24133606 | ||||||
chr2:24133656
|
A | G | 29 | a0001c0001t0001g0030a0001c0003t0001g0010a0002c0005t0001g0009others(26): Show | 29 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.100-1463A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24133656 | ||||||
chr2:24133858
|
G | A | 1 | a0001c0002t0001g0066 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.100-1261G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24133858 | ||||||
chr2:24134132
|
A | G | 1 | a0001c0003t0001g0244 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.100-987A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24134132 | ||||||
chr2:24134346
|
T | C | 1 | a0001c0002t0001g0066 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.100-773T>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24134346 | ||||||
chr2:24134373
|
C | T | 11 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0150others(8): Show | 13 | HG00621.hp1 HG02056.hp2 HG02074.hp2 others(10): Show |
intron_variant | MODIFIER | c.100-746C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24134373 | ||||||
chr2:24134593
|
G | A | 87 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0059others(84): Show | 89 | HG00099.hp2 HG00140.hp2 HG00735.hp1 others(86): Show |
intron_variant | MODIFIER | c.100-526G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24134593 | ||||||
chr2:24134594
|
T | G | 1 | a0001c0001t0001g0150 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.100-525T>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24134594 | ||||||
chr2:24134787
|
T | C | 87 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0059others(84): Show | 89 | HG00099.hp2 HG00140.hp2 HG00735.hp1 others(86): Show |
intron_variant | MODIFIER | c.100-332T>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24134787 | ||||||
chr2:24134932
|
G | A | 1 | a0001c0003t0001g0158 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.100-187G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24134932 | ||||||
chr2:24134941
|
A | G | 1 | a0002c0005t0001g0031 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.100-178A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24134941 | ||||||
chr2:24134956
|
G | A | 3 | a0001c0002t0001g0260a0001c0002t0001g0261a0001c0011t0001g0262 | 3 | HG03209.hp2 HG03453.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.100-163G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24134956 | ||||||
chr2:24135208
|
G | T | 2 | a0001c0001t0001g0149a0001c0001t0001g0206 | 2 | HG01346.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.168+21G>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 3/10 | chr2 | 24135208 | ||||||
chr2:24135290
|
A | C | 29 | a0001c0001t0001g0030a0001c0003t0001g0010a0002c0005t0001g0009others(26): Show | 29 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.168+103A>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 3/10 | chr2 | 24135290 | ||||||
chr2:24135474
|
C | T | 29 | a0001c0001t0001g0030a0001c0003t0001g0010a0002c0005t0001g0009others(26): Show | 29 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.168+287C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 3/10 | chr2 | 24135474 | ||||||
chr2:24135782
|
C | T | 129 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(126): Show | 136 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(133): Show |
intron_variant | MODIFIER | c.168+595C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 3/10 | chr2 | 24135782 | ||||||
chr2:24135804
|
A | T | 1 | a0001c0001t0001g0205 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.168+617A>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 3/10 | chr2 | 24135804 | ||||||
chr2:24135845
|
A | G | 1 | a0001c0008t0001g0238 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.168+658A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 3/10 | chr2 | 24135845 | ||||||
chr2:24135887
|
G | A | 3 | a0001c0001t0001g0068a0001c0002t0001g0069a0001c0002t0001g0070 | 3 | HG02622.hp1 HG02723.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.168+700G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 3/10 | chr2 | 24135887 | ||||||
chr2:24135916
|
C | T | 29 | a0001c0001t0001g0030a0001c0003t0001g0010a0002c0005t0001g0009others(26): Show | 29 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.168+729C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 3/10 | chr2 | 24135916 | ||||||
chr2:24135917
|
A | C | 29 | a0001c0001t0001g0030a0001c0003t0001g0010a0002c0005t0001g0009others(26): Show | 29 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.168+730A>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 3/10 | chr2 | 24135917 | ||||||
chr2:24135966
|
A | G | 279 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(276): Show | 288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.168+779A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 3/10 | chr2 | 24135966 | ||||||
chr2:24135976
|
G | GT | 47 | a0001c0001t0001g0038a0001c0001t0001g0068a0001c0001t0001g0113others(44): Show | 47 | HG00438.hp1 HG00438.hp2 HG01109.hp1 others(44): Show |
intron_variant | MODIFIER | c.168+807dupT | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr2 | 24135976 | |||||
chr2:24135976
|
GT | G | 28 | a0001c0003t0001g0010a0001c0003t0001g0085a0002c0005t0001g0009others(25): Show | 28 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.168+807delT | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr2 | 24135976 | |||||
chr2:24136048
|
C | A | 1 | a0001c0003t0001g0010 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.168+861C>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 3/10 | chr2 | 24136048 | ||||||
chr2:24136053
|
C | CT | 125 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(122): Show | 132 | HG00099.hp1 HG00323.hp1 HG00621.hp1 others(129): Show |
intron_variant | MODIFIER | c.168+892dupT | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr2 | 24136053 | |||||
chr2:24136053
|
C | CTT | 52 | a0001c0001t0001g0030a0001c0001t0001g0038a0001c0001t0001g0125others(49): Show | 52 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(49): Show |
intron_variant | MODIFIER | c.168+891_168+892dup others(2): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr2 | 24136053 | |||||
chr2:24136053
|
C | CTTT | 7 | a0001c0006t0001g0265a0001c0006t0001g0266a0001c0006t0001g0278others(4): Show | 7 | HG02486.hp1 HG03516.hp1 HG03927.hp1 others(4): Show |
intron_variant | MODIFIER | c.168+890_168+892dup others(3): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr2 | 24136053 | |||||
chr2:24136053
|
CT | C | 28 | a0001c0001t0001g0003a0001c0001t0001g0280a0001c0002t0001g0002others(25): Show | 30 | HG00140.hp2 HG00735.hp1 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.168+892delT | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr2 | 24136053 | |||||
chr2:24136092
|
C | T | 2 | a0002c0005t0001g0026a0002c0005t0001g0028 | 2 | NA18995.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.168+905C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 3/10 | chr2 | 24136092 | ||||||
chr2:24136551
|
C | T | 1 | a0001c0001t0001g0030 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.169-1358C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 3/10 | chr2 | 24136551 | ||||||
chr2:24136572
|
A | G | 3 | a0001c0001t0001g0068a0001c0002t0001g0069a0001c0002t0001g0070 | 3 | HG02622.hp1 HG02723.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.169-1337A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 3/10 | chr2 | 24136572 | ||||||
chr2:24136652
|
C | T | 1 | a0001c0001t0004g0196 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.169-1257C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 3/10 | chr2 | 24136652 | ||||||
chr2:24136755
|
G | A | 1 | a0001c0002t0001g0061 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.169-1154G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 3/10 | chr2 | 24136755 | ||||||
chr2:24136774
|
A | G | 4 | a0001c0001t0001g0214a0001c0001t0001g0223a0001c0001t0001g0224others(1): Show | 4 | HG02083.hp1 NA18949.hp2 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.169-1135A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 3/10 | chr2 | 24136774 | ||||||
chr2:24136852
|
C | T | 29 | a0001c0001t0001g0030a0001c0003t0001g0010a0002c0005t0001g0009others(26): Show | 29 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.169-1057C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 3/10 | chr2 | 24136852 | ||||||
chr2:24136880
|
T | G | 1 | a0001c0003t0001g0159 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.169-1029T>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 3/10 | chr2 | 24136880 | ||||||
chr2:24136925
|
T | C | 1 | a0001c0001t0004g0196 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.169-984T>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 3/10 | chr2 | 24136925 | ||||||
chr2:24137014
|
T | A | 16 | a0001c0001t0001g0263a0001c0001t0005g0270a0001c0006t0001g0264others(13): Show | 16 | HG01255.hp2 HG01361.hp1 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.169-895T>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 3/10 | chr2 | 24137014 | ||||||
chr2:24137054
|
T | C | 1 | a0001c0001t0001g0081 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.169-855T>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 3/10 | chr2 | 24137054 | ||||||
chr2:24137158
|
G | A | 1 | a0002c0005t0001g0036 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.169-751G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 3/10 | chr2 | 24137158 | ||||||
chr2:24137321
|
T | G | 1 | a0001c0001t0001g0215 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.169-588T>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 3/10 | chr2 | 24137321 | ||||||
chr2:24137516
|
G | A | 2 | a0001c0001t0001g0164a0001c0001t0001g0165 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.169-393G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 3/10 | chr2 | 24137516 | ||||||
chr2:24137641
|
C | T | 2 | a0001c0001t0001g0030a0001c0003t0001g0010 | 2 | HG01109.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.169-268C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 3/10 | chr2 | 24137641 | ||||||
chr2:24137859
|
C | T | 2 | a0001c0003t0001g0213a0001c0003t0001g0231 | 2 | HG01243.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.169-50C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 3/10 | chr2 | 24137859 | ||||||
chr2:24138200
|
C | G | 1 | a0001c0006t0001g0277 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.360+100C>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 4/10 | chr2 | 24138200 | ||||||
chr2:24138441
|
A | G | 1 | a0001c0003t0001g0159 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.360+341A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 4/10 | chr2 | 24138441 | ||||||
chr2:24138641
|
A | G | 1 | a0001c0001t0001g0195 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.360+541A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 4/10 | chr2 | 24138641 | ||||||
chr2:24138689
|
C | T | 16 | a0001c0001t0001g0263a0001c0001t0005g0270a0001c0006t0001g0264others(13): Show | 16 | HG01255.hp2 HG01361.hp1 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.360+589C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 4/10 | chr2 | 24138689 | ||||||
chr2:24138945
|
C | CA | 47 | a0001c0001t0001g0003a0001c0001t0001g0059a0001c0001t0001g0068others(44): Show | 49 | HG00140.hp2 HG00735.hp1 HG00735.hp2 others(46): Show |
intron_variant | MODIFIER | c.361-410dupA | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 24138945 | |||||
chr2:24138945
|
C | CAA | 28 | a0001c0001t0001g0030a0001c0003t0001g0010a0002c0005t0001g0009others(25): Show | 28 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.361-411_361-410dup others(2): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 24138945 | |||||
chr2:24138945
|
CA | C | 21 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0110others(18): Show | 21 | HG00140.hp1 HG00323.hp2 HG00642.hp1 others(18): Show |
intron_variant | MODIFIER | c.361-410delA | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 24138945 | |||||
chr2:24138947
|
A | C | 1 | a0003c0004t0001g0109 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.361-423A>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 4/10 | chr2 | 24138947 | ||||||
chr2:24139037
|
C | T | 1 | a0001c0003t0001g0237 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.361-333C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 4/10 | chr2 | 24139037 | ||||||
chr2:24139092
|
G | A | 127 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(124): Show | 134 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.361-278G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 4/10 | chr2 | 24139092 | ||||||
chr2:24139198
|
T | G | 3 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0168 | 3 | NA18952.hp2 NA19054.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.361-172T>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 4/10 | chr2 | 24139198 | ||||||
chr2:24139344
|
T | G | 1 | a0001c0001t0001g0169 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.361-26T>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 4/10 | chr2 | 24139344 | ||||||
chr2:24139566
|
T | A | 1 | a0001c0001t0001g0170 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.441+116T>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24139566 | ||||||
chr2:24139618
|
A | G | 1 | a0001c0001t0001g0136 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.441+168A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24139618 | ||||||
chr2:24139658
|
T | C | 16 | a0001c0001t0001g0263a0001c0001t0005g0270a0001c0006t0001g0264others(13): Show | 16 | HG01255.hp2 HG01361.hp1 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.441+208T>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24139658 | ||||||
chr2:24139660
|
G | A | 1 | a0001c0001t0001g0205 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.441+210G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24139660 | ||||||
chr2:24139666
|
T | C | 1 | a0003c0004t0001g0115 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.441+216T>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24139666 | ||||||
chr2:24139674
|
G | A | 2 | a0001c0001t0001g0171a0001c0001t0001g0197 | 2 | NA18971.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.441+224G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24139674 | ||||||
chr2:24140052
|
T | A | 2 | a0003c0004t0001g0098a0003c0004t0001g0111 | 2 | NA18943.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.441+602T>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24140052 | ||||||
chr2:24140095
|
A | G | 3 | a0001c0001t0001g0068a0001c0002t0001g0069a0001c0002t0001g0070 | 3 | HG02622.hp1 HG02723.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.441+645A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24140095 | ||||||
chr2:24140908
|
GC | G | 16 | a0001c0001t0001g0263a0001c0001t0005g0270a0001c0006t0001g0264others(13): Show | 16 | HG01255.hp2 HG01361.hp1 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.441+1460delC | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr2 | 24140908 | |||||
chr2:24141015
|
G | T | 2 | a0003c0004t0001g0098a0003c0004t0001g0111 | 2 | NA18943.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.441+1565G>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24141015 | ||||||
chr2:24141068
|
A | G | 29 | a0001c0001t0001g0030a0001c0003t0001g0010a0002c0005t0001g0009others(26): Show | 29 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.441+1618A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24141068 | ||||||
chr2:24141139
|
G | A | 154 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(151): Show | 161 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(158): Show |
intron_variant | MODIFIER | c.441+1689G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24141139 | ||||||
chr2:24141207
|
T | C | 2 | a0001c0001t0001g0030a0001c0003t0001g0010 | 2 | HG01109.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.441+1757T>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24141207 | ||||||
chr2:24141224
|
G | A | 3 | a0001c0002t0001g0052a0001c0002t0001g0062a0001c0002t0001g0064 | 3 | HG00741.hp2 HG01074.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.441+1774G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24141224 | ||||||
chr2:24141463
|
C | G | 1 | a0001c0002t0001g0051 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.441+2013C>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24141463 | ||||||
chr2:24141534
|
G | A | 1 | a0001c0001t0001g0172 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.441+2084G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24141534 | ||||||
chr2:24141687
|
G | T | 87 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0059others(84): Show | 89 | HG00099.hp2 HG00140.hp2 HG00735.hp1 others(86): Show |
intron_variant | MODIFIER | c.441+2237G>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24141687 | ||||||
chr2:24141709
|
G | A | 1 | a0003c0004t0001g0099 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.441+2259G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24141709 | ||||||
chr2:24141866
|
C | T | 42 | a0001c0001t0001g0003a0001c0001t0001g0059a0001c0001t0001g0068others(39): Show | 44 | HG00140.hp2 HG00735.hp1 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.441+2416C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24141866 | ||||||
chr2:24141925
|
A | G | 29 | a0001c0001t0001g0030a0001c0003t0001g0010a0002c0005t0001g0009others(26): Show | 29 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.441+2475A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24141925 | ||||||
chr2:24142084
|
C | T | 2 | a0001c0001t0001g0194a0001c0001t0001g0225 | 2 | NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.441+2634C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24142084 | ||||||
chr2:24142364
|
A | G | 4 | a0001c0001t0001g0146a0001c0001t0001g0221a0001c0001t0001g0222others(1): Show | 4 | HG00639.hp1 HG01081.hp1 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.441+2914A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24142364 | ||||||
chr2:24142390
|
C | A | 42 | a0001c0001t0001g0003a0001c0001t0001g0059a0001c0001t0001g0068others(39): Show | 44 | HG00140.hp2 HG00735.hp1 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.441+2940C>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24142390 | ||||||
chr2:24142403
|
T | G | 1 | a0001c0002t0001g0173 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.441+2953T>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24142403 | ||||||
chr2:24142599
|
A | G | 2 | a0001c0001t0001g0135a0001c0001t0001g0136 | 2 | NA19007.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.441+3149A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24142599 | ||||||
chr2:24143045
|
G | A | 1 | a0001c0002t0001g0064 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.441+3595G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24143045 | ||||||
chr2:24143118
|
C | T | 29 | a0001c0001t0001g0030a0001c0002t0001g0080a0001c0003t0001g0010others(26): Show | 29 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.442-3630C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24143118 | ||||||
chr2:24143262
|
C | G | 35 | a0001c0001t0001g0003a0001c0001t0001g0059a0001c0001t0001g0068others(32): Show | 37 | HG00140.hp2 HG00735.hp1 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.442-3486C>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24143262 | ||||||
chr2:24143319
|
T | C | 123 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(120): Show | 130 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.442-3429T>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24143319 | ||||||
chr2:24143326
|
GCC | G | 25 | a0001c0001t0001g0132a0001c0001t0001g0145a0001c0001t0001g0148others(22): Show | 25 | HG01074.hp2 HG01243.hp2 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.442-3420_442-3419d others(4): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr2 | 24143326 | |||||
chr2:24143328
|
C | A | 2 | a0001c0002t0001g0055a0001c0003t0001g0255 | 2 | HG03688.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.442-3420C>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24143328 | ||||||
chr2:24143328
|
C | G | 40 | a0001c0001t0001g0059a0001c0001t0001g0170a0001c0001t0001g0191others(37): Show | 41 | HG00735.hp2 HG00741.hp2 HG01074.hp1 others(38): Show |
intron_variant | MODIFIER | c.442-3420C>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24143328 | ||||||
chr2:24143328
|
C | T | 42 | a0001c0001t0001g0137a0001c0001t0001g0192a0001c0001t0001g0193others(39): Show | 42 | HG00099.hp2 HG00741.hp1 HG01069.hp2 others(39): Show |
intron_variant | MODIFIER | c.442-3420C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24143328 | ||||||
chr2:24143329
|
C | T | 41 | a0001c0001t0001g0059a0001c0001t0001g0170a0001c0001t0001g0191others(38): Show | 42 | HG00735.hp2 HG00741.hp2 HG01074.hp1 others(39): Show |
intron_variant | MODIFIER | c.442-3419C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24143329 | ||||||
chr2:24143330
|
G | A | 1 | a0001c0006t0003g0075 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.442-3418G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24143330 | ||||||
chr2:24143332
|
C | T | 26 | a0001c0001t0001g0132a0001c0001t0001g0145a0001c0001t0001g0148others(23): Show | 26 | HG01074.hp2 HG01243.hp2 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.442-3416C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24143332 | ||||||
chr2:24143341
|
C | T | 1 | a0001c0002t0001g0243 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.442-3407C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24143341 | ||||||
chr2:24143384
|
T | C | 28 | a0001c0001t0001g0078a0001c0001t0001g0100a0001c0001t0001g0101others(25): Show | 28 | HG00140.hp1 HG00323.hp2 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.442-3364T>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24143384 | ||||||
chr2:24143394
|
T | C | 99 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(96): Show | 103 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.442-3354T>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24143394 | ||||||
chr2:24143395
|
C | T | 97 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(94): Show | 101 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.442-3353C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24143395 | ||||||
chr2:24143400
|
T | C | 1 | a0001c0001t0001g0132 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.442-3348T>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24143400 | ||||||
chr2:24143401
|
A | G | 18 | a0001c0001t0001g0030a0001c0001t0001g0189a0001c0001t0001g0202others(15): Show | 18 | HG00099.hp2 HG01109.hp2 HG01261.hp2 others(15): Show |
intron_variant | MODIFIER | c.442-3347A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24143401 | ||||||
chr2:24143474
|
A | T | 1 | a0001c0002t0001g0066 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.442-3274A>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24143474 | ||||||
chr2:24143523
|
A | T | 1 | a0001c0001t0001g0280 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.442-3225A>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24143523 | ||||||
chr2:24143643
|
G | A | 2 | a0001c0001t0001g0076a0001c0001t0001g0081 | 2 | HG02109.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.442-3105G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24143643 | ||||||
chr2:24143746
|
TTAA | T | 7 | a0001c0002t0001g0239a0001c0002t0001g0240a0001c0002t0001g0241others(4): Show | 7 | HG01109.hp1 HG01358.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.442-2998_442-2996d others(5): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr2 | 24143746 | |||||
chr2:24143949
|
G | T | 16 | a0001c0002t0001g0080a0002c0005t0001g0009a0002c0005t0001g0013others(13): Show | 16 | HG00099.hp2 HG02040.hp1 HG02040.hp2 others(13): Show |
intron_variant | MODIFIER | c.442-2799G>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24143949 | ||||||
chr2:24143957
|
A | G | 2 | a0001c0001t0001g0219a0001c0001t0001g0227 | 2 | HG01346.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.442-2791A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24143957 | ||||||
chr2:24143959
|
G | A | 59 | a0001c0001t0001g0003a0001c0001t0001g0059a0001c0001t0001g0068others(56): Show | 61 | HG00099.hp2 HG00140.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.442-2789G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24143959 | ||||||
chr2:24143996
|
C | CA | 159 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(156): Show | 166 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(163): Show |
intron_variant | MODIFIER | c.442-2735dupA | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr2 | 24143996 | |||||
chr2:24144072
|
G | A | 1 | a0001c0011t0001g0262 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.442-2676G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24144072 | ||||||
chr2:24144090
|
G | A | 1 | a0001c0006t0003g0075 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.442-2658G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24144090 | ||||||
chr2:24144120
|
T | C | 1 | a0001c0001t0001g0119 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.442-2628T>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24144120 | ||||||
chr2:24144162
|
C | T | 1 | a0001c0002t0001g0067 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.442-2586C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24144162 | ||||||
chr2:24144252
|
C | A | 162 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(159): Show | 169 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(166): Show |
intron_variant | MODIFIER | c.442-2496C>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24144252 | ||||||
chr2:24144327
|
C | T | 1 | a0001c0002t0001g0066 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.442-2421C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24144327 | ||||||
chr2:24144329
|
C | T | 1 | a0001c0001t0001g0030 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.442-2419C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24144329 | ||||||
chr2:24144330
|
G | A | 1 | a0001c0006t0003g0075 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.442-2418G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24144330 | ||||||
chr2:24144335
|
G | T | 163 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(160): Show | 170 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(167): Show |
intron_variant | MODIFIER | c.442-2413G>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24144335 | ||||||
chr2:24144405
|
G | A | 61 | a0001c0001t0001g0003a0001c0001t0001g0059a0001c0001t0001g0068others(58): Show | 63 | HG00099.hp2 HG00140.hp2 HG00735.hp1 others(60): Show |
intron_variant | MODIFIER | c.442-2343G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24144405 | ||||||
chr2:24144670
|
C | T | 163 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(160): Show | 170 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(167): Show |
intron_variant | MODIFIER | c.442-2078C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24144670 | ||||||
chr2:24144699
|
C | T | 1 | a0001c0002t0001g0064 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.442-2049C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24144699 | ||||||
chr2:24144783
|
T | C | 10 | a0001c0001t0001g0039a0001c0001t0001g0118a0001c0001t0001g0120others(7): Show | 10 | HG01192.hp2 HG01243.hp1 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.442-1965T>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24144783 | ||||||
chr2:24144958
|
C | T | 162 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(159): Show | 169 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(166): Show |
intron_variant | MODIFIER | c.442-1790C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24144958 | ||||||
chr2:24144959
|
G | A | 1 | a0002c0005t0001g0036 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.442-1789G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24144959 | ||||||
chr2:24145042
|
G | C | 1 | a0001c0002t0001g0055 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.442-1706G>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24145042 | ||||||
chr2:24145124
|
G | A | 61 | a0001c0001t0001g0003a0001c0001t0001g0059a0001c0001t0001g0068others(58): Show | 63 | HG00099.hp2 HG00140.hp2 HG00735.hp1 others(60): Show |
intron_variant | MODIFIER | c.442-1624G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24145124 | ||||||
chr2:24145300
|
G | A | 6 | a0001c0003t0001g0208a0001c0003t0001g0209a0001c0003t0001g0210others(3): Show | 6 | HG01358.hp1 HG02055.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.442-1448G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24145300 | ||||||
chr2:24145560
|
C | T | 1 | a0002c0007t0001g0020 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.442-1188C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24145560 | ||||||
chr2:24145627
|
C | T | 1 | a0001c0001t0001g0143 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.442-1121C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24145627 | ||||||
chr2:24145706
|
CT | C | 214 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(211): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.442-1025delT | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr2 | 24145706 | |||||
chr2:24145728
|
C | T | 1 | a0001c0001t0001g0224 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.442-1020C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24145728 | ||||||
chr2:24145765
|
C | T | 1 | a0001c0003t0001g0244 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.442-983C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24145765 | ||||||
chr2:24145810
|
T | G | 10 | a0001c0003t0001g0084a0001c0003t0001g0085a0001c0003t0001g0086others(7): Show | 10 | HG01891.hp2 HG01934.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.442-938T>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24145810 | ||||||
chr2:24145841
|
A | G | 2 | a0001c0002t0001g0066a0001c0002t0001g0067 | 2 | HG02559.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.442-907A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24145841 | ||||||
chr2:24145879
|
C | T | 162 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(159): Show | 169 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(166): Show |
intron_variant | MODIFIER | c.442-869C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24145879 | ||||||
chr2:24145927
|
C | G | 223 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(220): Show | 232 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.442-821C>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24145927 | ||||||
chr2:24146008
|
T | G | 18 | a0003c0004t0001g0095a0003c0004t0001g0096a0003c0004t0001g0097others(15): Show | 18 | HG00140.hp1 HG00323.hp2 HG00642.hp1 others(15): Show |
intron_variant | MODIFIER | c.442-740T>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24146008 | ||||||
chr2:24146104
|
A | G | 2 | a0001c0002t0001g0260a0001c0002t0001g0261 | 2 | HG03209.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.442-644A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24146104 | ||||||
chr2:24146149
|
T | C | 162 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(159): Show | 169 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(166): Show |
intron_variant | MODIFIER | c.442-599T>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24146149 | ||||||
chr2:24146454
|
T | A | 1 | a0001c0001t0001g0279 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.442-294T>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24146454 | ||||||
chr2:24146535
|
C | G | 2 | a0001c0002t0001g0073a0001c0002t0001g0074 | 2 | HG02056.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.442-213C>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24146535 | ||||||
chr2:24146650
|
G | A | 1 | a0001c0006t0001g0277 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.442-98G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24146650 | ||||||
chr2:24147214
|
C | T | 16 | a0001c0002t0001g0080a0002c0005t0001g0009a0002c0005t0001g0013others(13): Show | 16 | HG00099.hp2 HG02040.hp1 HG02040.hp2 others(13): Show |
intron_variant | MODIFIER | c.686+128C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24147214 | ||||||
chr2:24147780
|
G | A | 2 | a0001c0001t0001g0249a0001c0001t0001g0257 | 2 | HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.686+694G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24147780 | ||||||
chr2:24147916
|
C | CT | 6 | a0002c0005t0001g0022a0002c0005t0001g0023a0003c0004t0001g0093others(3): Show | 6 | HG00642.hp1 HG02630.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.686+846dupT | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24147916 | |||||
chr2:24147916
|
CT | C | 171 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(168): Show | 179 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.686+846delT | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24147916 | |||||
chr2:24148236
|
A | T | 1 | a0002c0005t0001g0009 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.686+1150A>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24148236 | ||||||
chr2:24148821
|
T | C | 163 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(160): Show | 170 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(167): Show |
intron_variant | MODIFIER | c.686+1735T>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24148821 | ||||||
chr2:24148947
|
T | A | 3 | a0001c0003t0001g0086a0001c0003t0001g0087a0001c0003t0001g0088 | 3 | HG02922.hp1 HG03453.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.686+1861T>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24148947 | ||||||
chr2:24149055
|
G | A | 224 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(221): Show | 233 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.686+1969G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24149055 | ||||||
chr2:24149092
|
C | T | 162 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(159): Show | 169 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(166): Show |
intron_variant | MODIFIER | c.686+2006C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24149092 | ||||||
chr2:24149269
|
G | C | 163 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(160): Show | 170 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(167): Show |
intron_variant | MODIFIER | c.686+2183G>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24149269 | ||||||
chr2:24149549
|
C | G | 2 | a0002c0005t0001g0024a0002c0005t0001g0025 | 2 | HG00099.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.686+2463C>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24149549 | ||||||
chr2:24149579
|
C | T | 148 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(145): Show | 155 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(152): Show |
intron_variant | MODIFIER | c.686+2493C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24149579 | ||||||
chr2:24149651
|
T | G | 1 | a0001c0002t0001g0066 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.686+2565T>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24149651 | ||||||
chr2:24149797
|
G | A | 39 | a0001c0001t0001g0003a0001c0001t0001g0059a0001c0001t0001g0139others(36): Show | 41 | HG00140.hp2 HG00735.hp1 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.686+2711G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24149797 | ||||||
chr2:24149945
|
A | G | 163 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(160): Show | 170 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(167): Show |
intron_variant | MODIFIER | c.686+2859A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24149945 | ||||||
chr2:24150083
|
G | T | 16 | a0001c0002t0001g0080a0002c0005t0001g0009a0002c0005t0001g0013others(13): Show | 16 | HG00099.hp2 HG02040.hp1 HG02040.hp2 others(13): Show |
intron_variant | MODIFIER | c.686+2997G>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24150083 | ||||||
chr2:24150126
|
A | AG | 224 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(221): Show | 233 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.686+3040_686+3041i others(3): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24150126 | ||||||
chr2:24150143
|
G | T | 1 | a0003c0004t0001g0106 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.686+3057G>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24150143 | ||||||
chr2:24150280
|
A | G | 59 | a0001c0001t0001g0003a0001c0001t0001g0059a0001c0001t0001g0068others(56): Show | 61 | HG00099.hp2 HG00140.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.686+3194A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24150280 | ||||||
chr2:24150321
|
G | A | 2 | a0001c0002t0001g0050a0001c0002t0001g0051 | 2 | HG00735.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.686+3235G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24150321 | ||||||
chr2:24150627
|
A | T | 14 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0150others(11): Show | 16 | HG00621.hp1 HG02056.hp2 HG02074.hp2 others(13): Show |
intron_variant | MODIFIER | c.686+3541A>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24150627 | ||||||
chr2:24150633
|
C | T | 142 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(139): Show | 149 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(146): Show |
intron_variant | MODIFIER | c.686+3547C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24150633 | ||||||
chr2:24150799
|
T | C | 162 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(159): Show | 169 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(166): Show |
intron_variant | MODIFIER | c.686+3713T>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24150799 | ||||||
chr2:24151260
|
T | C | 4 | a0001c0001t0001g0100a0001c0001t0001g0137a0001c0001t0001g0192others(1): Show | 4 | HG00741.hp1 HG01099.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.686+4174T>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24151260 | ||||||
chr2:24151274
|
GTTTTGTT | G | 3 | a0001c0001t0001g0068a0001c0002t0001g0069a0001c0002t0001g0070 | 3 | HG02622.hp1 HG02723.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.686+4207_686+4213d others(9): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24151274 | |||||
chr2:24151444
|
C | T | 61 | a0001c0001t0001g0003a0001c0001t0001g0059a0001c0001t0001g0068others(58): Show | 63 | HG00099.hp2 HG00140.hp2 HG00735.hp1 others(60): Show |
intron_variant | MODIFIER | c.686+4358C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24151444 | ||||||
chr2:24151452
|
G | A | 11 | a0001c0002t0001g0002a0001c0002t0001g0040a0001c0002t0001g0041others(8): Show | 12 | NA18612.hp2 NA18945.hp1 NA18964.hp1 others(9): Show |
intron_variant | MODIFIER | c.686+4366G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24151452 | ||||||
chr2:24151534
|
C | T | 4 | a0001c0001t0001g0003a0001c0001t0001g0059a0001c0001t0001g0280others(1): Show | 5 | HG00140.hp2 HG00735.hp1 HG01106.hp2 others(2): Show |
intron_variant | MODIFIER | c.686+4448C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24151534 | ||||||
chr2:24151567
|
C | T | 1 | a0001c0002t0001g0067 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.686+4481C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24151567 | ||||||
chr2:24151583
|
C | T | 1 | a0001c0002t0001g0117 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.686+4497C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24151583 | ||||||
chr2:24151603
|
T | G | 16 | a0001c0002t0001g0080a0002c0005t0001g0009a0002c0005t0001g0013others(13): Show | 16 | HG00099.hp2 HG02040.hp1 HG02040.hp2 others(13): Show |
intron_variant | MODIFIER | c.686+4517T>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24151603 | ||||||
chr2:24151613
|
A | AT | 207 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(204): Show | 214 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.686+4543dupT | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24151613 | |||||
chr2:24151613
|
A | ATT | 14 | a0001c0001t0001g0068a0001c0001t0001g0081a0001c0001t0001g0157others(11): Show | 14 | HG00735.hp2 HG01099.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.686+4542_686+4543d others(4): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24151613 | |||||
chr2:24151613
|
A | ATTT | 50 | a0001c0001t0001g0003a0001c0001t0001g0139a0001c0001t0001g0280others(47): Show | 52 | HG00099.hp2 HG00140.hp2 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.686+4541_686+4543d others(5): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24151613 | |||||
chr2:24151687
|
C | G | 162 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(159): Show | 169 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(166): Show |
intron_variant | MODIFIER | c.686+4601C>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24151687 | ||||||
chr2:24151733
|
A | C | 1 | a0002c0005t0001g0031 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.686+4647A>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24151733 | ||||||
chr2:24151768
|
C | T | 61 | a0001c0001t0001g0003a0001c0001t0001g0059a0001c0001t0001g0068others(58): Show | 63 | HG00099.hp2 HG00140.hp2 HG00735.hp1 others(60): Show |
intron_variant | MODIFIER | c.686+4682C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24151768 | ||||||
chr2:24151859
|
T | C | 162 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(159): Show | 169 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(166): Show |
intron_variant | MODIFIER | c.686+4773T>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24151859 | ||||||
chr2:24151961
|
C | T | 7 | a0001c0001t0001g0003a0001c0001t0001g0059a0001c0001t0001g0280others(4): Show | 8 | HG00140.hp2 HG00735.hp1 HG00735.hp2 others(5): Show |
intron_variant | MODIFIER | c.686+4875C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24151961 | ||||||
chr2:24152004
|
G | T | 1 | a0001c0001t0001g0142 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.686+4918G>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24152004 | ||||||
chr2:24152022
|
C | T | 14 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0150others(11): Show | 16 | HG00621.hp1 HG02056.hp2 HG02074.hp2 others(13): Show |
intron_variant | MODIFIER | c.686+4936C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24152022 | ||||||
chr2:24152141
|
T | C | 38 | a0001c0001t0001g0003a0001c0001t0001g0059a0001c0001t0001g0139others(35): Show | 40 | HG00140.hp2 HG00735.hp1 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.686+5055T>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24152141 | ||||||
chr2:24152160
|
C | T | 2 | a0002c0005t0001g0024a0002c0005t0001g0025 | 2 | HG00099.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.686+5074C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24152160 | ||||||
chr2:24152181
|
T | A | 1 | a0001c0006t0003g0075 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.686+5095T>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24152181 | ||||||
chr2:24152360
|
A | G | 62 | a0001c0001t0001g0003a0001c0001t0001g0059a0001c0001t0001g0068others(59): Show | 64 | HG00099.hp2 HG00140.hp2 HG00735.hp1 others(61): Show |
intron_variant | MODIFIER | c.686+5274A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24152360 | ||||||
chr2:24152536
|
G | GTATTGCC others(16): Show |
1 | a0001c0001t0001g0263 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.686+5451_686+5473d others(25): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24152536 | |||||
chr2:24152593
|
G | A | 158 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(155): Show | 166 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.686+5507G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24152593 | ||||||
chr2:24152702
|
A | G | 62 | a0001c0001t0001g0100a0001c0001t0001g0139a0001c0001t0001g0222others(59): Show | 63 | HG00099.hp2 HG00735.hp2 HG00741.hp2 others(60): Show |
intron_variant | MODIFIER | c.686+5616A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24152702 | ||||||
chr2:24152983
|
C | G | 1 | a0001c0001t0001g0008 | 2 | HG00639.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.686+5897C>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24152983 | ||||||
chr2:24152984
|
T | C | 1 | a0001c0003t0001g0162 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.686+5898T>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24152984 | ||||||
chr2:24153127
|
C | T | 1 | a0001c0002t0001g0239 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.686+6041C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24153127 | ||||||
chr2:24153135
|
G | A | 4 | a0001c0003t0001g0131a0001c0003t0001g0134a0001c0003t0001g0162others(1): Show | 4 | HG02615.hp2 HG02723.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.686+6049G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24153135 | ||||||
chr2:24153264
|
G | A | 2 | a0001c0002t0001g0066a0001c0002t0001g0067 | 2 | HG02559.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.686+6178G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24153264 | ||||||
chr2:24153309
|
C | G | 7 | a0002c0007t0001g0012a0002c0007t0001g0017a0002c0007t0001g0018others(4): Show | 7 | HG01069.hp2 HG01071.hp1 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.686+6223C>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24153309 | ||||||
chr2:24153337
|
G | T | 1 | a0001c0003t0001g0163 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.686+6251G>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24153337 | ||||||
chr2:24153342
|
C | G | 2 | a0001c0001t0001g0234a0001c0001t0001g0235 | 2 | HG00099.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.686+6256C>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24153342 | ||||||
chr2:24153485
|
G | A | 1 | a0001c0002t0001g0064 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.686+6399G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24153485 | ||||||
chr2:24153515
|
G | A | 1 | a0001c0002t0001g0054 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.686+6429G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24153515 | ||||||
chr2:24153516
|
C | T | 1 | a0001c0001t0001g0254 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.686+6430C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24153516 | ||||||
chr2:24153590
|
C | T | 6 | a0001c0006t0001g0266a0001c0006t0001g0267a0001c0006t0001g0271others(3): Show | 6 | NA18949.hp1 NA18963.hp2 NA18980.hp1 others(3): Show |
intron_variant | MODIFIER | c.686+6504C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24153590 | ||||||
chr2:24153600
|
C | T | 15 | a0001c0006t0001g0218a0001c0006t0001g0264a0001c0006t0001g0265others(12): Show | 15 | HG01255.hp2 HG01361.hp1 HG01516.hp2 others(12): Show |
intron_variant | MODIFIER | c.686+6514C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24153600 | ||||||
chr2:24153761
|
T | C | 222 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(219): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.686+6675T>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24153761 | ||||||
chr2:24153780
|
T | C | 1 | a0003c0004t0001g0103 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.686+6694T>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24153780 | ||||||
chr2:24153789
|
T | A | 15 | a0001c0006t0001g0218a0001c0006t0001g0264a0001c0006t0001g0265others(12): Show | 15 | HG01255.hp2 HG01361.hp1 HG01516.hp2 others(12): Show |
intron_variant | MODIFIER | c.686+6703T>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24153789 | ||||||
chr2:24153840
|
C | T | 1 | a0001c0001t0001g0188 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.686+6754C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24153840 | ||||||
chr2:24153990
|
G | A | 15 | a0001c0006t0001g0218a0001c0006t0001g0264a0001c0006t0001g0265others(12): Show | 15 | HG01255.hp2 HG01361.hp1 HG01516.hp2 others(12): Show |
intron_variant | MODIFIER | c.686+6904G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24153990 | ||||||
chr2:24154061
|
C | T | 207 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(204): Show | 216 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.686+6975C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24154061 | ||||||
chr2:24154127
|
C | CA | 223 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(220): Show | 232 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.686+7042dupA | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24154127 | |||||
chr2:24154145
|
A | C | 2 | a0001c0001t0001g0122a0001c0001t0001g0172 | 2 | NA18969.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.686+7059A>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24154145 | ||||||
chr2:24154158
|
G | C | 15 | a0001c0006t0001g0218a0001c0006t0001g0264a0001c0006t0001g0265others(12): Show | 15 | HG01255.hp2 HG01361.hp1 HG01516.hp2 others(12): Show |
intron_variant | MODIFIER | c.686+7072G>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24154158 | ||||||
chr2:24154222
|
A | G | 15 | a0001c0006t0001g0218a0001c0006t0001g0264a0001c0006t0001g0265others(12): Show | 15 | HG01255.hp2 HG01361.hp1 HG01516.hp2 others(12): Show |
intron_variant | MODIFIER | c.686+7136A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24154222 | ||||||
chr2:24154684
|
G | T | 2 | a0001c0002t0001g0065a0001c0002t0001g0072 | 2 | HG03710.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.687-6822G>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24154684 | ||||||
chr2:24154977
|
T | G | 15 | a0001c0006t0001g0218a0001c0006t0001g0264a0001c0006t0001g0265others(12): Show | 15 | HG01255.hp2 HG01361.hp1 HG01516.hp2 others(12): Show |
intron_variant | MODIFIER | c.687-6529T>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24154977 | ||||||
chr2:24155231
|
C | A | 1 | a0001c0001t0001g0148 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.687-6275C>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24155231 | ||||||
chr2:24155237
|
T | G | 1 | a0001c0001t0001g0148 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.687-6269T>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24155237 | ||||||
chr2:24155290
|
T | C | 2 | a0001c0001t0001g0135a0001c0001t0001g0136 | 2 | NA19007.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.687-6216T>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24155290 | ||||||
chr2:24155361
|
A | G | 1 | a0001c0001t0001g0224 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.687-6145A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24155361 | ||||||
chr2:24155504
|
C | CAT | 5 | a0001c0003t0001g0084a0001c0003t0001g0085a0001c0003t0001g0089others(2): Show | 5 | HG02055.hp2 HG02109.hp1 HG02602.hp2 others(2): Show |
intron_variant | MODIFIER | c.687-5975_687-5974d others(4): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24155504 | |||||
chr2:24155504
|
C | CTT | 8 | a0001c0001t0001g0220a0002c0005t0001g0013a0002c0005t0001g0014others(5): Show | 8 | HG02040.hp2 HG02071.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.687-6002_687-6001i others(4): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24155504 | ||||||
chr2:24155504
|
C | CTTATATA others(3): Show |
1 | a0001c0002t0001g0175 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.687-6002_687-6001i others(12): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24155504 | ||||||
chr2:24155504
|
C | CTTATATA others(5): Show |
1 | a0001c0002t0001g0061 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.687-6002_687-6001i others(14): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24155504 | ||||||
chr2:24155504
|
C | CTTATATA others(9): Show |
1 | a0002c0005t0001g0025 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.687-6002_687-6001i others(18): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24155504 | ||||||
chr2:24155504
|
C | CTTATATA others(11): Show |
1 | a0001c0002t0001g0045 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.687-6002_687-6001i others(20): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24155504 | ||||||
chr2:24155504
|
C | CTTATATA others(23): Show |
1 | a0002c0005t0001g0024 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.687-6002_687-6001i others(32): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24155504 | ||||||
chr2:24155504
|
CATATATA others(5): Show |
C | 1 | a0001c0002t0001g0281 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.687-5985_687-5974d others(14): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24155504 | |||||
chr2:24155505
|
A | T | 191 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(188): Show | 200 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.687-6001A>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24155505 | ||||||
chr2:24155517
|
A | T | 1 | a0001c0002t0001g0281 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.687-5989A>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24155517 | ||||||
chr2:24155521
|
ATATATAT others(4): Show |
A | 1 | a0001c0002t0001g0241 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.687-5983_687-5973d others(13): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24155521 | |||||
chr2:24155521
|
ATATATAT others(5): Show |
A | 1 | a0001c0002t0001g0240 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.687-5983_687-5972d others(14): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24155521 | |||||
chr2:24155521
|
ATATATAT others(6): Show |
A | 1 | a0001c0002t0001g0239 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.687-5983_687-5971d others(15): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24155521 | |||||
chr2:24155523
|
ATATATAT others(5): Show |
A | 17 | a0001c0001t0001g0008a0001c0001t0001g0068a0001c0001t0001g0100others(14): Show | 18 | HG00099.hp1 HG00639.hp2 HG01099.hp1 others(15): Show |
intron_variant | MODIFIER | c.687-5981_687-5970d others(14): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24155523 | |||||
chr2:24155525
|
A | AT | 4 | a0001c0003t0001g0159a0001c0008t0001g0238a0003c0004t0001g0097others(1): Show | 4 | HG02071.hp2 HG02559.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.687-5980dupT | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24155525 | |||||
chr2:24155525
|
A | T | 1 | a0003c0004t0001g0109 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.687-5981A>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24155525 | ||||||
chr2:24155525
|
ATATATAT others(4): Show |
A | 8 | a0001c0001t0001g0121a0001c0001t0001g0146a0001c0001t0001g0152others(5): Show | 8 | HG00639.hp1 HG01081.hp1 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.687-5979_687-5969d others(13): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24155525 | |||||
chr2:24155525
|
ATATATAT others(5): Show |
A | 95 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(92): Show | 100 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.687-5979_687-5968d others(14): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24155525 | |||||
chr2:24155525
|
ATATATAT others(6): Show |
A | 6 | a0001c0001t0001g0128a0001c0001t0001g0166a0001c0001t0001g0248others(3): Show | 6 | HG01255.hp1 HG01516.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.687-5979_687-5967d others(15): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24155525 | |||||
chr2:24155527
|
A | AT | 11 | a0001c0002t0001g0243a0001c0003t0001g0133a0001c0003t0001g0158others(8): Show | 11 | HG02080.hp1 HG02257.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.687-5978dupT | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24155527 | |||||
chr2:24155527
|
A | T | 12 | a0001c0003t0001g0159a0001c0003t0001g0244a0001c0008t0001g0238others(9): Show | 12 | HG00140.hp1 HG00323.hp2 HG01069.hp1 others(9): Show |
intron_variant | MODIFIER | c.687-5979A>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24155527 | ||||||
chr2:24155527
|
ATATATTT others(3): Show |
A | 1 | a0001c0001t0001g0245 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.687-5977_687-5968d others(12): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24155527 | |||||
chr2:24155527
|
ATATATTT others(4): Show |
A | 3 | a0001c0001t0001g0138a0001c0001t0001g0177a0001c0001t0001g0259 | 3 | HG00642.hp2 NA18984.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.687-5977_687-5967d others(13): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24155527 | |||||
chr2:24155527
|
ATATATTT others(5): Show |
A | 11 | a0001c0001t0001g0001a0001c0001t0001g0078a0001c0001t0001g0127others(8): Show | 13 | HG01071.hp2 HG01361.hp2 HG02074.hp1 others(10): Show |
intron_variant | MODIFIER | c.687-5977_687-5966d others(14): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24155527 | |||||
chr2:24155527
|
ATATATTT others(7): Show |
A | 2 | a0001c0002t0001g0066a0001c0002t0001g0117 | 2 | HG02572.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.687-5977_687-5964d others(16): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24155527 | |||||
chr2:24155529
|
A | ATT | 4 | a0001c0003t0001g0088a0001c0003t0001g0131a0001c0008t0001g0160others(1): Show | 4 | HG02897.hp1 HG03041.hp1 NA18943.hp2 others(1): Show |
intron_variant | MODIFIER | c.687-5976_687-5975i others(4): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24155529 | |||||
chr2:24155529
|
A | T | 29 | a0001c0002t0001g0067a0001c0002t0001g0243a0001c0003t0001g0133others(26): Show | 29 | HG00140.hp1 HG00323.hp2 HG01069.hp1 others(26): Show |
intron_variant | MODIFIER | c.687-5977A>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24155529 | ||||||
chr2:24155529
|
ATATTTTT others(5): Show |
A | 1 | a0001c0001t0001g0246 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.687-5975_687-5964d others(14): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24155529 | |||||
chr2:24155529
|
ATATTTTT others(8): Show |
A | 1 | a0001c0006t0001g0275 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.687-5975_687-5961d others(17): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24155529 | |||||
chr2:24155531
|
A | ATATATAT others(6): Show |
1 | a0001c0002t0001g0040 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.687-5974_687-5973i others(15): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24155531 | |||||
chr2:24155531
|
A | ATATATAT others(10): Show |
1 | a0001c0002t0001g0049 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.687-5974_687-5973i others(19): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24155531 | |||||
chr2:24155531
|
A | ATATATAT others(8): Show |
2 | a0001c0002t0001g0042a0001c0002t0001g0074 | 2 | HG02135.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.687-5974_687-5973i others(17): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24155531 | |||||
chr2:24155531
|
A | ATATATAT others(6): Show |
4 | a0001c0002t0001g0002a0001c0002t0001g0046a0001c0002t0001g0047others(1): Show | 5 | HG02056.hp1 NA18964.hp1 NA18967.hp1 others(2): Show |
intron_variant | MODIFIER | c.687-5974_687-5973i others(15): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24155531 | |||||
chr2:24155531
|
A | ATATATAT others(8): Show |
1 | a0001c0002t0001g0043 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.687-5974_687-5973i others(17): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24155531 | |||||
chr2:24155531
|
A | ATATATAT others(6): Show |
4 | a0001c0002t0001g0041a0001c0002t0001g0044a0001c0002t0001g0048others(1): Show | 4 | HG01361.hp1 NA18945.hp1 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.687-5974_687-5973i others(15): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24155531 | |||||
chr2:24155531
|
A | ATATATAT others(2): Show |
6 | a0001c0002t0001g0050a0001c0002t0001g0051a0001c0002t0001g0054others(3): Show | 6 | HG00735.hp2 HG01099.hp2 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.687-5974_687-5973i others(11): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24155531 | |||||
chr2:24155531
|
A | ATATATAT others(3): Show |
2 | a0001c0002t0001g0057a0001c0002t0001g0070 | 2 | HG01257.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.687-5974_687-5973i others(12): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24155531 | |||||
chr2:24155531
|
A | ATATATAT others(6): Show |
1 | a0001c0006t0001g0269 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.687-5974_687-5973i others(15): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24155531 | |||||
chr2:24155531
|
A | ATATATTT others(3): Show |
1 | a0001c0002t0001g0173 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.687-5974_687-5973i others(12): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24155531 | |||||
chr2:24155531
|
A | ATATTTTT others(3): Show |
1 | a0001c0006t0001g0271 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.687-5974_687-5973i others(12): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24155531 | |||||
chr2:24155531
|
A | ATT | 6 | a0001c0003t0001g0087a0001c0003t0001g0090a0001c0003t0001g0091others(3): Show | 6 | HG01891.hp2 HG01934.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.687-5950_687-5949d others(4): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24155531 | |||||
chr2:24155531
|
A | T | 43 | a0001c0002t0001g0045a0001c0002t0001g0061a0001c0002t0001g0062others(40): Show | 43 | HG00140.hp1 HG00323.hp2 HG00741.hp2 others(40): Show |
intron_variant | MODIFIER | c.687-5975A>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24155531 | ||||||
chr2:24155531
|
ATTTTTTT others(3): Show |
A | 1 | a0001c0006t0003g0075 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.687-5958_687-5949d others(12): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24155531 | |||||
chr2:24155532
|
T | TA | 7 | a0001c0003t0001g0209a0001c0003t0001g0210a0001c0003t0001g0211others(4): Show | 7 | HG01358.hp1 HG02486.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.687-5974_687-5973i others(3): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24155532 | ||||||
chr2:24155533
|
T | A | 6 | a0001c0001t0001g0220a0001c0002t0001g0080a0001c0003t0001g0208others(3): Show | 6 | HG02040.hp1 HG02258.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.687-5973T>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24155533 | ||||||
chr2:24155539
|
T | A | 1 | a0001c0001t0001g0187 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.687-5967T>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24155539 | ||||||
chr2:24155541
|
T | A | 1 | a0002c0005t0001g0036 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.687-5965T>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24155541 | ||||||
chr2:24155542
|
T | A | 1 | a0001c0003t0001g0190 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.687-5964T>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24155542 | ||||||
chr2:24155543
|
T | A | 1 | a0001c0006t0003g0075 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.687-5963T>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24155543 | ||||||
chr2:24155545
|
T | A | 1 | a0001c0006t0003g0075 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.687-5961T>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24155545 | ||||||
chr2:24155547
|
T | A | 1 | a0001c0006t0003g0075 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.687-5959T>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24155547 | ||||||
chr2:24155571
|
G | A | 15 | a0001c0006t0001g0218a0001c0006t0001g0264a0001c0006t0001g0265others(12): Show | 15 | HG01255.hp2 HG01361.hp1 HG01516.hp2 others(12): Show |
intron_variant | MODIFIER | c.687-5935G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24155571 | ||||||
chr2:24155609
|
T | C | 19 | a0003c0004t0001g0095a0003c0004t0001g0096a0003c0004t0001g0097others(16): Show | 19 | HG00140.hp1 HG00323.hp2 HG00642.hp1 others(16): Show |
intron_variant | MODIFIER | c.687-5897T>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24155609 | ||||||
chr2:24155735
|
T | G | 1 | a0001c0002t0001g0260 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.687-5771T>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24155735 | ||||||
chr2:24155740
|
C | T | 1 | a0001c0006t0001g0271 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.687-5766C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24155740 | ||||||
chr2:24155752
|
G | T | 5 | a0001c0001t0001g0113a0001c0001t0001g0199a0001c0001t0001g0226others(2): Show | 5 | HG00438.hp1 HG02080.hp2 HG03834.hp2 others(2): Show |
intron_variant | MODIFIER | c.687-5754G>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24155752 | ||||||
chr2:24155924
|
T | C | 1 | a0001c0002t0001g0057 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.687-5582T>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24155924 | ||||||
chr2:24155930
|
G | A | 223 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(220): Show | 232 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.687-5576G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24155930 | ||||||
chr2:24156055
|
G | C | 208 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(205): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.687-5451G>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24156055 | ||||||
chr2:24156097
|
G | T | 1 | a0001c0001t0001g0132 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.687-5409G>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24156097 | ||||||
chr2:24156391
|
G | A | 2 | a0001c0001t0001g0178a0001c0001t0001g0204 | 2 | NA18955.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.687-5115G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24156391 | ||||||
chr2:24156770
|
TTCC | T | 4 | a0002c0005t0001g0022a0002c0005t0001g0023a0002c0005t0001g0031others(1): Show | 4 | HG02717.hp2 HG03041.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.687-4735_687-4733d others(5): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24156770 | ||||||
chr2:24156771
|
TCCG | T | 14 | a0001c0001t0001g0220a0001c0002t0001g0048a0001c0002t0001g0051others(11): Show | 14 | HG01099.hp2 HG01433.hp1 HG02040.hp1 others(11): Show |
intron_variant | MODIFIER | c.687-4732_687-4730d others(5): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24156771 | |||||
chr2:24156771
|
TCCGC | T | 34 | a0001c0002t0001g0002a0001c0002t0001g0040a0001c0002t0001g0041others(31): Show | 35 | HG00099.hp2 HG00735.hp2 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.687-4732_687-4729d others(6): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24156771 | |||||
chr2:24156771
|
TCCGCCC | T | 148 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(145): Show | 156 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.687-4732_687-4727d others(8): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24156771 | |||||
chr2:24156774
|
G | C | 5 | a0002c0005t0001g0022a0002c0005t0001g0023a0002c0005t0001g0031others(2): Show | 5 | HG02615.hp1 HG02717.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.687-4732G>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24156774 | ||||||
chr2:24156774
|
G | GC | 14 | a0001c0003t0001g0133a0001c0003t0001g0163a0001c0003t0001g0210others(11): Show | 14 | HG00323.hp2 HG01069.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.687-4719dupC | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24156774 | |||||
chr2:24156774
|
GC | G | 16 | a0001c0003t0001g0084a0001c0003t0001g0085a0001c0003t0001g0086others(13): Show | 16 | HG01891.hp2 HG01934.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.687-4719delC | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24156774 | |||||
chr2:24156776
|
C | T | 15 | a0001c0006t0001g0218a0001c0006t0001g0264a0001c0006t0001g0265others(12): Show | 15 | HG01255.hp2 HG01361.hp1 HG01516.hp2 others(12): Show |
intron_variant | MODIFIER | c.687-4730C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24156776 | ||||||
chr2:24156781
|
C | A | 1 | a0001c0006t0003g0075 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.687-4725C>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24156781 | ||||||
chr2:24156785
|
C | A | 11 | a0001c0003t0001g0084a0001c0003t0001g0085a0001c0003t0001g0086others(8): Show | 11 | HG01891.hp2 HG01934.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.687-4721C>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24156785 | ||||||
chr2:24156785
|
C | G | 1 | a0001c0001t0001g0184 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.687-4721C>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24156785 | ||||||
chr2:24156785
|
C | T | 1 | a0001c0001t0001g0169 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.687-4721C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24156785 | ||||||
chr2:24156787
|
C | A | 1 | a0001c0002t0001g0057 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.687-4719C>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24156787 | ||||||
chr2:24156818
|
T | C | 2 | a0001c0002t0001g0066a0001c0002t0001g0067 | 2 | HG02559.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.687-4688T>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24156818 | ||||||
chr2:24157029
|
T | C | 1 | a0001c0006t0003g0075 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.687-4477T>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24157029 | ||||||
chr2:24157067
|
G | A | 1 | a0001c0002t0001g0067 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.687-4439G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24157067 | ||||||
chr2:24157147
|
T | C | 15 | a0001c0006t0001g0218a0001c0006t0001g0264a0001c0006t0001g0265others(12): Show | 15 | HG01255.hp2 HG01361.hp1 HG01516.hp2 others(12): Show |
intron_variant | MODIFIER | c.687-4359T>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24157147 | ||||||
chr2:24157517
|
G | C | 223 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(220): Show | 232 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.687-3989G>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24157517 | ||||||
chr2:24157737
|
CA | C | 206 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(203): Show | 215 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(212): Show |
intron_variant | MODIFIER | c.687-3755delA | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24157737 | |||||
chr2:24157758
|
TC | T | 208 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(205): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.687-3745delC | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24157758 | |||||
chr2:24157845
|
C | T | 207 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(204): Show | 216 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.687-3661C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24157845 | ||||||
chr2:24157874
|
T | C | 2 | a0001c0002t0001g0065a0001c0002t0001g0072 | 2 | HG03710.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.687-3632T>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24157874 | ||||||
chr2:24157905
|
T | G | 19 | a0003c0004t0001g0095a0003c0004t0001g0096a0003c0004t0001g0097others(16): Show | 19 | HG00140.hp1 HG00323.hp2 HG00642.hp1 others(16): Show |
intron_variant | MODIFIER | c.687-3601T>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24157905 | ||||||
chr2:24158196
|
C | CT | 15 | a0001c0006t0001g0218a0001c0006t0001g0264a0001c0006t0001g0265others(12): Show | 15 | HG01255.hp2 HG01361.hp1 HG01516.hp2 others(12): Show |
intron_variant | MODIFIER | c.687-3293dupT | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24158196 | |||||
chr2:24158196
|
C | CTTT | 27 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0030others(24): Show | 30 | HG00642.hp2 HG01109.hp2 HG01884.hp2 others(27): Show |
intron_variant | MODIFIER | c.687-3295_687-3293d others(5): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24158196 | |||||
chr2:24158196
|
C | CTTTT | 7 | a0001c0001t0001g0005a0001c0001t0001g0138a0001c0001t0001g0156others(4): Show | 8 | HG00621.hp1 NA18955.hp2 NA18971.hp2 others(5): Show |
intron_variant | MODIFIER | c.687-3296_687-3293d others(6): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24158196 | |||||
chr2:24158196
|
C | CTTTTTT | 24 | a0001c0001t0001g0120a0001c0002t0001g0050a0001c0002t0001g0051others(21): Show | 24 | HG00099.hp2 HG00735.hp2 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.687-3298_687-3293d others(8): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24158196 | |||||
chr2:24158196
|
C | CTTTTTTT | 11 | a0001c0002t0001g0002a0001c0002t0001g0040a0001c0002t0001g0041others(8): Show | 12 | HG03834.hp1 NA18612.hp2 NA18945.hp1 others(9): Show |
intron_variant | MODIFIER | c.687-3299_687-3293d others(9): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24158196 | |||||
chr2:24158196
|
C | CTTTTTTT others(5): Show |
6 | a0001c0003t0001g0133a0001c0003t0001g0158a0001c0003t0001g0159others(3): Show | 6 | HG02257.hp2 HG06807.hp1 NA18952.hp1 others(3): Show |
intron_variant | MODIFIER | c.687-3304_687-3293d others(14): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24158196 | |||||
chr2:24158196
|
C | CTTTTTTT others(6): Show |
44 | a0001c0001t0001g0077a0001c0001t0001g0129a0001c0001t0001g0136others(41): Show | 44 | HG00140.hp1 HG00323.hp2 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.687-3305_687-3293d others(15): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24158196 | |||||
chr2:24158196
|
C | CTTTTTTT others(7): Show |
85 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(82): Show | 88 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.687-3306_687-3293d others(16): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24158196 | |||||
chr2:24158196
|
C | CTTTTTTT others(8): Show |
30 | a0001c0001t0001g0007a0001c0001t0001g0038a0001c0001t0001g0082others(27): Show | 31 | HG00438.hp1 HG00438.hp2 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.687-3307_687-3293d others(17): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24158196 | |||||
chr2:24158196
|
C | CTTTTTTT others(9): Show |
5 | a0001c0001t0001g0229a0001c0001t0001g0236a0001c0002t0001g0240others(2): Show | 5 | HG02080.hp2 HG02145.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.687-3308_687-3293d others(18): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24158196 | |||||
chr2:24158196
|
C | CTTTTTTT others(10): Show |
3 | a0001c0001t0001g0083a0001c0001t0001g0233a0001c0001t0001g0254 | 3 | HG02602.hp1 HG03471.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.687-3309_687-3293d others(19): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24158196 | |||||
chr2:24158196
|
C | CTTTTTTT others(13): Show |
6 | a0001c0002t0001g0243a0002c0005t0001g0013a0002c0005t0001g0015others(3): Show | 6 | HG02040.hp2 HG02615.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.687-3293_687-3292i others(22): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24158196 | |||||
chr2:24158196
|
C | CTTTTTTT others(14): Show |
5 | a0002c0005t0001g0014a0002c0005t0001g0021a0002c0005t0001g0023others(2): Show | 5 | HG02071.hp1 HG02717.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.687-3293_687-3292i others(23): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24158196 | |||||
chr2:24158196
|
C | CTTTTTTT others(15): Show |
2 | a0002c0005t0001g0009a0002c0005t0001g0022 | 2 | HG02922.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.687-3293_687-3292i others(24): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24158196 | |||||
chr2:24158196
|
C | CTTTTTTT others(16): Show |
1 | a0001c0002t0001g0067 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.687-3293_687-3292i others(25): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24158196 | |||||
chr2:24158196
|
C | CTTTTTTT others(17): Show |
1 | a0001c0002t0001g0080 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.687-3293_687-3292i others(26): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24158196 | |||||
chr2:24158214
|
C | T | 221 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(218): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.687-3292C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24158214 | ||||||
chr2:24158385
|
G | A | 1 | a0001c0006t0001g0269 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.687-3121G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24158385 | ||||||
chr2:24158608
|
C | A | 1 | a0001c0002t0001g0066 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.687-2898C>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24158608 | ||||||
chr2:24158919
|
C | T | 1 | a0001c0006t0003g0075 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.687-2587C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24158919 | ||||||
chr2:24159015
|
G | A | 1 | a0001c0006t0003g0075 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.687-2491G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24159015 | ||||||
chr2:24159051
|
C | T | 1 | a0001c0006t0003g0075 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.687-2455C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24159051 | ||||||
chr2:24159160
|
C | G | 153 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(150): Show | 161 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.687-2346C>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24159160 | ||||||
chr2:24159524
|
A | T | 1 | a0001c0002t0001g0067 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.687-1982A>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24159524 | ||||||
chr2:24159595
|
C | G | 1 | a0001c0002t0001g0066 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.687-1911C>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24159595 | ||||||
chr2:24159676
|
G | A | 154 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(151): Show | 162 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.687-1830G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24159676 | ||||||
chr2:24159688
|
A | G | 2 | a0003c0004t0001g0098a0003c0004t0001g0111 | 2 | NA18943.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.687-1818A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24159688 | ||||||
chr2:24159809
|
C | T | 1 | a0001c0006t0003g0075 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.687-1697C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24159809 | ||||||
chr2:24159811
|
C | G | 208 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(205): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.687-1695C>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24159811 | ||||||
chr2:24159989
|
AT | A | 12 | a0001c0001t0001g0127a0001c0001t0001g0183a0001c0001t0001g0280others(9): Show | 12 | HG01516.hp1 HG02040.hp2 HG02071.hp1 others(9): Show |
intron_variant | MODIFIER | c.687-1500delT | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24159989 | |||||
chr2:24160188
|
C | T | 2 | a0001c0002t0001g0066a0001c0002t0001g0067 | 2 | HG02559.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.687-1318C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24160188 | ||||||
chr2:24160189
|
C | T | 143 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(140): Show | 151 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.687-1317C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24160189 | ||||||
chr2:24160190
|
G | A | 5 | a0001c0003t0001g0208a0001c0003t0001g0209a0001c0003t0001g0210others(2): Show | 5 | HG02055.hp2 HG02630.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.687-1316G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24160190 | ||||||
chr2:24160269
|
C | T | 1 | a0001c0006t0003g0075 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.687-1237C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24160269 | ||||||
chr2:24161221
|
A | G | 208 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(205): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.687-285A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24161221 | ||||||
chr2:24161428
|
A | G | 1 | a0001c0006t0003g0075 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.687-78A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24161428 | ||||||
chr2:24161761
|
T | C | 1 | a0001c0001t0001g0245 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.794+148T>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 8/10 | chr2 | 24161761 | ||||||
chr2:24161869
|
C | T | 1 | a0001c0001t0001g0219 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.794+256C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 8/10 | chr2 | 24161869 | ||||||
chr2:24162275
|
T | C | 2 | a0001c0002t0001g0066a0001c0002t0001g0067 | 2 | HG02559.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.794+662T>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 8/10 | chr2 | 24162275 | ||||||
chr2:24162357
|
A | G | 1 | a0001c0001t0001g0235 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.794+744A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 8/10 | chr2 | 24162357 | ||||||
chr2:24162978
|
A | G | 1 | a0001c0001t0001g0195 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.795-1220A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 8/10 | chr2 | 24162978 | ||||||
chr2:24163160
|
C | T | 1 | a0001c0001t0001g0110 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.795-1038C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 8/10 | chr2 | 24163160 | ||||||
chr2:24163342
|
C | A | 207 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(204): Show | 216 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.795-856C>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 8/10 | chr2 | 24163342 | ||||||
chr2:24163686
|
G | T | 1 | a0001c0001t0001g0246 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.795-512G>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 8/10 | chr2 | 24163686 | ||||||
chr2:24163867
|
A | G | 1 | a0001c0006t0003g0075 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.795-331A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 8/10 | chr2 | 24163867 | ||||||
chr2:24164055
|
C | CA | 51 | a0001c0002t0001g0002a0001c0002t0001g0040a0001c0002t0001g0041others(48): Show | 52 | HG00099.hp2 HG00735.hp2 HG00741.hp2 others(49): Show |
intron_variant | MODIFIER | c.795-136dupA | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 24164055 | |||||
chr2:24164101
|
A | C | 1 | a0001c0001t0001g0113 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.795-97A>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 8/10 | chr2 | 24164101 | ||||||
chr2:24164473
|
T | A | 15 | a0001c0006t0001g0218a0001c0006t0001g0264a0001c0006t0001g0265others(12): Show | 15 | HG01255.hp2 HG01361.hp1 HG01516.hp2 others(12): Show |
intron_variant | MODIFIER | c.932+138T>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | chr2 | 24164473 | ||||||
chr2:24164520
|
GGCCCCCT others(22): Show |
G | 2 | a0003c0004t0001g0096a0003c0004t0001g0097 | 2 | NA19057.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.932+200_932+228del others(29): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 24164520 | |||||
chr2:24164520
|
GGCCCCCT others(51): Show |
G | 1 | a0001c0006t0001g0277 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.932+200_932+257del others(58): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 24164520 | |||||
chr2:24164535
|
TCACACGA others(22): Show |
T | 230 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(227): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.932+256_932+284del others(29): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 24164535 | |||||
chr2:24164568
|
A | G | 2 | a0001c0002t0001g0066a0001c0006t0003g0075 | 2 | HG02717.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.932+233A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | chr2 | 24164568 | ||||||
chr2:24164650
|
C | G | 1 | a0001c0006t0003g0075 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.932+315C>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | chr2 | 24164650 | ||||||
chr2:24164663
|
C | T | 52 | a0001c0001t0001g0189a0001c0002t0001g0002a0001c0002t0001g0040others(49): Show | 53 | HG00099.hp2 HG00735.hp2 HG00741.hp2 others(50): Show |
intron_variant | MODIFIER | c.932+328C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | chr2 | 24164663 | ||||||
chr2:24164704
|
G | A | 1 | a0001c0001t0001g0151 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.932+369G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | chr2 | 24164704 | ||||||
chr2:24164854
|
G | A | 2 | a0001c0001t0001g0149a0001c0001t0001g0206 | 2 | HG01346.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.932+519G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | chr2 | 24164854 | ||||||
chr2:24164990
|
G | A | 207 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(204): Show | 216 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.932+655G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | chr2 | 24164990 | ||||||
chr2:24165113
|
T | A | 1 | a0001c0002t0001g0046 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.932+778T>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | chr2 | 24165113 | ||||||
chr2:24165114
|
T | C | 1 | a0001c0002t0001g0046 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.932+779T>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | chr2 | 24165114 | ||||||
chr2:24165115
|
C | A | 1 | a0001c0002t0001g0046 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.932+780C>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | chr2 | 24165115 | ||||||
chr2:24165123
|
A | G | 1 | a0001c0002t0001g0046 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.932+788A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | chr2 | 24165123 | ||||||
chr2:24165126
|
G | C | 1 | a0001c0002t0001g0046 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.932+791G>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | chr2 | 24165126 | ||||||
chr2:24165128
|
G | C | 1 | a0001c0002t0001g0046 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.932+793G>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | chr2 | 24165128 | ||||||
chr2:24165129
|
A | G | 1 | a0001c0002t0001g0046 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.932+794A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | chr2 | 24165129 | ||||||
chr2:24165130
|
A | T | 1 | a0001c0002t0001g0046 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.932+795A>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | chr2 | 24165130 | ||||||
chr2:24165131
|
T | G | 1 | a0001c0002t0001g0046 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.932+796T>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | chr2 | 24165131 | ||||||
chr2:24165227
|
G | A | 207 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(204): Show | 216 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.932+892G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | chr2 | 24165227 | ||||||
chr2:24165304
|
GGCCCTAT others(7): Show |
G | 10 | a0001c0003t0001g0084a0001c0003t0001g0085a0001c0003t0001g0086others(7): Show | 10 | HG01891.hp2 HG01934.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.932+971_932+984del others(14): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 24165304 | |||||
chr2:24165326
|
C | T | 10 | a0001c0003t0001g0084a0001c0003t0001g0085a0001c0003t0001g0086others(7): Show | 10 | HG01891.hp2 HG01934.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.932+991C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | chr2 | 24165326 | ||||||
chr2:24165398
|
C | A | 1 | a0001c0001t0001g0179 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.932+1063C>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | chr2 | 24165398 | ||||||
chr2:24165499
|
C | T | 1 | a0001c0001t0001g0170 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.932+1164C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | chr2 | 24165499 | ||||||
chr2:24165740
|
T | G | 35 | a0001c0002t0001g0002a0001c0002t0001g0040a0001c0002t0001g0041others(32): Show | 36 | HG00099.hp2 HG00735.hp2 HG00741.hp2 others(33): Show |
intron_variant | MODIFIER | c.932+1405T>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | chr2 | 24165740 | ||||||
chr2:24165816
|
C | T | 1 | a0001c0001t0001g0206 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.932+1481C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | chr2 | 24165816 | ||||||
chr2:24165982
|
C | T | 1 | a0002c0005t0001g0021 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.933-1645C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | chr2 | 24165982 | ||||||
chr2:24165986
|
G | A | 1 | a0001c0002t0001g0066 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.933-1641G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | chr2 | 24165986 | ||||||
chr2:24166041
|
TA | T | 14 | a0001c0006t0001g0218a0001c0006t0001g0264a0001c0006t0001g0265others(11): Show | 14 | HG01255.hp2 HG01361.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.933-1572delA | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 24166041 | |||||
chr2:24166050
|
A | AATATATA others(3): Show |
3 | a0002c0005t0001g0022a0002c0005t0001g0023a0002c0005t0001g0031 | 3 | HG02717.hp2 HG03041.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.933-1576_933-1575i others(12): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 24166050 | |||||
chr2:24166052
|
A | AAGAAATA others(9): Show |
1 | a0001c0001t0001g0155 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.933-1574_933-1573i others(18): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 24166052 | |||||
chr2:24166052
|
A | AAT | 14 | a0001c0002t0001g0070a0001c0003t0001g0102a0001c0003t0001g0133others(11): Show | 14 | HG01243.hp2 HG01358.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.933-1574_933-1573i others(4): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 24166052 | |||||
chr2:24166052
|
A | AATAT | 7 | a0001c0002t0001g0066a0001c0003t0001g0131a0001c0003t0001g0134others(4): Show | 7 | HG02615.hp2 HG02647.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.933-1574_933-1573i others(6): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 24166052 | |||||
chr2:24166052
|
A | AATATATA others(3): Show |
5 | a0002c0005t0001g0014a0002c0005t0001g0015a0002c0005t0001g0021others(2): Show | 5 | HG02071.hp1 NA18995.hp2 NA19074.hp1 others(2): Show |
intron_variant | MODIFIER | c.933-1574_933-1573i others(12): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 24166052 | |||||
chr2:24166052
|
A | AATATATA others(5): Show |
1 | a0002c0005t0001g0013 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.933-1574_933-1573i others(14): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 24166052 | |||||
chr2:24166052
|
A | AATATATA others(7): Show |
1 | a0002c0005t0001g0034 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.933-1574_933-1573i others(16): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 24166052 | |||||
chr2:24166052
|
A | AATATATA others(13): Show |
1 | a0001c0001t0001g0279 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.933-1574_933-1573i others(22): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 24166052 | |||||
chr2:24166052
|
A | AT | 6 | a0001c0003t0001g0084a0001c0003t0001g0085a0001c0003t0001g0091others(3): Show | 6 | HG01516.hp2 HG01891.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.933-1575_933-1574i others(3): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | chr2 | 24166052 | ||||||
chr2:24166052
|
A | ATATAT | 3 | a0001c0002t0001g0073a0001c0002t0001g0074a0001c0002t0001g0175 | 3 | HG02056.hp1 HG02135.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.933-1575_933-1574i others(7): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | chr2 | 24166052 | ||||||
chr2:24166052
|
A | ATATATAT others(14): Show |
1 | a0001c0001t0001g0228 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.933-1575_933-1574i others(23): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | chr2 | 24166052 | ||||||
chr2:24166052
|
A | T | 10 | a0001c0002t0001g0069a0001c0003t0001g0209a0001c0006t0001g0277others(7): Show | 10 | HG00323.hp2 HG01255.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.933-1575A>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | chr2 | 24166052 | ||||||
chr2:24166054
|
A | AAAAAAAT others(10): Show |
1 | a0001c0001t0001g0258 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.933-1572_933-1571i others(19): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 24166054 | |||||
chr2:24166054
|
A | AAAAATAT others(4): Show |
1 | a0001c0002t0001g0261 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.933-1572_933-1571i others(13): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 24166054 | |||||
chr2:24166054
|
A | AAAAATAT others(8): Show |
12 | a0001c0001t0001g0101a0001c0001t0001g0118a0001c0001t0001g0123others(9): Show | 12 | HG01192.hp2 HG01243.hp1 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.933-1572_933-1571i others(17): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 24166054 | |||||
chr2:24166054
|
A | AAAAATAT others(10): Show |
1 | a0001c0001t0001g0130 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.933-1572_933-1571i others(19): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 24166054 | |||||
chr2:24166054
|
A | AAAATATA others(7): Show |
3 | a0001c0001t0001g0120a0001c0001t0001g0194a0001c0001t0001g0219 | 3 | HG01978.hp2 NA19068.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.933-1572_933-1571i others(16): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 24166054 | |||||
chr2:24166054
|
A | AAATAATA others(9): Show |
1 | a0001c0001t0001g0147 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.933-1572_933-1571i others(18): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 24166054 | |||||
chr2:24166054
|
A | AAATATAT others(4): Show |
1 | a0001c0002t0001g0260 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.933-1572_933-1571i others(13): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 24166054 | |||||
chr2:24166054
|
A | AAATATAT others(6): Show |
17 | a0001c0001t0001g0008a0001c0001t0001g0068a0001c0001t0001g0146others(14): Show | 18 | HG00639.hp1 HG00639.hp2 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.933-1572_933-1571i others(15): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 24166054 | |||||
chr2:24166054
|
A | AAATATAT others(8): Show |
46 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(43): Show | 51 | HG00621.hp1 HG01106.hp1 HG01192.hp1 others(48): Show |
intron_variant | MODIFIER | c.933-1572_933-1571i others(17): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 24166054 | |||||
chr2:24166054
|
A | AAATATAT others(10): Show |
15 | a0001c0001t0001g0078a0001c0001t0001g0122a0001c0001t0001g0137others(12): Show | 15 | HG00642.hp2 HG00741.hp1 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.933-1572_933-1571i others(19): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 24166054 | |||||
chr2:24166054
|
A | AAATATAT others(12): Show |
9 | a0001c0001t0001g0077a0001c0001t0001g0100a0001c0001t0001g0176others(6): Show | 9 | HG01099.hp1 HG01169.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.933-1572_933-1571i others(21): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 24166054 | |||||
chr2:24166054
|
A | AAATATAT others(14): Show |
3 | a0001c0001t0001g0193a0001c0001t0001g0250a0001c0001t0001g0257 | 3 | HG01257.hp1 HG02258.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.933-1572_933-1571i others(23): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 24166054 | |||||
chr2:24166054
|
A | AAATATAT others(16): Show |
5 | a0001c0001t0001g0076a0001c0001t0001g0079a0001c0001t0001g0081others(2): Show | 5 | HG02109.hp2 HG02647.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.933-1572_933-1571i others(25): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 24166054 | |||||
chr2:24166054
|
A | AAATATAT others(18): Show |
2 | a0002c0007t0001g0012a0002c0007t0001g0027 | 2 | HG03492.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.933-1572_933-1571i others(27): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 24166054 | |||||
chr2:24166054
|
A | AAATATAT others(20): Show |
1 | a0002c0007t0001g0017 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.933-1572_933-1571i others(29): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 24166054 | |||||
chr2:24166054
|
A | AATATATA others(5): Show |
1 | a0001c0002t0001g0117 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.933-1566_933-1555d others(14): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 24166054 | |||||
chr2:24166054
|
A | AATATATA others(7): Show |
2 | a0001c0001t0001g0186a0001c0001t0001g0201 | 2 | HG00323.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.933-1568_933-1555d others(16): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 24166054 | |||||
chr2:24166054
|
A | AATATATA others(9): Show |
9 | a0001c0001t0001g0110a0001c0001t0001g0119a0001c0001t0001g0182others(6): Show | 9 | HG00099.hp1 HG00621.hp2 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.933-1570_933-1555d others(18): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 24166054 | |||||
chr2:24166054
|
A | AATATATA others(11): Show |
4 | a0001c0001t0001g0007a0001c0001t0001g0030a0001c0001t0001g0177others(1): Show | 5 | HG01109.hp2 NA18612.hp1 NA18955.hp1 others(2): Show |
intron_variant | MODIFIER | c.933-1572_933-1555d others(20): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 24166054 | |||||
chr2:24166054
|
A | AATATATA others(13): Show |
2 | a0001c0001t0001g0233a0001c0011t0001g0262 | 2 | HG03453.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.933-1555_933-1554i others(22): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 24166054 | |||||
chr2:24166054
|
A | AATATATA others(19): Show |
2 | a0002c0007t0001g0019a0002c0007t0001g0029 | 2 | HG01069.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.933-1555_933-1554i others(28): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 24166054 | |||||
chr2:24166054
|
A | ATATAT | 27 | a0001c0002t0001g0002a0001c0002t0001g0040a0001c0002t0001g0041others(24): Show | 28 | HG00099.hp2 HG00741.hp2 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.933-1573_933-1572i others(7): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | chr2 | 24166054 | ||||||
chr2:24166054
|
A | ATATATAT others(8): Show |
3 | a0001c0001t0001g0003a0001c0001t0001g0059a0001c0001t0001g0136 | 4 | HG00140.hp2 HG00735.hp1 HG01106.hp2 others(1): Show |
intron_variant | MODIFIER | c.933-1573_933-1572i others(17): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | chr2 | 24166054 | ||||||
chr2:24166054
|
A | ATATATAT others(10): Show |
2 | a0001c0001t0001g0263a0001c0001t0001g0280 | 2 | HG01496.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.933-1573_933-1572i others(19): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | chr2 | 24166054 | ||||||
chr2:24166054
|
A | ATATATAT others(14): Show |
2 | a0001c0001t0001g0224a0001c0001t0001g0252 | 2 | HG02083.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.933-1573_933-1572i others(23): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | chr2 | 24166054 | ||||||
chr2:24166054
|
A | ATATATAT others(16): Show |
1 | a0001c0001t0001g0038 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.933-1573_933-1572i others(25): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | chr2 | 24166054 | ||||||
chr2:24166054
|
A | ATATATAT others(18): Show |
2 | a0002c0007t0001g0016a0002c0007t0001g0018 | 2 | HG01071.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.933-1573_933-1572i others(27): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | chr2 | 24166054 | ||||||
chr2:24166054
|
A | T | 90 | a0001c0001t0001g0155a0001c0001t0001g0228a0001c0001t0001g0279others(87): Show | 90 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.933-1573A>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | chr2 | 24166054 | ||||||
chr2:24166056
|
T | A | 1 | a0003c0004t0001g0093 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.933-1571T>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | chr2 | 24166056 | ||||||
chr2:24166210
|
G | A | 1 | a0001c0006t0003g0075 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.933-1417G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | chr2 | 24166210 | ||||||
chr2:24166341
|
A | G | 1 | a0001c0006t0001g0218 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.933-1286A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | chr2 | 24166341 | ||||||
chr2:24166409
|
A | C | 33 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(30): Show | 37 | HG00621.hp1 HG00642.hp2 HG01109.hp2 others(34): Show |
intron_variant | MODIFIER | c.933-1218A>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | chr2 | 24166409 | ||||||
chr2:24166496
|
G | GTGCT | 36 | a0001c0002t0001g0050a0001c0002t0001g0051a0001c0002t0001g0052others(33): Show | 36 | HG00099.hp2 HG00735.hp2 HG00741.hp2 others(33): Show |
intron_variant | MODIFIER | c.933-1117_933-1114d others(6): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 24166496 | |||||
chr2:24166600
|
C | T | 1 | a0001c0006t0003g0075 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.933-1027C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | chr2 | 24166600 | ||||||
chr2:24166669
|
G | T | 6 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0079others(3): Show | 6 | HG02109.hp2 HG02258.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.933-958G>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | chr2 | 24166669 | ||||||
chr2:24166806
|
G | A | 207 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(204): Show | 216 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.933-821G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | chr2 | 24166806 | ||||||
chr2:24167214
|
C | T | 1 | a0001c0006t0003g0075 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.933-413C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | chr2 | 24167214 | ||||||
chr2:24167283
|
G | A | 2 | a0001c0002t0001g0260a0001c0002t0001g0261 | 2 | HG03209.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.933-344G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | chr2 | 24167283 | ||||||
chr2:24167382
|
G | A | 1 | a0001c0001t0001g0233 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.933-245G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | chr2 | 24167382 | ||||||
chr2:24167424
|
G | C | 1 | a0002c0007t0001g0017 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.933-203G>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | chr2 | 24167424 | ||||||
chr2:24167519
|
G | A | 1 | a0001c0006t0003g0075 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.933-108G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | chr2 | 24167519 | ||||||
chr2:24167780
|
G | A | 1 | a0001c0001t0001g0143 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.*14+97G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 10/10 | chr2 | 24167780 | ||||||
chr2:24167787
|
A | G | 1 | a0001c0006t0003g0075 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.*14+104A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 10/10 | chr2 | 24167787 | ||||||
chr2:24167971
|
G | C | 223 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(220): Show | 232 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.*14+288G>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 10/10 | chr2 | 24167971 | ||||||
chr2:24168157
|
C | T | 1 | a0001c0006t0003g0075 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.*14+474C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 10/10 | chr2 | 24168157 | ||||||
chr2:24168260
|
A | G | 153 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(150): Show | 161 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.*14+577A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 10/10 | chr2 | 24168260 | ||||||
chr2:24168669
|
A | G | 1 | a0001c0006t0003g0075 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.*15-687A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 10/10 | chr2 | 24168669 | ||||||
chr2:24168810
|
G | T | 1 | a0001c0001t0001g0189 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.*15-546G>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 10/10 | chr2 | 24168810 | ||||||
chr2:24168851
|
T | C | 223 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(220): Show | 232 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.*15-505T>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 10/10 | chr2 | 24168851 | ||||||
chr2:24168864
|
A | G | 223 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(220): Show | 232 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.*15-492A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 10/10 | chr2 | 24168864 | ||||||
chr2:24168878
|
C | T | 1 | a0001c0006t0003g0075 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.*15-478C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 10/10 | chr2 | 24168878 | ||||||
chr2:24168955
|
G | A | 1 | a0002c0005t0001g0023 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.*15-401G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 10/10 | chr2 | 24168955 | ||||||
chr2:24169025
|
A | G | 15 | a0001c0006t0001g0218a0001c0006t0001g0264a0001c0006t0001g0265others(12): Show | 15 | HG01255.hp2 HG01361.hp1 HG01516.hp2 others(12): Show |
intron_variant | MODIFIER | c.*15-331A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 10/10 | chr2 | 24169025 | ||||||
chr2:24169091
|
C | T | 2 | a0001c0002t0001g0054a0001c0002t0001g0060 | 2 | HG02698.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.*15-265C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 10/10 | chr2 | 24169091 | ||||||
chr2:24169177
|
C | T | 16 | a0001c0002t0001g0080a0001c0006t0001g0218a0001c0006t0001g0264others(13): Show | 16 | HG01255.hp2 HG01361.hp1 HG01516.hp2 others(13): Show |
intron_variant | MODIFIER | c.*15-179C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 10/10 | chr2 | 24169177 | ||||||
chr2:24169235
|
C | T | 1 | a0001c0001t0001g0113 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.*15-121C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 10/10 | chr2 | 24169235 |