geneid | 11036 |
---|---|
ensemblid | ENSG00000242441.8 |
hgncid | 30727 |
symbol | GTF2A1L |
name | general transcription factor IIA subunit 1 like |
refseq_nuc | NM_006872.5 |
refseq_prot | NP_006863.2 |
ensembl_nuc | ENST00000403751.8 |
ensembl_prot | ENSP00000384597.3 |
mane_status | MANE Select |
chr | chr2 |
start | 48617856 |
end | 48679604 |
strand | + |
ver | v1.2 |
region | chr2:48617856-48679604 |
region5000 | chr2:48612856-48684604 |
regionname0 | GTF2A1L_chr2_48617856_48679604 |
regionname5000 | GTF2A1L_chr2_48612856_48684604 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 478 | 265 | 79 | 49 | 94 | 10 | 31 | 67 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | copy fasta | chr2 | 48612856 | 48684604 |
a0002 | 0/0 | 478 | 67 | 8 | 13 | 33 | 4 | 9 | 24 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | copy fasta | chr2 | 48612856 | 48684604 |
a0003 | 0/0 | 478 | 3 | 1 | 2 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | copy fasta | chr2 | 48612856 | 48684604 |
a0004 | 0/0 | 478 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | copy fasta | chr2 | 48612856 | 48684604 |
a0005 | 0/0 | 478 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | copy fasta | chr2 | 48612856 | 48684604 |
a0006 | 0/0 | 478 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | copy fasta | chr2 | 48612856 | 48684604 |
a0007 | 0/0 | 478 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | copy fasta | chr2 | 48612856 | 48684604 |
a0008 | 0/0 | 478 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | copy fasta | chr2 | 48612856 | 48684604 |
a0009 | 0/0 | 478 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | copy fasta | chr2 | 48612856 | 48684604 |
a0010 | 0/0 | 478 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | copy fasta | chr2 | 48612856 | 48684604 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 1437 | 243 | 62 | 48 | 93 | 9 | 30 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | copy fasta | chr2 | 48612856 | 48684604 |
c0002 | 0/0 | 1437 | 63 | 8 | 13 | 30 | 4 | 8 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | copy fasta | chr2 | 48612856 | 48684604 |
c0003 | 0/0 | 1437 | 18 | 17 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | copy fasta | chr2 | 48612856 | 48684604 |
c0004 | 0/0 | 1437 | 3 | 1 | 2 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | copy fasta | chr2 | 48612856 | 48684604 |
c0005 | 1/0 | 1437 | 3 | 0 | 0 | 0 | 1 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | copy fasta | chr2 | 48612856 | 48684604 |
c0006 | 0/0 | 1437 | 3 | 0 | 0 | 3 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | copy fasta | chr2 | 48612856 | 48684604 |
c0007 | 0/0 | 1437 | 2 | 0 | 2 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | copy fasta | chr2 | 48612856 | 48684604 |
c0008 | 0/0 | 1437 | 2 | 2 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | copy fasta | chr2 | 48612856 | 48684604 |
c0009 | 0/0 | 1437 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | copy fasta | chr2 | 48612856 | 48684604 |
c0010 | 0/0 | 1437 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | copy fasta | chr2 | 48612856 | 48684604 |
c0011 | 0/0 | 1437 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | copy fasta | chr2 | 48612856 | 48684604 |
c0012 | 0/0 | 1437 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | copy fasta | chr2 | 48612856 | 48684604 |
c0013 | 0/0 | 1437 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | copy fasta | chr2 | 48612856 | 48684604 |
c0014 | 0/0 | 1437 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | copy fasta | chr2 | 48612856 | 48684604 |
c0015 | 0/0 | 1437 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | copy fasta | chr2 | 48612856 | 48684604 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 182 | 319 | 72 | 64 | 128 | 13 | 41 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | copy fasta | chr2 | 48612856 | 48684604 |
t0002 | 0/0 | 182 | 19 | 18 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | copy fasta | chr2 | 48612856 | 48684604 |
t0003 | 1/0 | 182 | 3 | 0 | 0 | 0 | 1 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | copy fasta | chr2 | 48612856 | 48684604 |
t0004 | 0/0 | 182 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | copy fasta | chr2 | 48612856 | 48684604 |
t0005 | 0/0 | 182 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | copy fasta | chr2 | 48612856 | 48684604 |
t0006 | 0/0 | 182 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | copy fasta | chr2 | 48612856 | 48684604 |
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 | 0/1 | 4 | 0 | 0 | 1 | 1 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0002 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0003 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0007 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0008 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0010 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0016 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0083 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0308 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 1437 | 243 | 62 | 48 | 93 | 9 | 30 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | copy fasta | chr2 | 48612856 | 48684604 |
a0001c0003 | 0/0 | 1437 | 18 | 17 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | copy fasta | chr2 | 48612856 | 48684604 |
a0001c0005 | 1/0 | 1437 | 3 | 0 | 0 | 0 | 1 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | copy fasta | chr2 | 48612856 | 48684604 |
a0001c0012 | 0/0 | 1437 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | copy fasta | chr2 | 48612856 | 48684604 |
a0002c0002 | 0/0 | 1437 | 63 | 8 | 13 | 30 | 4 | 8 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | copy fasta | chr2 | 48612856 | 48684604 |
a0002c0006 | 0/0 | 1437 | 3 | 0 | 0 | 3 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | copy fasta | chr2 | 48612856 | 48684604 |
a0002c0014 | 0/0 | 1437 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | copy fasta | chr2 | 48612856 | 48684604 |
a0003c0004 | 0/0 | 1437 | 3 | 1 | 2 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | copy fasta | chr2 | 48612856 | 48684604 |
a0004c0008 | 0/0 | 1437 | 2 | 2 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | copy fasta | chr2 | 48612856 | 48684604 |
a0005c0007 | 0/0 | 1437 | 2 | 0 | 2 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | copy fasta | chr2 | 48612856 | 48684604 |
a0006c0010 | 0/0 | 1437 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | copy fasta | chr2 | 48612856 | 48684604 |
a0007c0011 | 0/0 | 1437 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | copy fasta | chr2 | 48612856 | 48684604 |
a0008c0009 | 0/0 | 1437 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | copy fasta | chr2 | 48612856 | 48684604 |
a0009c0013 | 0/0 | 1437 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | copy fasta | chr2 | 48612856 | 48684604 |
a0010c0015 | 0/0 | 1437 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | copy fasta | chr2 | 48612856 | 48684604 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 1618 | 223 | 44 | 46 | 93 | 9 | 30 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | copy fasta | chr2 | 48612856 | 48684604 |
a0001c0001t0002 | 0/0 | 1618 | 17 | 16 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | copy fasta | chr2 | 48612856 | 48684604 |
a0001c0001t0004 | 0/0 | 1618 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | copy fasta | chr2 | 48612856 | 48684604 |
a0001c0001t0005 | 0/0 | 1618 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | copy fasta | chr2 | 48612856 | 48684604 |
a0001c0001t0006 | 0/0 | 1618 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | copy fasta | chr2 | 48612856 | 48684604 |
a0001c0003t0001 | 0/0 | 1618 | 18 | 17 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | copy fasta | chr2 | 48612856 | 48684604 |
a0001c0005t0003 | 1/0 | 1618 | 3 | 0 | 0 | 0 | 1 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | copy fasta | chr2 | 48612856 | 48684604 |
a0001c0012t0001 | 0/0 | 1618 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | copy fasta | chr2 | 48612856 | 48684604 |
a0002c0002t0001 | 0/0 | 1618 | 63 | 8 | 13 | 30 | 4 | 8 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | copy fasta | chr2 | 48612856 | 48684604 |
a0002c0006t0001 | 0/0 | 1618 | 3 | 0 | 0 | 3 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | copy fasta | chr2 | 48612856 | 48684604 |
a0002c0014t0001 | 0/0 | 1618 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | copy fasta | chr2 | 48612856 | 48684604 |
a0003c0004t0001 | 0/0 | 1618 | 3 | 1 | 2 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | copy fasta | chr2 | 48612856 | 48684604 |
a0004c0008t0002 | 0/0 | 1618 | 2 | 2 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | copy fasta | chr2 | 48612856 | 48684604 |
a0005c0007t0001 | 0/0 | 1618 | 2 | 0 | 2 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | copy fasta | chr2 | 48612856 | 48684604 |
a0006c0010t0001 | 0/0 | 1618 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | copy fasta | chr2 | 48612856 | 48684604 |
a0007c0011t0001 | 0/0 | 1618 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | copy fasta | chr2 | 48612856 | 48684604 |
a0008c0009t0001 | 0/0 | 1618 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | copy fasta | chr2 | 48612856 | 48684604 |
a0009c0013t0001 | 0/0 | 1618 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | copy fasta | chr2 | 48612856 | 48684604 |
a0010c0015t0001 | 0/0 | 1618 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | copy fasta | chr2 | 48612856 | 48684604 |
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 | 0/1 | 4 | 0 | 0 | 1 | 1 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0003 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0002g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0002g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0002g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0004g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0005g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0001t0006g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0003t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0003t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0003t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0003t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0003t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0003t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0003t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0003t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0003t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0003t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0003t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0003t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0003t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0003t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0003t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0003t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0003t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0003t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0005t0003g0083 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0005t0003g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0005t0003g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0001c0012t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0002c0002t0001g0002 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0002c0002t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0002c0002t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0002c0002t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0002c0002t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0002c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0002c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0002c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0002c0002t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0002c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0002c0002t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0002c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0002c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0002c0002t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0002c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0002c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0002c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0002c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0002c0002t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0002c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0002c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0002c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0002c0002t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0002c0002t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0002c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0002c0002t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0002c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0002c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0002c0002t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0002c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0002c0002t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0002c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0002c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0002c0002t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0002c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0002c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0002c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0002c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0002c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0002c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0002c0002t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0002c0002t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0002c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0002c0002t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0002c0002t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0002c0002t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0002c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0002c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0002c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0002c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0002c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0002c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0002c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0002c0002t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0002c0002t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0002c0006t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0002c0006t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0002c0006t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0002c0014t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0003c0004t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0003c0004t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0003c0004t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0004c0008t0002g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0004c0008t0002g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0005c0007t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0005c0007t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0006c0010t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0007c0011t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0008c0009t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0009c0013t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
a0010c0015t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0033 | EUR | GBR | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0134 | EUR | GBR | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG00140 | hp1 | a0002 | c0002 | t0001 | g0114 | EUR | GBR | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0185 | EUR | GBR | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0037 | EUR | FIN | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0052 | EUR | FIN | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | CHS | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | CHS | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | CHS | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | CHS | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | CHS | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | CHS | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | CHS | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | CHS | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | CHS | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG00609 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | CHS | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | CHS | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | CHS | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0311 | AMR | PUR | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG00733 | hp1 | a0005 | c0007 | t0001 | g0027 | AMR | PUR | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG00733 | hp2 | a0002 | c0002 | t0001 | g0139 | AMR | PUR | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG00735 | hp2 | a0002 | c0002 | t0001 | g0227 | AMR | PUR | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0281 | AMR | PUR | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG00741 | hp1 | a0001 | c0001 | t0005 | g0129 | AMR | PUR | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG00741 | hp2 | a0002 | c0002 | t0001 | g0113 | AMR | PUR | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG01070 | hp1 | a0003 | c0004 | t0001 | g0063 | AMR | PUR | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0292 | AMR | PUR | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG01081 | hp2 | a0002 | c0002 | t0001 | g0206 | AMR | PUR | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0223 | AMR | PUR | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0271 | AMR | PUR | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0296 | AMR | PUR | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG01168 | hp1 | a0002 | c0002 | t0001 | g0203 | AMR | PUR | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG01168 | hp2 | a0005 | c0007 | t0001 | g0028 | AMR | PUR | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | PUR | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0279 | AMR | PUR | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | PUR | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG01243 | hp1 | a0001 | c0003 | t0001 | g0072 | AMR | PUR | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG01243 | hp2 | a0001 | c0001 | t0002 | g0092 | AMR | PUR | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | CLM | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | CLM | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG01256 | hp1 | a0002 | c0002 | t0001 | g0262 | AMR | CLM | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | CLM | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG01257 | hp2 | a0002 | c0002 | t0001 | g0218 | AMR | CLM | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0221 | AMR | CLM | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | CLM | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | CLM | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG01361 | hp1 | a0002 | c0002 | t0001 | g0226 | AMR | CLM | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0307 | AMR | CLM | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0270 | AMR | CLM | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG01433 | hp2 | a0002 | c0002 | t0001 | g0188 | AMR | CLM | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG01496 | hp1 | a0002 | c0002 | t0001 | g0219 | AMR | CLM | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG01496 | hp2 | a0002 | c0002 | t0001 | g0142 | AMR | CLM | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG01515 | hp1 | a0002 | c0002 | t0001 | g0112 | EUR | IBS | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0016 | EUR | IBS | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG01517 | hp1 | a0002 | c0002 | t0001 | g0210 | EUR | IBS | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0016 | EUR | IBS | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG01891 | hp1 | a0001 | c0003 | t0001 | g0061 | AFR | ACB | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG01891 | hp2 | a0001 | c0001 | t0004 | g0174 | AFR | ACB | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | PEL | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0278 | AMR | PEL | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | PEL | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0255 | AMR | PEL | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG01981 | hp1 | a0002 | c0002 | t0001 | g0194 | AMR | PEL | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0251 | AMR | PEL | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0275 | AMR | PEL | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PEL | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PEL | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | KHV | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | KHV | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | KHV | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG02027 | hp2 | a0002 | c0002 | t0001 | g0012 | EAS | KHV | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG02040 | hp1 | a0002 | c0002 | t0001 | g0216 | EAS | KHV | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | KHV | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG02055 | hp1 | a0001 | c0001 | t0002 | g0161 | AFR | ACB | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0282 | AFR | ACB | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | KHV | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | KHV | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG02083 | hp1 | a0002 | c0002 | t0001 | g0207 | EAS | KHV | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | KHV | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | KHV | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG02129 | hp2 | a0002 | c0006 | t0001 | g0093 | EAS | KHV | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG02132 | hp1 | a0002 | c0002 | t0001 | g0229 | EAS | KHV | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | KHV | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG02135 | hp1 | a0002 | c0002 | t0001 | g0213 | EAS | KHV | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | KHV | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0285 | AFR | ACB | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0318 | AFR | ACB | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | CDX | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG02165 | hp2 | a0002 | c0002 | t0001 | g0237 | EAS | CDX | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | ACB | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0309 | AFR | ACB | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG02280 | hp1 | a0002 | c0002 | t0001 | g0228 | AFR | ACB | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0306 | AFR | ACB | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0301 | AFR | ACB | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0257 | AFR | ACB | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG02523 | hp1 | a0001 | c0012 | t0001 | g0242 | EAS | KHV | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | KHV | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG02572 | hp2 | a0002 | c0002 | t0001 | g0002 | AFR | GWD | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0269 | SAS | PJL | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG02602 | hp2 | a0008 | c0009 | t0001 | g0152 | SAS | PJL | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0294 | AFR | GWD | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG02615 | hp2 | a0001 | c0003 | t0001 | g0018 | AFR | GWD | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG02622 | hp1 | a0001 | c0001 | t0002 | g0090 | AFR | GWD | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG02622 | hp2 | a0001 | c0003 | t0001 | g0077 | AFR | GWD | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0284 | AFR | GWD | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0319 | AFR | GWD | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG02647 | hp1 | a0001 | c0001 | t0002 | g0176 | AFR | GWD | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0316 | AFR | GWD | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0313 | SAS | PJL | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG02683 | hp2 | a0002 | c0002 | t0001 | g0209 | SAS | PJL | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0138 | SAS | PJL | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0317 | AFR | GWD | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG02717 | hp2 | a0009 | c0013 | t0001 | g0280 | AFR | GWD | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0288 | AFR | GWD | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG02723 | hp2 | a0001 | c0003 | t0001 | g0069 | AFR | GWD | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG02735 | hp1 | a0002 | c0002 | t0001 | g0225 | SAS | PJL | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0268 | SAS | PJL | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG02738 | hp2 | a0002 | c0002 | t0001 | g0144 | SAS | PJL | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG02809 | hp1 | a0001 | c0003 | t0001 | g0076 | AFR | GWD | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG02809 | hp2 | a0002 | c0002 | t0001 | g0211 | AFR | GWD | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG02818 | hp1 | a0001 | c0003 | t0001 | g0075 | AFR | GWD | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG02818 | hp2 | a0002 | c0002 | t0001 | g0002 | AFR | GWD | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0290 | AFR | GWD | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | GWD | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0220 | AFR | GWD | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0298 | AFR | GWD | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG02896 | hp1 | a0001 | c0003 | t0001 | g0079 | AFR | GWD | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0320 | AFR | GWD | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0299 | AFR | GWD | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG02897 | hp2 | a0001 | c0003 | t0001 | g0078 | AFR | GWD | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG02922 | hp1 | a0001 | c0003 | t0001 | g0066 | AFR | ESN | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG02922 | hp2 | a0001 | c0001 | t0002 | g0178 | AFR | ESN | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0321 | AFR | ESN | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG02970 | hp2 | a0001 | c0001 | t0002 | g0082 | AFR | ESN | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG02976 | hp1 | a0004 | c0008 | t0002 | g0303 | AFR | ESN | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG02976 | hp2 | a0001 | c0001 | t0002 | g0172 | AFR | ESN | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG03017 | hp1 | a0002 | c0002 | t0001 | g0098 | SAS | PJL | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0046 | SAS | PJL | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0293 | AFR | GWD | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG03041 | hp2 | a0002 | c0002 | t0001 | g0193 | AFR | GWD | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG03098 | hp1 | a0004 | c0008 | t0002 | g0302 | AFR | MSL | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG03098 | hp2 | a0001 | c0003 | t0001 | g0062 | AFR | MSL | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG03130 | hp1 | a0002 | c0002 | t0001 | g0002 | AFR | ESN | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | ESN | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG03139 | hp1 | a0001 | c0001 | t0002 | g0260 | AFR | ESN | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG03139 | hp2 | a0001 | c0001 | t0002 | g0179 | AFR | ESN | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0286 | AFR | ESN | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG03209 | hp1 | a0001 | c0001 | t0002 | g0102 | AFR | MSL | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG03225 | hp1 | a0001 | c0001 | t0002 | g0182 | AFR | MSL | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0315 | AFR | MSL | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG03239 | hp1 | a0002 | c0002 | t0001 | g0191 | SAS | PJL | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG03486 | hp1 | a0001 | c0001 | t0002 | g0177 | AFR | MSL | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | MSL | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG03516 | hp1 | a0002 | c0002 | t0001 | g0208 | AFR | ESN | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG03516 | hp2 | a0001 | c0001 | t0002 | g0081 | AFR | ESN | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0291 | AFR | GWD | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0310 | AFR | GWD | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0287 | AFR | MSL | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0261 | AFR | MSL | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0265 | SAS | PJL | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG03654 | hp2 | a0002 | c0014 | t0001 | g0195 | SAS | PJL | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0047 | SAS | PJL | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0304 | SAS | PJL | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0050 | SAS | PJL | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0273 | SAS | PJL | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0156 | SAS | PJL | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0120 | SAS | PJL | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG03831 | hp1 | a0002 | c0002 | t0001 | g0217 | SAS | BEB | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0305 | SAS | BEB | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0051 | SAS | BEB | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | BEB | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | BEB | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0312 | SAS | BEB | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG04115 | hp1 | a0001 | c0005 | t0003 | g0087 | SAS | STU | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0088 | SAS | STU | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0023 | SAS | BEB | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG04184 | hp2 | a0002 | c0002 | t0001 | g0141 | SAS | BEB | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0157 | SAS | STU | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0049 | SAS | STU | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0054 | SAS | STU | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0314 | SAS | STU | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0035 | SAS | STU | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG04228 | hp2 | a0007 | c0011 | t0001 | g0048 | SAS | STU | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA18522 | hp1 | a0001 | c0003 | t0001 | g0064 | AFR | YRI | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | YRI | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | CHB | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | CHB | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | CHB | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA18747 | hp2 | a0002 | c0002 | t0001 | g0235 | EAS | CHB | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA18906 | hp1 | a0001 | c0003 | t0001 | g0067 | AFR | YRI | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0283 | AFR | YRI | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA18940 | hp2 | a0002 | c0006 | t0001 | g0091 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA18941 | hp1 | a0002 | c0002 | t0001 | g0187 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA18947 | hp1 | a0002 | c0002 | t0001 | g0171 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA18950 | hp2 | a0002 | c0002 | t0001 | g0215 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA18951 | hp1 | a0002 | c0002 | t0001 | g0236 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA18953 | hp2 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA18954 | hp2 | a0002 | c0002 | t0001 | g0256 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA18960 | hp1 | a0002 | c0002 | t0001 | g0214 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA18961 | hp1 | a0002 | c0002 | t0001 | g0200 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA18962 | hp1 | a0002 | c0002 | t0001 | g0014 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA18968 | hp2 | a0002 | c0002 | t0001 | g0159 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA18969 | hp2 | a0002 | c0002 | t0001 | g0205 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA18970 | hp2 | a0002 | c0002 | t0001 | g0204 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA18971 | hp2 | a0002 | c0002 | t0001 | g0233 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA18975 | hp2 | a0002 | c0002 | t0001 | g0189 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA18982 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA18998 | hp1 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA19000 | hp2 | a0002 | c0002 | t0001 | g0192 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA19002 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA19010 | hp2 | a0010 | c0015 | t0001 | g0164 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA19030 | hp1 | a0001 | c0001 | t0002 | g0181 | AFR | LWK | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA19030 | hp2 | a0001 | c0003 | t0001 | g0071 | AFR | LWK | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA19043 | hp1 | a0001 | c0001 | t0006 | g0289 | AFR | LWK | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0258 | AFR | LWK | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA19063 | hp2 | a0002 | c0002 | t0001 | g0212 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA19079 | hp1 | a0002 | c0006 | t0001 | g0094 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA19080 | hp1 | a0002 | c0002 | t0001 | g0014 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA19085 | hp1 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA19087 | hp1 | a0002 | c0002 | t0001 | g0232 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA19240 | hp1 | a0002 | c0002 | t0001 | g0002 | AFR | YRI | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | YRI | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0300 | AFR | ASW | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ASW | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA20752 | hp1 | a0001 | c0005 | t0003 | g0084 | EUR | TSI | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA20805 | hp1 | a0002 | c0002 | t0001 | g0140 | EUR | TSI | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0308 | EUR | TSI | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA20905 | hp1 | a0002 | c0002 | t0001 | g0111 | SAS | GIH | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0234 | SAS | GIH | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG01123 | hp1 | a0003 | c0004 | t0001 | g0080 | AMR | CLM | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG01123 | hp2 | a0002 | c0002 | t0001 | g0263 | AMR | CLM | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | ACB | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG02486 | hp2 | a0001 | c0003 | t0001 | g0074 | AFR | ACB | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0295 | AFR | ACB | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG02559 | hp2 | a0001 | c0001 | t0002 | g0180 | AFR | ACB | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG03471 | hp1 | a0001 | c0003 | t0001 | g0070 | AFR | MSL | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG03471 | hp2 | a0001 | c0001 | t0002 | g0104 | AFR | MSL | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG06807 | hp1 | a0001 | c0001 | t0002 | g0175 | AFR | USA | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
HG06807 | hp2 | a0001 | c0003 | t0001 | g0073 | AFR | USA | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA20300 | hp1 | a0001 | c0003 | t0001 | g0068 | AFR | USA | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA20300 | hp2 | a0006 | c0010 | t0001 | g0297 | AFR | USA | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA21309 | hp1 | a0003 | c0004 | t0001 | g0065 | AFR | LWK | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0259 | AFR | LWK | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0001 | REF | REF | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
homoSapiens_grch38 | hp1 | a0001 | c0005 | t0003 | g0083 | REF | REF | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:48645091
|
C | T | 1 | a0010 | 1 | NA19010.hp2 | missense_variant | MODERATE | c.362C>T | p.Ala121Val | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 5/9 | 381/1618 | 362/1437 | 121/478 | chr2 | 48645091 | ||
chr2:48646746
|
G | T | 1 | a0004 | 2 | HG02976.hp1 HG03098.hp1 |
missense_variant | MODERATE | c.682G>T | p.Val228Leu | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/9 | 701/1618 | 682/1437 | 228/478 | chr2 | 48646746 | ||
chr2:48646786
|
A | G | 1 | a0003 | 3 | HG01070.hp1 HG01123.hp1 NA21309.hp1 |
missense_variant | MODERATE | c.722A>G | p.Tyr241Cys | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/9 | 741/1618 | 722/1437 | 241/478 | chr2 | 48646786 | ||
chr2:48646839
|
A | G | 1 | a0002 | 67 | HG00140.hp1 HG00609.hp2 HG00733.hp2 others(64): Show |
missense_variant | MODERATE | c.775A>G | p.Asn259Asp | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/9 | 794/1618 | 775/1437 | 259/478 | chr2 | 48646839 | ||
chr2:48646921
|
C | T | 1 | a0009 | 1 | HG02717.hp2 | missense_variant | MODERATE | c.857C>T | p.Ala286Val | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/9 | 876/1618 | 857/1437 | 286/478 | chr2 | 48646921 | ||
chr2:48669758
|
A | G | 1 | a0005 | 2 | HG00733.hp1 HG01168.hp2 |
missense_variant | MODERATE | c.1015A>G | p.Thr339Ala | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 7/9 | 1034/1618 | 1015/1437 | 339/478 | chr2 | 48669758 | ||
chr2:48669776
|
G | A | 1 | a0008 | 1 | HG02602.hp2 | missense_variant | MODERATE | c.1033G>A | p.Glu345Lys | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 7/9 | 1052/1618 | 1033/1437 | 345/478 | chr2 | 48669776 | ||
chr2:48669798
|
G | A | 1 | a0006 | 1 | NA20300.hp2 | missense_variant | MODERATE | c.1055G>A | p.Ser352Asn | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 7/9 | 1074/1618 | 1055/1437 | 352/478 | chr2 | 48669798 | ||
chr2:48669908
|
G | A | 1 | a0007 | 1 | HG04228.hp2 | missense_variant | MODERATE | c.1165G>A | p.Asp389Asn | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 7/9 | 1184/1618 | 1165/1437 | 389/478 | chr2 | 48669908 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:48620904
|
A | T | 1 | a0002c0006 | 3 | HG02129.hp2 NA18940.hp2 NA19079.hp1 |
synonymous_variant | LOW | c.75A>T | p.Leu25Leu | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 2/9 | 94/1618 | 75/1437 | 25/478 | chr2 | 48620904 | ||
chr2:48646523
|
T | C | 2 | a0001c0003a0003c0004 | 21 | HG01070.hp1 HG01123.hp1 HG01243.hp1 others(18): Show |
synonymous_variant | LOW | c.459T>C | p.His153His | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/9 | 478/1618 | 459/1437 | 153/478 | chr2 | 48646523 | ||
chr2:48646868
|
T | C | 1 | a0002c0014 | 1 | HG03654.hp2 | synonymous_variant | LOW | c.804T>C | p.Ala268Ala | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/9 | 823/1618 | 804/1437 | 268/478 | chr2 | 48646868 | ||
chr2:48669874
|
C | T | 1 | a0001c0012 | 1 | HG02523.hp1 | synonymous_variant | LOW | c.1131C>T | p.Asp377Asp | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 7/9 | 1150/1618 | 1131/1437 | 377/478 | chr2 | 48669874 | ||
chr2:48671659
|
T | A | 14 | a0001c0001a0001c0003a0001c0012others(11): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
synonymous_variant | LOW | c.1308T>A | p.Val436Val | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/9 | 1327/1618 | 1308/1437 | 436/478 | chr2 | 48671659 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:48617856
|
A | T | 1 | a0001c0001t0006 | 1 | NA19043.hp1 | 5_prime_UTR_variant | MODIFIER | c.-19A>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 1/9 | 19 | chr2 | 48617856 | |||||
chr2:48617862
|
T | C | 1 | a0001c0001t0004 | 1 | HG01891.hp2 | 5_prime_UTR_variant | MODIFIER | c.-13T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 1/9 | 13 | chr2 | 48617862 | |||||
chr2:48679459
|
A | G | 1 | a0001c0001t0005 | 1 | HG00741.hp1 | 3_prime_UTR_variant | MODIFIER | c.*17A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 9/9 | 17 | chr2 | 48679459 | |||||
chr2:48679486
|
T | C | 18 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(15): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
3_prime_UTR_variant | MODIFIER | c.*44T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 9/9 | 44 | chr2 | 48679486 | |||||
chr2:48679554
|
G | T | 3 | a0001c0001t0002a0001c0001t0004a0004c0008t0002 | 20 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*112G>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 9/9 | 112 | chr2 | 48679554 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:48617980
|
C | T | 1 | a0001c0001t0001g0321 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.21+85C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 1/8 | chr2 | 48617980 | ||||||
chr2:48618093
|
G | A | 1 | a0001c0001t0001g0017 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.21+198G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 1/8 | chr2 | 48618093 | ||||||
chr2:48618108
|
A | G | 18 | a0001c0001t0001g0016a0001c0001t0001g0304a0001c0001t0001g0305others(15): Show | 19 | HG00642.hp1 HG01361.hp2 HG01515.hp2 others(16): Show |
intron_variant | MODIFIER | c.21+213A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 1/8 | chr2 | 48618108 | ||||||
chr2:48618244
|
C | T | 2 | a0004c0008t0002g0302a0004c0008t0002g0303 | 2 | HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.21+349C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 1/8 | chr2 | 48618244 | ||||||
chr2:48618522
|
C | A | 65 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0019others(62): Show | 69 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(66): Show |
intron_variant | MODIFIER | c.21+627C>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 1/8 | chr2 | 48618522 | ||||||
chr2:48618523
|
C | G | 65 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0019others(62): Show | 69 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(66): Show |
intron_variant | MODIFIER | c.21+628C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 1/8 | chr2 | 48618523 | ||||||
chr2:48618567
|
C | T | 42 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(39): Show | 46 | HG00642.hp1 HG01074.hp1 HG01109.hp2 others(43): Show |
intron_variant | MODIFIER | c.21+672C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 1/8 | chr2 | 48618567 | ||||||
chr2:48618754
|
A | T | 18 | a0001c0001t0001g0016a0001c0001t0001g0304a0001c0001t0001g0305others(15): Show | 19 | HG00642.hp1 HG01361.hp2 HG01515.hp2 others(16): Show |
intron_variant | MODIFIER | c.21+859A>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 1/8 | chr2 | 48618754 | ||||||
chr2:48618867
|
C | G | 2 | a0004c0008t0002g0302a0004c0008t0002g0303 | 2 | HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.21+972C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 1/8 | chr2 | 48618867 | ||||||
chr2:48618879
|
C | T | 109 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(106): Show | 117 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(114): Show |
intron_variant | MODIFIER | c.21+984C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 1/8 | chr2 | 48618879 | ||||||
chr2:48618945
|
G | GT | 7 | a0001c0001t0001g0015a0001c0001t0001g0274a0001c0001t0001g0275others(4): Show | 8 | HG01175.hp2 HG01934.hp1 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.21+1056dupT | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 48618945 | |||||
chr2:48618957
|
G | A | 1 | a0009c0013t0001g0280 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.21+1062G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 1/8 | chr2 | 48618957 | ||||||
chr2:48619049
|
A | C | 1 | a0002c0002t0001g0014 | 2 | NA18962.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.21+1154A>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 1/8 | chr2 | 48619049 | ||||||
chr2:48619069
|
T | G | 2 | a0001c0001t0002g0081a0001c0001t0002g0082 | 2 | HG02970.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.21+1174T>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 1/8 | chr2 | 48619069 | ||||||
chr2:48619134
|
C | A | 1 | a0001c0003t0001g0018 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.21+1239C>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 1/8 | chr2 | 48619134 | ||||||
chr2:48619224
|
C | T | 315 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(312): Show | 338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.21+1329C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 1/8 | chr2 | 48619224 | ||||||
chr2:48619343
|
G | A | 2 | a0004c0008t0002g0302a0004c0008t0002g0303 | 2 | HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.21+1448G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 1/8 | chr2 | 48619343 | ||||||
chr2:48619360
|
C | T | 1 | a0001c0001t0001g0301 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.21+1465C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 1/8 | chr2 | 48619360 | ||||||
chr2:48619432
|
C | T | 315 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(312): Show | 338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.22-1419C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 1/8 | chr2 | 48619432 | ||||||
chr2:48619469
|
C | CA | 54 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0019others(51): Show | 58 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.22-1369dupA | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 48619469 | |||||
chr2:48619477
|
A | T | 1 | a0009c0013t0001g0280 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.22-1374A>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 1/8 | chr2 | 48619477 | ||||||
chr2:48619480
|
A | T | 20 | a0001c0001t0001g0016a0001c0001t0001g0272a0001c0001t0001g0273others(17): Show | 21 | HG00597.hp2 HG00642.hp1 HG01361.hp2 others(18): Show |
intron_variant | MODIFIER | c.22-1371A>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 1/8 | chr2 | 48619480 | ||||||
chr2:48619483
|
T | A | 22 | a0001c0001t0001g0003a0001c0001t0001g0019a0001c0001t0001g0020others(19): Show | 25 | HG00597.hp1 HG00738.hp2 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.22-1368T>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 1/8 | chr2 | 48619483 | ||||||
chr2:48619486
|
T | A | 4 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0001t0001g0284others(1): Show | 4 | HG02055.hp2 HG02145.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.22-1365T>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 1/8 | chr2 | 48619486 | ||||||
chr2:48619496
|
A | T | 1 | a0003c0004t0001g0080 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.22-1355A>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 1/8 | chr2 | 48619496 | ||||||
chr2:48619498
|
A | T | 39 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(36): Show | 43 | HG00642.hp1 HG01074.hp1 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.22-1353A>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 1/8 | chr2 | 48619498 | ||||||
chr2:48619508
|
C | T | 3 | a0001c0001t0006g0289a0004c0008t0002g0302a0004c0008t0002g0303 | 3 | HG02976.hp1 HG03098.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.22-1343C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 1/8 | chr2 | 48619508 | ||||||
chr2:48619551
|
T | G | 1 | a0001c0001t0001g0023 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.22-1300T>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 1/8 | chr2 | 48619551 | ||||||
chr2:48619582
|
G | A | 1 | a0001c0001t0001g0024 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.22-1269G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 1/8 | chr2 | 48619582 | ||||||
chr2:48619685
|
G | C | 3 | a0001c0001t0006g0289a0004c0008t0002g0302a0004c0008t0002g0303 | 3 | HG02976.hp1 HG03098.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.22-1166G>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 1/8 | chr2 | 48619685 | ||||||
chr2:48619758
|
G | A | 3 | a0001c0001t0006g0289a0004c0008t0002g0302a0004c0008t0002g0303 | 3 | HG02976.hp1 HG03098.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.22-1093G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 1/8 | chr2 | 48619758 | ||||||
chr2:48619833
|
G | T | 1 | a0001c0001t0001g0058 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.22-1018G>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 1/8 | chr2 | 48619833 | ||||||
chr2:48619913
|
A | T | 12 | a0001c0001t0001g0017a0001c0001t0001g0290a0001c0001t0001g0291others(9): Show | 12 | HG01074.hp1 HG01109.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.22-938A>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 1/8 | chr2 | 48619913 | ||||||
chr2:48619929
|
G | A | 7 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0001t0001g0284others(4): Show | 7 | HG02055.hp2 HG02145.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.22-922G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 1/8 | chr2 | 48619929 | ||||||
chr2:48619958
|
C | T | 2 | a0001c0001t0001g0270a0001c0001t0001g0271 | 2 | HG01106.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.22-893C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 1/8 | chr2 | 48619958 | ||||||
chr2:48620035
|
G | A | 12 | a0001c0001t0001g0016a0001c0001t0001g0304a0001c0001t0001g0305others(9): Show | 13 | HG00642.hp1 HG01361.hp2 HG01515.hp2 others(10): Show |
intron_variant | MODIFIER | c.22-816G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 1/8 | chr2 | 48620035 | ||||||
chr2:48620218
|
A | G | 3 | a0001c0001t0006g0289a0004c0008t0002g0302a0004c0008t0002g0303 | 3 | HG02976.hp1 HG03098.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.22-633A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 1/8 | chr2 | 48620218 | ||||||
chr2:48620394
|
T | C | 2 | a0001c0001t0001g0006a0001c0001t0001g0100 | 3 | NA18942.hp1 NA18974.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.22-457T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 1/8 | chr2 | 48620394 | ||||||
chr2:48620487
|
G | A | 3 | a0001c0001t0006g0289a0004c0008t0002g0302a0004c0008t0002g0303 | 3 | HG02976.hp1 HG03098.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.22-364G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 1/8 | chr2 | 48620487 | ||||||
chr2:48620593
|
CA | C | 3 | a0001c0001t0006g0289a0004c0008t0002g0302a0004c0008t0002g0303 | 3 | HG02976.hp1 HG03098.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.22-257delA | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 1/8 | chr2 | 48620593 | ||||||
chr2:48620729
|
T | A | 47 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0019others(44): Show | 51 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(48): Show |
intron_variant | MODIFIER | c.22-122T>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 1/8 | chr2 | 48620729 | ||||||
chr2:48620731
|
C | T | 2 | a0001c0001t0001g0268a0001c0001t0001g0269 | 2 | HG02602.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.22-120C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 1/8 | chr2 | 48620731 | ||||||
chr2:48620779
|
G | GAATA | 111 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(108): Show | 122 | HG00140.hp2 HG00423.hp2 HG00609.hp2 others(119): Show |
intron_variant | MODIFIER | c.22-33_22-30dupTAAA | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 48620779 | |||||
chr2:48620779
|
G | GAATAAAT others(1): Show |
46 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0095others(43): Show | 50 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.22-37_22-30dupTAAA others(4): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 48620779 | |||||
chr2:48620779
|
G | GAATAAAT others(5): Show |
4 | a0001c0001t0001g0264a0001c0001t0001g0265a0001c0001t0001g0266others(1): Show | 4 | HG03654.hp1 NA19000.hp1 NA19063.hp1 others(1): Show |
intron_variant | MODIFIER | c.22-41_22-30dupTAAA others(8): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 48620779 | |||||
chr2:48620779
|
GAATA | G | 53 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0019others(50): Show | 57 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(54): Show |
intron_variant | MODIFIER | c.22-33_22-30delTAAA | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 48620779 | |||||
chr2:48620779
|
GAATAAAT others(5): Show |
G | 1 | a0001c0001t0001g0101 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.22-41_22-30delTAAA others(8): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 48620779 | |||||
chr2:48621018
|
T | C | 12 | a0001c0001t0001g0017a0001c0001t0001g0290a0001c0001t0001g0291others(9): Show | 12 | HG01074.hp1 HG01109.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.123+66T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 2/8 | chr2 | 48621018 | ||||||
chr2:48621146
|
CT | C | 12 | a0001c0001t0001g0017a0001c0001t0001g0290a0001c0001t0001g0291others(9): Show | 12 | HG01074.hp1 HG01109.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.124-12delT | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 48621146 | |||||
chr2:48621156
|
C | T | 47 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0019others(44): Show | 51 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(48): Show |
intron_variant | MODIFIER | c.124-11C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 2/8 | chr2 | 48621156 | ||||||
chr2:48621376
|
G | C | 66 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0086others(63): Show | 68 | HG00140.hp2 HG00423.hp2 HG00597.hp1 others(65): Show |
intron_variant | MODIFIER | c.247+86G>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48621376 | ||||||
chr2:48621409
|
C | G | 2 | a0004c0008t0002g0302a0004c0008t0002g0303 | 2 | HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.247+119C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48621409 | ||||||
chr2:48621501
|
T | C | 208 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(205): Show | 223 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.247+211T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48621501 | ||||||
chr2:48621657
|
G | A | 2 | a0004c0008t0002g0302a0004c0008t0002g0303 | 2 | HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.247+367G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48621657 | ||||||
chr2:48621695
|
G | A | 4 | a0001c0003t0001g0018a0001c0003t0001g0070a0001c0003t0001g0071others(1): Show | 4 | HG01243.hp1 HG02615.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.247+405G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48621695 | ||||||
chr2:48621927
|
C | G | 248 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(245): Show | 267 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.247+637C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48621927 | ||||||
chr2:48621985
|
A | G | 47 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0019others(44): Show | 51 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(48): Show |
intron_variant | MODIFIER | c.247+695A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48621985 | ||||||
chr2:48622014
|
C | T | 5 | a0002c0002t0001g0012a0002c0002t0001g0159a0002c0002t0001g0235others(2): Show | 6 | HG02027.hp2 HG02165.hp2 NA18747.hp2 others(3): Show |
intron_variant | MODIFIER | c.247+724C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48622014 | ||||||
chr2:48622206
|
G | T | 8 | a0001c0001t0001g0017a0001c0001t0001g0290a0001c0001t0001g0291others(5): Show | 8 | HG01074.hp1 HG01884.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.247+916G>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48622206 | ||||||
chr2:48622415
|
A | G | 12 | a0001c0001t0001g0016a0001c0001t0001g0304a0001c0001t0001g0305others(9): Show | 13 | HG00642.hp1 HG01361.hp2 HG01515.hp2 others(10): Show |
intron_variant | MODIFIER | c.247+1125A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48622415 | ||||||
chr2:48622499
|
A | T | 1 | a0009c0013t0001g0280 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.247+1209A>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48622499 | ||||||
chr2:48622505
|
G | GT | 6 | a0001c0001t0001g0315a0001c0001t0001g0316a0001c0001t0001g0317others(3): Show | 6 | HG02145.hp2 HG02630.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.247+1222dupT | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 48622505 | |||||
chr2:48622689
|
C | T | 1 | a0001c0001t0001g0293 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.247+1399C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48622689 | ||||||
chr2:48622694
|
C | T | 2 | a0004c0008t0002g0302a0004c0008t0002g0303 | 2 | HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.247+1404C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48622694 | ||||||
chr2:48622790
|
C | T | 1 | a0001c0001t0001g0255 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.247+1500C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48622790 | ||||||
chr2:48622809
|
G | A | 1 | a0001c0001t0001g0107 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.247+1519G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48622809 | ||||||
chr2:48622812
|
C | T | 39 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(36): Show | 43 | HG00642.hp1 HG01074.hp1 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.247+1522C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48622812 | ||||||
chr2:48622833
|
T | TA | 106 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(103): Show | 112 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.247+1560dupA | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 48622833 | |||||
chr2:48622943
|
A | AAT | 315 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(312): Show | 338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.247+1654_247+1655i others(4): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 48622943 | |||||
chr2:48623091
|
T | G | 86 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(83): Show | 94 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.247+1801T>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48623091 | ||||||
chr2:48623095
|
A | G | 2 | a0001c0001t0001g0085a0001c0001t0001g0086 | 2 | NA18940.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.247+1805A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48623095 | ||||||
chr2:48623326
|
C | T | 12 | a0001c0001t0001g0017a0001c0001t0001g0290a0001c0001t0001g0291others(9): Show | 12 | HG01074.hp1 HG01109.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.247+2036C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48623326 | ||||||
chr2:48623469
|
G | A | 1 | a0001c0001t0001g0025 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.247+2179G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48623469 | ||||||
chr2:48623615
|
T | C | 1 | a0001c0001t0001g0026 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.247+2325T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48623615 | ||||||
chr2:48623630
|
A | G | 1 | a0001c0001t0001g0184 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.247+2340A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48623630 | ||||||
chr2:48623650
|
C | G | 1 | a0001c0001t0001g0184 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.247+2360C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48623650 | ||||||
chr2:48623675
|
G | C | 207 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(204): Show | 222 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.247+2385G>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48623675 | ||||||
chr2:48623775
|
G | T | 1 | a0001c0001t0001g0158 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.247+2485G>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48623775 | ||||||
chr2:48623787
|
A | G | 1 | a0009c0013t0001g0280 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.247+2497A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48623787 | ||||||
chr2:48623872
|
G | A | 2 | a0004c0008t0002g0302a0004c0008t0002g0303 | 2 | HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.247+2582G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48623872 | ||||||
chr2:48623944
|
C | T | 1 | a0001c0001t0001g0054 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.247+2654C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48623944 | ||||||
chr2:48624024
|
G | A | 2 | a0004c0008t0002g0302a0004c0008t0002g0303 | 2 | HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.247+2734G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48624024 | ||||||
chr2:48624045
|
C | G | 3 | a0002c0006t0001g0091a0002c0006t0001g0093a0002c0006t0001g0094 | 3 | HG02129.hp2 NA18940.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.247+2755C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48624045 | ||||||
chr2:48624051
|
CTAAACCC others(6755): Show |
C | 45 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0019others(42): Show | 49 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(46): Show |
intron_variant | MODIFIER | c.247+2764_247+9525d others(2): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 48624051 | |||||
chr2:48624233
|
TAAAAC | T | 2 | a0002c0002t0001g0002a0002c0002t0001g0188 | 5 | HG01433.hp2 HG02572.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.247+2948_247+2952d others(7): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 48624233 | |||||
chr2:48624378
|
T | C | 41 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(38): Show | 45 | HG00642.hp1 HG01074.hp1 HG01109.hp2 others(42): Show |
intron_variant | MODIFIER | c.247+3088T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48624378 | ||||||
chr2:48624381
|
C | A | 2 | a0004c0008t0002g0302a0004c0008t0002g0303 | 2 | HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.247+3091C>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48624381 | ||||||
chr2:48624402
|
T | C | 3 | a0001c0001t0001g0190a0002c0002t0001g0189a0002c0002t0001g0256 | 3 | NA18953.hp1 NA18954.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.247+3112T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48624402 | ||||||
chr2:48624457
|
G | C | 1 | a0002c0002t0001g0191 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.247+3167G>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48624457 | ||||||
chr2:48624459
|
T | TATAGATA others(9): Show |
1 | a0004c0008t0002g0303 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.247+3182_247+3197d others(18): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 48624459 | |||||
chr2:48624459
|
T | TATAGATA others(13): Show |
1 | a0004c0008t0002g0302 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.247+3178_247+3197d others(22): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 48624459 | |||||
chr2:48624459
|
TATAG | T | 205 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(202): Show | 220 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.247+3194_247+3197d others(6): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 48624459 | |||||
chr2:48624467
|
G | T | 3 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0234 | 3 | HG03710.hp1 HG04199.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.247+3177G>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48624467 | ||||||
chr2:48624681
|
G | T | 267 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(264): Show | 286 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(283): Show |
intron_variant | MODIFIER | c.247+3391G>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48624681 | ||||||
chr2:48624762
|
GTT | G | 267 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(264): Show | 286 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(283): Show |
intron_variant | MODIFIER | c.247+3483_247+3484d others(4): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 48624762 | |||||
chr2:48624999
|
G | A | 1 | a0001c0001t0001g0273 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.247+3709G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48624999 | ||||||
chr2:48625331
|
G | C | 1 | a0002c0002t0001g0193 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.247+4041G>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48625331 | ||||||
chr2:48625393
|
T | A | 1 | a0001c0001t0001g0096 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.247+4103T>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48625393 | ||||||
chr2:48625421
|
T | C | 1 | a0001c0001t0001g0238 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.247+4131T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48625421 | ||||||
chr2:48625604
|
G | A | 2 | a0004c0008t0002g0302a0004c0008t0002g0303 | 2 | HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.247+4314G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48625604 | ||||||
chr2:48625639
|
G | A | 3 | a0001c0001t0001g0017a0001c0001t0001g0290a0001c0001t0001g0291 | 3 | HG01884.hp1 HG02886.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.247+4349G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48625639 | ||||||
chr2:48625696
|
C | A | 1 | a0001c0001t0001g0273 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.247+4406C>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48625696 | ||||||
chr2:48625713
|
A | G | 1 | a0001c0001t0001g0155 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.247+4423A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48625713 | ||||||
chr2:48625788
|
G | A | 2 | a0001c0003t0001g0073a0001c0003t0001g0074 | 2 | HG02486.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.247+4498G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48625788 | ||||||
chr2:48625845
|
A | T | 3 | a0002c0002t0001g0011a0002c0002t0001g0232a0002c0002t0001g0233 | 4 | NA18971.hp2 NA18998.hp1 NA19085.hp1 others(1): Show |
intron_variant | MODIFIER | c.247+4555A>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48625845 | ||||||
chr2:48625869
|
G | A | 6 | a0001c0001t0001g0315a0001c0001t0001g0316a0001c0001t0001g0317others(3): Show | 6 | HG02145.hp2 HG02630.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.247+4579G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48625869 | ||||||
chr2:48625893
|
C | T | 7 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0001t0001g0284others(4): Show | 7 | HG02055.hp2 HG02145.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.247+4603C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48625893 | ||||||
chr2:48625906
|
C | T | 2 | a0004c0008t0002g0302a0004c0008t0002g0303 | 2 | HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.247+4616C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48625906 | ||||||
chr2:48626218
|
C | A | 2 | a0001c0001t0001g0108a0001c0001t0001g0109 | 2 | HG00558.hp2 NA18956.hp2 |
intron_variant | MODIFIER | c.247+4928C>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48626218 | ||||||
chr2:48626221
|
C | T | 19 | a0001c0001t0001g0006a0001c0001t0001g0096a0001c0001t0001g0097others(16): Show | 20 | HG00423.hp1 HG02015.hp1 HG02056.hp2 others(17): Show |
intron_variant | MODIFIER | c.247+4931C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48626221 | ||||||
chr2:48626251
|
A | G | 1 | a0002c0002t0001g0229 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.247+4961A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48626251 | ||||||
chr2:48626388
|
C | A | 269 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(266): Show | 288 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(285): Show |
intron_variant | MODIFIER | c.247+5098C>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48626388 | ||||||
chr2:48626388
|
C | T | 1 | a0001c0001t0001g0276 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.247+5098C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48626388 | ||||||
chr2:48626469
|
A | G | 39 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(36): Show | 43 | HG00642.hp1 HG01074.hp1 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.247+5179A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48626469 | ||||||
chr2:48626474
|
C | G | 3 | a0002c0006t0001g0091a0002c0006t0001g0093a0002c0006t0001g0094 | 3 | HG02129.hp2 NA18940.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.247+5184C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48626474 | ||||||
chr2:48626492
|
T | C | 1 | a0001c0001t0001g0160 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.247+5202T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48626492 | ||||||
chr2:48626657
|
C | A | 1 | a0002c0002t0001g0194 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.247+5367C>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48626657 | ||||||
chr2:48626690
|
G | A | 1 | a0002c0014t0001g0195 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.247+5400G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48626690 | ||||||
chr2:48626758
|
G | A | 1 | a0001c0001t0001g0110 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.247+5468G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48626758 | ||||||
chr2:48626782
|
C | T | 1 | a0009c0013t0001g0280 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.247+5492C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48626782 | ||||||
chr2:48626922
|
T | C | 18 | a0001c0001t0001g0016a0001c0001t0001g0304a0001c0001t0001g0305others(15): Show | 19 | HG00642.hp1 HG01361.hp2 HG01515.hp2 others(16): Show |
intron_variant | MODIFIER | c.247+5632T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48626922 | ||||||
chr2:48626959
|
C | G | 270 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(267): Show | 289 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(286): Show |
intron_variant | MODIFIER | c.247+5669C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48626959 | ||||||
chr2:48627094
|
C | T | 1 | a0001c0001t0001g0281 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.247+5804C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48627094 | ||||||
chr2:48627108
|
T | C | 2 | a0004c0008t0002g0302a0004c0008t0002g0303 | 2 | HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.247+5818T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48627108 | ||||||
chr2:48627114
|
T | A | 1 | a0001c0001t0001g0310 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.247+5824T>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48627114 | ||||||
chr2:48627154
|
T | A | 1 | a0002c0002t0001g0189 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.247+5864T>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48627154 | ||||||
chr2:48627372
|
A | T | 1 | a0001c0001t0001g0281 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.247+6082A>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48627372 | ||||||
chr2:48627490
|
C | A | 4 | a0002c0002t0001g0111a0002c0002t0001g0112a0002c0002t0001g0113others(1): Show | 4 | HG00140.hp1 HG00741.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.247+6200C>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48627490 | ||||||
chr2:48627502
|
T | G | 3 | a0001c0001t0001g0006a0001c0001t0001g0100a0001c0001t0001g0145 | 4 | NA18942.hp1 NA18974.hp2 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.247+6212T>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48627502 | ||||||
chr2:48627503
|
G | C | 8 | a0001c0001t0001g0013a0001c0001t0001g0196a0001c0001t0001g0197others(5): Show | 9 | HG02451.hp2 HG02886.hp2 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.247+6213G>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48627503 | ||||||
chr2:48627538
|
C | A | 20 | a0001c0003t0001g0018a0001c0003t0001g0062a0001c0003t0001g0064others(17): Show | 20 | HG01070.hp1 HG01123.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.247+6248C>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48627538 | ||||||
chr2:48627546
|
G | C | 267 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(264): Show | 286 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(283): Show |
intron_variant | MODIFIER | c.247+6256G>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48627546 | ||||||
chr2:48627616
|
T | A | 20 | a0001c0003t0001g0018a0001c0003t0001g0062a0001c0003t0001g0064others(17): Show | 20 | HG01070.hp1 HG01123.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.247+6326T>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48627616 | ||||||
chr2:48627641
|
A | C | 1 | a0001c0001t0001g0272 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.247+6351A>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48627641 | ||||||
chr2:48627652
|
C | G | 3 | a0002c0006t0001g0091a0002c0006t0001g0093a0002c0006t0001g0094 | 3 | HG02129.hp2 NA18940.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.247+6362C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48627652 | ||||||
chr2:48627761
|
A | G | 3 | a0002c0006t0001g0091a0002c0006t0001g0093a0002c0006t0001g0094 | 3 | HG02129.hp2 NA18940.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.247+6471A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48627761 | ||||||
chr2:48627772
|
A | G | 2 | a0004c0008t0002g0302a0004c0008t0002g0303 | 2 | HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.247+6482A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48627772 | ||||||
chr2:48627930
|
T | C | 21 | a0001c0003t0001g0018a0001c0003t0001g0061a0001c0003t0001g0062others(18): Show | 21 | HG01070.hp1 HG01123.hp1 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.247+6640T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48627930 | ||||||
chr2:48628061
|
G | T | 2 | a0001c0001t0001g0089a0001c0001t0001g0095 | 2 | HG00597.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.247+6771G>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48628061 | ||||||
chr2:48628075
|
C | G | 2 | a0001c0003t0001g0078a0001c0003t0001g0079 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.247+6785C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48628075 | ||||||
chr2:48628150
|
A | C | 1 | a0001c0001t0001g0281 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.247+6860A>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48628150 | ||||||
chr2:48628156
|
T | C | 2 | a0001c0001t0001g0003a0001c0001t0001g0288 | 5 | HG01884.hp2 HG02723.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.247+6866T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48628156 | ||||||
chr2:48628183
|
A | C | 19 | a0001c0001t0001g0006a0001c0001t0001g0096a0001c0001t0001g0097others(16): Show | 20 | HG00423.hp1 HG02015.hp1 HG02056.hp2 others(17): Show |
intron_variant | MODIFIER | c.247+6893A>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48628183 | ||||||
chr2:48628406
|
A | G | 1 | a0009c0013t0001g0280 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.247+7116A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48628406 | ||||||
chr2:48628477
|
G | A | 246 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(243): Show | 265 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.247+7187G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48628477 | ||||||
chr2:48628507
|
C | T | 2 | a0001c0001t0001g0003a0001c0001t0001g0288 | 5 | HG01884.hp2 HG02723.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.247+7217C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48628507 | ||||||
chr2:48628515
|
T | C | 1 | a0001c0001t0002g0092 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.247+7225T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48628515 | ||||||
chr2:48628540
|
C | A | 2 | a0001c0001t0002g0090a0001c0001t0002g0102 | 2 | HG02622.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.247+7250C>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48628540 | ||||||
chr2:48628627
|
A | G | 18 | a0001c0003t0001g0018a0001c0003t0001g0061a0001c0003t0001g0064others(15): Show | 18 | HG01243.hp1 HG01891.hp1 HG02486.hp2 others(15): Show |
intron_variant | MODIFIER | c.247+7337A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48628627 | ||||||
chr2:48628631
|
G | A | 2 | a0004c0008t0002g0302a0004c0008t0002g0303 | 2 | HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.247+7341G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48628631 | ||||||
chr2:48628638
|
G | A | 27 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0282others(24): Show | 31 | HG00642.hp1 HG01361.hp2 HG01515.hp2 others(28): Show |
intron_variant | MODIFIER | c.247+7348G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48628638 | ||||||
chr2:48628674
|
A | G | 1 | a0001c0003t0001g0069 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.247+7384A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48628674 | ||||||
chr2:48628897
|
G | C | 1 | a0009c0013t0001g0280 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.247+7607G>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48628897 | ||||||
chr2:48629000
|
T | C | 2 | a0004c0008t0002g0302a0004c0008t0002g0303 | 2 | HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.247+7710T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48629000 | ||||||
chr2:48629030
|
A | T | 2 | a0004c0008t0002g0302a0004c0008t0002g0303 | 2 | HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.247+7740A>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48629030 | ||||||
chr2:48629045
|
C | G | 2 | a0004c0008t0002g0302a0004c0008t0002g0303 | 2 | HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.247+7755C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48629045 | ||||||
chr2:48629079
|
A | G | 3 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0088 | 3 | HG04115.hp2 NA18940.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.247+7789A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48629079 | ||||||
chr2:48629317
|
T | A | 1 | a0001c0001t0001g0115 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.247+8027T>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48629317 | ||||||
chr2:48629372
|
C | T | 1 | a0002c0002t0001g0228 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.247+8082C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48629372 | ||||||
chr2:48629434
|
C | T | 27 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0282others(24): Show | 31 | HG00642.hp1 HG01361.hp2 HG01515.hp2 others(28): Show |
intron_variant | MODIFIER | c.247+8144C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48629434 | ||||||
chr2:48629440
|
A | T | 27 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0282others(24): Show | 31 | HG00642.hp1 HG01361.hp2 HG01515.hp2 others(28): Show |
intron_variant | MODIFIER | c.247+8150A>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48629440 | ||||||
chr2:48629479
|
G | A | 12 | a0001c0001t0001g0017a0001c0001t0001g0290a0001c0001t0001g0291others(9): Show | 12 | HG01074.hp1 HG01109.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.247+8189G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48629479 | ||||||
chr2:48629610
|
A | G | 2 | a0004c0008t0002g0302a0004c0008t0002g0303 | 2 | HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.247+8320A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48629610 | ||||||
chr2:48629631
|
G | A | 246 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(243): Show | 265 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.247+8341G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48629631 | ||||||
chr2:48629707
|
G | C | 1 | a0009c0013t0001g0280 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.247+8417G>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48629707 | ||||||
chr2:48629709
|
C | T | 1 | a0001c0001t0001g0281 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.247+8419C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48629709 | ||||||
chr2:48629867
|
C | A | 2 | a0004c0008t0002g0302a0004c0008t0002g0303 | 2 | HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.247+8577C>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48629867 | ||||||
chr2:48629885
|
G | A | 1 | a0001c0001t0002g0161 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.247+8595G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48629885 | ||||||
chr2:48629925
|
G | T | 3 | a0002c0002t0001g0227a0002c0002t0001g0262a0002c0002t0001g0263 | 3 | HG00735.hp2 HG01123.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.247+8635G>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48629925 | ||||||
chr2:48629996
|
G | T | 1 | a0001c0001t0001g0183 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.247+8706G>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48629996 | ||||||
chr2:48629997
|
C | G | 2 | a0004c0008t0002g0302a0004c0008t0002g0303 | 2 | HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.247+8707C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48629997 | ||||||
chr2:48630099
|
G | C | 6 | a0001c0003t0001g0064a0001c0003t0001g0075a0001c0003t0001g0076others(3): Show | 6 | HG02622.hp2 HG02809.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.247+8809G>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48630099 | ||||||
chr2:48630188
|
A | G | 15 | a0001c0003t0001g0018a0001c0003t0001g0064a0001c0003t0001g0066others(12): Show | 15 | HG01243.hp1 HG02486.hp2 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.247+8898A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48630188 | ||||||
chr2:48630199
|
T | G | 271 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(268): Show | 290 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(287): Show |
intron_variant | MODIFIER | c.247+8909T>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48630199 | ||||||
chr2:48630254
|
G | A | 2 | a0001c0001t0001g0270a0001c0001t0001g0271 | 2 | HG01106.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.247+8964G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48630254 | ||||||
chr2:48630330
|
C | G | 21 | a0001c0003t0001g0018a0001c0003t0001g0061a0001c0003t0001g0062others(18): Show | 21 | HG01070.hp1 HG01123.hp1 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.247+9040C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48630330 | ||||||
chr2:48630352
|
C | G | 1 | a0001c0001t0001g0096 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.247+9062C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48630352 | ||||||
chr2:48630581
|
G | C | 2 | a0004c0008t0002g0302a0004c0008t0002g0303 | 2 | HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.247+9291G>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48630581 | ||||||
chr2:48630700
|
G | A | 2 | a0004c0008t0002g0302a0004c0008t0002g0303 | 2 | HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.247+9410G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48630700 | ||||||
chr2:48631001
|
A | T | 86 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(83): Show | 94 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.247+9711A>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48631001 | ||||||
chr2:48631053
|
C | G | 2 | a0002c0002t0001g0225a0002c0002t0001g0226 | 2 | HG01361.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.247+9763C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48631053 | ||||||
chr2:48631080
|
T | G | 2 | a0004c0008t0002g0302a0004c0008t0002g0303 | 2 | HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.247+9790T>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48631080 | ||||||
chr2:48631121
|
C | T | 1 | a0001c0001t0001g0270 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.247+9831C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48631121 | ||||||
chr2:48631188
|
T | G | 1 | a0001c0001t0001g0281 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.247+9898T>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48631188 | ||||||
chr2:48631306
|
G | A | 1 | a0001c0001t0001g0023 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.247+10016G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48631306 | ||||||
chr2:48631421
|
C | G | 6 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0222others(3): Show | 6 | HG01099.hp2 HG01175.hp1 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.247+10131C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48631421 | ||||||
chr2:48631797
|
C | T | 6 | a0001c0001t0001g0315a0001c0001t0001g0316a0001c0001t0001g0317others(3): Show | 6 | HG02145.hp2 HG02630.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.247+10507C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48631797 | ||||||
chr2:48631985
|
C | G | 291 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(288): Show | 314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.248-10417C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48631985 | ||||||
chr2:48632098
|
G | A | 1 | a0001c0001t0001g0162 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.248-10304G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48632098 | ||||||
chr2:48632135
|
G | A | 2 | a0004c0008t0002g0302a0004c0008t0002g0303 | 2 | HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.248-10267G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48632135 | ||||||
chr2:48632306
|
A | G | 7 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0001t0001g0284others(4): Show | 7 | HG02055.hp2 HG02145.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.248-10096A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48632306 | ||||||
chr2:48632391
|
G | GT | 8 | a0001c0001t0001g0053a0001c0001t0001g0143a0001c0001t0001g0238others(5): Show | 8 | HG00738.hp1 HG01175.hp2 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.248-9999dupT | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 48632391 | |||||
chr2:48632532
|
A | T | 1 | a0002c0006t0001g0091 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.248-9870A>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48632532 | ||||||
chr2:48632672
|
C | T | 1 | a0001c0001t0001g0183 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.248-9730C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48632672 | ||||||
chr2:48632743
|
G | T | 1 | a0001c0001t0001g0281 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.248-9659G>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48632743 | ||||||
chr2:48632808
|
A | C | 1 | a0001c0003t0001g0068 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.248-9594A>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48632808 | ||||||
chr2:48632832
|
C | A | 1 | a0002c0002t0001g0191 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.248-9570C>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48632832 | ||||||
chr2:48632992
|
C | T | 9 | a0001c0001t0001g0003a0001c0001t0001g0282a0001c0001t0001g0283others(6): Show | 12 | HG01884.hp2 HG02055.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.248-9410C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48632992 | ||||||
chr2:48633240
|
A | G | 1 | a0001c0001t0001g0287 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.248-9162A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48633240 | ||||||
chr2:48633257
|
C | A | 1 | a0001c0001t0001g0286 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.248-9145C>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48633257 | ||||||
chr2:48633259
|
C | T | 1 | a0001c0001t0001g0234 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.248-9143C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48633259 | ||||||
chr2:48633372
|
G | C | 4 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0118others(1): Show | 4 | HG00621.hp2 HG02040.hp2 HG02083.hp2 others(1): Show |
intron_variant | MODIFIER | c.248-9030G>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48633372 | ||||||
chr2:48633378
|
C | T | 1 | a0001c0001t0001g0053 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.248-9024C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48633378 | ||||||
chr2:48633379
|
G | A | 1 | a0001c0001t0001g0198 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.248-9023G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48633379 | ||||||
chr2:48633477
|
C | G | 39 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(36): Show | 43 | HG00642.hp1 HG01074.hp1 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.248-8925C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48633477 | ||||||
chr2:48633699
|
C | T | 1 | a0009c0013t0001g0280 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.248-8703C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48633699 | ||||||
chr2:48633729
|
C | T | 1 | a0001c0001t0001g0058 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.248-8673C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48633729 | ||||||
chr2:48633731
|
A | T | 1 | a0001c0001t0001g0058 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.248-8671A>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48633731 | ||||||
chr2:48633756
|
C | T | 2 | a0001c0001t0001g0105a0001c0001t0001g0106 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.248-8646C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48633756 | ||||||
chr2:48633759
|
A | G | 65 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0019others(62): Show | 69 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(66): Show |
intron_variant | MODIFIER | c.248-8643A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48633759 | ||||||
chr2:48633773
|
G | A | 1 | a0001c0001t0001g0287 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.248-8629G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48633773 | ||||||
chr2:48633784
|
C | G | 6 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0222others(3): Show | 6 | HG01099.hp2 HG01175.hp1 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.248-8618C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48633784 | ||||||
chr2:48633812
|
G | A | 2 | a0005c0007t0001g0027a0005c0007t0001g0028 | 2 | HG00733.hp1 HG01168.hp2 |
intron_variant | MODIFIER | c.248-8590G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48633812 | ||||||
chr2:48633897
|
G | GTCT | 295 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(292): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.248-8504_248-8503i others(5): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 48633897 | |||||
chr2:48633914
|
T | G | 39 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(36): Show | 43 | HG00642.hp1 HG01074.hp1 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.248-8488T>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48633914 | ||||||
chr2:48633979
|
G | C | 18 | a0001c0001t0001g0016a0001c0001t0001g0304a0001c0001t0001g0305others(15): Show | 19 | HG00642.hp1 HG01361.hp2 HG01515.hp2 others(16): Show |
intron_variant | MODIFIER | c.248-8423G>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48633979 | ||||||
chr2:48634012
|
A | T | 1 | a0001c0001t0001g0058 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.248-8390A>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48634012 | ||||||
chr2:48634143
|
T | C | 1 | a0001c0001t0001g0287 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.248-8259T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48634143 | ||||||
chr2:48634151
|
C | T | 20 | a0001c0001t0001g0173a0001c0001t0002g0081a0001c0001t0002g0082others(17): Show | 20 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.248-8251C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48634151 | ||||||
chr2:48634199
|
G | A | 1 | a0001c0001t0001g0301 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.248-8203G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48634199 | ||||||
chr2:48634201
|
C | T | 1 | a0001c0003t0001g0068 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.248-8201C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48634201 | ||||||
chr2:48634204
|
C | T | 45 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0019others(42): Show | 49 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(46): Show |
intron_variant | MODIFIER | c.248-8198C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48634204 | ||||||
chr2:48634265
|
C | A | 1 | a0001c0001t0001g0120 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.248-8137C>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48634265 | ||||||
chr2:48634300
|
C | T | 1 | a0001c0001t0002g0182 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.248-8102C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48634300 | ||||||
chr2:48634376
|
G | T | 1 | a0001c0001t0001g0003 | 4 | HG01884.hp2 HG03195.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.248-8026G>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48634376 | ||||||
chr2:48634578
|
A | G | 12 | a0001c0001t0001g0017a0001c0001t0001g0290a0001c0001t0001g0291others(9): Show | 12 | HG01074.hp1 HG01109.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.248-7824A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48634578 | ||||||
chr2:48634621
|
C | G | 1 | a0001c0001t0001g0288 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.248-7781C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48634621 | ||||||
chr2:48634765
|
C | T | 44 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0019others(41): Show | 48 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(45): Show |
intron_variant | MODIFIER | c.248-7637C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48634765 | ||||||
chr2:48634780
|
G | T | 2 | a0004c0008t0002g0302a0004c0008t0002g0303 | 2 | HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.248-7622G>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48634780 | ||||||
chr2:48635034
|
A | G | 3 | a0001c0003t0001g0061a0001c0003t0001g0069a0003c0004t0001g0065 | 3 | HG01891.hp1 HG02723.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.248-7368A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48635034 | ||||||
chr2:48635070
|
A | G | 6 | a0001c0001t0001g0315a0001c0001t0001g0316a0001c0001t0001g0317others(3): Show | 6 | HG02145.hp2 HG02630.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.248-7332A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48635070 | ||||||
chr2:48635073
|
G | C | 2 | a0001c0001t0001g0059a0001c0001t0001g0060 | 2 | HG00544.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.248-7329G>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48635073 | ||||||
chr2:48635090
|
G | A | 1 | a0001c0003t0001g0068 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.248-7312G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48635090 | ||||||
chr2:48635171
|
G | C | 65 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0019others(62): Show | 69 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(66): Show |
intron_variant | MODIFIER | c.248-7231G>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48635171 | ||||||
chr2:48635359
|
A | G | 45 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0019others(42): Show | 49 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(46): Show |
intron_variant | MODIFIER | c.248-7043A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48635359 | ||||||
chr2:48635498
|
C | T | 2 | a0003c0004t0001g0063a0003c0004t0001g0080 | 2 | HG01070.hp1 HG01123.hp1 |
intron_variant | MODIFIER | c.248-6904C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48635498 | ||||||
chr2:48635691
|
C | T | 1 | a0002c0002t0001g0219 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.248-6711C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48635691 | ||||||
chr2:48635744
|
T | C | 18 | a0001c0001t0001g0173a0001c0001t0002g0081a0001c0001t0002g0082others(15): Show | 18 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.248-6658T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48635744 | ||||||
chr2:48635763
|
C | T | 45 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0019others(42): Show | 49 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(46): Show |
intron_variant | MODIFIER | c.248-6639C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48635763 | ||||||
chr2:48636095
|
C | T | 1 | a0009c0013t0001g0280 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.248-6307C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48636095 | ||||||
chr2:48636135
|
C | G | 1 | a0001c0001t0001g0301 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.248-6267C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48636135 | ||||||
chr2:48636272
|
T | G | 1 | a0001c0001t0001g0270 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.248-6130T>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48636272 | ||||||
chr2:48636308
|
C | G | 1 | a0009c0013t0001g0280 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.248-6094C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48636308 | ||||||
chr2:48636643
|
A | G | 1 | a0001c0001t0002g0181 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.248-5759A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48636643 | ||||||
chr2:48636722
|
G | A | 1 | a0001c0001t0006g0289 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.248-5680G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48636722 | ||||||
chr2:48636731
|
T | C | 12 | a0001c0001t0001g0017a0001c0001t0001g0290a0001c0001t0001g0291others(9): Show | 12 | HG01074.hp1 HG01109.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.248-5671T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48636731 | ||||||
chr2:48636770
|
G | A | 294 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(291): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.248-5632G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48636770 | ||||||
chr2:48636917
|
A | T | 294 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(291): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.248-5485A>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48636917 | ||||||
chr2:48636925
|
A | G | 2 | a0001c0001t0001g0298a0001c0001t0001g0299 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.248-5477A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48636925 | ||||||
chr2:48636957
|
G | A | 45 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0019others(42): Show | 49 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(46): Show |
intron_variant | MODIFIER | c.248-5445G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48636957 | ||||||
chr2:48637041
|
A | G | 2 | a0001c0001t0001g0270a0001c0001t0001g0271 | 2 | HG01106.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.248-5361A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48637041 | ||||||
chr2:48637080
|
G | T | 39 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(36): Show | 43 | HG00642.hp1 HG01074.hp1 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.248-5322G>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48637080 | ||||||
chr2:48637152
|
C | T | 1 | a0001c0001t0001g0254 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.248-5250C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48637152 | ||||||
chr2:48637177
|
T | A | 45 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0019others(42): Show | 49 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(46): Show |
intron_variant | MODIFIER | c.248-5225T>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48637177 | ||||||
chr2:48637265
|
C | T | 1 | a0001c0001t0001g0052 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.248-5137C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48637265 | ||||||
chr2:48637377
|
G | A | 294 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(291): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.248-5025G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48637377 | ||||||
chr2:48637392
|
T | A | 1 | a0001c0001t0001g0185 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.248-5010T>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48637392 | ||||||
chr2:48637425
|
A | G | 6 | a0001c0001t0001g0315a0001c0001t0001g0316a0001c0001t0001g0317others(3): Show | 6 | HG02145.hp2 HG02630.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.248-4977A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48637425 | ||||||
chr2:48637448
|
C | G | 1 | a0002c0002t0001g0228 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.248-4954C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48637448 | ||||||
chr2:48637461
|
A | G | 1 | a0009c0013t0001g0280 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.248-4941A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48637461 | ||||||
chr2:48637565
|
T | A | 1 | a0001c0001t0001g0281 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.248-4837T>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48637565 | ||||||
chr2:48637574
|
C | A | 1 | a0002c0002t0001g0192 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.248-4828C>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48637574 | ||||||
chr2:48637610
|
G | A | 1 | a0001c0001t0001g0315 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.248-4792G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48637610 | ||||||
chr2:48637625
|
A | G | 39 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(36): Show | 43 | HG00642.hp1 HG01074.hp1 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.248-4777A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48637625 | ||||||
chr2:48637687
|
T | C | 2 | a0004c0008t0002g0302a0004c0008t0002g0303 | 2 | HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.248-4715T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48637687 | ||||||
chr2:48637690
|
G | C | 2 | a0004c0008t0002g0302a0004c0008t0002g0303 | 2 | HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.248-4712G>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48637690 | ||||||
chr2:48637731
|
A | G | 39 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(36): Show | 43 | HG00642.hp1 HG01074.hp1 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.248-4671A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48637731 | ||||||
chr2:48637780
|
T | C | 3 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0234 | 3 | HG03710.hp1 HG04199.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.248-4622T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48637780 | ||||||
chr2:48638153
|
G | A | 47 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0019others(44): Show | 51 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(48): Show |
intron_variant | MODIFIER | c.248-4249G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48638153 | ||||||
chr2:48638289
|
G | A | 268 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(265): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.248-4113G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48638289 | ||||||
chr2:48638344
|
C | T | 1 | a0001c0001t0001g0296 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.248-4058C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48638344 | ||||||
chr2:48638480
|
C | T | 1 | a0002c0002t0001g0228 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.248-3922C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48638480 | ||||||
chr2:48638707
|
T | A | 3 | a0004c0008t0002g0302a0004c0008t0002g0303a0009c0013t0001g0280 | 3 | HG02717.hp2 HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.248-3695T>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48638707 | ||||||
chr2:48638792
|
T | G | 5 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(2): Show | 5 | HG02129.hp1 NA18951.hp2 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.248-3610T>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48638792 | ||||||
chr2:48638834
|
G | A | 9 | a0001c0001t0001g0016a0001c0001t0001g0304a0001c0001t0001g0305others(6): Show | 10 | HG00642.hp1 HG01361.hp2 HG01515.hp2 others(7): Show |
intron_variant | MODIFIER | c.248-3568G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48638834 | ||||||
chr2:48638885
|
A | G | 6 | a0001c0003t0001g0064a0001c0003t0001g0075a0001c0003t0001g0076others(3): Show | 6 | HG02622.hp2 HG02809.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.248-3517A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48638885 | ||||||
chr2:48638969
|
A | G | 45 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0019others(42): Show | 49 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(46): Show |
intron_variant | MODIFIER | c.248-3433A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48638969 | ||||||
chr2:48639143
|
G | T | 309 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(306): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.248-3259G>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48639143 | ||||||
chr2:48639208
|
C | T | 48 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0019others(45): Show | 52 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.248-3194C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48639208 | ||||||
chr2:48639328
|
G | T | 45 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0019others(42): Show | 49 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(46): Show |
intron_variant | MODIFIER | c.248-3074G>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48639328 | ||||||
chr2:48639342
|
C | G | 7 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0001t0001g0284others(4): Show | 7 | HG02055.hp2 HG02145.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.248-3060C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48639342 | ||||||
chr2:48639347
|
A | G | 39 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(36): Show | 43 | HG00642.hp1 HG01074.hp1 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.248-3055A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48639347 | ||||||
chr2:48639407
|
C | T | 1 | a0002c0002t0001g0218 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.248-2995C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48639407 | ||||||
chr2:48639421
|
C | G | 5 | a0001c0001t0001g0238a0001c0001t0001g0252a0001c0001t0001g0253others(2): Show | 5 | NA18960.hp2 NA19000.hp1 NA19003.hp2 others(2): Show |
intron_variant | MODIFIER | c.248-2981C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48639421 | ||||||
chr2:48639499
|
C | T | 5 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0001t0001g0284others(2): Show | 5 | HG02055.hp2 HG02145.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.248-2903C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48639499 | ||||||
chr2:48639636
|
A | G | 1 | a0001c0001t0001g0026 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.248-2766A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48639636 | ||||||
chr2:48639765
|
C | A | 201 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(198): Show | 216 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.248-2637C>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48639765 | ||||||
chr2:48640010
|
C | T | 58 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0011others(55): Show | 66 | HG00140.hp1 HG00609.hp2 HG00733.hp2 others(63): Show |
intron_variant | MODIFIER | c.248-2392C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48640010 | ||||||
chr2:48640269
|
T | C | 8 | a0001c0001t0001g0017a0001c0001t0001g0290a0001c0001t0001g0291others(5): Show | 8 | HG01074.hp1 HG01884.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.248-2133T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48640269 | ||||||
chr2:48640290
|
C | G | 18 | a0001c0001t0001g0173a0001c0001t0002g0081a0001c0001t0002g0082others(15): Show | 18 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.248-2112C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48640290 | ||||||
chr2:48640309
|
T | A | 289 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(286): Show | 312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.248-2093T>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48640309 | ||||||
chr2:48640378
|
A | G | 2 | a0001c0001t0001g0105a0001c0001t0001g0106 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.248-2024A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48640378 | ||||||
chr2:48640378
|
A | T | 39 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(36): Show | 43 | HG00642.hp1 HG01074.hp1 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.248-2024A>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48640378 | ||||||
chr2:48640641
|
C | G | 1 | a0001c0001t0001g0054 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.248-1761C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48640641 | ||||||
chr2:48640703
|
A | T | 39 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(36): Show | 43 | HG00642.hp1 HG01074.hp1 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.248-1699A>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48640703 | ||||||
chr2:48640725
|
C | T | 20 | a0001c0001t0001g0173a0001c0001t0002g0081a0001c0001t0002g0082others(17): Show | 20 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.248-1677C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48640725 | ||||||
chr2:48640770
|
T | C | 104 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(101): Show | 112 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.248-1632T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48640770 | ||||||
chr2:48640779
|
T | C | 1 | a0001c0001t0001g0033 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.248-1623T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48640779 | ||||||
chr2:48640900
|
CTTGTTAG others(1): Show |
C | 45 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0019others(42): Show | 49 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(46): Show |
intron_variant | MODIFIER | c.248-1499_248-1492d others(10): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 48640900 | |||||
chr2:48640980
|
C | T | 1 | a0001c0001t0001g0051 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.248-1422C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48640980 | ||||||
chr2:48641060
|
C | T | 1 | a0001c0001t0001g0254 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.248-1342C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48641060 | ||||||
chr2:48641101
|
A | C | 8 | a0002c0002t0001g0004a0002c0002t0001g0171a0002c0002t0001g0212others(5): Show | 10 | HG00609.hp2 HG02040.hp1 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.248-1301A>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48641101 | ||||||
chr2:48641303
|
G | C | 20 | a0001c0001t0001g0173a0001c0001t0002g0081a0001c0001t0002g0082others(17): Show | 20 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.248-1099G>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48641303 | ||||||
chr2:48641372
|
G | C | 39 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(36): Show | 43 | HG00642.hp1 HG01074.hp1 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.248-1030G>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48641372 | ||||||
chr2:48641649
|
C | A | 1 | a0001c0001t0001g0097 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.248-753C>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48641649 | ||||||
chr2:48641668
|
T | G | 1 | a0001c0001t0001g0199 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.248-734T>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48641668 | ||||||
chr2:48641674
|
C | T | 1 | a0009c0013t0001g0280 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.248-728C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48641674 | ||||||
chr2:48641846
|
T | C | 1 | a0002c0002t0001g0111 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.248-556T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48641846 | ||||||
chr2:48641850
|
A | G | 1 | a0002c0002t0001g0211 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.248-552A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48641850 | ||||||
chr2:48642056
|
T | C | 1 | a0001c0001t0002g0172 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.248-346T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48642056 | ||||||
chr2:48642059
|
A | G | 201 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(198): Show | 216 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.248-343A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48642059 | ||||||
chr2:48642258
|
C | T | 2 | a0001c0001t0001g0319a0001c0001t0001g0320 | 2 | HG02630.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.248-144C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48642258 | ||||||
chr2:48642262
|
CTTGGAAT others(8): Show |
C | 1 | a0001c0001t0001g0292 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.248-137_248-123del others(15): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 48642262 | |||||
chr2:48642278
|
T | A | 1 | a0001c0001t0001g0292 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.248-124T>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48642278 | ||||||
chr2:48642324
|
T | A | 4 | a0001c0001t0001g0008a0001c0001t0001g0103a0001c0001t0001g0105others(1): Show | 5 | HG01070.hp2 HG01071.hp2 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.248-78T>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48642324 | ||||||
chr2:48642361
|
T | C | 8 | a0001c0001t0001g0017a0001c0001t0001g0290a0001c0001t0001g0291others(5): Show | 8 | HG01074.hp1 HG01884.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.248-41T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48642361 | ||||||
chr2:48642583
|
G | A | 1 | a0001c0001t0001g0146 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.303+126G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 4/8 | chr2 | 48642583 | ||||||
chr2:48642592
|
C | T | 2 | a0001c0001t0001g0268a0001c0001t0001g0269 | 2 | HG02602.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.303+135C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 4/8 | chr2 | 48642592 | ||||||
chr2:48642731
|
T | C | 4 | a0003c0004t0001g0063a0003c0004t0001g0065a0003c0004t0001g0080others(1): Show | 4 | HG01070.hp1 HG01123.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.303+274T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 4/8 | chr2 | 48642731 | ||||||
chr2:48642856
|
C | G | 39 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(36): Show | 43 | HG00642.hp1 HG01074.hp1 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.303+399C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 4/8 | chr2 | 48642856 | ||||||
chr2:48642858
|
A | G | 2 | a0004c0008t0002g0302a0004c0008t0002g0303 | 2 | HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.303+401A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 4/8 | chr2 | 48642858 | ||||||
chr2:48642860
|
GA | G | 208 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(205): Show | 226 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(223): Show |
intron_variant | MODIFIER | c.303+416delA | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 48642860 | |||||
chr2:48642876
|
TGTG | T | 39 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(36): Show | 43 | HG00642.hp1 HG01074.hp1 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.303+422_303+424del others(3): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 48642876 | |||||
chr2:48642978
|
A | G | 1 | a0001c0001t0001g0050 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.303+521A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 4/8 | chr2 | 48642978 | ||||||
chr2:48643063
|
T | C | 2 | a0001c0001t0001g0268a0001c0001t0001g0269 | 2 | HG02602.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.303+606T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 4/8 | chr2 | 48643063 | ||||||
chr2:48643067
|
A | G | 45 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0019others(42): Show | 49 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(46): Show |
intron_variant | MODIFIER | c.303+610A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 4/8 | chr2 | 48643067 | ||||||
chr2:48643226
|
C | T | 45 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0019others(42): Show | 49 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(46): Show |
intron_variant | MODIFIER | c.303+769C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 4/8 | chr2 | 48643226 | ||||||
chr2:48643228
|
C | G | 1 | a0001c0001t0001g0315 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.303+771C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 4/8 | chr2 | 48643228 | ||||||
chr2:48643470
|
T | G | 1 | a0001c0001t0001g0160 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.303+1013T>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 4/8 | chr2 | 48643470 | ||||||
chr2:48643568
|
A | T | 86 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(83): Show | 94 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.303+1111A>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 4/8 | chr2 | 48643568 | ||||||
chr2:48643693
|
A | AT | 60 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0019others(57): Show | 64 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.303+1259dupT | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 48643693 | |||||
chr2:48643693
|
A | ATT | 7 | a0001c0001t0001g0032a0001c0001t0001g0049a0001c0001t0001g0057others(4): Show | 7 | HG01978.hp1 HG02055.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.303+1258_303+1259d others(4): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 48643693 | |||||
chr2:48643693
|
AT | A | 10 | a0001c0001t0001g0145a0001c0001t0001g0147a0001c0001t0001g0163others(7): Show | 10 | HG00733.hp2 HG02523.hp2 HG02735.hp1 others(7): Show |
intron_variant | MODIFIER | c.303+1259delT | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 48643693 | |||||
chr2:48643693
|
ATTTTTTT others(6): Show |
A | 39 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(36): Show | 43 | HG00642.hp1 HG01074.hp1 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.303+1247_303+1259d others(15): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 48643693 | |||||
chr2:48643741
|
C | G | 1 | a0001c0001t0001g0138 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.303+1284C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 4/8 | chr2 | 48643741 | ||||||
chr2:48643749
|
G | T | 39 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(36): Show | 43 | HG00642.hp1 HG01074.hp1 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.304-1284G>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 4/8 | chr2 | 48643749 | ||||||
chr2:48643843
|
C | T | 18 | a0001c0003t0001g0018a0001c0003t0001g0061a0001c0003t0001g0062others(15): Show | 18 | HG01243.hp1 HG01891.hp1 HG02486.hp2 others(15): Show |
intron_variant | MODIFIER | c.304-1190C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 4/8 | chr2 | 48643843 | ||||||
chr2:48643844
|
G | A | 7 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0001t0001g0284others(4): Show | 7 | HG02055.hp2 HG02145.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.304-1189G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 4/8 | chr2 | 48643844 | ||||||
chr2:48643929
|
C | T | 8 | a0001c0001t0001g0013a0001c0001t0001g0196a0001c0001t0001g0197others(5): Show | 9 | HG02451.hp2 HG02886.hp2 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.304-1104C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 4/8 | chr2 | 48643929 | ||||||
chr2:48644013
|
T | A | 20 | a0001c0001t0001g0173a0001c0001t0002g0081a0001c0001t0002g0082others(17): Show | 20 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.304-1020T>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 4/8 | chr2 | 48644013 | ||||||
chr2:48644014
|
T | A | 20 | a0001c0001t0001g0173a0001c0001t0002g0081a0001c0001t0002g0082others(17): Show | 20 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.304-1019T>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 4/8 | chr2 | 48644014 | ||||||
chr2:48644015
|
A | T | 5 | a0002c0002t0001g0012a0002c0002t0001g0159a0002c0002t0001g0235others(2): Show | 6 | HG02027.hp2 HG02165.hp2 NA18747.hp2 others(3): Show |
intron_variant | MODIFIER | c.304-1018A>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 4/8 | chr2 | 48644015 | ||||||
chr2:48644093
|
C | T | 1 | a0002c0014t0001g0195 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.304-940C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 4/8 | chr2 | 48644093 | ||||||
chr2:48644094
|
C | A | 1 | a0002c0014t0001g0195 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.304-939C>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 4/8 | chr2 | 48644094 | ||||||
chr2:48644095
|
T | C | 1 | a0002c0014t0001g0195 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.304-938T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 4/8 | chr2 | 48644095 | ||||||
chr2:48644096
|
C | A | 1 | a0002c0014t0001g0195 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.304-937C>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 4/8 | chr2 | 48644096 | ||||||
chr2:48644151
|
A | G | 1 | a0001c0001t0001g0101 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.304-882A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 4/8 | chr2 | 48644151 | ||||||
chr2:48644404
|
C | A | 1 | a0001c0001t0001g0036 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.304-629C>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 4/8 | chr2 | 48644404 | ||||||
chr2:48644445
|
G | C | 2 | a0004c0008t0002g0302a0004c0008t0002g0303 | 2 | HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.304-588G>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 4/8 | chr2 | 48644445 | ||||||
chr2:48644694
|
C | T | 18 | a0001c0001t0001g0006a0001c0001t0001g0096a0001c0001t0001g0097others(15): Show | 19 | HG00423.hp1 HG02015.hp1 HG02056.hp2 others(16): Show |
intron_variant | MODIFIER | c.304-339C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 4/8 | chr2 | 48644694 | ||||||
chr2:48644730
|
C | G | 2 | a0001c0001t0001g0085a0001c0001t0001g0086 | 2 | NA18940.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.304-303C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 4/8 | chr2 | 48644730 | ||||||
chr2:48644769
|
G | A | 2 | a0001c0001t0001g0121a0001c0001t0001g0272 | 2 | HG00544.hp1 HG00597.hp2 |
intron_variant | MODIFIER | c.304-264G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 4/8 | chr2 | 48644769 | ||||||
chr2:48644893
|
A | G | 7 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(4): Show | 7 | HG00738.hp2 HG01106.hp2 HG01928.hp2 others(4): Show |
intron_variant | MODIFIER | c.304-140A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 4/8 | chr2 | 48644893 | ||||||
chr2:48644974
|
A | G | 22 | a0001c0001t0001g0016a0001c0001t0001g0294a0001c0001t0001g0295others(19): Show | 23 | HG00642.hp1 HG01109.hp2 HG01361.hp2 others(20): Show |
intron_variant | MODIFIER | c.304-59A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 4/8 | chr2 | 48644974 | ||||||
chr2:48644996
|
C | G | 1 | a0001c0001t0001g0168 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.304-37C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 4/8 | chr2 | 48644996 | ||||||
chr2:48645192
|
T | A | 1 | a0009c0013t0001g0280 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.388+75T>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 5/8 | chr2 | 48645192 | ||||||
chr2:48645310
|
G | C | 1 | a0001c0001t0001g0122 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.388+193G>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 5/8 | chr2 | 48645310 | ||||||
chr2:48645326
|
A | T | 1 | a0001c0001t0001g0137 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.388+209A>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 5/8 | chr2 | 48645326 | ||||||
chr2:48645369
|
T | C | 2 | a0005c0007t0001g0027a0005c0007t0001g0028 | 2 | HG00733.hp1 HG01168.hp2 |
intron_variant | MODIFIER | c.388+252T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 5/8 | chr2 | 48645369 | ||||||
chr2:48645472
|
A | T | 309 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(306): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.388+355A>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 5/8 | chr2 | 48645472 | ||||||
chr2:48645646
|
C | G | 21 | a0001c0003t0001g0018a0001c0003t0001g0061a0001c0003t0001g0062others(18): Show | 21 | HG01070.hp1 HG01123.hp1 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.388+529C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 5/8 | chr2 | 48645646 | ||||||
chr2:48645677
|
C | G | 2 | a0004c0008t0002g0302a0004c0008t0002g0303 | 2 | HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.388+560C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 5/8 | chr2 | 48645677 | ||||||
chr2:48645937
|
C | T | 1 | a0001c0001t0001g0153 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.389-516C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 5/8 | chr2 | 48645937 | ||||||
chr2:48645939
|
C | T | 1 | a0001c0003t0001g0069 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.389-514C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 5/8 | chr2 | 48645939 | ||||||
chr2:48645947
|
C | CT | 48 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0019others(45): Show | 52 | HG00099.hp1 HG00544.hp2 HG00642.hp2 others(49): Show |
intron_variant | MODIFIER | c.389-493dupT | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 48645947 | |||||
chr2:48645947
|
CT | C | 8 | a0001c0001t0001g0017a0001c0001t0001g0290a0001c0001t0001g0291others(5): Show | 8 | HG01074.hp1 HG01884.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.389-493delT | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 48645947 | |||||
chr2:48646018
|
C | A | 1 | a0001c0001t0001g0321 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.389-435C>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 5/8 | chr2 | 48646018 | ||||||
chr2:48646118
|
C | T | 44 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0019others(41): Show | 48 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(45): Show |
intron_variant | MODIFIER | c.389-335C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 5/8 | chr2 | 48646118 | ||||||
chr2:48646179
|
A | T | 2 | a0001c0001t0001g0085a0001c0001t0001g0086 | 2 | NA18940.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.389-274A>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 5/8 | chr2 | 48646179 | ||||||
chr2:48646204
|
G | A | 2 | a0001c0001t0001g0183a0010c0015t0001g0164 | 2 | NA18942.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.389-249G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 5/8 | chr2 | 48646204 | ||||||
chr2:48646373
|
A | AT | 6 | a0001c0001t0001g0047a0001c0001t0001g0136a0001c0001t0001g0163others(3): Show | 6 | HG01099.hp1 HG02145.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.389-65dupT | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 48646373 | |||||
chr2:48646373
|
AT | A | 6 | a0001c0001t0001g0173a0001c0001t0001g0198a0001c0001t0001g0301others(3): Show | 6 | HG01358.hp1 HG02451.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.389-65delT | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 48646373 | |||||
chr2:48646387
|
T | G | 1 | a0001c0003t0001g0062 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.389-66T>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 5/8 | chr2 | 48646387 | ||||||
chr2:48646443
|
C | T | 39 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(36): Show | 43 | HG00642.hp1 HG01074.hp1 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.389-10C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 5/8 | chr2 | 48646443 | ||||||
chr2:48647155
|
T | G | 2 | a0001c0001t0001g0089a0001c0001t0001g0095 | 2 | HG00597.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.978+113T>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48647155 | ||||||
chr2:48647218
|
A | G | 1 | a0001c0001t0001g0168 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.978+176A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48647218 | ||||||
chr2:48647297
|
A | T | 39 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(36): Show | 43 | HG00642.hp1 HG01074.hp1 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.978+255A>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48647297 | ||||||
chr2:48647391
|
A | G | 9 | a0001c0001t0001g0173a0001c0001t0002g0081a0001c0001t0002g0082others(6): Show | 9 | HG01243.hp2 HG01891.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.978+349A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48647391 | ||||||
chr2:48647517
|
C | T | 1 | a0001c0001t0001g0026 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.978+475C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48647517 | ||||||
chr2:48647527
|
G | A | 318 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(315): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.978+485G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48647527 | ||||||
chr2:48647563
|
T | C | 1 | a0009c0013t0001g0280 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.978+521T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48647563 | ||||||
chr2:48647565
|
T | C | 2 | a0001c0001t0001g0123a0001c0001t0001g0124 | 2 | NA18954.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.978+523T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48647565 | ||||||
chr2:48647643
|
C | T | 2 | a0004c0008t0002g0302a0004c0008t0002g0303 | 2 | HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.978+601C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48647643 | ||||||
chr2:48647682
|
C | A | 184 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(181): Show | 199 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.978+640C>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48647682 | ||||||
chr2:48647880
|
A | G | 44 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0019others(41): Show | 48 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(45): Show |
intron_variant | MODIFIER | c.978+838A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48647880 | ||||||
chr2:48647923
|
A | C | 11 | a0001c0003t0001g0064a0001c0003t0001g0066a0001c0003t0001g0067others(8): Show | 11 | HG02486.hp2 HG02622.hp2 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.978+881A>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48647923 | ||||||
chr2:48647969
|
G | A | 1 | a0002c0002t0001g0142 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.978+927G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48647969 | ||||||
chr2:48648011
|
C | T | 1 | a0002c0002t0001g0111 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.978+969C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48648011 | ||||||
chr2:48648222
|
G | GT | 19 | a0001c0001t0001g0016a0001c0001t0001g0135a0001c0001t0001g0304others(16): Show | 20 | HG00642.hp1 HG01361.hp2 HG01515.hp2 others(17): Show |
intron_variant | MODIFIER | c.978+1188dupT | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 48648222 | |||||
chr2:48648286
|
A | T | 1 | a0002c0002t0001g0139 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.978+1244A>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48648286 | ||||||
chr2:48648326
|
T | G | 18 | a0001c0001t0001g0016a0001c0001t0001g0304a0001c0001t0001g0305others(15): Show | 19 | HG00642.hp1 HG01361.hp2 HG01515.hp2 others(16): Show |
intron_variant | MODIFIER | c.978+1284T>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48648326 | ||||||
chr2:48648523
|
G | A | 20 | a0001c0003t0001g0018a0001c0003t0001g0062a0001c0003t0001g0064others(17): Show | 20 | HG01070.hp1 HG01123.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.978+1481G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48648523 | ||||||
chr2:48648703
|
C | T | 1 | a0002c0002t0001g0229 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.978+1661C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48648703 | ||||||
chr2:48648799
|
G | A | 56 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0011others(53): Show | 63 | HG00140.hp1 HG00609.hp2 HG00733.hp2 others(60): Show |
intron_variant | MODIFIER | c.978+1757G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48648799 | ||||||
chr2:48648840
|
T | C | 45 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0019others(42): Show | 49 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(46): Show |
intron_variant | MODIFIER | c.978+1798T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48648840 | ||||||
chr2:48648851
|
T | G | 1 | a0009c0013t0001g0280 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.978+1809T>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48648851 | ||||||
chr2:48648995
|
C | G | 2 | a0001c0001t0001g0270a0001c0001t0001g0271 | 2 | HG01106.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.978+1953C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48648995 | ||||||
chr2:48649060
|
T | A | 1 | a0001c0001t0006g0289 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.978+2018T>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48649060 | ||||||
chr2:48649100
|
A | G | 309 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(306): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.978+2058A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48649100 | ||||||
chr2:48649131
|
T | C | 20 | a0001c0001t0001g0173a0001c0001t0002g0081a0001c0001t0002g0082others(17): Show | 20 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.978+2089T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48649131 | ||||||
chr2:48649230
|
A | G | 20 | a0001c0001t0001g0173a0001c0001t0002g0081a0001c0001t0002g0082others(17): Show | 20 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.978+2188A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48649230 | ||||||
chr2:48649238
|
C | T | 18 | a0001c0001t0001g0016a0001c0001t0001g0304a0001c0001t0001g0305others(15): Show | 19 | HG00642.hp1 HG01361.hp2 HG01515.hp2 others(16): Show |
intron_variant | MODIFIER | c.978+2196C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48649238 | ||||||
chr2:48649277
|
G | A | 3 | a0001c0001t0001g0240a0001c0001t0001g0241a0001c0012t0001g0242 | 3 | HG02523.hp1 NA18941.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.978+2235G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48649277 | ||||||
chr2:48649326
|
G | C | 39 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(36): Show | 43 | HG00642.hp1 HG01074.hp1 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.978+2284G>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48649326 | ||||||
chr2:48649374
|
C | T | 20 | a0001c0003t0001g0018a0001c0003t0001g0062a0001c0003t0001g0064others(17): Show | 20 | HG01070.hp1 HG01123.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.978+2332C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48649374 | ||||||
chr2:48649405
|
A | G | 1 | a0001c0001t0001g0168 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.978+2363A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48649405 | ||||||
chr2:48649435
|
C | G | 20 | a0001c0001t0001g0173a0001c0001t0002g0081a0001c0001t0002g0082others(17): Show | 20 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.978+2393C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48649435 | ||||||
chr2:48649486
|
A | T | 1 | a0001c0003t0001g0062 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.978+2444A>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48649486 | ||||||
chr2:48649655
|
A | T | 4 | a0001c0001t0001g0294a0001c0001t0001g0295a0001c0001t0001g0296others(1): Show | 4 | HG01109.hp2 HG02559.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.978+2613A>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48649655 | ||||||
chr2:48649744
|
C | G | 5 | a0001c0001t0001g0304a0001c0001t0001g0305a0001c0001t0001g0306others(2): Show | 5 | HG02280.hp2 HG02683.hp1 HG03669.hp2 others(2): Show |
intron_variant | MODIFIER | c.978+2702C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48649744 | ||||||
chr2:48649993
|
G | A | 20 | a0001c0001t0001g0173a0001c0001t0002g0081a0001c0001t0002g0082others(17): Show | 20 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.978+2951G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48649993 | ||||||
chr2:48650117
|
G | A | 1 | a0001c0001t0001g0055 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.978+3075G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48650117 | ||||||
chr2:48650131
|
C | T | 20 | a0001c0001t0001g0173a0001c0001t0002g0081a0001c0001t0002g0082others(17): Show | 20 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.978+3089C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48650131 | ||||||
chr2:48650221
|
A | G | 1 | a0001c0001t0001g0293 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.978+3179A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48650221 | ||||||
chr2:48650297
|
C | T | 1 | a0005c0007t0001g0028 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.978+3255C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48650297 | ||||||
chr2:48650332
|
A | G | 9 | a0001c0001t0001g0003a0001c0001t0001g0282a0001c0001t0001g0283others(6): Show | 12 | HG01884.hp2 HG02055.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.978+3290A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48650332 | ||||||
chr2:48650361
|
A | G | 64 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0019others(61): Show | 68 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(65): Show |
intron_variant | MODIFIER | c.978+3319A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48650361 | ||||||
chr2:48650518
|
C | G | 3 | a0002c0002t0001g0011a0002c0002t0001g0232a0002c0002t0001g0233 | 4 | NA18971.hp2 NA18998.hp1 NA19085.hp1 others(1): Show |
intron_variant | MODIFIER | c.978+3476C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48650518 | ||||||
chr2:48650563
|
A | G | 20 | a0001c0001t0001g0173a0001c0001t0002g0081a0001c0001t0002g0082others(17): Show | 20 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.978+3521A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48650563 | ||||||
chr2:48650741
|
A | C | 2 | a0001c0001t0001g0223a0001c0001t0001g0224 | 2 | HG01099.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.978+3699A>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48650741 | ||||||
chr2:48650850
|
A | G | 12 | a0001c0001t0001g0016a0001c0001t0001g0304a0001c0001t0001g0305others(9): Show | 13 | HG00642.hp1 HG01361.hp2 HG01515.hp2 others(10): Show |
intron_variant | MODIFIER | c.978+3808A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48650850 | ||||||
chr2:48651084
|
C | G | 6 | a0001c0001t0001g0315a0001c0001t0001g0316a0001c0001t0001g0317others(3): Show | 6 | HG02145.hp2 HG02630.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.978+4042C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48651084 | ||||||
chr2:48651115
|
A | G | 2 | a0001c0001t0001g0089a0001c0001t0001g0095 | 2 | HG00597.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.978+4073A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48651115 | ||||||
chr2:48651144
|
A | G | 1 | a0002c0002t0001g0219 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.978+4102A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48651144 | ||||||
chr2:48651162
|
G | A | 1 | a0002c0002t0001g0112 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.978+4120G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48651162 | ||||||
chr2:48651307
|
T | A | 44 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0019others(41): Show | 48 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(45): Show |
intron_variant | MODIFIER | c.978+4265T>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48651307 | ||||||
chr2:48651409
|
C | T | 1 | a0001c0001t0001g0046 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.978+4367C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48651409 | ||||||
chr2:48651416
|
G | T | 1 | a0001c0001t0001g0261 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.978+4374G>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48651416 | ||||||
chr2:48651422
|
T | C | 2 | a0001c0001t0001g0274a0001c0001t0001g0276 | 2 | NA18975.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.978+4380T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48651422 | ||||||
chr2:48651436
|
C | CT | 51 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(48): Show | 55 | HG00621.hp2 HG01074.hp1 HG01109.hp2 others(52): Show |
intron_variant | MODIFIER | c.978+4412dupT | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 48651436 | |||||
chr2:48651436
|
CT | C | 52 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0019others(49): Show | 56 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.978+4412delT | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 48651436 | |||||
chr2:48651436
|
CTTTT | C | 20 | a0001c0001t0001g0173a0001c0001t0002g0081a0001c0001t0002g0082others(17): Show | 20 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.978+4409_978+4412d others(6): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 48651436 | |||||
chr2:48651455
|
A | T | 3 | a0001c0001t0001g0240a0001c0001t0001g0241a0001c0012t0001g0242 | 3 | HG02523.hp1 NA18941.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.978+4413A>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48651455 | ||||||
chr2:48651576
|
G | A | 20 | a0001c0001t0001g0173a0001c0001t0002g0081a0001c0001t0002g0082others(17): Show | 20 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.978+4534G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48651576 | ||||||
chr2:48651586
|
A | C | 20 | a0001c0001t0001g0173a0001c0001t0002g0081a0001c0001t0002g0082others(17): Show | 20 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.978+4544A>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48651586 | ||||||
chr2:48651588
|
T | A | 191 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(188): Show | 206 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(203): Show |
intron_variant | MODIFIER | c.978+4546T>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48651588 | ||||||
chr2:48651605
|
A | G | 20 | a0001c0001t0001g0173a0001c0001t0002g0081a0001c0001t0002g0082others(17): Show | 20 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.978+4563A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48651605 | ||||||
chr2:48651681
|
C | T | 1 | a0002c0002t0001g0210 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.978+4639C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48651681 | ||||||
chr2:48651696
|
G | C | 1 | a0009c0013t0001g0280 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.978+4654G>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48651696 | ||||||
chr2:48651786
|
AGCCCTTG others(6): Show |
A | 1 | a0002c0002t0001g0212 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.978+4745_978+4757d others(15): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48651786 | ||||||
chr2:48652064
|
A | G | 6 | a0001c0001t0001g0315a0001c0001t0001g0316a0001c0001t0001g0317others(3): Show | 6 | HG02145.hp2 HG02630.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.978+5022A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48652064 | ||||||
chr2:48652228
|
C | G | 20 | a0001c0001t0001g0173a0001c0001t0002g0081a0001c0001t0002g0082others(17): Show | 20 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.978+5186C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48652228 | ||||||
chr2:48652234
|
C | T | 1 | a0001c0001t0001g0008 | 2 | HG01261.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.978+5192C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48652234 | ||||||
chr2:48652279
|
G | A | 64 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0019others(61): Show | 68 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(65): Show |
intron_variant | MODIFIER | c.978+5237G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48652279 | ||||||
chr2:48652380
|
C | T | 44 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0019others(41): Show | 48 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(45): Show |
intron_variant | MODIFIER | c.978+5338C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48652380 | ||||||
chr2:48652402
|
G | A | 20 | a0001c0001t0001g0173a0001c0001t0002g0081a0001c0001t0002g0082others(17): Show | 20 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.978+5360G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48652402 | ||||||
chr2:48652418
|
C | G | 1 | a0001c0001t0002g0179 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.978+5376C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48652418 | ||||||
chr2:48652431
|
C | T | 2 | a0001c0001t0001g0156a0001c0001t0001g0157 | 2 | HG03710.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.978+5389C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48652431 | ||||||
chr2:48652445
|
G | A | 20 | a0001c0001t0001g0173a0001c0001t0002g0081a0001c0001t0002g0082others(17): Show | 20 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.978+5403G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48652445 | ||||||
chr2:48652475
|
G | A | 2 | a0001c0001t0002g0090a0001c0001t0002g0102 | 2 | HG02622.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.978+5433G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48652475 | ||||||
chr2:48652508
|
C | T | 2 | a0001c0001t0001g0308a0001c0001t0001g0311 | 2 | HG00642.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.978+5466C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48652508 | ||||||
chr2:48652520
|
C | T | 1 | a0002c0002t0001g0144 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.978+5478C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48652520 | ||||||
chr2:48652560
|
A | C | 6 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0222others(3): Show | 6 | HG01099.hp2 HG01175.hp1 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.978+5518A>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48652560 | ||||||
chr2:48652576
|
C | T | 2 | a0001c0003t0001g0062a0001c0003t0001g0069 | 2 | HG02723.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.978+5534C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48652576 | ||||||
chr2:48652577
|
T | G | 2 | a0001c0003t0001g0062a0001c0003t0001g0069 | 2 | HG02723.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.978+5535T>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48652577 | ||||||
chr2:48652763
|
C | T | 43 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0019others(40): Show | 47 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(44): Show |
intron_variant | MODIFIER | c.978+5721C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48652763 | ||||||
chr2:48652776
|
C | A | 8 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(5): Show | 8 | HG00738.hp2 HG01106.hp2 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.978+5734C>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48652776 | ||||||
chr2:48652780
|
T | C | 20 | a0001c0001t0001g0173a0001c0001t0002g0081a0001c0001t0002g0082others(17): Show | 20 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.978+5738T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48652780 | ||||||
chr2:48652815
|
G | C | 315 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(312): Show | 338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.978+5773G>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48652815 | ||||||
chr2:48652951
|
C | G | 4 | a0001c0001t0001g0294a0001c0001t0001g0295a0001c0001t0001g0296others(1): Show | 4 | HG01109.hp2 HG02559.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.978+5909C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48652951 | ||||||
chr2:48653089
|
C | A | 12 | a0001c0001t0001g0017a0001c0001t0001g0290a0001c0001t0001g0291others(9): Show | 12 | HG01074.hp1 HG01109.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.978+6047C>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48653089 | ||||||
chr2:48653095
|
G | C | 315 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(312): Show | 338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.978+6053G>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48653095 | ||||||
chr2:48653189
|
C | G | 1 | a0001c0001t0001g0170 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.978+6147C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48653189 | ||||||
chr2:48653211
|
A | G | 1 | a0001c0001t0001g0292 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.978+6169A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48653211 | ||||||
chr2:48653220
|
C | CA | 59 | a0001c0001t0001g0003a0001c0001t0001g0169a0001c0001t0001g0170others(56): Show | 66 | HG00597.hp2 HG00609.hp2 HG00735.hp2 others(63): Show |
intron_variant | MODIFIER | c.978+6198dupA | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 48653220 | |||||
chr2:48653220
|
CA | C | 11 | a0001c0001t0001g0024a0001c0001t0001g0058a0001c0001t0001g0122others(8): Show | 11 | HG00738.hp1 HG01934.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.978+6198delA | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 48653220 | |||||
chr2:48653220
|
CAA | C | 61 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0019others(58): Show | 65 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.978+6197_978+6198d others(4): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 48653220 | |||||
chr2:48653320
|
A | G | 1 | a0001c0003t0001g0064 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.978+6278A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48653320 | ||||||
chr2:48653447
|
A | G | 1 | a0001c0003t0001g0061 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.978+6405A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48653447 | ||||||
chr2:48653533
|
C | G | 6 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0222others(3): Show | 6 | HG01099.hp2 HG01175.hp1 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.978+6491C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48653533 | ||||||
chr2:48653920
|
C | CA | 38 | a0001c0001t0001g0103a0001c0001t0001g0106a0001c0001t0001g0162others(35): Show | 38 | HG01070.hp2 HG01243.hp1 HG01243.hp2 others(35): Show |
intron_variant | MODIFIER | c.978+6901dupA | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 48653920 | |||||
chr2:48653920
|
C | CAA | 112 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(109): Show | 123 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.978+6900_978+6901d others(4): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 48653920 | |||||
chr2:48653920
|
C | CAAA | 19 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0020others(16): Show | 19 | HG00735.hp1 HG00738.hp1 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.978+6899_978+6901d others(5): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 48653920 | |||||
chr2:48653920
|
CAAAAAA | C | 7 | a0001c0001t0001g0013a0001c0001t0001g0127a0001c0001t0001g0128others(4): Show | 8 | HG02523.hp2 HG02886.hp2 HG03516.hp1 others(5): Show |
intron_variant | MODIFIER | c.978+6896_978+6901d others(8): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 48653920 | |||||
chr2:48653920
|
CAAAAAAA | C | 133 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(130): Show | 144 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(141): Show |
intron_variant | MODIFIER | c.978+6895_978+6901d others(9): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 48653920 | |||||
chr2:48653954
|
C | G | 1 | a0001c0001t0001g0170 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.978+6912C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48653954 | ||||||
chr2:48653995
|
G | A | 1 | a0001c0001t0001g0198 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.978+6953G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48653995 | ||||||
chr2:48654024
|
C | T | 20 | a0001c0001t0001g0173a0001c0001t0002g0081a0001c0001t0002g0082others(17): Show | 20 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.978+6982C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48654024 | ||||||
chr2:48654195
|
G | C | 1 | a0001c0001t0001g0281 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.978+7153G>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48654195 | ||||||
chr2:48654222
|
C | T | 20 | a0001c0001t0001g0173a0001c0001t0002g0081a0001c0001t0002g0082others(17): Show | 20 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.978+7180C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48654222 | ||||||
chr2:48654242
|
T | C | 20 | a0001c0001t0001g0173a0001c0001t0002g0081a0001c0001t0002g0082others(17): Show | 20 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.978+7200T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48654242 | ||||||
chr2:48654249
|
C | A | 315 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(312): Show | 338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.978+7207C>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48654249 | ||||||
chr2:48654472
|
C | T | 46 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0019others(43): Show | 51 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(48): Show |
intron_variant | MODIFIER | c.978+7430C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48654472 | ||||||
chr2:48654606
|
C | T | 2 | a0001c0001t0001g0268a0001c0001t0001g0269 | 2 | HG02602.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.978+7564C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48654606 | ||||||
chr2:48654870
|
C | G | 1 | a0001c0001t0001g0168 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.978+7828C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48654870 | ||||||
chr2:48654904
|
T | C | 8 | a0001c0001t0001g0017a0001c0001t0001g0290a0001c0001t0001g0291others(5): Show | 8 | HG01074.hp1 HG01884.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.978+7862T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48654904 | ||||||
chr2:48655014
|
G | T | 1 | a0009c0013t0001g0280 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.978+7972G>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48655014 | ||||||
chr2:48655044
|
A | G | 1 | a0001c0001t0001g0126 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.978+8002A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48655044 | ||||||
chr2:48655117
|
C | T | 1 | a0001c0001t0002g0161 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.978+8075C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48655117 | ||||||
chr2:48655126
|
G | T | 19 | a0001c0001t0002g0081a0001c0001t0002g0082a0001c0001t0002g0090others(16): Show | 19 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.978+8084G>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48655126 | ||||||
chr2:48655201
|
A | G | 315 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(312): Show | 338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.978+8159A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48655201 | ||||||
chr2:48655223
|
AT | A | 5 | a0001c0001t0002g0104a0001c0001t0002g0172a0001c0001t0002g0175others(2): Show | 5 | HG01891.hp2 HG02647.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.978+8182delT | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48655223 | ||||||
chr2:48655225
|
C | G | 1 | a0001c0001t0002g0161 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.978+8183C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48655225 | ||||||
chr2:48655385
|
C | G | 186 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(183): Show | 200 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.978+8343C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48655385 | ||||||
chr2:48655430
|
C | G | 19 | a0001c0001t0002g0081a0001c0001t0002g0082a0001c0001t0002g0090others(16): Show | 19 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.978+8388C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48655430 | ||||||
chr2:48655609
|
T | A | 40 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(37): Show | 44 | HG00642.hp1 HG01074.hp1 HG01109.hp2 others(41): Show |
intron_variant | MODIFIER | c.978+8567T>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48655609 | ||||||
chr2:48655666
|
T | C | 1 | a0001c0001t0001g0266 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.978+8624T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48655666 | ||||||
chr2:48655667
|
C | T | 1 | a0001c0001t0001g0266 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.978+8625C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48655667 | ||||||
chr2:48655718
|
T | C | 2 | a0001c0001t0001g0108a0001c0001t0001g0109 | 2 | HG00558.hp2 NA18956.hp2 |
intron_variant | MODIFIER | c.978+8676T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48655718 | ||||||
chr2:48655739
|
A | G | 67 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0019others(64): Show | 72 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(69): Show |
intron_variant | MODIFIER | c.978+8697A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48655739 | ||||||
chr2:48656105
|
C | T | 8 | a0001c0001t0002g0081a0001c0001t0002g0082a0001c0001t0002g0092others(5): Show | 8 | HG01243.hp2 HG01891.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.978+9063C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48656105 | ||||||
chr2:48656126
|
A | G | 40 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(37): Show | 44 | HG00642.hp1 HG01074.hp1 HG01109.hp2 others(41): Show |
intron_variant | MODIFIER | c.978+9084A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48656126 | ||||||
chr2:48656165
|
T | A | 40 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(37): Show | 44 | HG00642.hp1 HG01074.hp1 HG01109.hp2 others(41): Show |
intron_variant | MODIFIER | c.978+9123T>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48656165 | ||||||
chr2:48656255
|
A | G | 1 | a0001c0001t0001g0168 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.978+9213A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48656255 | ||||||
chr2:48656339
|
T | A | 140 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(137): Show | 152 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.978+9297T>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48656339 | ||||||
chr2:48656348
|
G | GT | 12 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0085others(9): Show | 15 | HG01884.hp1 HG01884.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.978+9335dupT | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 48656348 | |||||
chr2:48656348
|
G | GTT | 7 | a0001c0001t0001g0086a0001c0001t0001g0292a0001c0001t0001g0294others(4): Show | 7 | HG01074.hp1 HG01109.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.978+9334_978+9335d others(4): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 48656348 | |||||
chr2:48656348
|
GT | G | 191 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(188): Show | 205 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(202): Show |
intron_variant | MODIFIER | c.978+9335delT | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 48656348 | |||||
chr2:48656348
|
GTT | G | 50 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0019others(47): Show | 55 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(52): Show |
intron_variant | MODIFIER | c.978+9334_978+9335d others(4): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 48656348 | |||||
chr2:48656348
|
GTTTTTTT others(1): Show |
G | 19 | a0001c0001t0002g0081a0001c0001t0002g0082a0001c0001t0002g0090others(16): Show | 19 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.978+9328_978+9335d others(10): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 48656348 | |||||
chr2:48656359
|
T | G | 3 | a0001c0001t0001g0133a0001c0001t0001g0240a0002c0014t0001g0195 | 3 | HG03654.hp2 NA19012.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.978+9317T>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48656359 | ||||||
chr2:48656360
|
T | G | 183 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(180): Show | 197 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(194): Show |
intron_variant | MODIFIER | c.978+9318T>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48656360 | ||||||
chr2:48656361
|
T | G | 47 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0019others(44): Show | 52 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.978+9319T>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48656361 | ||||||
chr2:48656362
|
T | G | 1 | a0005c0007t0001g0028 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.978+9320T>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48656362 | ||||||
chr2:48656367
|
T | G | 3 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0234 | 3 | HG03710.hp1 HG04199.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.978+9325T>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48656367 | ||||||
chr2:48656368
|
T | G | 19 | a0001c0001t0002g0081a0001c0001t0002g0082a0001c0001t0002g0090others(16): Show | 19 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.978+9326T>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48656368 | ||||||
chr2:48656391
|
C | A | 1 | a0001c0001t0001g0201 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.978+9349C>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48656391 | ||||||
chr2:48656517
|
C | T | 60 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0222others(57): Show | 67 | HG00140.hp1 HG00609.hp2 HG00733.hp2 others(64): Show |
intron_variant | MODIFIER | c.978+9475C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48656517 | ||||||
chr2:48656828
|
G | T | 19 | a0001c0001t0001g0006a0001c0001t0001g0096a0001c0001t0001g0097others(16): Show | 20 | HG00423.hp1 HG02015.hp1 HG02056.hp2 others(17): Show |
intron_variant | MODIFIER | c.978+9786G>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48656828 | ||||||
chr2:48656870
|
G | A | 2 | a0001c0001t0001g0003a0001c0001t0001g0288 | 5 | HG01884.hp2 HG02723.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.978+9828G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48656870 | ||||||
chr2:48657032
|
T | C | 315 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(312): Show | 338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.978+9990T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48657032 | ||||||
chr2:48657086
|
A | G | 1 | a0001c0001t0001g0279 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.978+10044A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48657086 | ||||||
chr2:48657092
|
A | G | 49 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0054others(46): Show | 51 | HG00140.hp2 HG00423.hp2 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.978+10050A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48657092 | ||||||
chr2:48657251
|
C | T | 12 | a0001c0001t0001g0017a0001c0001t0001g0290a0001c0001t0001g0291others(9): Show | 12 | HG01074.hp1 HG01109.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.978+10209C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48657251 | ||||||
chr2:48657280
|
A | G | 49 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0054others(46): Show | 51 | HG00140.hp2 HG00423.hp2 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.978+10238A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48657280 | ||||||
chr2:48657308
|
C | T | 1 | a0001c0001t0001g0020 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.978+10266C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48657308 | ||||||
chr2:48657367
|
G | A | 10 | a0001c0003t0001g0064a0001c0003t0001g0066a0001c0003t0001g0068others(7): Show | 10 | HG02486.hp2 HG02622.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.978+10325G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48657367 | ||||||
chr2:48657409
|
T | G | 47 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0019others(44): Show | 52 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.978+10367T>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48657409 | ||||||
chr2:48657672
|
A | G | 1 | a0001c0001t0001g0110 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.978+10630A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48657672 | ||||||
chr2:48657763
|
GT | G | 279 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(276): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.978+10733delT | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 48657763 | |||||
chr2:48658235
|
A | G | 296 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(293): Show | 319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.978+11193A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48658235 | ||||||
chr2:48658303
|
T | G | 2 | a0001c0001t0001g0085a0001c0001t0001g0086 | 2 | NA18940.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.978+11261T>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48658303 | ||||||
chr2:48658318
|
A | G | 48 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0019others(45): Show | 53 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(50): Show |
intron_variant | MODIFIER | c.978+11276A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48658318 | ||||||
chr2:48658345
|
T | A | 18 | a0001c0003t0001g0018a0001c0003t0001g0062a0001c0003t0001g0064others(15): Show | 18 | HG01243.hp1 HG02486.hp2 HG02615.hp2 others(15): Show |
intron_variant | MODIFIER | c.978+11303T>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48658345 | ||||||
chr2:48658358
|
A | G | 2 | a0001c0001t0001g0003a0001c0001t0001g0288 | 5 | HG01884.hp2 HG02723.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.978+11316A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48658358 | ||||||
chr2:48658407
|
G | A | 1 | a0001c0001t0001g0167 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.979-11315G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48658407 | ||||||
chr2:48658501
|
G | A | 1 | a0001c0001t0001g0107 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.979-11221G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48658501 | ||||||
chr2:48658561
|
T | C | 19 | a0001c0001t0002g0081a0001c0001t0002g0082a0001c0001t0002g0090others(16): Show | 19 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.979-11161T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48658561 | ||||||
chr2:48658714
|
A | G | 315 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(312): Show | 338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.979-11008A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48658714 | ||||||
chr2:48658816
|
T | C | 21 | a0001c0001t0001g0003a0001c0001t0001g0288a0001c0001t0002g0081others(18): Show | 24 | HG01243.hp2 HG01884.hp2 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.979-10906T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48658816 | ||||||
chr2:48658847
|
T | G | 1 | a0001c0003t0001g0064 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.979-10875T>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48658847 | ||||||
chr2:48658850
|
T | TC | 107 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(104): Show | 116 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.979-10872_979-1087 others(5): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48658850 | ||||||
chr2:48659090
|
C | T | 315 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(312): Show | 338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.979-10632C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48659090 | ||||||
chr2:48659134
|
T | A | 315 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(312): Show | 338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.979-10588T>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48659134 | ||||||
chr2:48659289
|
G | T | 1 | a0009c0013t0001g0280 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.979-10433G>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48659289 | ||||||
chr2:48659318
|
T | G | 1 | a0008c0009t0001g0152 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.979-10404T>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48659318 | ||||||
chr2:48659456
|
G | C | 1 | a0001c0001t0002g0161 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.979-10266G>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48659456 | ||||||
chr2:48659636
|
A | C | 2 | a0002c0002t0001g0216a0002c0002t0001g0217 | 2 | HG02040.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.979-10086A>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48659636 | ||||||
chr2:48659726
|
G | A | 66 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0019others(63): Show | 71 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.979-9996G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48659726 | ||||||
chr2:48659743
|
A | T | 18 | a0001c0003t0001g0018a0001c0003t0001g0062a0001c0003t0001g0064others(15): Show | 18 | HG01243.hp1 HG02486.hp2 HG02615.hp2 others(15): Show |
intron_variant | MODIFIER | c.979-9979A>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48659743 | ||||||
chr2:48659904
|
A | G | 2 | a0001c0001t0001g0309a0001c0001t0001g0310 | 2 | HG02258.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.979-9818A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48659904 | ||||||
chr2:48659908
|
A | G | 1 | a0001c0001t0001g0122 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.979-9814A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48659908 | ||||||
chr2:48659912
|
G | A | 4 | a0001c0001t0001g0016a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 5 | HG00642.hp1 HG01361.hp2 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.979-9810G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48659912 | ||||||
chr2:48660093
|
A | AC | 32 | a0001c0001t0001g0006a0001c0001t0001g0096a0001c0001t0001g0097others(29): Show | 33 | HG00423.hp1 HG00741.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.979-9629_979-9628i others(3): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48660093 | ||||||
chr2:48660095
|
T | G | 32 | a0001c0001t0001g0006a0001c0001t0001g0096a0001c0001t0001g0097others(29): Show | 33 | HG00423.hp1 HG00741.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.979-9627T>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48660095 | ||||||
chr2:48660095
|
T | TG | 286 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(283): Show | 308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.979-9627_979-9626i others(3): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48660095 | ||||||
chr2:48660311
|
T | C | 1 | a0001c0001t0001g0276 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.979-9411T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48660311 | ||||||
chr2:48660312
|
T | C | 1 | a0001c0001t0001g0276 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.979-9410T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48660312 | ||||||
chr2:48660397
|
G | T | 4 | a0001c0001t0001g0097a0001c0001t0001g0150a0001c0001t0001g0151others(1): Show | 4 | HG02015.hp1 HG02056.hp2 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.979-9325G>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48660397 | ||||||
chr2:48660454
|
G | A | 4 | a0001c0001t0001g0097a0001c0001t0001g0150a0001c0001t0001g0151others(1): Show | 4 | HG02015.hp1 HG02056.hp2 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.979-9268G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48660454 | ||||||
chr2:48660506
|
G | A | 1 | a0001c0003t0001g0069 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.979-9216G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48660506 | ||||||
chr2:48660560
|
T | G | 1 | a0001c0001t0004g0174 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.979-9162T>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48660560 | ||||||
chr2:48660650
|
T | C | 1 | a0001c0001t0001g0274 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.979-9072T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48660650 | ||||||
chr2:48660659
|
T | C | 3 | a0001c0001t0001g0025a0001c0001t0001g0052a0001c0001t0001g0056 | 3 | HG00323.hp2 HG01074.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.979-9063T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48660659 | ||||||
chr2:48660677
|
C | T | 47 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0019others(44): Show | 52 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.979-9045C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48660677 | ||||||
chr2:48660917
|
A | C | 1 | a0009c0013t0001g0280 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.979-8805A>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48660917 | ||||||
chr2:48660918
|
G | C | 1 | a0009c0013t0001g0280 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.979-8804G>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48660918 | ||||||
chr2:48660952
|
T | G | 1 | a0001c0001t0001g0038 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.979-8770T>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48660952 | ||||||
chr2:48661247
|
C | CT | 104 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0013others(101): Show | 112 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.979-8447dupT | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 48661247 | |||||
chr2:48661247
|
C | CTT | 92 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(89): Show | 98 | HG00099.hp2 HG00423.hp1 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.979-8448_979-8447d others(4): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 48661247 | |||||
chr2:48661247
|
C | CTTT | 11 | a0001c0001t0001g0100a0001c0001t0001g0119a0001c0001t0001g0125others(8): Show | 11 | HG00621.hp2 HG01069.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.979-8449_979-8447d others(5): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 48661247 | |||||
chr2:48661247
|
C | CTTTT | 8 | a0001c0001t0001g0003a0001c0001t0001g0282a0001c0001t0001g0283others(5): Show | 11 | HG01109.hp2 HG01884.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.979-8450_979-8447d others(6): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 48661247 | |||||
chr2:48661247
|
C | CTTTTT | 7 | a0001c0001t0001g0284a0001c0001t0001g0285a0001c0001t0001g0295others(4): Show | 7 | HG02145.hp1 HG02145.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.979-8451_979-8447d others(7): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 48661247 | |||||
chr2:48661247
|
CT | C | 38 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0019others(35): Show | 43 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(40): Show |
intron_variant | MODIFIER | c.979-8447delT | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 48661247 | |||||
chr2:48661247
|
CTTTTTTT others(3): Show |
C | 2 | a0001c0001t0001g0085a0001c0001t0001g0086 | 2 | NA18940.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.979-8456_979-8447d others(12): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 48661247 | |||||
chr2:48661247
|
CTTTTTTT others(4): Show |
C | 13 | a0001c0001t0001g0016a0001c0001t0001g0273a0001c0001t0001g0304others(10): Show | 14 | HG00642.hp1 HG01361.hp2 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.979-8457_979-8447d others(13): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 48661247 | |||||
chr2:48661394
|
T | C | 65 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0019others(62): Show | 70 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.979-8328T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48661394 | ||||||
chr2:48661414
|
T | C | 1 | a0002c0002t0001g0213 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.979-8308T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48661414 | ||||||
chr2:48661696
|
A | AT | 47 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0019others(44): Show | 52 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.979-8018dupT | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 48661696 | |||||
chr2:48661740
|
A | G | 2 | a0001c0001t0001g0265a0001c0003t0001g0075 | 2 | HG02818.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.979-7982A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48661740 | ||||||
chr2:48661758
|
A | C | 48 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0019others(45): Show | 53 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(50): Show |
intron_variant | MODIFIER | c.979-7964A>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48661758 | ||||||
chr2:48661868
|
T | G | 3 | a0001c0001t0001g0169a0001c0001t0001g0251a0001c0001t0001g0255 | 3 | HG01928.hp1 HG01978.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.979-7854T>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48661868 | ||||||
chr2:48661892
|
C | T | 1 | a0002c0002t0001g0140 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.979-7830C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48661892 | ||||||
chr2:48661909
|
G | A | 46 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0019others(43): Show | 51 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(48): Show |
intron_variant | MODIFIER | c.979-7813G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48661909 | ||||||
chr2:48661932
|
C | T | 1 | a0001c0001t0001g0287 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.979-7790C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48661932 | ||||||
chr2:48661990
|
C | T | 2 | a0001c0001t0001g0003a0001c0001t0001g0288 | 5 | HG01884.hp2 HG02723.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.979-7732C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48661990 | ||||||
chr2:48662111
|
T | G | 19 | a0001c0001t0002g0081a0001c0001t0002g0082a0001c0001t0002g0090others(16): Show | 19 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.979-7611T>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48662111 | ||||||
chr2:48662114
|
A | C | 1 | a0001c0001t0001g0255 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.979-7608A>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48662114 | ||||||
chr2:48662204
|
T | A | 1 | a0001c0001t0001g0266 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.979-7518T>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48662204 | ||||||
chr2:48662307
|
A | T | 188 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(185): Show | 202 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(199): Show |
intron_variant | MODIFIER | c.979-7415A>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48662307 | ||||||
chr2:48662445
|
C | T | 320 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(317): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.979-7277C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48662445 | ||||||
chr2:48662594
|
G | C | 47 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0019others(44): Show | 52 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.979-7128G>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48662594 | ||||||
chr2:48662652
|
C | CT | 36 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0089others(33): Show | 39 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.979-7050dupT | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 48662652 | |||||
chr2:48662652
|
CT | C | 41 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0017others(38): Show | 43 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(40): Show |
intron_variant | MODIFIER | c.979-7050delT | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 48662652 | |||||
chr2:48662652
|
CTT | C | 70 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0019others(67): Show | 77 | HG00099.hp1 HG00323.hp2 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.979-7051_979-7050d others(4): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 48662652 | |||||
chr2:48662799
|
T | C | 6 | a0001c0001t0001g0315a0001c0001t0001g0316a0001c0001t0001g0317others(3): Show | 6 | HG02145.hp2 HG02630.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.979-6923T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48662799 | ||||||
chr2:48662828
|
A | G | 37 | a0001c0001t0001g0006a0001c0001t0001g0096a0001c0001t0001g0097others(34): Show | 38 | HG00423.hp1 HG00741.hp1 HG01069.hp2 others(35): Show |
intron_variant | MODIFIER | c.979-6894A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48662828 | ||||||
chr2:48662869
|
C | G | 1 | a0001c0001t0001g0054 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.979-6853C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48662869 | ||||||
chr2:48662898
|
C | T | 1 | a0001c0001t0001g0281 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.979-6824C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48662898 | ||||||
chr2:48662915
|
G | A | 1 | a0001c0001t0001g0137 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.979-6807G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48662915 | ||||||
chr2:48662955
|
C | T | 48 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0019others(45): Show | 53 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(50): Show |
intron_variant | MODIFIER | c.979-6767C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48662955 | ||||||
chr2:48662959
|
G | A | 21 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0282others(18): Show | 24 | HG01074.hp1 HG01109.hp2 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.979-6763G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48662959 | ||||||
chr2:48663037
|
C | T | 19 | a0001c0003t0001g0018a0001c0003t0001g0061a0001c0003t0001g0062others(16): Show | 19 | HG01243.hp1 HG01891.hp1 HG02486.hp2 others(16): Show |
intron_variant | MODIFIER | c.979-6685C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48663037 | ||||||
chr2:48663118
|
A | G | 19 | a0001c0001t0001g0016a0001c0001t0001g0273a0001c0001t0001g0304others(16): Show | 20 | HG00642.hp1 HG01361.hp2 HG01515.hp2 others(17): Show |
intron_variant | MODIFIER | c.979-6604A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48663118 | ||||||
chr2:48663191
|
T | C | 13 | a0001c0001t0001g0016a0001c0001t0001g0273a0001c0001t0001g0304others(10): Show | 14 | HG00642.hp1 HG01361.hp2 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.979-6531T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48663191 | ||||||
chr2:48663328
|
C | T | 1 | a0001c0001t0001g0183 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.979-6394C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48663328 | ||||||
chr2:48663393
|
A | G | 315 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(312): Show | 338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.979-6329A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48663393 | ||||||
chr2:48663611
|
A | C | 1 | a0001c0001t0001g0021 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.979-6111A>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48663611 | ||||||
chr2:48663637
|
A | T | 1 | a0001c0001t0001g0155 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.979-6085A>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48663637 | ||||||
chr2:48663774
|
G | A | 1 | a0001c0001t0001g0120 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.979-5948G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48663774 | ||||||
chr2:48663824
|
G | T | 1 | a0001c0001t0001g0035 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.979-5898G>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48663824 | ||||||
chr2:48664019
|
C | T | 21 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0282others(18): Show | 24 | HG01074.hp1 HG01109.hp2 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.979-5703C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48664019 | ||||||
chr2:48664079
|
A | G | 21 | a0001c0003t0001g0018a0001c0003t0001g0061a0001c0003t0001g0062others(18): Show | 21 | HG01070.hp1 HG01123.hp1 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.979-5643A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48664079 | ||||||
chr2:48664095
|
A | T | 1 | a0002c0002t0001g0210 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.979-5627A>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48664095 | ||||||
chr2:48664145
|
T | C | 19 | a0001c0001t0001g0016a0001c0001t0001g0273a0001c0001t0001g0304others(16): Show | 20 | HG00642.hp1 HG01361.hp2 HG01515.hp2 others(17): Show |
intron_variant | MODIFIER | c.979-5577T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48664145 | ||||||
chr2:48664148
|
C | T | 47 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0019others(44): Show | 52 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.979-5574C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48664148 | ||||||
chr2:48664228
|
C | A | 12 | a0001c0001t0001g0017a0001c0001t0001g0290a0001c0001t0001g0291others(9): Show | 12 | HG01074.hp1 HG01109.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.979-5494C>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48664228 | ||||||
chr2:48664265
|
T | G | 1 | a0001c0001t0001g0301 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.979-5457T>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48664265 | ||||||
chr2:48664298
|
C | A | 86 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(83): Show | 94 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.979-5424C>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48664298 | ||||||
chr2:48664318
|
T | G | 19 | a0001c0001t0002g0081a0001c0001t0002g0082a0001c0001t0002g0090others(16): Show | 19 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.979-5404T>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48664318 | ||||||
chr2:48664415
|
C | T | 3 | a0001c0001t0001g0010a0001c0001t0001g0134a0001c0001t0001g0158 | 4 | HG00099.hp2 HG01192.hp2 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.979-5307C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48664415 | ||||||
chr2:48664590
|
G | A | 4 | a0001c0001t0001g0294a0001c0001t0001g0295a0001c0001t0001g0296others(1): Show | 4 | HG01109.hp2 HG02559.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.979-5132G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48664590 | ||||||
chr2:48664689
|
G | A | 1 | a0001c0001t0001g0281 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.979-5033G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48664689 | ||||||
chr2:48664952
|
ACT | A | 4 | a0001c0001t0001g0316a0001c0001t0001g0318a0001c0001t0001g0319others(1): Show | 4 | HG02145.hp2 HG02630.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.979-4767_979-4766d others(4): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 48664952 | |||||
chr2:48665022
|
C | T | 6 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0001t0001g0284others(3): Show | 6 | HG02055.hp2 HG02145.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.979-4700C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48665022 | ||||||
chr2:48665032
|
G | C | 1 | a0002c0002t0001g0014 | 2 | NA18962.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.979-4690G>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48665032 | ||||||
chr2:48665046
|
C | T | 1 | a0001c0001t0001g0287 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.979-4676C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48665046 | ||||||
chr2:48665055
|
G | A | 19 | a0001c0001t0002g0081a0001c0001t0002g0082a0001c0001t0002g0090others(16): Show | 19 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.979-4667G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48665055 | ||||||
chr2:48665203
|
C | T | 12 | a0001c0001t0001g0017a0001c0001t0001g0290a0001c0001t0001g0291others(9): Show | 12 | HG01074.hp1 HG01109.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.979-4519C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48665203 | ||||||
chr2:48665257
|
G | A | 315 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(312): Show | 338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.979-4465G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48665257 | ||||||
chr2:48665276
|
TTC | T | 5 | a0001c0001t0001g0315a0001c0001t0001g0316a0001c0001t0001g0317others(2): Show | 5 | HG02145.hp2 HG02630.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.979-4436_979-4435d others(4): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 48665276 | |||||
chr2:48665286
|
C | CT | 67 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0019others(64): Show | 72 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(69): Show |
intron_variant | MODIFIER | c.979-4421dupT | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 48665286 | |||||
chr2:48665286
|
CT | C | 25 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0085others(22): Show | 28 | HG01074.hp1 HG01109.hp2 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.979-4421delT | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 48665286 | |||||
chr2:48665349
|
T | TTCCTCCT others(22): Show |
1 | a0001c0001t0001g0100 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.979-4372_979-4344d others(31): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 48665349 | |||||
chr2:48665550
|
A | T | 1 | a0001c0001t0001g0050 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.979-4172A>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48665550 | ||||||
chr2:48665623
|
A | G | 49 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0019others(46): Show | 54 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.979-4099A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48665623 | ||||||
chr2:48665626
|
T | C | 1 | a0001c0001t0001g0039 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.979-4096T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48665626 | ||||||
chr2:48665632
|
A | G | 19 | a0001c0001t0002g0081a0001c0001t0002g0082a0001c0001t0002g0090others(16): Show | 19 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.979-4090A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48665632 | ||||||
chr2:48665668
|
T | C | 6 | a0001c0001t0001g0238a0001c0001t0001g0252a0001c0001t0001g0253others(3): Show | 6 | NA18960.hp2 NA19000.hp1 NA19003.hp2 others(3): Show |
intron_variant | MODIFIER | c.979-4054T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48665668 | ||||||
chr2:48665762
|
C | T | 1 | a0001c0001t0001g0307 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.979-3960C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48665762 | ||||||
chr2:48665974
|
A | G | 2 | a0004c0008t0002g0302a0004c0008t0002g0303 | 2 | HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.979-3748A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48665974 | ||||||
chr2:48666168
|
T | C | 69 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0019others(66): Show | 74 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.979-3554T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48666168 | ||||||
chr2:48666193
|
G | T | 12 | a0001c0001t0001g0016a0001c0001t0001g0304a0001c0001t0001g0305others(9): Show | 13 | HG00642.hp1 HG01361.hp2 HG01515.hp2 others(10): Show |
intron_variant | MODIFIER | c.979-3529G>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48666193 | ||||||
chr2:48666211
|
CT | C | 12 | a0001c0003t0001g0018a0001c0003t0001g0061a0001c0003t0001g0062others(9): Show | 12 | HG01243.hp1 HG01891.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.979-3499delT | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 48666211 | |||||
chr2:48666348
|
G | C | 12 | a0001c0001t0001g0017a0001c0001t0001g0290a0001c0001t0001g0291others(9): Show | 12 | HG01074.hp1 HG01109.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.979-3374G>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48666348 | ||||||
chr2:48666505
|
C | T | 68 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0019others(65): Show | 73 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.979-3217C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48666505 | ||||||
chr2:48666523
|
A | G | 1 | a0001c0001t0001g0023 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.979-3199A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48666523 | ||||||
chr2:48666584
|
G | GGT | 142 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(139): Show | 155 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.979-3111_979-3110d others(4): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 48666584 | |||||
chr2:48666584
|
G | GGTGT | 43 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0015others(40): Show | 47 | HG00099.hp2 HG00544.hp1 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.979-3113_979-3110d others(6): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 48666584 | |||||
chr2:48666584
|
G | GGTGTGT | 4 | a0001c0001t0001g0127a0001c0001t0001g0272a0001c0001t0001g0278others(1): Show | 4 | HG00597.hp2 HG01934.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.979-3115_979-3110d others(8): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 48666584 | |||||
chr2:48666584
|
G | GTGT | 5 | a0001c0001t0001g0222a0001c0001t0001g0269a0001c0001t0001g0316others(2): Show | 5 | HG01175.hp1 HG02165.hp2 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.979-3138_979-3137i others(5): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48666584 | ||||||
chr2:48666584
|
GGTGT | G | 7 | a0001c0001t0001g0003a0001c0001t0001g0288a0001c0001t0001g0294others(4): Show | 10 | HG01109.hp2 HG01884.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.979-3113_979-3110d others(6): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 48666584 | |||||
chr2:48666584
|
GGTGTGT | G | 15 | a0001c0001t0001g0017a0001c0001t0001g0282a0001c0001t0001g0283others(12): Show | 15 | HG01074.hp1 HG01884.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.979-3115_979-3110d others(8): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 48666584 | |||||
chr2:48666613
|
T | G | 1 | a0002c0002t0001g0204 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.979-3109T>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48666613 | ||||||
chr2:48666691
|
T | C | 1 | a0001c0001t0001g0042 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.979-3031T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48666691 | ||||||
chr2:48666874
|
T | C | 1 | a0001c0001t0005g0129 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.979-2848T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48666874 | ||||||
chr2:48667115
|
A | AT | 203 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(200): Show | 217 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.979-2592dupT | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 48667115 | |||||
chr2:48667115
|
A | ATT | 8 | a0001c0001t0001g0170a0001c0001t0001g0238a0001c0001t0001g0252others(5): Show | 8 | HG04184.hp2 NA18941.hp1 NA18960.hp2 others(5): Show |
intron_variant | MODIFIER | c.979-2593_979-2592d others(4): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 48667115 | |||||
chr2:48667115
|
AT | A | 44 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0043others(41): Show | 47 | HG00544.hp2 HG01074.hp1 HG01109.hp2 others(44): Show |
intron_variant | MODIFIER | c.979-2592delT | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 48667115 | |||||
chr2:48667166
|
C | T | 17 | a0001c0001t0002g0081a0001c0001t0002g0082a0001c0001t0002g0090others(14): Show | 17 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.979-2556C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48667166 | ||||||
chr2:48667202
|
G | T | 12 | a0001c0001t0001g0017a0001c0001t0001g0290a0001c0001t0001g0291others(9): Show | 12 | HG01074.hp1 HG01109.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.979-2520G>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48667202 | ||||||
chr2:48667343
|
C | G | 1 | a0001c0001t0001g0275 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.979-2379C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48667343 | ||||||
chr2:48667465
|
A | G | 71 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(68): Show | 77 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.979-2257A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48667465 | ||||||
chr2:48667682
|
A | T | 1 | a0001c0001t0001g0292 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.979-2040A>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48667682 | ||||||
chr2:48667996
|
C | G | 18 | a0001c0001t0002g0081a0001c0001t0002g0082a0001c0001t0002g0090others(15): Show | 18 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.979-1726C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48667996 | ||||||
chr2:48668017
|
C | T | 9 | a0001c0001t0001g0003a0001c0001t0001g0282a0001c0001t0001g0283others(6): Show | 12 | HG01884.hp2 HG02055.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.979-1705C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48668017 | ||||||
chr2:48668018
|
G | A | 1 | a0001c0001t0001g0099 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.979-1704G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48668018 | ||||||
chr2:48668109
|
C | T | 1 | a0009c0013t0001g0280 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.979-1613C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48668109 | ||||||
chr2:48668115
|
C | T | 1 | a0001c0001t0001g0110 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.979-1607C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48668115 | ||||||
chr2:48668299
|
A | G | 1 | a0001c0001t0001g0199 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.979-1423A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48668299 | ||||||
chr2:48668661
|
C | G | 1 | a0001c0001t0001g0281 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.979-1061C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48668661 | ||||||
chr2:48668696
|
A | G | 49 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0019others(46): Show | 54 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.979-1026A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48668696 | ||||||
chr2:48668837
|
A | AAAAT | 7 | a0001c0001t0001g0088a0001c0001t0001g0150a0002c0002t0001g0004others(4): Show | 9 | HG00609.hp2 HG02015.hp1 HG02135.hp1 others(6): Show |
intron_variant | MODIFIER | c.979-859_979-856dup others(4): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 48668837 | |||||
chr2:48668837
|
A | AAAATAAA others(5): Show |
3 | a0001c0001t0002g0092a0001c0001t0002g0176a0004c0008t0002g0303 | 3 | HG01243.hp2 HG02647.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.979-867_979-856dup others(12): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 48668837 | |||||
chr2:48668837
|
A | AAAATAAA others(9): Show |
13 | a0001c0001t0002g0081a0001c0001t0002g0082a0001c0001t0002g0090others(10): Show | 13 | HG01891.hp2 HG02055.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.979-871_979-856dup others(16): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 48668837 | |||||
chr2:48668837
|
A | AAAATAAA others(13): Show |
3 | a0001c0001t0002g0177a0001c0001t0002g0179a0001c0001t0002g0182 | 3 | HG03139.hp2 HG03225.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.979-875_979-856dup others(20): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 48668837 | |||||
chr2:48668837
|
AAAAT | A | 50 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0019others(47): Show | 55 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(52): Show |
intron_variant | MODIFIER | c.979-859_979-856del others(4): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 48668837 | |||||
chr2:48669069
|
A | G | 1 | a0001c0001t0001g0281 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.979-653A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48669069 | ||||||
chr2:48669310
|
T | A | 46 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0089others(43): Show | 48 | HG00140.hp2 HG00423.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.979-412T>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48669310 | ||||||
chr2:48669679
|
C | T | 1 | a0002c0002t0001g0215 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.979-43C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48669679 | ||||||
chr2:48670120
|
C | T | 1 | a0001c0001t0001g0183 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1239+138C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 7/8 | chr2 | 48670120 | ||||||
chr2:48670133
|
A | C | 112 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(109): Show | 122 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.1239+151A>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 7/8 | chr2 | 48670133 | ||||||
chr2:48670248
|
G | A | 7 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0001t0001g0284others(4): Show | 7 | HG02055.hp2 HG02145.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.1239+266G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 7/8 | chr2 | 48670248 | ||||||
chr2:48670256
|
TG | T | 20 | a0001c0001t0002g0081a0001c0001t0002g0082a0001c0001t0002g0090others(17): Show | 20 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.1239+276delG | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr2 | 48670256 | |||||
chr2:48670379
|
T | TA | 56 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(53): Show | 62 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.1239+409dupA | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr2 | 48670379 | |||||
chr2:48670398
|
T | A | 12 | a0001c0001t0001g0017a0001c0001t0001g0290a0001c0001t0001g0291others(9): Show | 12 | HG01074.hp1 HG01109.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.1239+416T>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 7/8 | chr2 | 48670398 | ||||||
chr2:48670786
|
G | T | 1 | a0001c0003t0001g0064 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1239+804G>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 7/8 | chr2 | 48670786 | ||||||
chr2:48670802
|
A | G | 40 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(37): Show | 44 | HG00642.hp1 HG01074.hp1 HG01109.hp2 others(41): Show |
intron_variant | MODIFIER | c.1240-789A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 7/8 | chr2 | 48670802 | ||||||
chr2:48670816
|
C | CA | 73 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(70): Show | 79 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(76): Show |
intron_variant | MODIFIER | c.1240-775_1240-774i others(3): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 7/8 | chr2 | 48670816 | ||||||
chr2:48670914
|
C | T | 1 | a0001c0001t0006g0289 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1240-677C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 7/8 | chr2 | 48670914 | ||||||
chr2:48670918
|
G | A | 73 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(70): Show | 79 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(76): Show |
intron_variant | MODIFIER | c.1240-673G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 7/8 | chr2 | 48670918 | ||||||
chr2:48670926
|
T | C | 73 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(70): Show | 79 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(76): Show |
intron_variant | MODIFIER | c.1240-665T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 7/8 | chr2 | 48670926 | ||||||
chr2:48670970
|
C | T | 1 | a0001c0001t0006g0289 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1240-621C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 7/8 | chr2 | 48670970 | ||||||
chr2:48671075
|
G | A | 2 | a0001c0001t0001g0105a0001c0001t0001g0106 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1240-516G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 7/8 | chr2 | 48671075 | ||||||
chr2:48671078
|
T | A | 1 | a0004c0008t0002g0303 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1240-513T>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 7/8 | chr2 | 48671078 | ||||||
chr2:48671261
|
G | C | 53 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(50): Show | 59 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.1240-330G>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 7/8 | chr2 | 48671261 | ||||||
chr2:48671400
|
C | T | 73 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(70): Show | 79 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(76): Show |
intron_variant | MODIFIER | c.1240-191C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 7/8 | chr2 | 48671400 | ||||||
chr2:48671479
|
T | C | 1 | a0001c0001t0001g0275 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1240-112T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 7/8 | chr2 | 48671479 | ||||||
chr2:48671582
|
C | T | 2 | a0004c0008t0002g0302a0004c0008t0002g0303 | 2 | HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1240-9C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 7/8 | chr2 | 48671582 | ||||||
chr2:48671710
|
T | G | 1 | a0001c0001t0001g0036 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1329+30T>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48671710 | ||||||
chr2:48672011
|
G | A | 181 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(178): Show | 194 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(191): Show |
intron_variant | MODIFIER | c.1329+331G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48672011 | ||||||
chr2:48672052
|
A | G | 20 | a0001c0001t0002g0081a0001c0001t0002g0082a0001c0001t0002g0090others(17): Show | 20 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.1329+372A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48672052 | ||||||
chr2:48672147
|
G | A | 21 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0282others(18): Show | 24 | HG01074.hp1 HG01109.hp2 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.1329+467G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48672147 | ||||||
chr2:48672377
|
C | G | 51 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(48): Show | 57 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(54): Show |
intron_variant | MODIFIER | c.1329+697C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48672377 | ||||||
chr2:48672563
|
G | A | 1 | a0001c0001t0001g0116 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1329+883G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48672563 | ||||||
chr2:48672668
|
C | T | 35 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0015others(32): Show | 38 | HG00099.hp2 HG00544.hp1 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.1329+988C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48672668 | ||||||
chr2:48672722
|
T | C | 70 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(67): Show | 76 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(73): Show |
intron_variant | MODIFIER | c.1329+1042T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48672722 | ||||||
chr2:48672727
|
G | A | 1 | a0001c0001t0001g0269 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1329+1047G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48672727 | ||||||
chr2:48672728
|
T | A | 21 | a0001c0003t0001g0018a0001c0003t0001g0061a0001c0003t0001g0062others(18): Show | 21 | HG01070.hp1 HG01123.hp1 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.1329+1048T>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48672728 | ||||||
chr2:48672783
|
G | T | 2 | a0001c0001t0001g0003a0001c0001t0001g0288 | 5 | HG01884.hp2 HG02723.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1329+1103G>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48672783 | ||||||
chr2:48672867
|
C | T | 18 | a0001c0001t0001g0016a0001c0001t0001g0304a0001c0001t0001g0305others(15): Show | 19 | HG00642.hp1 HG01361.hp2 HG01515.hp2 others(16): Show |
intron_variant | MODIFIER | c.1329+1187C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48672867 | ||||||
chr2:48672917
|
T | C | 1 | a0001c0001t0001g0245 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1329+1237T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48672917 | ||||||
chr2:48673000
|
A | G | 72 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(69): Show | 78 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(75): Show |
intron_variant | MODIFIER | c.1329+1320A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48673000 | ||||||
chr2:48673038
|
T | C | 2 | a0002c0002t0001g0200a0002c0002t0001g0205 | 2 | NA18961.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.1329+1358T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48673038 | ||||||
chr2:48673084
|
G | T | 2 | a0002c0002t0001g0140a0002c0002t0001g0142 | 2 | HG01496.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1329+1404G>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48673084 | ||||||
chr2:48673104
|
T | C | 1 | a0001c0001t0001g0294 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1329+1424T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48673104 | ||||||
chr2:48673189
|
C | T | 20 | a0001c0001t0002g0081a0001c0001t0002g0082a0001c0001t0002g0090others(17): Show | 20 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.1329+1509C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48673189 | ||||||
chr2:48673310
|
A | G | 1 | a0001c0001t0001g0109 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1329+1630A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48673310 | ||||||
chr2:48673359
|
C | CT | 169 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(166): Show | 181 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(178): Show |
intron_variant | MODIFIER | c.1329+1700dupT | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 48673359 | |||||
chr2:48673359
|
C | CTT | 7 | a0001c0001t0001g0119a0001c0001t0001g0122a0001c0001t0001g0123others(4): Show | 7 | HG00140.hp2 HG00621.hp2 HG02083.hp1 others(4): Show |
intron_variant | MODIFIER | c.1329+1699_1329+170 others(6): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 48673359 | |||||
chr2:48673359
|
CT | C | 49 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0290others(46): Show | 50 | HG00642.hp1 HG01070.hp1 HG01074.hp1 others(47): Show |
intron_variant | MODIFIER | c.1329+1700delT | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 48673359 | |||||
chr2:48673359
|
CTT | C | 19 | a0001c0001t0001g0100a0001c0001t0002g0082a0001c0001t0002g0090others(16): Show | 19 | HG01243.hp2 HG01891.hp2 HG02559.hp2 others(16): Show |
intron_variant | MODIFIER | c.1329+1699_1329+170 others(6): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 48673359 | |||||
chr2:48673359
|
CTTT | C | 52 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(49): Show | 58 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.1329+1698_1329+170 others(7): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 48673359 | |||||
chr2:48673507
|
C | T | 39 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(36): Show | 43 | HG00642.hp1 HG01074.hp1 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.1329+1827C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48673507 | ||||||
chr2:48673592
|
T | C | 73 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(70): Show | 79 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(76): Show |
intron_variant | MODIFIER | c.1329+1912T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48673592 | ||||||
chr2:48673663
|
A | C | 73 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(70): Show | 79 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(76): Show |
intron_variant | MODIFIER | c.1329+1983A>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48673663 | ||||||
chr2:48673720
|
G | A | 6 | a0002c0002t0001g0004a0002c0002t0001g0171a0002c0002t0001g0212others(3): Show | 8 | HG00609.hp2 HG02135.hp1 NA18947.hp1 others(5): Show |
intron_variant | MODIFIER | c.1329+2040G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48673720 | ||||||
chr2:48673850
|
A | G | 20 | a0001c0001t0002g0081a0001c0001t0002g0082a0001c0001t0002g0090others(17): Show | 20 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.1329+2170A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48673850 | ||||||
chr2:48673912
|
C | T | 180 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(177): Show | 193 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.1329+2232C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48673912 | ||||||
chr2:48674125
|
T | C | 1 | a0001c0001t0001g0266 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1329+2445T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48674125 | ||||||
chr2:48674173
|
A | C | 1 | a0001c0001t0001g0165 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1329+2493A>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48674173 | ||||||
chr2:48674174
|
T | A | 1 | a0001c0001t0001g0165 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1329+2494T>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48674174 | ||||||
chr2:48674174
|
T | C | 73 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(70): Show | 79 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(76): Show |
intron_variant | MODIFIER | c.1329+2494T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48674174 | ||||||
chr2:48674175
|
T | C | 1 | a0001c0001t0001g0165 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1329+2495T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48674175 | ||||||
chr2:48674177
|
G | C | 1 | a0001c0001t0001g0165 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1329+2497G>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48674177 | ||||||
chr2:48674178
|
A | G | 1 | a0001c0001t0001g0165 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1329+2498A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48674178 | ||||||
chr2:48674183
|
T | A | 1 | a0001c0001t0001g0165 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1329+2503T>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48674183 | ||||||
chr2:48674346
|
A | G | 1 | a0001c0001t0006g0289 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1329+2666A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48674346 | ||||||
chr2:48674356
|
C | G | 1 | a0001c0001t0006g0289 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1329+2676C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48674356 | ||||||
chr2:48674379
|
T | G | 3 | a0001c0001t0001g0282a0001c0001t0001g0284a0001c0001t0001g0285 | 3 | HG02055.hp2 HG02145.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.1329+2699T>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48674379 | ||||||
chr2:48674500
|
C | T | 2 | a0003c0004t0001g0063a0003c0004t0001g0080 | 2 | HG01070.hp1 HG01123.hp1 |
intron_variant | MODIFIER | c.1329+2820C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48674500 | ||||||
chr2:48674529
|
A | T | 1 | a0001c0003t0001g0061 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1329+2849A>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48674529 | ||||||
chr2:48674758
|
G | A | 1 | a0001c0003t0001g0067 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1329+3078G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48674758 | ||||||
chr2:48674833
|
G | A | 21 | a0001c0003t0001g0018a0001c0003t0001g0061a0001c0003t0001g0062others(18): Show | 21 | HG01070.hp1 HG01123.hp1 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.1329+3153G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48674833 | ||||||
chr2:48675309
|
G | C | 1 | a0001c0001t0006g0289 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1329+3629G>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48675309 | ||||||
chr2:48675322
|
A | G | 1 | a0001c0001t0006g0289 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1329+3642A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48675322 | ||||||
chr2:48675387
|
A | G | 1 | a0001c0001t0001g0221 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1329+3707A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48675387 | ||||||
chr2:48675428
|
A | C | 3 | a0001c0001t0001g0169a0001c0001t0001g0251a0001c0001t0001g0255 | 3 | HG01928.hp1 HG01978.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.1329+3748A>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48675428 | ||||||
chr2:48675439
|
A | G | 59 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(56): Show | 65 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.1329+3759A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48675439 | ||||||
chr2:48675451
|
G | C | 1 | a0001c0001t0001g0126 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1329+3771G>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48675451 | ||||||
chr2:48675487
|
A | G | 12 | a0001c0001t0001g0017a0001c0001t0001g0290a0001c0001t0001g0291others(9): Show | 12 | HG01074.hp1 HG01109.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.1329+3807A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48675487 | ||||||
chr2:48675617
|
C | T | 4 | a0001c0001t0001g0316a0001c0001t0001g0318a0001c0001t0001g0319others(1): Show | 4 | HG02145.hp2 HG02630.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.1330-3718C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48675617 | ||||||
chr2:48675618
|
G | A | 18 | a0001c0001t0002g0081a0001c0001t0002g0082a0001c0001t0002g0090others(15): Show | 18 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.1330-3717G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48675618 | ||||||
chr2:48675728
|
G | A | 1 | a0001c0001t0001g0146 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1330-3607G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48675728 | ||||||
chr2:48675729
|
T | C | 5 | a0001c0003t0001g0075a0001c0003t0001g0076a0001c0003t0001g0077others(2): Show | 5 | HG02622.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1330-3606T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48675729 | ||||||
chr2:48675870
|
G | A | 316 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(313): Show | 339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.1330-3465G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48675870 | ||||||
chr2:48675932
|
G | A | 1 | a0001c0001t0001g0134 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1330-3403G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48675932 | ||||||
chr2:48676248
|
C | G | 12 | a0001c0001t0001g0017a0001c0001t0001g0290a0001c0001t0001g0291others(9): Show | 12 | HG01074.hp1 HG01109.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.1330-3087C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48676248 | ||||||
chr2:48676536
|
C | G | 1 | a0001c0012t0001g0242 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1330-2799C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48676536 | ||||||
chr2:48676833
|
C | CATCTAT | 3 | a0001c0001t0001g0238a0001c0001t0001g0274a0001c0001t0001g0276 | 3 | NA18975.hp1 NA19075.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.1330-2481_1330-247 others(10): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 48676833 | |||||
chr2:48676925
|
AT | A | 58 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(55): Show | 64 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.1330-2399delT | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 48676925 | |||||
chr2:48676930
|
T | A | 1 | a0001c0001t0001g0246 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1330-2405T>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48676930 | ||||||
chr2:48676931
|
T | A | 4 | a0001c0001t0001g0003a0001c0001t0001g0281a0001c0001t0001g0288others(1): Show | 7 | HG00738.hp1 HG01884.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1330-2404T>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48676931 | ||||||
chr2:48677050
|
T | C | 1 | a0001c0001t0001g0148 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1330-2285T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48677050 | ||||||
chr2:48677128
|
G | A | 315 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(312): Show | 338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.1330-2207G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48677128 | ||||||
chr2:48677223
|
T | C | 3 | a0001c0001t0001g0197a0001c0001t0001g0258a0001c0001t0001g0261 | 3 | HG03486.hp2 HG03579.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1330-2112T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48677223 | ||||||
chr2:48677231
|
A | T | 79 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(76): Show | 85 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.1330-2104A>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48677231 | ||||||
chr2:48677262
|
C | T | 2 | a0001c0001t0001g0173a0001c0001t0001g0321 | 2 | HG02970.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1330-2073C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48677262 | ||||||
chr2:48677311
|
G | C | 1 | a0001c0001t0001g0126 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1330-2024G>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48677311 | ||||||
chr2:48677338
|
G | A | 2 | a0001c0001t0001g0108a0001c0001t0001g0109 | 2 | HG00558.hp2 NA18956.hp2 |
intron_variant | MODIFIER | c.1330-1997G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48677338 | ||||||
chr2:48677411
|
T | C | 81 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(78): Show | 87 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.1330-1924T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48677411 | ||||||
chr2:48677423
|
G | A | 7 | a0001c0001t0001g0315a0001c0001t0001g0316a0001c0001t0001g0317others(4): Show | 7 | HG02145.hp2 HG02630.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1330-1912G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48677423 | ||||||
chr2:48677470
|
C | T | 58 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(55): Show | 64 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.1330-1865C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48677470 | ||||||
chr2:48677520
|
A | G | 60 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(57): Show | 66 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.1330-1815A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48677520 | ||||||
chr2:48677571
|
T | C | 1 | a0001c0001t0001g0137 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1330-1764T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48677571 | ||||||
chr2:48677671
|
C | G | 12 | a0001c0001t0001g0016a0001c0001t0001g0304a0001c0001t0001g0305others(9): Show | 13 | HG00642.hp1 HG01361.hp2 HG01515.hp2 others(10): Show |
intron_variant | MODIFIER | c.1330-1664C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48677671 | ||||||
chr2:48677697
|
G | T | 1 | a0001c0001t0001g0312 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1330-1638G>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48677697 | ||||||
chr2:48677699
|
G | C | 1 | a0001c0001t0001g0148 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1330-1636G>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48677699 | ||||||
chr2:48677700
|
G | C | 12 | a0001c0001t0001g0016a0001c0001t0001g0304a0001c0001t0001g0305others(9): Show | 13 | HG00642.hp1 HG01361.hp2 HG01515.hp2 others(10): Show |
intron_variant | MODIFIER | c.1330-1635G>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48677700 | ||||||
chr2:48677703
|
A | G | 286 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(283): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.1330-1632A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48677703 | ||||||
chr2:48677892
|
A | G | 1 | a0001c0001t0001g0110 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1330-1443A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48677892 | ||||||
chr2:48677896
|
G | A | 7 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0001t0001g0284others(4): Show | 7 | HG02055.hp2 HG02145.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.1330-1439G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48677896 | ||||||
chr2:48677978
|
G | GGT | 30 | a0001c0001t0001g0259a0001c0001t0001g0270a0001c0001t0001g0271others(27): Show | 30 | HG00738.hp1 HG01070.hp1 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.1330-1326_1330-132 others(6): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 48677978 | |||||
chr2:48677978
|
GGT | G | 178 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(175): Show | 187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.1330-1326_1330-132 others(6): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 48677978 | |||||
chr2:48677978
|
GGTGT | G | 84 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(81): Show | 97 | HG00323.hp2 HG00544.hp2 HG00642.hp1 others(94): Show |
intron_variant | MODIFIER | c.1330-1328_1330-132 others(8): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 48677978 | |||||
chr2:48678009
|
G | A | 1 | a0001c0001t0001g0088 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1330-1326G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48678009 | ||||||
chr2:48678129
|
A | C | 1 | a0001c0001t0001g0250 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1330-1206A>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48678129 | ||||||
chr2:48678150
|
G | C | 2 | a0001c0001t0001g0003a0001c0001t0001g0288 | 5 | HG01884.hp2 HG02723.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1330-1185G>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48678150 | ||||||
chr2:48678172
|
T | C | 5 | a0002c0002t0001g0012a0002c0002t0001g0159a0002c0002t0001g0235others(2): Show | 6 | HG02027.hp2 HG02165.hp2 NA18747.hp2 others(3): Show |
intron_variant | MODIFIER | c.1330-1163T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48678172 | ||||||
chr2:48678191
|
T | C | 2 | a0001c0001t0002g0161a0001c0001t0002g0181 | 2 | HG02055.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1330-1144T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48678191 | ||||||
chr2:48678266
|
G | T | 1 | a0001c0001t0001g0281 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1330-1069G>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48678266 | ||||||
chr2:48678290
|
T | A | 1 | a0001c0001t0001g0287 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1330-1045T>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48678290 | ||||||
chr2:48678543
|
G | A | 1 | a0001c0001t0001g0261 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1330-792G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48678543 | ||||||
chr2:48678659
|
A | G | 1 | a0001c0005t0003g0087 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1330-676A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48678659 | ||||||
chr2:48678803
|
T | C | 1 | a0001c0001t0001g0055 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1330-532T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48678803 | ||||||
chr2:48678805
|
T | C | 1 | a0001c0001t0001g0055 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1330-530T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48678805 | ||||||
chr2:48678806
|
T | A | 1 | a0001c0001t0001g0055 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1330-529T>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48678806 | ||||||
chr2:48678808
|
C | G | 1 | a0001c0001t0001g0055 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1330-527C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48678808 | ||||||
chr2:48678809
|
T | C | 1 | a0001c0001t0001g0055 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1330-526T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48678809 | ||||||
chr2:48678810
|
T | G | 1 | a0001c0001t0001g0055 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1330-525T>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48678810 | ||||||
chr2:48678811
|
T | C | 1 | a0001c0001t0001g0055 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1330-524T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48678811 | ||||||
chr2:48678815
|
G | T | 1 | a0001c0001t0001g0055 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1330-520G>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48678815 | ||||||
chr2:48678817
|
C | T | 224 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(221): Show | 241 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(238): Show |
intron_variant | MODIFIER | c.1330-518C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48678817 | ||||||
chr2:48678818
|
A | T | 1 | a0001c0001t0001g0055 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1330-517A>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48678818 | ||||||
chr2:48678856
|
G | A | 1 | a0001c0001t0001g0258 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1330-479G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48678856 | ||||||
chr2:48678910
|
A | C | 317 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(314): Show | 340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.1330-425A>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48678910 | ||||||
chr2:48679003
|
G | A | 1 | a0001c0001t0001g0051 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1330-332G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48679003 | ||||||
chr2:48679055
|
A | AT | 275 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(272): Show | 298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.1330-272dupT | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 48679055 | |||||
chr2:48679095
|
A | G | 1 | a0001c0001t0001g0301 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1330-240A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48679095 | ||||||
chr2:48679179
|
C | G | 1 | a0001c0001t0001g0089 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1330-156C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48679179 | ||||||
chr2:48679220
|
A | C | 1 | a0001c0001t0001g0103 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1330-115A>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48679220 | ||||||
chr2:48679221
|
A | G | 295 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(292): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.1330-114A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48679221 |