geneid | 8907 |
---|---|
ensemblid | ENSG00000072958.9 |
hgncid | 13667 |
symbol | AP1M1 |
name | adaptor related protein complex 1 subunit mu 1 |
refseq_nuc | NM_032493.4 |
refseq_prot | NP_115882.1 |
ensembl_nuc | ENST00000291439.8 |
ensembl_prot | ENSP00000291439.2 |
mane_status | MANE Select |
chr | chr19 |
start | 16197911 |
end | 16245906 |
strand | + |
ver | v1.2 |
region | chr19:16197911-16245906 |
region5000 | chr19:16192911-16250906 |
regionname0 | AP1M1_chr19_16197911_16245906 |
regionname5000 | AP1M1_chr19_16192911_16250906 |
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 | 423 | 308 | 86 | 62 | 112 | 8 | 38 | 82 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1272 | 207 | 75 | 32 | 73 | 2 | 23 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
c0002 | 0/0 | 1272 | 98 | 10 | 29 | 38 | 6 | 15 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
c0003 | 0/0 | 1272 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
c0004 | 0/0 | 1272 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
c0005 | 0/0 | 1272 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 11551 | 28 | 1 | 9 | 14 | 0 | 4 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0002 | 0/0 | 11570 | 20 | 2 | 2 | 11 | 2 | 3 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0003 | 0/0 | 11589 | 9 | 0 | 2 | 2 | 0 | 5 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0004 | 0/0 | 11615 | 9 | 0 | 1 | 8 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0005 | 0/0 | 11571 | 6 | 0 | 3 | 1 | 0 | 2 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0006 | 0/0 | 11556 | 6 | 6 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0007 | 0/0 | 11574 | 5 | 0 | 3 | 2 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0008 | 0/0 | 11620 | 5 | 0 | 0 | 5 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0009 | 0/0 | 11556 | 5 | 5 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0010 | 0/0 | 11569 | 4 | 0 | 1 | 3 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0011 | 0/0 | 11572 | 4 | 0 | 3 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0012 | 0/0 | 11575 | 4 | 0 | 3 | 0 | 1 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0013 | 0/0 | 11592 | 4 | 0 | 2 | 1 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0014 | 0/0 | 11550 | 4 | 0 | 1 | 3 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0015 | 0/0 | 11570 | 3 | 0 | 0 | 3 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0016 | 0/0 | 11575 | 3 | 0 | 0 | 3 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0017 | 0/0 | 11572 | 3 | 0 | 2 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0018 | 0/0 | 11552 | 3 | 0 | 0 | 3 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0019 | 0/0 | 11552 | 3 | 0 | 1 | 2 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0020 | 0/0 | 11615 | 3 | 3 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0021 | 0/0 | 11573 | 2 | 0 | 0 | 0 | 0 | 2 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0022 | 0/0 | 11571 | 2 | 0 | 2 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0023 | 0/0 | 11568 | 2 | 1 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0024 | 0/0 | 11579 | 2 | 2 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0025 | 0/0 | 11574 | 2 | 0 | 0 | 0 | 0 | 2 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0026 | 0/0 | 11591 | 2 | 2 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0027 | 0/0 | 11599 | 2 | 1 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0028 | 0/0 | 11602 | 2 | 2 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0029 | 0/0 | 11612 | 2 | 1 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0030 | 0/0 | 11613 | 2 | 1 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0031 | 0/0 | 11618 | 2 | 0 | 0 | 2 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0032 | 0/0 | 11621 | 2 | 0 | 0 | 2 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0033 | 0/0 | 11622 | 2 | 0 | 0 | 2 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0034 | 0/0 | 11546 | 2 | 2 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0035 | 0/0 | 11549 | 2 | 2 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0036 | 0/0 | 11623 | 2 | 2 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0037 | 0/0 | 11592 | 2 | 2 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0038 | 0/0 | 11546 | 2 | 2 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0039 | 0/0 | 11558 | 2 | 1 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0040 | 0/0 | 11564 | 2 | 2 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0041 | 0/0 | 11572 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0042 | 0/0 | 11581 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0043 | 0/0 | 11558 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0044 | 0/0 | 11574 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0045 | 0/0 | 11574 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0046 | 0/0 | 11569 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0047 | 0/0 | 11570 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0048 | 0/0 | 11571 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0049 | 0/0 | 11573 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0050 | 0/0 | 11579 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0051 | 0/0 | 11547 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0052 | 0/0 | 11558 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0053 | 0/0 | 11560 | 1 | 0 | 0 | 0 | 1 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0054 | 0/0 | 11559 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0055 | 0/0 | 11560 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0056 | 0/0 | 11559 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0057 | 0/0 | 11567 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0058 | 0/0 | 11572 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0059 | 0/0 | 11572 | 1 | 0 | 0 | 0 | 1 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0060 | 0/0 | 11558 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0061 | 0/0 | 11566 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0062 | 0/0 | 11567 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0063 | 0/0 | 11573 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0064 | 0/0 | 11571 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0065 | 0/0 | 11572 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0066 | 0/0 | 11571 | 1 | 0 | 0 | 0 | 1 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0067 | 0/0 | 11576 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0068 | 0/0 | 11570 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0069 | 0/0 | 11568 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0070 | 0/0 | 11575 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0071 | 0/0 | 11569 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0072 | 0/0 | 11574 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0073 | 0/0 | 11569 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0074 | 0/0 | 11570 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0075 | 0/0 | 11571 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0076 | 0/0 | 11576 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0077 | 0/0 | 11578 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0078 | 0/0 | 11580 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0079 | 0/0 | 11576 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0080 | 0/0 | 11561 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0081 | 0/0 | 11572 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0082 | 0/0 | 11544 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0083 | 0/0 | 11565 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0084 | 0/0 | 11570 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0085 | 0/0 | 11588 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0086 | 0/0 | 11588 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0087 | 0/0 | 11589 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0088 | 1/0 | 11588 | 1 | 0 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0089 | 0/0 | 11589 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0090 | 0/0 | 11591 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0091 | 0/0 | 11598 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0092 | 0/0 | 11590 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0093 | 0/1 | 11591 | 1 | 0 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0094 | 0/0 | 11592 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0095 | 0/0 | 11593 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0096 | 0/0 | 11597 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0097 | 0/0 | 11590 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0098 | 0/0 | 11592 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0099 | 0/0 | 11593 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0100 | 0/0 | 11591 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0101 | 0/0 | 11593 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0102 | 0/0 | 11589 | 1 | 0 | 0 | 0 | 1 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0103 | 0/0 | 11590 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0104 | 0/0 | 11598 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0105 | 0/0 | 11579 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0106 | 0/0 | 11591 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0107 | 0/0 | 11578 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0108 | 0/0 | 11593 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0109 | 0/0 | 11589 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0110 | 0/0 | 11599 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0111 | 0/0 | 11585 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0112 | 0/0 | 11557 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0113 | 0/0 | 11569 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0114 | 0/0 | 11554 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0115 | 0/0 | 11597 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0116 | 0/0 | 11617 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0117 | 0/0 | 11624 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0118 | 0/0 | 11597 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0119 | 0/0 | 11622 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0120 | 0/0 | 11612 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0121 | 0/0 | 11618 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0122 | 0/0 | 11620 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0123 | 0/0 | 11619 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0124 | 0/0 | 11585 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0125 | 0/0 | 11584 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0126 | 0/0 | 11591 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0127 | 0/0 | 11593 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0128 | 0/0 | 11613 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0129 | 0/0 | 11618 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0130 | 0/0 | 11616 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0131 | 0/0 | 11618 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0132 | 0/0 | 11617 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0133 | 0/0 | 11617 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0134 | 0/0 | 11620 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0135 | 0/0 | 11619 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0136 | 0/0 | 11620 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0137 | 0/0 | 11617 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0138 | 0/0 | 11616 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0139 | 0/0 | 11615 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0140 | 0/0 | 11618 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0141 | 0/0 | 11619 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0142 | 0/0 | 11614 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0143 | 0/0 | 11616 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0144 | 0/0 | 11621 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0145 | 0/0 | 11624 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0146 | 0/0 | 11616 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0147 | 0/0 | 11617 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0148 | 0/0 | 11619 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0149 | 0/0 | 11616 | 1 | 0 | 0 | 0 | 1 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0150 | 0/0 | 11595 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0151 | 0/0 | 11615 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0152 | 0/0 | 11578 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0153 | 0/0 | 11590 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0154 | 0/0 | 11554 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0155 | 0/0 | 11558 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0156 | 0/0 | 11552 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0157 | 0/0 | 11553 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0158 | 0/0 | 11553 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0159 | 0/0 | 11557 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0160 | 0/0 | 11556 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0161 | 0/0 | 11551 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0162 | 0/0 | 11556 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0163 | 0/0 | 11555 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0164 | 0/0 | 11558 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0165 | 0/0 | 11588 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0166 | 0/0 | 11555 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0167 | 0/0 | 11561 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0168 | 0/0 | 11556 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0169 | 0/0 | 11559 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0170 | 0/0 | 11558 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0171 | 0/0 | 11557 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0172 | 0/0 | 11552 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0173 | 0/0 | 11558 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0174 | 0/0 | 11561 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0175 | 0/0 | 11559 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0176 | 0/0 | 11562 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
t0177 | 0/0 | 11581 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0002 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0006 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0007 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0203 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0207 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1272 | 207 | 75 | 32 | 73 | 2 | 23 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0002 | 0/0 | 1272 | 98 | 10 | 29 | 38 | 6 | 15 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0003 | 0/0 | 1272 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0004 | 0/0 | 1272 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0005 | 0/0 | 1272 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 12822 | 28 | 1 | 9 | 14 | 0 | 4 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0003 | 0/0 | 12860 | 9 | 0 | 2 | 2 | 0 | 5 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0004 | 0/0 | 12886 | 9 | 0 | 1 | 8 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0006 | 0/0 | 12827 | 6 | 6 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0008 | 0/0 | 12891 | 5 | 0 | 0 | 5 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0009 | 0/0 | 12827 | 5 | 5 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0013 | 0/0 | 12863 | 4 | 0 | 2 | 1 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0014 | 0/0 | 12821 | 4 | 0 | 1 | 3 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0018 | 0/0 | 12823 | 3 | 0 | 0 | 3 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0019 | 0/0 | 12823 | 3 | 0 | 1 | 2 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0020 | 0/0 | 12886 | 3 | 3 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0024 | 0/0 | 12850 | 2 | 2 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0025 | 0/0 | 12845 | 2 | 0 | 0 | 0 | 0 | 2 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0026 | 0/0 | 12862 | 2 | 2 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0027 | 0/0 | 12870 | 2 | 1 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0028 | 0/0 | 12873 | 2 | 2 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0029 | 0/0 | 12883 | 2 | 1 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0030 | 0/0 | 12884 | 2 | 1 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0031 | 0/0 | 12889 | 2 | 0 | 0 | 2 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0032 | 0/0 | 12892 | 2 | 0 | 0 | 2 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0033 | 0/0 | 12893 | 2 | 0 | 0 | 2 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0034 | 0/0 | 12817 | 2 | 2 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0035 | 0/0 | 12820 | 2 | 2 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0036 | 0/0 | 12894 | 2 | 2 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0037 | 0/0 | 12863 | 2 | 2 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0038 | 0/0 | 12817 | 2 | 2 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0039 | 0/0 | 12829 | 2 | 1 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0040 | 0/0 | 12835 | 2 | 2 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0041 | 0/0 | 12843 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0042 | 0/0 | 12852 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0083 | 0/0 | 12836 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0084 | 0/0 | 12841 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0085 | 0/0 | 12859 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0086 | 0/0 | 12859 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0087 | 0/0 | 12860 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0088 | 1/0 | 12859 | 1 | 0 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0089 | 0/0 | 12860 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0090 | 0/0 | 12862 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0091 | 0/0 | 12869 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0092 | 0/0 | 12861 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0093 | 0/1 | 12862 | 1 | 0 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0094 | 0/0 | 12863 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0095 | 0/0 | 12864 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0096 | 0/0 | 12868 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0097 | 0/0 | 12861 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0099 | 0/0 | 12864 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0100 | 0/0 | 12862 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0101 | 0/0 | 12864 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0102 | 0/0 | 12860 | 1 | 0 | 0 | 0 | 1 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0103 | 0/0 | 12861 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0104 | 0/0 | 12869 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0105 | 0/0 | 12850 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0106 | 0/0 | 12862 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0107 | 0/0 | 12849 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0108 | 0/0 | 12864 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0109 | 0/0 | 12860 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0110 | 0/0 | 12870 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0111 | 0/0 | 12856 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0113 | 0/0 | 12840 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0114 | 0/0 | 12825 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0115 | 0/0 | 12868 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0116 | 0/0 | 12888 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0117 | 0/0 | 12895 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0118 | 0/0 | 12868 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0119 | 0/0 | 12893 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0120 | 0/0 | 12883 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0122 | 0/0 | 12891 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0123 | 0/0 | 12890 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0124 | 0/0 | 12856 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0125 | 0/0 | 12855 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0126 | 0/0 | 12862 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0127 | 0/0 | 12864 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0128 | 0/0 | 12884 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0129 | 0/0 | 12889 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0130 | 0/0 | 12887 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0131 | 0/0 | 12889 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0132 | 0/0 | 12888 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0133 | 0/0 | 12888 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0134 | 0/0 | 12891 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0135 | 0/0 | 12890 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0136 | 0/0 | 12891 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0137 | 0/0 | 12888 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0138 | 0/0 | 12887 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0139 | 0/0 | 12886 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0140 | 0/0 | 12889 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0141 | 0/0 | 12890 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0142 | 0/0 | 12885 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0143 | 0/0 | 12887 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0144 | 0/0 | 12892 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0145 | 0/0 | 12895 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0146 | 0/0 | 12887 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0147 | 0/0 | 12888 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0148 | 0/0 | 12890 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0149 | 0/0 | 12887 | 1 | 0 | 0 | 0 | 1 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0150 | 0/0 | 12866 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0151 | 0/0 | 12886 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0152 | 0/0 | 12849 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0153 | 0/0 | 12861 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0154 | 0/0 | 12825 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0155 | 0/0 | 12829 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0156 | 0/0 | 12823 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0157 | 0/0 | 12824 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0158 | 0/0 | 12824 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0159 | 0/0 | 12828 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0160 | 0/0 | 12827 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0161 | 0/0 | 12822 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0162 | 0/0 | 12827 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0163 | 0/0 | 12826 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0164 | 0/0 | 12829 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0165 | 0/0 | 12859 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0166 | 0/0 | 12826 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0167 | 0/0 | 12832 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0168 | 0/0 | 12827 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0169 | 0/0 | 12830 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0170 | 0/0 | 12829 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0171 | 0/0 | 12828 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0172 | 0/0 | 12823 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0173 | 0/0 | 12829 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0174 | 0/0 | 12832 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0175 | 0/0 | 12830 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0176 | 0/0 | 12833 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0001t0177 | 0/0 | 12852 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0002t0002 | 0/0 | 12841 | 20 | 2 | 2 | 11 | 2 | 3 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0002t0005 | 0/0 | 12842 | 6 | 0 | 3 | 1 | 0 | 2 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0002t0007 | 0/0 | 12845 | 5 | 0 | 3 | 2 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0002t0010 | 0/0 | 12840 | 4 | 0 | 1 | 3 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0002t0011 | 0/0 | 12843 | 4 | 0 | 3 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0002t0012 | 0/0 | 12846 | 4 | 0 | 3 | 0 | 1 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0002t0015 | 0/0 | 12841 | 3 | 0 | 0 | 3 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0002t0016 | 0/0 | 12846 | 3 | 0 | 0 | 3 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0002t0017 | 0/0 | 12843 | 3 | 0 | 2 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0002t0021 | 0/0 | 12844 | 2 | 0 | 0 | 0 | 0 | 2 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0002t0022 | 0/0 | 12842 | 2 | 0 | 2 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0002t0023 | 0/0 | 12839 | 2 | 1 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0002t0043 | 0/0 | 12829 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0002t0044 | 0/0 | 12845 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0002t0045 | 0/0 | 12845 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0002t0046 | 0/0 | 12840 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0002t0047 | 0/0 | 12841 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0002t0048 | 0/0 | 12842 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0002t0049 | 0/0 | 12844 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0002t0050 | 0/0 | 12850 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0002t0051 | 0/0 | 12818 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0002t0052 | 0/0 | 12829 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0002t0053 | 0/0 | 12831 | 1 | 0 | 0 | 0 | 1 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0002t0054 | 0/0 | 12830 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0002t0055 | 0/0 | 12831 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0002t0056 | 0/0 | 12830 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0002t0057 | 0/0 | 12838 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0002t0058 | 0/0 | 12843 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0002t0059 | 0/0 | 12843 | 1 | 0 | 0 | 0 | 1 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0002t0060 | 0/0 | 12829 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0002t0061 | 0/0 | 12837 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0002t0062 | 0/0 | 12838 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0002t0063 | 0/0 | 12844 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0002t0064 | 0/0 | 12842 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0002t0065 | 0/0 | 12843 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0002t0066 | 0/0 | 12842 | 1 | 0 | 0 | 0 | 1 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0002t0067 | 0/0 | 12847 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0002t0068 | 0/0 | 12841 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0002t0069 | 0/0 | 12839 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0002t0070 | 0/0 | 12846 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0002t0071 | 0/0 | 12840 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0002t0072 | 0/0 | 12845 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0002t0073 | 0/0 | 12840 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0002t0074 | 0/0 | 12841 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0002t0075 | 0/0 | 12842 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0002t0077 | 0/0 | 12849 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0002t0078 | 0/0 | 12851 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0002t0079 | 0/0 | 12847 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0002t0080 | 0/0 | 12832 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0002t0081 | 0/0 | 12843 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0002t0082 | 0/0 | 12815 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0002t0112 | 0/0 | 12828 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0003t0098 | 0/0 | 12863 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0004t0121 | 0/0 | 12889 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
a0001c0005t0076 | 0/0 | 12847 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | copy fasta | chr19 | 16192911 | 16250906 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0003g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0003g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0003g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0003g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0003g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0003g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0004g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0004g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0004g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0004g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0004g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0004g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0004g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0004g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0004g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0006g0001 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0006g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0006g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0008g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0008g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0008g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0008g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0008g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0009g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0009g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0009g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0009g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0009g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0013g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0013g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0013g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0013g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0014g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0014g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0014g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0014g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0018g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0018g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0018g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0019g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0019g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0019g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0020g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0020g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0020g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0024g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0024g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0025g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0026g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0026g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0027g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0027g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0028g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0028g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0029g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0029g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0030g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0030g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0031g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0031g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0032g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0032g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0033g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0033g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0034g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0034g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0035g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0035g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0036g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0036g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0037g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0037g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0038g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0039g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0039g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0040g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0040g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0041g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0042g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0083g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0084g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0085g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0086g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0087g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0088g0207 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0089g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0090g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0091g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0092g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0093g0203 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0094g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0095g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0096g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0097g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0099g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0100g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0101g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0102g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0103g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0104g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0105g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0106g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0107g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0108g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0109g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0110g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0111g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0113g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0114g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0115g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0116g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0117g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0118g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0119g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0120g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0122g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0123g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0124g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0125g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0126g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0127g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0128g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0129g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0130g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0131g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0132g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0133g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0134g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0135g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0136g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0137g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0138g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0139g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0140g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0141g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0142g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0143g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0144g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0145g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0146g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0147g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0148g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0149g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0150g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0151g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0152g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0153g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0154g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0155g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0156g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0157g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0158g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0159g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0160g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0161g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0162g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0163g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0164g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0165g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0166g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0167g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0168g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0169g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0170g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0171g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0172g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0173g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0174g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0175g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0176g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0001t0177g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0002g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0002g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0002g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0002g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0002g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0002g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0005g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0005g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0005g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0005g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0005g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0005g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0007g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0007g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0007g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0007g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0007g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0010g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0010g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0010g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0010g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0011g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0011g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0011g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0011g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0012g0006 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0012g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0012g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0012g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0015g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0015g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0015g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0016g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0016g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0016g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0017g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0017g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0017g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0021g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0021g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0022g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0022g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0023g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0023g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0043g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0044g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0045g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0046g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0047g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0048g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0049g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0050g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0051g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0052g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0053g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0054g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0055g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0056g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0057g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0058g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0059g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0060g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0061g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0062g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0063g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0064g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0065g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0066g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0067g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0068g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0069g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0070g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0071g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0072g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0073g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0074g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0075g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0077g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0078g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0079g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0080g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0081g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0082g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0002t0112g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0003t0098g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0004t0121g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
a0001c0005t0076g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0002 | t0002 | g0149 | EUR | GBR | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG00099 | hp2 | a0001 | c0001 | t0149 | g0231 | EUR | GBR | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG00140 | hp1 | a0001 | c0002 | t0053 | g0134 | EUR | GBR | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG00140 | hp2 | a0001 | c0002 | t0059 | g0148 | EUR | GBR | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG00423 | hp1 | a0001 | c0001 | t0018 | g0072 | EAS | CHS | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG00423 | hp2 | a0001 | c0001 | t0004 | g0241 | EAS | CHS | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG00438 | hp1 | a0001 | c0001 | t0158 | g0063 | EAS | CHS | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG00438 | hp2 | a0001 | c0001 | t0133 | g0235 | EAS | CHS | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG00544 | hp1 | a0001 | c0001 | t0116 | g0251 | EAS | CHS | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG00544 | hp2 | a0001 | c0001 | t0101 | g0209 | EAS | CHS | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG00558 | hp1 | a0001 | c0001 | t0031 | g0247 | EAS | CHS | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | CHS | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG00597 | hp2 | a0001 | c0002 | t0002 | g0175 | EAS | CHS | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG00609 | hp1 | a0001 | c0001 | t0004 | g0237 | EAS | CHS | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG00609 | hp2 | a0001 | c0002 | t0063 | g0116 | EAS | CHS | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG00673 | hp1 | a0001 | c0002 | t0016 | g0156 | EAS | CHS | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG00673 | hp2 | a0001 | c0001 | t0004 | g0229 | EAS | CHS | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG00735 | hp1 | a0001 | c0001 | t0030 | g0020 | AMR | PUR | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG00735 | hp2 | a0001 | c0001 | t0019 | g0086 | AMR | PUR | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG00738 | hp1 | a0001 | c0001 | t0003 | g0181 | AMR | PUR | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG00738 | hp2 | a0001 | c0002 | t0007 | g0106 | AMR | PUR | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG01069 | hp1 | a0001 | c0001 | t0004 | g0226 | AMR | PUR | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG01069 | hp2 | a0001 | c0001 | t0014 | g0061 | AMR | PUR | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG01071 | hp1 | a0001 | c0002 | t0056 | g0102 | AMR | PUR | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG01074 | hp1 | a0001 | c0002 | t0011 | g0140 | AMR | PUR | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG01074 | hp2 | a0001 | c0002 | t0007 | g0139 | AMR | PUR | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG01081 | hp1 | a0001 | c0001 | t0084 | g0185 | AMR | PUR | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG01099 | hp1 | a0001 | c0002 | t0022 | g0170 | AMR | PUR | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG01099 | hp2 | a0001 | c0001 | t0089 | g0184 | AMR | PUR | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG01109 | hp1 | a0001 | c0001 | t0029 | g0017 | AMR | PUR | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG01109 | hp2 | a0001 | c0001 | t0141 | g0267 | AMR | PUR | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG01167 | hp1 | a0001 | c0001 | t0171 | g0034 | AMR | PUR | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG01167 | hp2 | a0001 | c0002 | t0057 | g0128 | AMR | PUR | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG01169 | hp1 | a0001 | c0002 | t0065 | g0167 | AMR | PUR | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG01169 | hp2 | a0001 | c0001 | t0173 | g0054 | AMR | PUR | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG01192 | hp1 | a0001 | c0002 | t0005 | g0138 | AMR | PUR | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG01243 | hp1 | a0001 | c0001 | t0142 | g0266 | AMR | PUR | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG01243 | hp2 | a0001 | c0002 | t0017 | g0127 | AMR | PUR | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG01255 | hp1 | a0001 | c0002 | t0017 | g0096 | AMR | CLM | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG01256 | hp1 | a0001 | c0002 | t0007 | g0092 | AMR | CLM | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG01256 | hp2 | a0001 | c0001 | t0086 | g0201 | AMR | CLM | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG01257 | hp1 | a0001 | c0002 | t0002 | g0132 | AMR | CLM | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG01257 | hp2 | a0001 | c0001 | t0013 | g0193 | AMR | CLM | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG01258 | hp1 | a0001 | c0001 | t0013 | g0194 | AMR | CLM | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG01258 | hp2 | a0001 | c0001 | t0003 | g0202 | AMR | CLM | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG01261 | hp1 | a0001 | c0002 | t0002 | g0158 | AMR | CLM | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | CLM | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG01346 | hp1 | a0001 | c0005 | t0076 | g0142 | AMR | CLM | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG01346 | hp2 | a0001 | c0001 | t0114 | g0067 | AMR | CLM | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG01358 | hp1 | a0001 | c0001 | t0134 | g0243 | AMR | CLM | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG01358 | hp2 | a0001 | c0002 | t0011 | g0113 | AMR | CLM | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG01361 | hp1 | a0001 | c0001 | t0169 | g0223 | AMR | CLM | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG01361 | hp2 | a0001 | c0002 | t0044 | g0099 | AMR | CLM | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG01433 | hp1 | a0001 | c0002 | t0047 | g0174 | AMR | CLM | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG01433 | hp2 | a0001 | c0002 | t0062 | g0163 | AMR | CLM | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG01496 | hp1 | a0001 | c0002 | t0064 | g0169 | AMR | CLM | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | CLM | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG01884 | hp1 | a0001 | c0001 | t0153 | g0033 | AFR | ACB | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG01884 | hp2 | a0001 | c0001 | t0029 | g0018 | AFR | ACB | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG01891 | hp1 | a0001 | c0003 | t0098 | g0195 | AFR | ACB | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG01891 | hp2 | a0001 | c0001 | t0120 | g0270 | AFR | ACB | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG01928 | hp1 | a0001 | c0002 | t0005 | g0094 | AMR | PEL | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG01928 | hp2 | a0001 | c0001 | t0138 | g0242 | AMR | PEL | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG01934 | hp1 | a0001 | c0001 | t0027 | g0191 | AMR | PEL | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG01934 | hp2 | a0001 | c0002 | t0012 | g0104 | AMR | PEL | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | PEL | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG01975 | hp2 | a0001 | c0002 | t0011 | g0093 | AMR | PEL | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG01978 | hp1 | a0001 | c0002 | t0005 | g0129 | AMR | PEL | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG01978 | hp2 | a0001 | c0001 | t0143 | g0265 | AMR | PEL | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG01993 | hp1 | a0001 | c0002 | t0010 | g0165 | AMR | PEL | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG01993 | hp2 | a0001 | c0002 | t0048 | g0130 | AMR | PEL | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02015 | hp1 | a0001 | c0001 | t0004 | g0257 | EAS | KHV | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02015 | hp2 | a0001 | c0001 | t0003 | g0196 | EAS | KHV | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02055 | hp1 | a0001 | c0001 | t0028 | g0003 | AFR | ACB | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02055 | hp2 | a0001 | c0001 | t0152 | g0079 | AFR | ACB | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | KHV | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02080 | hp2 | a0001 | c0001 | t0148 | g0254 | EAS | KHV | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | KHV | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02083 | hp2 | a0001 | c0002 | t0045 | g0122 | EAS | KHV | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02132 | hp1 | a0001 | c0001 | t0032 | g0283 | EAS | KHV | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | KHV | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02135 | hp1 | a0001 | c0002 | t0050 | g0117 | EAS | KHV | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | KHV | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02145 | hp1 | a0001 | c0001 | t0006 | g0025 | AFR | ACB | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02145 | hp2 | a0001 | c0001 | t0118 | g0282 | AFR | ACB | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02155 | hp1 | a0001 | c0001 | t0154 | g0066 | EAS | CDX | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02155 | hp2 | a0001 | c0002 | t0058 | g0166 | EAS | CDX | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02165 | hp1 | a0001 | c0002 | t0002 | g0157 | EAS | CDX | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | CDX | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02257 | hp1 | a0001 | c0001 | t0174 | g0080 | AFR | ACB | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02257 | hp2 | a0001 | c0001 | t0042 | g0016 | AFR | ACB | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02258 | hp1 | a0001 | c0001 | t0034 | g0048 | AFR | ACB | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02258 | hp2 | a0001 | c0001 | t0172 | g0055 | AFR | ACB | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | PEL | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02273 | hp2 | a0001 | c0002 | t0012 | g0105 | AMR | PEL | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02280 | hp1 | a0001 | c0001 | t0026 | g0008 | AFR | ACB | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02280 | hp2 | a0001 | c0001 | t0020 | g0278 | AFR | ACB | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02293 | hp2 | a0001 | c0002 | t0022 | g0159 | AMR | PEL | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02300 | hp1 | a0001 | c0002 | t0046 | g0150 | AMR | PEL | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02300 | hp2 | a0001 | c0002 | t0012 | g0107 | AMR | PEL | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02451 | hp1 | a0001 | c0002 | t0080 | g0176 | AFR | ACB | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02451 | hp2 | a0001 | c0001 | t0110 | g0187 | AFR | ACB | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | KHV | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02523 | hp2 | a0001 | c0001 | t0170 | g0057 | EAS | KHV | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02572 | hp1 | a0001 | c0001 | t0040 | g0052 | AFR | GWD | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02572 | hp2 | a0001 | c0001 | t0119 | g0271 | AFR | GWD | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02602 | hp1 | a0001 | c0002 | t0002 | g0029 | SAS | PJL | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02602 | hp2 | a0001 | c0001 | t0175 | g0083 | SAS | PJL | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02615 | hp1 | a0001 | c0001 | t0037 | g0234 | AFR | GWD | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02615 | hp2 | a0001 | c0001 | t0009 | g0219 | AFR | GWD | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02630 | hp1 | a0001 | c0001 | t0109 | g0003 | AFR | GWD | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02630 | hp2 | a0001 | c0001 | t0034 | g0050 | AFR | GWD | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02647 | hp1 | a0001 | c0001 | t0024 | g0289 | AFR | GWD | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02647 | hp2 | a0001 | c0001 | t0020 | g0280 | AFR | GWD | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02683 | hp1 | a0001 | c0002 | t0052 | g0098 | SAS | PJL | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02683 | hp2 | a0001 | c0001 | t0003 | g0009 | SAS | PJL | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02717 | hp1 | a0001 | c0002 | t0075 | g0121 | AFR | GWD | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02717 | hp2 | a0001 | c0001 | t0038 | g0004 | AFR | GWD | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02723 | hp1 | a0001 | c0001 | t0160 | g0220 | AFR | GWD | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02723 | hp2 | a0001 | c0001 | t0150 | g0015 | AFR | GWD | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02735 | hp1 | a0001 | c0002 | t0021 | g0097 | SAS | PJL | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02735 | hp2 | a0001 | c0002 | t0021 | g0101 | SAS | PJL | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02738 | hp1 | a0001 | c0001 | t0095 | g0211 | SAS | PJL | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02738 | hp2 | a0001 | c0002 | t0112 | g0151 | SAS | PJL | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02809 | hp2 | a0001 | c0001 | t0030 | g0019 | AFR | GWD | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02818 | hp1 | a0001 | c0001 | t0091 | g0022 | AFR | GWD | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02818 | hp2 | a0001 | c0002 | t0074 | g0109 | AFR | GWD | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02886 | hp1 | a0001 | c0001 | t0090 | g0027 | AFR | GWD | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02886 | hp2 | a0001 | c0001 | t0028 | g0186 | AFR | GWD | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02895 | hp1 | a0001 | c0001 | t0124 | g0011 | AFR | GWD | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02895 | hp2 | a0001 | c0001 | t0037 | g0233 | AFR | GWD | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02896 | hp1 | a0001 | c0001 | t0105 | g0287 | AFR | GWD | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02896 | hp2 | a0001 | c0001 | t0009 | g0214 | AFR | GWD | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02897 | hp1 | a0001 | c0001 | t0009 | g0215 | AFR | GWD | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02897 | hp2 | a0001 | c0001 | t0125 | g0013 | AFR | GWD | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02922 | hp1 | a0001 | c0001 | t0104 | g0021 | AFR | ESN | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02922 | hp2 | a0001 | c0001 | t0165 | g0032 | AFR | ESN | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02965 | hp1 | a0001 | c0002 | t0061 | g0114 | AFR | ESN | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02965 | hp2 | a0001 | c0001 | t0111 | g0190 | AFR | ESN | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02976 | hp1 | a0001 | c0002 | t0073 | g0091 | AFR | ESN | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02976 | hp2 | a0001 | c0001 | t0006 | g0001 | AFR | ESN | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG03098 | hp1 | a0001 | c0001 | t0026 | g0192 | AFR | MSL | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG03098 | hp2 | a0001 | c0001 | t0115 | g0224 | AFR | MSL | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG03130 | hp1 | a0001 | c0001 | t0006 | g0001 | AFR | ESN | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG03130 | hp2 | a0001 | c0001 | t0036 | g0281 | AFR | ESN | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG03139 | hp1 | a0001 | c0002 | t0060 | g0178 | AFR | ESN | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG03139 | hp2 | a0001 | c0001 | t0009 | g0217 | AFR | ESN | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG03195 | hp1 | a0001 | c0001 | t0040 | g0058 | AFR | ESN | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG03195 | hp2 | a0001 | c0001 | t0006 | g0001 | AFR | ESN | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG03209 | hp1 | a0001 | c0001 | t0024 | g0290 | AFR | MSL | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG03209 | hp2 | a0001 | c0001 | t0164 | g0293 | AFR | MSL | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG03239 | hp1 | a0001 | c0002 | t0077 | g0284 | SAS | PJL | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG03239 | hp2 | a0001 | c0001 | t0097 | g0007 | SAS | PJL | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG03453 | hp1 | a0001 | c0001 | t0096 | g0291 | AFR | MSL | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG03453 | hp2 | a0001 | c0001 | t0127 | g0012 | AFR | MSL | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG03486 | hp1 | a0001 | c0001 | t0159 | g0222 | AFR | MSL | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG03486 | hp2 | a0001 | c0001 | t0126 | g0014 | AFR | MSL | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG03490 | hp1 | a0001 | c0001 | t0013 | g0009 | SAS | PJL | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG03490 | hp2 | a0001 | c0001 | t0025 | g0010 | SAS | PJL | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG03491 | hp1 | a0001 | c0001 | t0085 | g0197 | SAS | PJL | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG03491 | hp2 | a0001 | c0002 | t0011 | g0123 | SAS | PJL | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG03492 | hp1 | a0001 | c0001 | t0025 | g0010 | SAS | PJL | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG03492 | hp2 | a0001 | c0001 | t0087 | g0200 | SAS | PJL | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG03516 | hp1 | a0001 | c0001 | t0020 | g0279 | AFR | ESN | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG03516 | hp2 | a0001 | c0001 | t0168 | g0221 | AFR | ESN | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG03540 | hp1 | a0001 | c0001 | t0155 | g0056 | AFR | GWD | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG03540 | hp2 | a0001 | c0002 | t0051 | g0173 | AFR | GWD | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG03579 | hp1 | a0001 | c0001 | t0108 | g0188 | AFR | MSL | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG03579 | hp2 | a0001 | c0002 | t0002 | g0285 | AFR | MSL | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0042 | SAS | PJL | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG03669 | hp2 | a0001 | c0001 | t0092 | g0205 | SAS | PJL | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0044 | SAS | STU | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG03688 | hp2 | a0001 | c0002 | t0017 | g0147 | SAS | STU | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG03710 | hp1 | a0001 | c0002 | t0023 | g0177 | SAS | PJL | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG03710 | hp2 | a0001 | c0001 | t0003 | g0183 | SAS | PJL | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG03831 | hp1 | a0001 | c0001 | t0003 | g0204 | SAS | BEB | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG03831 | hp2 | a0001 | c0001 | t0161 | g0045 | SAS | BEB | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0075 | SAS | BEB | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG03834 | hp2 | a0001 | c0002 | t0005 | g0119 | SAS | BEB | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG03927 | hp1 | a0001 | c0001 | t0003 | g0213 | SAS | BEB | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG03927 | hp2 | a0001 | c0002 | t0005 | g0161 | SAS | BEB | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG03942 | hp1 | a0001 | c0001 | t0156 | g0047 | SAS | BEB | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG03942 | hp2 | a0001 | c0001 | t0039 | g0084 | SAS | BEB | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG04115 | hp1 | a0001 | c0002 | t0055 | g0120 | SAS | STU | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG04115 | hp2 | a0001 | c0002 | t0054 | g0136 | SAS | STU | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG04184 | hp1 | a0001 | c0001 | t0094 | g0198 | SAS | BEB | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0070 | SAS | BEB | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG04204 | hp1 | a0001 | c0001 | t0103 | g0007 | SAS | STU | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG04204 | hp2 | a0001 | c0002 | t0002 | g0125 | SAS | STU | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA18522 | hp1 | a0001 | c0001 | t0035 | g0049 | AFR | YRI | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA18522 | hp2 | a0001 | c0001 | t0035 | g0030 | AFR | YRI | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA18906 | hp1 | a0001 | c0001 | t0106 | g0189 | AFR | YRI | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA18906 | hp2 | a0001 | c0001 | t0009 | g0218 | AFR | YRI | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA18939 | hp1 | a0001 | c0002 | t0071 | g0179 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA18939 | hp2 | a0001 | c0001 | t0136 | g0250 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA18943 | hp1 | a0001 | c0002 | t0016 | g0160 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA18943 | hp2 | a0001 | c0001 | t0033 | g0276 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA18944 | hp1 | a0001 | c0002 | t0015 | g0090 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA18944 | hp2 | a0001 | c0001 | t0140 | g0245 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA18945 | hp1 | a0001 | c0001 | t0004 | g0239 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA18945 | hp2 | a0001 | c0002 | t0068 | g0115 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA18947 | hp1 | a0001 | c0001 | t0008 | g0260 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA18947 | hp2 | a0001 | c0002 | t0002 | g0171 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA18948 | hp1 | a0001 | c0002 | t0002 | g0143 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA18948 | hp2 | a0001 | c0001 | t0014 | g0036 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA18949 | hp1 | a0001 | c0002 | t0079 | g0131 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA18949 | hp2 | a0001 | c0001 | t0130 | g0225 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA18951 | hp1 | a0001 | c0002 | t0043 | g0141 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA18951 | hp2 | a0001 | c0001 | t0008 | g0262 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA18954 | hp1 | a0001 | c0001 | t0003 | g0199 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA18954 | hp2 | a0001 | c0001 | t0117 | g0244 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA18957 | hp1 | a0001 | c0002 | t0007 | g0110 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA18957 | hp2 | a0001 | c0001 | t0128 | g0238 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA18962 | hp1 | a0001 | c0001 | t0157 | g0292 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA18962 | hp2 | a0001 | c0001 | t0132 | g0230 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA18964 | hp1 | a0001 | c0002 | t0015 | g0088 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA18964 | hp2 | a0001 | c0001 | t0004 | g0256 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA18965 | hp1 | a0001 | c0001 | t0018 | g0038 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA18965 | hp2 | a0001 | c0002 | t0002 | g0135 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA18968 | hp1 | a0001 | c0002 | t0002 | g0124 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA18968 | hp2 | a0001 | c0001 | t0135 | g0272 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA18969 | hp1 | a0001 | c0001 | t0008 | g0263 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA18969 | hp2 | a0001 | c0001 | t0014 | g0035 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA18971 | hp1 | a0001 | c0001 | t0131 | g0236 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA18971 | hp2 | a0001 | c0001 | t0008 | g0261 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA18978 | hp1 | a0001 | c0002 | t0002 | g0028 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA18981 | hp2 | a0001 | c0002 | t0002 | g0100 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA18982 | hp1 | a0001 | c0002 | t0010 | g0146 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA18982 | hp2 | a0001 | c0001 | t0113 | g0182 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA18983 | hp1 | a0001 | c0001 | t0129 | g0232 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA18983 | hp2 | a0001 | c0001 | t0144 | g0269 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA18984 | hp1 | a0001 | c0001 | t0014 | g0039 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA18984 | hp2 | a0001 | c0004 | t0121 | g0249 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA18985 | hp1 | a0001 | c0001 | t0122 | g0274 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA18985 | hp2 | a0001 | c0001 | t0019 | g0068 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA18986 | hp1 | a0001 | c0002 | t0067 | g0133 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA18986 | hp2 | a0001 | c0001 | t0032 | g0273 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA18988 | hp1 | a0001 | c0001 | t0137 | g0248 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA18988 | hp2 | a0001 | c0002 | t0072 | g0168 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA18997 | hp1 | a0001 | c0002 | t0002 | g0103 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA18997 | hp2 | a0001 | c0001 | t0147 | g0240 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA19002 | hp1 | a0001 | c0001 | t0041 | g0246 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA19002 | hp2 | a0001 | c0002 | t0015 | g0089 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA19007 | hp1 | a0001 | c0001 | t0099 | g0210 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA19007 | hp2 | a0001 | c0002 | t0002 | g0155 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA19011 | hp1 | a0001 | c0001 | t0018 | g0081 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA19011 | hp2 | a0001 | c0002 | t0002 | g0164 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA19054 | hp1 | a0001 | c0002 | t0081 | g0118 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA19056 | hp1 | a0001 | c0002 | t0010 | g0095 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA19056 | hp2 | a0001 | c0001 | t0008 | g0228 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA19058 | hp2 | a0001 | c0001 | t0151 | g0227 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA19064 | hp1 | a0001 | c0001 | t0100 | g0208 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA19079 | hp1 | a0001 | c0002 | t0005 | g0137 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA19079 | hp2 | a0001 | c0001 | t0004 | g0252 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA19080 | hp1 | a0001 | c0002 | t0007 | g0144 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA19080 | hp2 | a0001 | c0001 | t0123 | g0259 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA19082 | hp1 | a0001 | c0002 | t0082 | g0006 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA19082 | hp2 | a0001 | c0001 | t0013 | g0206 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA19084 | hp2 | a0001 | c0002 | t0016 | g0126 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA19086 | hp1 | a0001 | c0002 | t0049 | g0152 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA19086 | hp2 | a0001 | c0001 | t0139 | g0275 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA19088 | hp1 | a0001 | c0001 | t0033 | g0264 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA19088 | hp2 | a0001 | c0001 | t0146 | g0255 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA19089 | hp1 | a0001 | c0002 | t0010 | g0145 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA19089 | hp2 | a0001 | c0001 | t0019 | g0046 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA19090 | hp1 | a0001 | c0002 | t0070 | g0153 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA19090 | hp2 | a0001 | c0001 | t0031 | g0258 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA19240 | hp1 | a0001 | c0001 | t0145 | g0268 | AFR | YRI | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA19240 | hp2 | a0001 | c0001 | t0038 | g0004 | AFR | YRI | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA20129 | hp1 | a0001 | c0001 | t0162 | g0051 | AFR | ASW | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA20129 | hp2 | a0001 | c0001 | t0006 | g0024 | AFR | ASW | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA20752 | hp1 | a0001 | c0002 | t0002 | g0154 | EUR | TSI | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA20752 | hp2 | a0001 | c0002 | t0066 | g0112 | EUR | TSI | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA20805 | hp1 | a0001 | c0001 | t0102 | g0180 | EUR | TSI | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA20805 | hp2 | a0001 | c0002 | t0012 | g0006 | EUR | TSI | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA20905 | hp1 | a0001 | c0001 | t0003 | g0212 | SAS | GIH | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA20905 | hp2 | a0001 | c0002 | t0002 | g0026 | SAS | GIH | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG01123 | hp1 | a0001 | c0002 | t0078 | g0108 | AMR | CLM | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG01123 | hp2 | a0001 | c0001 | t0163 | g0031 | AMR | CLM | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02486 | hp1 | a0001 | c0001 | t0166 | g0286 | AFR | ACB | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02486 | hp2 | a0001 | c0001 | t0167 | g0023 | AFR | ACB | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02559 | hp1 | a0001 | c0001 | t0039 | g0041 | AFR | ACB | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG02559 | hp2 | a0001 | c0001 | t0036 | g0277 | AFR | ACB | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG03471 | hp1 | a0001 | c0001 | t0027 | g0008 | AFR | MSL | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG03471 | hp2 | a0001 | c0002 | t0023 | g0172 | AFR | MSL | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG06807 | hp1 | a0001 | c0001 | t0176 | g0053 | AFR | USA | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
HG06807 | hp2 | a0001 | c0002 | t0002 | g0111 | AFR | USA | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA18955 | hp1 | a0001 | c0001 | t0004 | g0253 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA18955 | hp2 | a0001 | c0002 | t0069 | g0162 | EAS | JPT | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA20300 | hp1 | a0001 | c0001 | t0006 | g0001 | AFR | USA | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA20300 | hp2 | a0001 | c0001 | t0177 | g0216 | AFR | USA | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA21309 | hp1 | a0001 | c0001 | t0107 | g0003 | AFR | LWK | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
NA21309 | hp2 | a0001 | c0001 | t0083 | g0288 | AFR | LWK | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0093 | g0203 | REF | REF | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0088 | g0207 | REF | REF | AP1M1_chr19_16192911_16250906 | AP1M1 | chr19 | 16192911 | 16250906 |
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 |
---|
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:16209087
|
C | T | 1 | a0001c0005 | 1 | HG01346.hp1 | synonymous_variant | LOW | c.456C>T | p.Thr152Thr | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/12 | 572/12859 | 456/1272 | 152/423 | chr19 | 16209087 | ||
chr19:16227648
|
C | A | 1 | a0001c0003 | 1 | HG01891.hp1 | synonymous_variant | LOW | c.774C>A | p.Pro258Pro | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 7/12 | 890/12859 | 774/1272 | 258/423 | chr19 | 16227648 | ||
chr19:16228904
|
C | T | 2 | a0001c0002a0001c0005 | 99 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(96): Show |
synonymous_variant | LOW | c.1023C>T | p.Ile341Ile | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/12 | 1139/12859 | 1023/1272 | 341/423 | chr19 | 16228904 | ||
chr19:16233609
|
C | T | 1 | a0001c0004 | 1 | NA18984.hp2 | synonymous_variant | LOW | c.1164C>T | p.Ser388Ser | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 10/12 | 1280/12859 | 1164/1272 | 388/423 | chr19 | 16233609 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:16197975
|
T | TCGCTGCC others(18): Show |
83 | a0001c0001t0001a0001c0001t0004a0001c0001t0006others(80): Show | 152 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(149): Show |
5_prime_UTR_variant | MODIFIER | c.-43_-19dupCCGCCACC others(17): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/12 | 18 | INFO_REALIGN_3_PRIME | chr19 | 16197975 | ||||
chr19:16197975
|
T | TCGCTGCC others(43): Show |
1 | a0001c0001t0177 | 1 | NA20300.hp2 | 5_prime_UTR_variant | MODIFIER | c.-19_-18insCCGCCACC others(42): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/12 | 18 | INFO_REALIGN_3_PRIME | chr19 | 16197975 | ||||
chr19:16198008
|
G | GCCGCCAC others(18): Show |
1 | a0001c0001t0114 | 1 | HG01346.hp2 | 5_prime_UTR_variant | MODIFIER | c.-19_-18insCCGCCACC others(17): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/12 | 18 | chr19 | 16198008 | |||||
chr19:16234653
|
G | A | 1 | a0001c0001t0115 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*218G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 218 | chr19 | 16234653 | |||||
chr19:16234702
|
C | T | 1 | a0001c0001t0113 | 1 | NA18982.hp2 | 3_prime_UTR_variant | MODIFIER | c.*267C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 267 | chr19 | 16234702 | |||||
chr19:16234822
|
G | A | 1 | a0001c0001t0041 | 1 | NA19002.hp1 | 3_prime_UTR_variant | MODIFIER | c.*387G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 387 | chr19 | 16234822 | |||||
chr19:16234837
|
C | T | 9 | a0001c0001t0039a0001c0001t0040a0001c0001t0170others(6): Show | 11 | HG01167.hp1 HG01169.hp2 HG02257.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*402C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 402 | chr19 | 16234837 | |||||
chr19:16234934
|
C | G | 1 | a0001c0002t0112 | 1 | HG02738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*499C>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 499 | chr19 | 16234934 | |||||
chr19:16234972
|
T | C | 1 | a0001c0001t0170 | 1 | HG02523.hp2 | 3_prime_UTR_variant | MODIFIER | c.*537T>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 537 | chr19 | 16234972 | |||||
chr19:16235011
|
G | A | 98 | a0001c0001t0004a0001c0001t0008a0001c0001t0029others(95): Show | 161 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(158): Show |
3_prime_UTR_variant | MODIFIER | c.*576G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 576 | chr19 | 16235011 | |||||
chr19:16235013
|
C | T | 1 | a0001c0001t0038 | 2 | HG02717.hp2 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*578C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 578 | chr19 | 16235013 | |||||
chr19:16235020
|
C | T | 1 | a0001c0001t0151 | 1 | NA19058.hp2 | 3_prime_UTR_variant | MODIFIER | c.*585C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 585 | chr19 | 16235020 | |||||
chr19:16235021
|
G | T | 11 | a0001c0001t0026a0001c0001t0027a0001c0001t0028others(8): Show | 14 | HG01361.hp1 HG01934.hp1 HG02055.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*586G>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 586 | chr19 | 16235021 | |||||
chr19:16235039
|
G | A | 1 | a0001c0001t0106 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*604G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 604 | chr19 | 16235039 | |||||
chr19:16235058
|
G | A | 1 | a0001c0001t0042 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*623G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 623 | chr19 | 16235058 | |||||
chr19:16235073
|
T | A | 1 | a0001c0002t0043 | 1 | NA18951.hp1 | 3_prime_UTR_variant | MODIFIER | c.*638T>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 638 | chr19 | 16235073 | |||||
chr19:16235079
|
G | A | 1 | a0001c0001t0152 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*644G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 644 | chr19 | 16235079 | |||||
chr19:16235092
|
C | G | 1 | a0001c0001t0105 | 1 | HG02896.hp1 | 3_prime_UTR_variant | MODIFIER | c.*657C>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 657 | chr19 | 16235092 | |||||
chr19:16235118
|
G | A | 2 | a0001c0001t0115a0001c0001t0153 | 2 | HG01884.hp1 HG03098.hp2 |
3_prime_UTR_variant | MODIFIER | c.*683G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 683 | chr19 | 16235118 | |||||
chr19:16235365
|
A | G | 106 | a0001c0001t0004a0001c0001t0008a0001c0001t0020others(103): Show | 173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
3_prime_UTR_variant | MODIFIER | c.*930A>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 930 | chr19 | 16235365 | |||||
chr19:16235494
|
G | A | 1 | a0001c0001t0154 | 1 | HG02155.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1059G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 1059 | chr19 | 16235494 | |||||
chr19:16235561
|
G | T | 1 | a0001c0001t0041 | 1 | NA19002.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1126G>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 1126 | chr19 | 16235561 | |||||
chr19:16235680
|
T | A | 1 | a0001c0002t0044 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1245T>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 1245 | chr19 | 16235680 | |||||
chr19:16235824
|
C | T | 1 | a0001c0001t0103 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1389C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 1389 | chr19 | 16235824 | |||||
chr19:16235940
|
C | T | 33 | a0001c0001t0001a0001c0001t0009a0001c0001t0014others(30): Show | 76 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(73): Show |
3_prime_UTR_variant | MODIFIER | c.*1505C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 1505 | chr19 | 16235940 | |||||
chr19:16235965
|
C | T | 1 | a0001c0001t0102 | 1 | NA20805.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1530C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 1530 | chr19 | 16235965 | |||||
chr19:16235992
|
C | T | 10 | a0001c0001t0039a0001c0001t0040a0001c0001t0155others(7): Show | 12 | HG01167.hp1 HG01169.hp2 HG02257.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1557C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 1557 | chr19 | 16235992 | |||||
chr19:16235998
|
C | T | 3 | a0001c0001t0099a0001c0001t0100a0001c0001t0101 | 3 | HG00544.hp2 NA19007.hp1 NA19064.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1563C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 1563 | chr19 | 16235998 | |||||
chr19:16236036
|
G | T | 1 | a0001c0001t0150 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1601G>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 1601 | chr19 | 16236036 | |||||
chr19:16236101
|
TATC | T | 32 | a0001c0001t0001a0001c0001t0006a0001c0001t0009others(29): Show | 80 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(77): Show |
3_prime_UTR_variant | MODIFIER | c.*1668_*1670delTCA | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 1668 | INFO_REALIGN_3_PRIME | chr19 | 16236101 | ||||
chr19:16236103
|
T | G | 1 | a0001c0001t0163 | 1 | HG01123.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1668T>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 1668 | chr19 | 16236103 | |||||
chr19:16236204
|
C | T | 1 | a0001c0001t0149 | 1 | HG00099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1769C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 1769 | chr19 | 16236204 | |||||
chr19:16236421
|
T | G | 1 | a0001c0001t0083 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1986T>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 1986 | chr19 | 16236421 | |||||
chr19:16236426
|
G | A | 1 | a0001c0001t0116 | 1 | HG00544.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1991G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 1991 | chr19 | 16236426 | |||||
chr19:16236428
|
G | A | 1 | a0001c0001t0115 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1993G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 1993 | chr19 | 16236428 | |||||
chr19:16236438
|
G | A | 55 | a0001c0001t0029a0001c0001t0030a0001c0002t0002others(52): Show | 103 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(100): Show |
3_prime_UTR_variant | MODIFIER | c.*2003G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 2003 | chr19 | 16236438 | |||||
chr19:16236474
|
C | T | 1 | a0001c0001t0037 | 2 | HG02615.hp1 HG02895.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2039C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 2039 | chr19 | 16236474 | |||||
chr19:16236546
|
T | A | 1 | a0001c0002t0045 | 1 | HG02083.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2111T>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 2111 | chr19 | 16236546 | |||||
chr19:16236607
|
T | C | 1 | a0001c0001t0006 | 6 | HG02145.hp1 HG02976.hp2 HG03130.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2172T>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 2172 | chr19 | 16236607 | |||||
chr19:16236772
|
A | G | 1 | a0001c0001t0006 | 6 | HG02145.hp1 HG02976.hp2 HG03130.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2337A>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 2337 | chr19 | 16236772 | |||||
chr19:16236789
|
C | T | 1 | a0001c0003t0098 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2354C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 2354 | chr19 | 16236789 | |||||
chr19:16236901
|
CG | C | 39 | a0001c0001t0001a0001c0001t0006a0001c0001t0009others(36): Show | 87 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*2467delG | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 2467 | chr19 | 16236901 | |||||
chr19:16236902
|
GAACTTCA others(29): Show |
G | 1 | a0001c0002t0082 | 1 | NA19082.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2469_*2504delACTT others(32): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 2469 | INFO_REALIGN_3_PRIME | chr19 | 16236902 | ||||
chr19:16237197
|
G | T | 12 | a0001c0001t0039a0001c0001t0040a0001c0001t0155others(9): Show | 14 | HG01167.hp1 HG01169.hp2 HG02257.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*2762G>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 2762 | chr19 | 16237197 | |||||
chr19:16237231
|
C | T | 1 | a0001c0001t0167 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2796C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 2796 | chr19 | 16237231 | |||||
chr19:16237316
|
C | T | 1 | a0001c0001t0166 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2881C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 2881 | chr19 | 16237316 | |||||
chr19:16237376
|
G | T | 3 | a0001c0001t0115a0001c0001t0153a0001c0001t0165 | 3 | HG01884.hp1 HG02922.hp2 HG03098.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2941G>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 2941 | chr19 | 16237376 | |||||
chr19:16237388
|
A | T | 1 | a0001c0001t0041 | 1 | NA19002.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2953A>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 2953 | chr19 | 16237388 | |||||
chr19:16237458
|
C | T | 1 | a0001c0001t0148 | 1 | HG02080.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3023C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 3023 | chr19 | 16237458 | |||||
chr19:16237602
|
G | A | 1 | a0001c0001t0042 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3167G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 3167 | chr19 | 16237602 | |||||
chr19:16237771
|
C | G | 93 | a0001c0001t0001a0001c0001t0006a0001c0001t0009others(90): Show | 187 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(184): Show |
3_prime_UTR_variant | MODIFIER | c.*3336C>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 3336 | chr19 | 16237771 | |||||
chr19:16237796
|
ACCAAGAC others(18): Show |
A | 1 | a0001c0001t0041 | 1 | NA19002.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3362_*3386delCCAA others(21): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 3362 | chr19 | 16237796 | |||||
chr19:16237842
|
A | C | 1 | a0001c0001t0161 | 1 | HG03831.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3407A>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 3407 | chr19 | 16237842 | |||||
chr19:16237849
|
T | A | 7 | a0001c0001t0029a0001c0001t0030a0001c0001t0102others(4): Show | 9 | HG00735.hp1 HG01109.hp1 HG01884.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3414T>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 3414 | chr19 | 16237849 | |||||
chr19:16237926
|
C | G | 3 | a0001c0001t0115a0001c0001t0153a0001c0001t0165 | 3 | HG01884.hp1 HG02922.hp2 HG03098.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3491C>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 3491 | chr19 | 16237926 | |||||
chr19:16237927
|
G | A | 1 | a0001c0001t0152 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3492G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 3492 | chr19 | 16237927 | |||||
chr19:16238039
|
C | T | 54 | a0001c0001t0083a0001c0002t0002a0001c0002t0005others(51): Show | 100 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*3604C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 3604 | chr19 | 16238039 | |||||
chr19:16238119
|
C | T | 1 | a0001c0001t0166 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3684C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 3684 | chr19 | 16238119 | |||||
chr19:16238135
|
A | C | 39 | a0001c0001t0001a0001c0001t0006a0001c0001t0009others(36): Show | 87 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*3700A>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 3700 | chr19 | 16238135 | |||||
chr19:16238137
|
G | A | 1 | a0001c0001t0155 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3702G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 3702 | chr19 | 16238137 | |||||
chr19:16238255
|
C | G | 5 | a0001c0001t0009a0001c0001t0160a0001c0001t0168others(2): Show | 9 | HG01361.hp1 HG02615.hp2 HG02723.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3820C>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 3820 | chr19 | 16238255 | |||||
chr19:16238308
|
T | TA | 54 | a0001c0001t0083a0001c0002t0002a0001c0002t0005others(51): Show | 100 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*3874dupA | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 3875 | INFO_REALIGN_3_PRIME | chr19 | 16238308 | ||||
chr19:16238382
|
T | C | 39 | a0001c0001t0001a0001c0001t0006a0001c0001t0009others(36): Show | 87 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*3947T>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 3947 | chr19 | 16238382 | |||||
chr19:16238440
|
T | C | 54 | a0001c0001t0083a0001c0002t0002a0001c0002t0005others(51): Show | 100 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*4005T>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 4005 | chr19 | 16238440 | |||||
chr19:16238475
|
A | G | 54 | a0001c0001t0083a0001c0002t0002a0001c0002t0005others(51): Show | 100 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*4040A>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 4040 | chr19 | 16238475 | |||||
chr19:16238519
|
G | A | 3 | a0001c0002t0046a0001c0002t0047a0001c0002t0048 | 3 | HG01433.hp1 HG01993.hp2 HG02300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4084G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 4084 | chr19 | 16238519 | |||||
chr19:16238542
|
G | A | 8 | a0001c0001t0026a0001c0001t0027a0001c0001t0028others(5): Show | 11 | HG01934.hp1 HG02055.hp1 HG02280.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*4107G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 4107 | chr19 | 16238542 | |||||
chr19:16238722
|
C | CT | 19 | a0001c0001t0001a0001c0001t0014a0001c0001t0018others(16): Show | 52 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*4304dupT | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 4305 | INFO_REALIGN_3_PRIME | chr19 | 16238722 | ||||
chr19:16238722
|
C | CTT | 27 | a0001c0001t0009a0001c0001t0019a0001c0001t0034others(24): Show | 38 | HG00438.hp1 HG00735.hp2 HG01123.hp2 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*4303_*4304dupTT | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 4305 | INFO_REALIGN_3_PRIME | chr19 | 16238722 | ||||
chr19:16238722
|
C | CTTT | 3 | a0001c0001t0006a0001c0001t0166a0001c0001t0176 | 8 | HG02145.hp1 HG02486.hp1 HG02976.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*4302_*4304dupTTT | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 4305 | INFO_REALIGN_3_PRIME | chr19 | 16238722 | ||||
chr19:16238722
|
CT | C | 60 | a0001c0001t0008a0001c0001t0083a0001c0001t0117others(57): Show | 110 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(107): Show |
3_prime_UTR_variant | MODIFIER | c.*4304delT | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 4304 | INFO_REALIGN_3_PRIME | chr19 | 16238722 | ||||
chr19:16238789
|
G | A | 3 | a0001c0001t0141a0001c0001t0142a0001c0001t0143 | 3 | HG01109.hp2 HG01243.hp1 HG01978.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4354G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 4354 | chr19 | 16238789 | |||||
chr19:16238789
|
G | GGCTCACT others(5): Show |
1 | a0001c0001t0117 | 1 | NA18954.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4355_*4366dupGCTC others(8): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 4367 | INFO_REALIGN_3_PRIME | chr19 | 16238789 | ||||
chr19:16238930
|
G | T | 1 | a0001c0002t0082 | 1 | NA19082.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4495G>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 4495 | chr19 | 16238930 | |||||
chr19:16239239
|
C | CT | 19 | a0001c0001t0008a0001c0001t0031a0001c0001t0032others(16): Show | 26 | HG00558.hp1 HG01243.hp1 HG01891.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*4844dupT | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 4845 | INFO_REALIGN_3_PRIME | chr19 | 16239239 | ||||
chr19:16239239
|
C | CTTTTTTT others(1): Show |
5 | a0001c0001t0027a0001c0001t0036a0001c0001t0096others(2): Show | 7 | HG01934.hp1 HG02451.hp2 HG02559.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*4837_*4844dupTTTT others(4): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 4845 | INFO_REALIGN_3_PRIME | chr19 | 16239239 | ||||
chr19:16239239
|
C | CTTTTTTT others(4): Show |
1 | a0001c0001t0028 | 2 | HG02055.hp1 HG02886.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4834_*4844dupTTTT others(7): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 4845 | INFO_REALIGN_3_PRIME | chr19 | 16239239 | ||||
chr19:16239239
|
CT | C | 5 | a0001c0001t0029a0001c0001t0085a0001c0001t0086others(2): Show | 6 | HG00099.hp2 HG01109.hp1 HG01256.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4844delT | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 4844 | INFO_REALIGN_3_PRIME | chr19 | 16239239 | ||||
chr19:16239239
|
CTTTTT | C | 12 | a0001c0002t0005a0001c0002t0012a0001c0002t0017others(9): Show | 23 | HG01192.hp1 HG01243.hp2 HG01255.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*4840_*4844delTTTT others(1): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 4840 | INFO_REALIGN_3_PRIME | chr19 | 16239239 | ||||
chr19:16239239
|
CTTTTTT | C | 18 | a0001c0001t0111a0001c0002t0002a0001c0002t0007others(15): Show | 49 | HG00099.hp1 HG00597.hp2 HG00609.hp2 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*4839_*4844delTTTT others(2): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 4839 | INFO_REALIGN_3_PRIME | chr19 | 16239239 | ||||
chr19:16239239
|
CTTTTTTT | C | 9 | a0001c0002t0010a0001c0002t0021a0001c0002t0046others(6): Show | 13 | HG00140.hp2 HG01071.hp1 HG01167.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*4838_*4844delTTTT others(3): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 4838 | INFO_REALIGN_3_PRIME | chr19 | 16239239 | ||||
chr19:16239239
|
CTTTTTTT others(4): Show |
C | 5 | a0001c0001t0024a0001c0001t0105a0001c0001t0115others(2): Show | 6 | HG01884.hp1 HG02647.hp1 HG02896.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4834_*4844delTTTT others(7): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 4834 | INFO_REALIGN_3_PRIME | chr19 | 16239239 | ||||
chr19:16239239
|
CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0107 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4832_*4844delTTTT others(9): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 4832 | INFO_REALIGN_3_PRIME | chr19 | 16239239 | ||||
chr19:16239239
|
CTTTTTTT others(7): Show |
C | 1 | a0001c0001t0159 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4831_*4844delTTTT others(10): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 4831 | INFO_REALIGN_3_PRIME | chr19 | 16239239 | ||||
chr19:16239239
|
CTTTTTTT others(8): Show |
C | 13 | a0001c0001t0009a0001c0001t0018a0001c0001t0042others(10): Show | 19 | HG00423.hp1 HG00438.hp1 HG01361.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*4830_*4844delTTTT others(11): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 4830 | INFO_REALIGN_3_PRIME | chr19 | 16239239 | ||||
chr19:16239239
|
CTTTTTTT others(9): Show |
C | 20 | a0001c0001t0001a0001c0001t0006a0001c0001t0019others(17): Show | 59 | HG00558.hp2 HG00597.hp1 HG00735.hp2 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*4829_*4844delTTTT others(12): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 4829 | INFO_REALIGN_3_PRIME | chr19 | 16239239 | ||||
chr19:16239239
|
CTTTTTTT others(10): Show |
C | 3 | a0001c0001t0014a0001c0001t0166a0001c0001t0171 | 6 | HG01069.hp2 HG01167.hp1 HG02486.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4828_*4844delTTTT others(13): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 4828 | INFO_REALIGN_3_PRIME | chr19 | 16239239 | ||||
chr19:16239239
|
CTTTTTTT others(11): Show |
C | 2 | a0001c0002t0043a0001c0002t0055 | 2 | HG04115.hp1 NA18951.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4827_*4844delTTTT others(14): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 4827 | INFO_REALIGN_3_PRIME | chr19 | 16239239 | ||||
chr19:16239239
|
CTTTTTTT others(12): Show |
C | 10 | a0001c0001t0037a0001c0001t0084a0001c0001t0124others(7): Show | 11 | HG00140.hp1 HG01081.hp1 HG02615.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*4826_*4844delTTTT others(15): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 4826 | INFO_REALIGN_3_PRIME | chr19 | 16239239 | ||||
chr19:16239239
|
CTTTTTTT others(13): Show |
C | 1 | a0001c0002t0052 | 1 | HG02683.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4825_*4844delTTTT others(16): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 4825 | INFO_REALIGN_3_PRIME | chr19 | 16239239 | ||||
chr19:16239239
|
CTTTTTTT others(19): Show |
C | 1 | a0001c0002t0051 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4819_*4844delTTTT others(22): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 4819 | INFO_REALIGN_3_PRIME | chr19 | 16239239 | ||||
chr19:16239245
|
T | C | 1 | a0001c0002t0050 | 1 | HG02135.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4810T>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 4810 | chr19 | 16239245 | |||||
chr19:16239246
|
T | C | 1 | a0001c0002t0049 | 1 | NA19086.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4811T>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 4811 | chr19 | 16239246 | |||||
chr19:16239273
|
T | G | 5 | a0001c0001t0009a0001c0001t0160a0001c0001t0168others(2): Show | 9 | HG01361.hp1 HG02615.hp2 HG02723.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*4838T>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 4838 | chr19 | 16239273 | |||||
chr19:16239341
|
G | A | 2 | a0001c0001t0153a0001c0001t0165 | 2 | HG01884.hp1 HG02922.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4906G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 4906 | chr19 | 16239341 | |||||
chr19:16239419
|
C | A | 39 | a0001c0001t0001a0001c0001t0006a0001c0001t0009others(36): Show | 87 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*4984C>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 4984 | chr19 | 16239419 | |||||
chr19:16239429
|
C | G | 6 | a0001c0001t0009a0001c0001t0159a0001c0001t0160others(3): Show | 10 | HG01361.hp1 HG02615.hp2 HG02723.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*4994C>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 4994 | chr19 | 16239429 | |||||
chr19:16239562
|
C | G | 1 | a0001c0001t0037 | 2 | HG02615.hp1 HG02895.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5127C>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 5127 | chr19 | 16239562 | |||||
chr19:16239666
|
T | C | 1 | a0001c0001t0163 | 1 | HG01123.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5231T>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 5231 | chr19 | 16239666 | |||||
chr19:16239671
|
G | A | 6 | a0001c0001t0009a0001c0001t0159a0001c0001t0160others(3): Show | 10 | HG01361.hp1 HG02615.hp2 HG02723.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*5236G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 5236 | chr19 | 16239671 | |||||
chr19:16239809
|
T | C | 93 | a0001c0001t0001a0001c0001t0006a0001c0001t0009others(90): Show | 187 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(184): Show |
3_prime_UTR_variant | MODIFIER | c.*5374T>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 5374 | chr19 | 16239809 | |||||
chr19:16239819
|
T | G | 1 | a0001c0001t0141 | 1 | HG01109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5384T>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 5384 | chr19 | 16239819 | |||||
chr19:16239825
|
A | G | 54 | a0001c0001t0083a0001c0002t0002a0001c0002t0005others(51): Show | 100 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*5390A>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 5390 | chr19 | 16239825 | |||||
chr19:16239861
|
G | A | 1 | a0001c0002t0046 | 1 | HG02300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5426G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 5426 | chr19 | 16239861 | |||||
chr19:16239978
|
A | G | 141 | a0001c0001t0001a0001c0001t0004a0001c0001t0006others(138): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
3_prime_UTR_variant | MODIFIER | c.*5543A>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 5543 | chr19 | 16239978 | |||||
chr19:16239997
|
A | AG | 2 | a0001c0001t0024a0001c0001t0105 | 3 | HG02647.hp1 HG02896.hp1 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5562_*5563insG | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 5563 | chr19 | 16239997 | |||||
chr19:16240041
|
G | T | 39 | a0001c0001t0001a0001c0001t0006a0001c0001t0009others(36): Show | 87 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*5606G>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 5606 | chr19 | 16240041 | |||||
chr19:16240059
|
A | C | 3 | a0001c0001t0083a0001c0002t0060a0001c0002t0080 | 3 | HG02451.hp1 HG03139.hp1 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5624A>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 5624 | chr19 | 16240059 | |||||
chr19:16240109
|
A | G | 1 | a0001c0001t0006 | 6 | HG02145.hp1 HG02976.hp2 HG03130.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*5674A>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 5674 | chr19 | 16240109 | |||||
chr19:16240199
|
G | A | 1 | a0001c0001t0167 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5764G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 5764 | chr19 | 16240199 | |||||
chr19:16240240
|
CTCTGTGT others(13): Show |
C | 2 | a0001c0002t0068a0001c0002t0079 | 2 | NA18945.hp2 NA18949.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5807_*5826delCTGT others(16): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 5807 | INFO_REALIGN_3_PRIME | chr19 | 16240240 | ||||
chr19:16240242
|
C | CTG | 12 | a0001c0001t0026a0001c0001t0027a0001c0001t0028others(9): Show | 15 | HG01891.hp1 HG01934.hp1 HG02055.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*5837_*5838dupGT | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 5839 | INFO_REALIGN_3_PRIME | chr19 | 16240242 | ||||
chr19:16240242
|
C | CTGTG | 4 | a0001c0001t0091a0001c0001t0104a0001c0001t0108others(1): Show | 4 | HG02723.hp2 HG02818.hp1 HG02922.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5835_*5838dupGTGT | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 5839 | INFO_REALIGN_3_PRIME | chr19 | 16240242 | ||||
chr19:16240248
|
GTGTGTGT others(19): Show |
G | 3 | a0001c0001t0083a0001c0002t0060a0001c0002t0080 | 3 | HG02451.hp1 HG03139.hp1 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5839_*5864delATGT others(22): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 5839 | INFO_REALIGN_3_PRIME | chr19 | 16240248 | ||||
chr19:16240250
|
GTGTGTGT others(17): Show |
G | 3 | a0001c0002t0056a0001c0002t0061a0001c0002t0073 | 3 | HG01071.hp1 HG02965.hp1 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5839_*5862delATGT others(20): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 5839 | INFO_REALIGN_3_PRIME | chr19 | 16240250 | ||||
chr19:16240252
|
GTGTGTGT others(15): Show |
G | 2 | a0001c0002t0074a0001c0002t0075 | 2 | HG02717.hp1 HG02818.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5839_*5860delATGT others(18): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 5839 | INFO_REALIGN_3_PRIME | chr19 | 16240252 | ||||
chr19:16240254
|
GTGTGTGT others(13): Show |
G | 30 | a0001c0001t0113a0001c0002t0002a0001c0002t0005others(27): Show | 64 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*5839_*5858delATGT others(16): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 5839 | INFO_REALIGN_3_PRIME | chr19 | 16240254 | ||||
chr19:16240256
|
GTGTGTGT others(11): Show |
G | 11 | a0001c0001t0025a0001c0002t0011a0001c0002t0016others(8): Show | 17 | HG00673.hp1 HG01074.hp1 HG01358.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*5839_*5856delATGT others(14): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 5839 | INFO_REALIGN_3_PRIME | chr19 | 16240256 | ||||
chr19:16240258
|
G | C | 36 | a0001c0001t0001a0001c0001t0006a0001c0001t0009others(33): Show | 84 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(81): Show |
3_prime_UTR_variant | MODIFIER | c.*5823G>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 5823 | chr19 | 16240258 | |||||
chr19:16240258
|
GTGTGTGT others(9): Show |
G | 4 | a0001c0002t0007a0001c0002t0012a0001c0002t0045others(1): Show | 11 | HG00738.hp2 HG01074.hp2 HG01123.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*5839_*5854delATGT others(12): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 5839 | INFO_REALIGN_3_PRIME | chr19 | 16240258 | ||||
chr19:16240260
|
GTGTGTGT others(7): Show |
G | 1 | a0001c0002t0082 | 1 | NA19082.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5839_*5852delATGT others(10): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 5839 | INFO_REALIGN_3_PRIME | chr19 | 16240260 | ||||
chr19:16240266
|
GTGTGTGT others(1): Show |
G | 2 | a0001c0001t0037a0001c0001t0115 | 3 | HG02615.hp1 HG02895.hp2 HG03098.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5839_*5846delATGT others(4): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 5839 | INFO_REALIGN_3_PRIME | chr19 | 16240266 | ||||
chr19:16240267
|
TGTGTGTA others(34): Show |
T | 36 | a0001c0001t0001a0001c0001t0006a0001c0001t0009others(33): Show | 84 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(81): Show |
3_prime_UTR_variant | MODIFIER | c.*5839_*5879delATGT others(37): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 5839 | INFO_REALIGN_3_PRIME | chr19 | 16240267 | ||||
chr19:16240268
|
GTGTGTA | G | 3 | a0001c0001t0124a0001c0001t0125a0001c0001t0165 | 3 | HG02895.hp1 HG02897.hp2 HG02922.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5839_*5844delATGT others(2): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 5839 | INFO_REALIGN_3_PRIME | chr19 | 16240268 | ||||
chr19:16240270
|
GTGTA | G | 3 | a0001c0001t0118a0001c0001t0120a0001c0001t0153 | 3 | HG01884.hp1 HG01891.hp2 HG02145.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5839_*5842delATGT | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 5839 | INFO_REALIGN_3_PRIME | chr19 | 16240270 | ||||
chr19:16240272
|
G | A | 1 | a0001c0001t0024 | 2 | HG02647.hp1 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5837G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 5837 | chr19 | 16240272 | |||||
chr19:16240272
|
GTA | G | 21 | a0001c0001t0004a0001c0001t0020a0001c0001t0033others(18): Show | 33 | HG00423.hp2 HG00609.hp1 HG00673.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*5839_*5840delAT | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 5839 | INFO_REALIGN_3_PRIME | chr19 | 16240272 | ||||
chr19:16240274
|
A | G | 27 | a0001c0001t0008a0001c0001t0024a0001c0001t0029others(24): Show | 36 | HG00099.hp2 HG00438.hp2 HG00544.hp1 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*5839A>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 5839 | chr19 | 16240274 | |||||
chr19:16240276
|
G | A | 3 | a0001c0001t0029a0001c0001t0030a0001c0001t0037 | 6 | HG00735.hp1 HG01109.hp1 HG01884.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*5841G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 5841 | chr19 | 16240276 | |||||
chr19:16240278
|
G | A | 3 | a0001c0001t0042a0001c0001t0116a0001c0001t0132 | 3 | HG00544.hp1 HG02257.hp2 NA18962.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5843G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 5843 | chr19 | 16240278 | |||||
chr19:16240280
|
G | A | 27 | a0001c0001t0004a0001c0001t0020a0001c0001t0031others(24): Show | 40 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*5845G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 5845 | chr19 | 16240280 | |||||
chr19:16240280
|
G | GTA | 7 | a0001c0001t0008a0001c0001t0032a0001c0001t0123others(4): Show | 12 | HG02080.hp2 HG02132.hp1 NA18939.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*5846_*5847insAT | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 5847 | INFO_REALIGN_3_PRIME | chr19 | 16240280 | ||||
chr19:16240598
|
C | T | 1 | a0001c0002t0059 | 1 | HG00140.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6163C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 6163 | chr19 | 16240598 | |||||
chr19:16240699
|
T | C | 1 | a0001c0001t0166 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6264T>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 6264 | chr19 | 16240699 | |||||
chr19:16240707
|
C | G | 1 | a0001c0001t0117 | 1 | NA18954.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6272C>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 6272 | chr19 | 16240707 | |||||
chr19:16240916
|
T | C | 39 | a0001c0001t0001a0001c0001t0006a0001c0001t0009others(36): Show | 87 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*6481T>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 6481 | chr19 | 16240916 | |||||
chr19:16241010
|
A | T | 39 | a0001c0001t0001a0001c0001t0006a0001c0001t0009others(36): Show | 87 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*6575A>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 6575 | chr19 | 16241010 | |||||
chr19:16241023
|
T | C | 1 | a0001c0001t0042 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6588T>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 6588 | chr19 | 16241023 | |||||
chr19:16241033
|
A | G | 1 | a0001c0002t0082 | 1 | NA19082.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6598A>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 6598 | chr19 | 16241033 | |||||
chr19:16241054
|
C | G | 1 | a0001c0003t0098 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6619C>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 6619 | chr19 | 16241054 | |||||
chr19:16241059
|
G | A | 2 | a0001c0001t0153a0001c0001t0165 | 2 | HG01884.hp1 HG02922.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6624G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 6624 | chr19 | 16241059 | |||||
chr19:16241067
|
T | G | 1 | a0001c0001t0042 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6632T>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 6632 | chr19 | 16241067 | |||||
chr19:16241186
|
C | T | 1 | a0001c0001t0006 | 6 | HG02145.hp1 HG02976.hp2 HG03130.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*6751C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 6751 | chr19 | 16241186 | |||||
chr19:16241253
|
C | T | 1 | a0001c0001t0131 | 1 | NA18971.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6818C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 6818 | chr19 | 16241253 | |||||
chr19:16241269
|
C | T | 11 | a0001c0001t0039a0001c0001t0040a0001c0001t0155others(8): Show | 13 | HG01167.hp1 HG01169.hp2 HG02257.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*6834C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 6834 | chr19 | 16241269 | |||||
chr19:16241309
|
C | CAA | 52 | a0001c0001t0083a0001c0002t0002a0001c0002t0005others(49): Show | 98 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(95): Show |
3_prime_UTR_variant | MODIFIER | c.*6886_*6887dupAA | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 6888 | INFO_REALIGN_3_PRIME | chr19 | 16241309 | ||||
chr19:16241309
|
CA | C | 7 | a0001c0001t0029a0001c0001t0030a0001c0001t0100others(4): Show | 9 | HG00735.hp1 HG01109.hp1 HG01884.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*6887delA | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 6887 | INFO_REALIGN_3_PRIME | chr19 | 16241309 | ||||
chr19:16241592
|
C | T | 93 | a0001c0001t0001a0001c0001t0006a0001c0001t0009others(90): Show | 187 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(184): Show |
3_prime_UTR_variant | MODIFIER | c.*7157C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 7157 | chr19 | 16241592 | |||||
chr19:16241621
|
C | A | 1 | a0001c0001t0166 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7186C>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 7186 | chr19 | 16241621 | |||||
chr19:16241655
|
CT | C | 59 | a0001c0001t0083a0001c0001t0115a0001c0001t0152others(56): Show | 105 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(102): Show |
3_prime_UTR_variant | MODIFIER | c.*7224delT | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 7224 | INFO_REALIGN_3_PRIME | chr19 | 16241655 | ||||
chr19:16241673
|
G | A | 54 | a0001c0001t0083a0001c0002t0002a0001c0002t0005others(51): Show | 100 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*7238G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 7238 | chr19 | 16241673 | |||||
chr19:16241716
|
T | C | 93 | a0001c0001t0001a0001c0001t0006a0001c0001t0009others(90): Show | 187 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(184): Show |
3_prime_UTR_variant | MODIFIER | c.*7281T>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 7281 | chr19 | 16241716 | |||||
chr19:16241792
|
C | A | 54 | a0001c0001t0083a0001c0002t0002a0001c0002t0005others(51): Show | 100 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*7357C>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 7357 | chr19 | 16241792 | |||||
chr19:16241949
|
C | T | 54 | a0001c0001t0083a0001c0002t0002a0001c0002t0005others(51): Show | 100 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*7514C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 7514 | chr19 | 16241949 | |||||
chr19:16242309
|
CA | C | 79 | a0001c0001t0001a0001c0001t0004a0001c0001t0006others(76): Show | 146 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(143): Show |
3_prime_UTR_variant | MODIFIER | c.*7886delA | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 7886 | INFO_REALIGN_3_PRIME | chr19 | 16242309 | ||||
chr19:16242309
|
CAA | C | 54 | a0001c0001t0083a0001c0001t0117a0001c0002t0002others(51): Show | 100 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*7885_*7886delAA | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 7885 | INFO_REALIGN_3_PRIME | chr19 | 16242309 | ||||
chr19:16242608
|
T | C | 2 | a0001c0001t0085a0001c0001t0087 | 2 | HG03491.hp1 HG03492.hp2 |
3_prime_UTR_variant | MODIFIER | c.*8173T>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 8173 | chr19 | 16242608 | |||||
chr19:16242688
|
G | T | 3 | a0001c0001t0115a0001c0001t0153a0001c0001t0165 | 3 | HG01884.hp1 HG02922.hp2 HG03098.hp2 |
3_prime_UTR_variant | MODIFIER | c.*8253G>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 8253 | chr19 | 16242688 | |||||
chr19:16242827
|
T | C | 54 | a0001c0001t0083a0001c0002t0002a0001c0002t0005others(51): Show | 100 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*8392T>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 8392 | chr19 | 16242827 | |||||
chr19:16242846
|
C | T | 1 | a0001c0001t0167 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8411C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 8411 | chr19 | 16242846 | |||||
chr19:16242979
|
C | T | 2 | a0001c0001t0085a0001c0001t0087 | 2 | HG03491.hp1 HG03492.hp2 |
3_prime_UTR_variant | MODIFIER | c.*8544C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 8544 | chr19 | 16242979 | |||||
chr19:16243246
|
TTTTTTG | T | 134 | a0001c0001t0001a0001c0001t0004a0001c0001t0006others(131): Show | 244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
3_prime_UTR_variant | MODIFIER | c.*8846_*8851delTGTT others(2): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 8846 | INFO_REALIGN_3_PRIME | chr19 | 16243246 | ||||
chr19:16243246
|
TTTTTTGT others(5): Show |
T | 5 | a0001c0001t0034a0001c0001t0035a0001c0001t0038others(2): Show | 8 | HG01884.hp1 HG02258.hp1 HG02630.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*8840_*8851delTGTT others(8): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 8840 | INFO_REALIGN_3_PRIME | chr19 | 16243246 | ||||
chr19:16243432
|
C | CTT | 41 | a0001c0002t0002a0001c0002t0005a0001c0002t0007others(38): Show | 83 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(80): Show |
3_prime_UTR_variant | MODIFIER | c.*8998_*8999insTT | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 8999 | INFO_REALIGN_3_PRIME | chr19 | 16243432 | ||||
chr19:16243432
|
C | CTTT | 11 | a0001c0001t0083a0001c0002t0017a0001c0002t0021others(8): Show | 14 | HG01169.hp1 HG01243.hp2 HG01255.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*8998_*8999insTTT | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 8999 | INFO_REALIGN_3_PRIME | chr19 | 16243432 | ||||
chr19:16243434
|
A | AT | 13 | a0001c0001t0008a0001c0001t0032a0001c0001t0093others(10): Show | 18 | HG02055.hp2 HG02080.hp2 HG02132.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*9015dupT | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 9016 | INFO_REALIGN_3_PRIME | chr19 | 16243434 | ||||
chr19:16243434
|
A | T | 54 | a0001c0001t0083a0001c0002t0002a0001c0002t0005others(51): Show | 100 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*8999A>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 8999 | chr19 | 16243434 | |||||
chr19:16243434
|
ATT | A | 33 | a0001c0001t0001a0001c0001t0006a0001c0001t0009others(30): Show | 81 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*9014_*9015delTT | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 9014 | INFO_REALIGN_3_PRIME | chr19 | 16243434 | ||||
chr19:16243445
|
T | G | 33 | a0001c0001t0001a0001c0001t0006a0001c0001t0009others(30): Show | 81 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*9010T>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 9010 | chr19 | 16243445 | |||||
chr19:16243447
|
T | G | 33 | a0001c0001t0001a0001c0001t0006a0001c0001t0009others(30): Show | 81 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*9012T>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 9012 | chr19 | 16243447 | |||||
chr19:16243449
|
T | G | 33 | a0001c0001t0001a0001c0001t0006a0001c0001t0009others(30): Show | 81 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*9014T>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 9014 | chr19 | 16243449 | |||||
chr19:16243453
|
A | G | 33 | a0001c0001t0001a0001c0001t0006a0001c0001t0009others(30): Show | 81 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*9018A>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 9018 | chr19 | 16243453 | |||||
chr19:16243775
|
C | T | 1 | a0001c0001t0160 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9340C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 9340 | chr19 | 16243775 | |||||
chr19:16243898
|
G | A | 2 | a0001c0001t0142a0001c0001t0143 | 2 | HG01243.hp1 HG01978.hp2 |
3_prime_UTR_variant | MODIFIER | c.*9463G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 9463 | chr19 | 16243898 | |||||
chr19:16243945
|
A | G | 1 | a0001c0002t0015 | 3 | NA18944.hp1 NA18964.hp1 NA19002.hp2 |
3_prime_UTR_variant | MODIFIER | c.*9510A>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 9510 | chr19 | 16243945 | |||||
chr19:16244324
|
A | G | 56 | a0001c0001t0083a0001c0001t0152a0001c0001t0167others(53): Show | 102 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(99): Show |
3_prime_UTR_variant | MODIFIER | c.*9889A>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 9889 | chr19 | 16244324 | |||||
chr19:16244342
|
C | G | 1 | a0001c0001t0156 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9907C>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 9907 | chr19 | 16244342 | |||||
chr19:16244627
|
G | A | 33 | a0001c0001t0001a0001c0001t0006a0001c0001t0009others(30): Show | 81 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*10192G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 10192 | chr19 | 16244627 | |||||
chr19:16244647
|
G | A | 54 | a0001c0001t0083a0001c0002t0002a0001c0002t0005others(51): Show | 100 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*10212G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 10212 | chr19 | 16244647 | |||||
chr19:16244687
|
G | A | 2 | a0001c0001t0029a0001c0001t0030 | 4 | HG00735.hp1 HG01109.hp1 HG01884.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*10252G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 10252 | chr19 | 16244687 | |||||
chr19:16244703
|
G | A | 57 | a0001c0001t0083a0001c0001t0115a0001c0001t0153others(54): Show | 103 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(100): Show |
3_prime_UTR_variant | MODIFIER | c.*10268G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 10268 | chr19 | 16244703 | |||||
chr19:16244755
|
G | A | 57 | a0001c0001t0083a0001c0001t0115a0001c0001t0153others(54): Show | 103 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(100): Show |
3_prime_UTR_variant | MODIFIER | c.*10320G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 10320 | chr19 | 16244755 | |||||
chr19:16244792
|
TGCAGTCC | T | 3 | a0001c0001t0115a0001c0001t0153a0001c0001t0165 | 3 | HG01884.hp1 HG02922.hp2 HG03098.hp2 |
3_prime_UTR_variant | MODIFIER | c.*10366_*10372delCA others(5): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 10366 | INFO_REALIGN_3_PRIME | chr19 | 16244792 | ||||
chr19:16244803
|
G | C | 3 | a0001c0001t0115a0001c0001t0153a0001c0001t0165 | 3 | HG01884.hp1 HG02922.hp2 HG03098.hp2 |
3_prime_UTR_variant | MODIFIER | c.*10368G>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 10368 | chr19 | 16244803 | |||||
chr19:16244807
|
G | A | 3 | a0001c0001t0115a0001c0001t0153a0001c0001t0165 | 3 | HG01884.hp1 HG02922.hp2 HG03098.hp2 |
3_prime_UTR_variant | MODIFIER | c.*10372G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 10372 | chr19 | 16244807 | |||||
chr19:16244837
|
A | AAAAT | 38 | a0001c0001t0004a0001c0001t0008a0001c0001t0020others(35): Show | 55 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*10425_*10428dupAT others(2): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 10429 | INFO_REALIGN_3_PRIME | chr19 | 16244837 | ||||
chr19:16244837
|
A | AAAATAAA others(1): Show |
4 | a0001c0001t0033a0001c0001t0115a0001c0001t0144others(1): Show | 5 | HG03098.hp2 NA18943.hp2 NA18983.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*10421_*10428dupAT others(6): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 10429 | INFO_REALIGN_3_PRIME | chr19 | 16244837 | ||||
chr19:16244841
|
T | A | 84 | a0001c0001t0001a0001c0001t0006a0001c0001t0009others(81): Show | 178 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(175): Show |
3_prime_UTR_variant | MODIFIER | c.*10406T>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 10406 | chr19 | 16244841 | |||||
chr19:16244845
|
T | A | 1 | a0001c0001t0162 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10410T>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 10410 | chr19 | 16244845 | |||||
chr19:16244881
|
G | GTTT | 6 | a0001c0001t0124a0001c0001t0125a0001c0001t0126others(3): Show | 6 | HG02486.hp1 HG02723.hp2 HG02895.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*10447_*10449dupTT others(1): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 10450 | INFO_REALIGN_3_PRIME | chr19 | 16244881 | ||||
chr19:16244881
|
G | T | 28 | a0001c0001t0004a0001c0001t0008a0001c0001t0031others(25): Show | 42 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*10446G>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 10446 | chr19 | 16244881 | |||||
chr19:16244882
|
T | TTTG | 5 | a0001c0001t0013a0001c0001t0025a0001c0001t0099others(2): Show | 9 | HG00544.hp2 HG01257.hp2 HG01258.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*10478_*10480dupTT others(1): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 10481 | INFO_REALIGN_3_PRIME | chr19 | 16244882 | ||||
chr19:16244882
|
T | TTTGTTG | 24 | a0001c0001t0004a0001c0001t0008a0001c0001t0031others(21): Show | 38 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*10475_*10480dupTT others(4): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 10481 | INFO_REALIGN_3_PRIME | chr19 | 16244882 | ||||
chr19:16244882
|
T | TTTGTTGT others(2): Show |
5 | a0001c0001t0122a0001c0001t0129a0001c0001t0131others(2): Show | 5 | HG01358.hp1 NA18955.hp2 NA18971.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*10472_*10480dupTT others(7): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 10481 | INFO_REALIGN_3_PRIME | chr19 | 16244882 | ||||
chr19:16244882
|
T | TTTGTTGT others(5): Show |
1 | a0001c0001t0162 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10469_*10480dupTT others(10): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 10481 | INFO_REALIGN_3_PRIME | chr19 | 16244882 | ||||
chr19:16244882
|
T | TTTTTTG | 24 | a0001c0001t0001a0001c0001t0014a0001c0001t0018others(21): Show | 63 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*10449_*10450insTT others(4): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 10450 | INFO_REALIGN_3_PRIME | chr19 | 16244882 | ||||
chr19:16244882
|
T | TTTTTTGT others(2): Show |
17 | a0001c0001t0006a0001c0001t0009a0001c0001t0035others(14): Show | 28 | HG01346.hp2 HG01433.hp2 HG02145.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*10449_*10450insTT others(7): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 10450 | INFO_REALIGN_3_PRIME | chr19 | 16244882 | ||||
chr19:16244882
|
T | TTTTTTGT others(5): Show |
41 | a0001c0001t0037a0001c0001t0039a0001c0001t0152others(38): Show | 84 | HG00099.hp1 HG00597.hp2 HG00738.hp2 others(81): Show |
3_prime_UTR_variant | MODIFIER | c.*10449_*10450insTT others(10): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 10450 | INFO_REALIGN_3_PRIME | chr19 | 16244882 | ||||
chr19:16244882
|
T | TTTTTTGT others(8): Show |
14 | a0001c0001t0174a0001c0001t0176a0001c0002t0016others(11): Show | 18 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*10449_*10450insTT others(13): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 10450 | INFO_REALIGN_3_PRIME | chr19 | 16244882 | ||||
chr19:16244882
|
T | TTTTTTGT others(11): Show |
1 | a0001c0001t0040 | 2 | HG02572.hp1 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*10449_*10450insTT others(16): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 10450 | INFO_REALIGN_3_PRIME | chr19 | 16244882 | ||||
chr19:16244882
|
T | TTTTTTTG | 7 | a0001c0001t0033a0001c0001t0091a0001c0001t0104others(4): Show | 8 | HG01109.hp2 HG01243.hp1 HG01978.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*10449_*10450insTT others(5): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 10450 | INFO_REALIGN_3_PRIME | chr19 | 16244882 | ||||
chr19:16244882
|
T | TTTTTTTG others(3): Show |
1 | a0001c0001t0145 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10449_*10450insTT others(8): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 10450 | INFO_REALIGN_3_PRIME | chr19 | 16244882 | ||||
chr19:16244885
|
G | T | 14 | a0001c0001t0024a0001c0001t0026a0001c0001t0027others(11): Show | 20 | HG00735.hp1 HG01109.hp1 HG01884.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*10450G>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 10450 | chr19 | 16244885 | |||||
chr19:16244888
|
G | T | 1 | a0001c0001t0110 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*10453G>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 10453 | chr19 | 16244888 | |||||
chr19:16245011
|
C | T | 1 | a0001c0005t0076 | 1 | HG01346.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10576C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 10576 | chr19 | 16245011 | |||||
chr19:16245040
|
C | G | 176 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(173): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
3_prime_UTR_variant | MODIFIER | c.*10605C>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 10605 | chr19 | 16245040 | |||||
chr19:16245041
|
G | GC | 175 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(172): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
3_prime_UTR_variant | MODIFIER | c.*10606_*10607insC | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 10607 | chr19 | 16245041 | |||||
chr19:16245143
|
G | A | 54 | a0001c0001t0083a0001c0002t0002a0001c0002t0005others(51): Show | 100 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*10708G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 10708 | chr19 | 16245143 | |||||
chr19:16245148
|
G | A | 54 | a0001c0001t0083a0001c0002t0002a0001c0002t0005others(51): Show | 100 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*10713G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 10713 | chr19 | 16245148 | |||||
chr19:16245170
|
A | G | 2 | a0001c0001t0152a0001c0001t0167 | 2 | HG02055.hp2 HG02486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*10735A>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 10735 | chr19 | 16245170 | |||||
chr19:16245245
|
C | T | 1 | a0001c0001t0162 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10810C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 10810 | chr19 | 16245245 | |||||
chr19:16245275
|
C | T | 92 | a0001c0001t0001a0001c0001t0006a0001c0001t0009others(89): Show | 186 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(183): Show |
3_prime_UTR_variant | MODIFIER | c.*10840C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 10840 | chr19 | 16245275 | |||||
chr19:16245364
|
C | T | 2 | a0001c0001t0135a0001c0001t0140 | 2 | NA18944.hp2 NA18968.hp2 |
3_prime_UTR_variant | MODIFIER | c.*10929C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 10929 | chr19 | 16245364 | |||||
chr19:16245414
|
C | T | 92 | a0001c0001t0001a0001c0001t0006a0001c0001t0009others(89): Show | 186 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(183): Show |
3_prime_UTR_variant | MODIFIER | c.*10979C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 10979 | chr19 | 16245414 | |||||
chr19:16245682
|
C | G | 1 | a0001c0001t0164 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11247C>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 11247 | chr19 | 16245682 | |||||
chr19:16245710
|
T | C | 1 | a0001c0001t0089 | 1 | HG01099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11275T>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 11275 | chr19 | 16245710 | |||||
chr19:16245720
|
G | A | 33 | a0001c0001t0001a0001c0001t0006a0001c0001t0009others(30): Show | 81 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*11285G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 11285 | chr19 | 16245720 | |||||
chr19:16245739
|
G | A | 92 | a0001c0001t0001a0001c0001t0006a0001c0001t0009others(89): Show | 186 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(183): Show |
3_prime_UTR_variant | MODIFIER | c.*11304G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 11304 | chr19 | 16245739 | |||||
chr19:16245795
|
G | A | 92 | a0001c0001t0001a0001c0001t0006a0001c0001t0009others(89): Show | 186 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(183): Show |
3_prime_UTR_variant | MODIFIER | c.*11360G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 11360 | chr19 | 16245795 | |||||
chr19:16245874
|
G | T | 3 | a0001c0001t0152a0001c0001t0164a0001c0001t0167 | 3 | HG02055.hp2 HG02486.hp2 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*11439G>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 12/12 | 11439 | chr19 | 16245874 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:16198079
|
C | T | 1 | a0001c0001t0164g0293 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.42+11C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/11 | chr19 | 16198079 | ||||||
chr19:16198211
|
C | T | 1 | a0001c0001t0157g0292 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.42+143C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/11 | chr19 | 16198211 | ||||||
chr19:16198237
|
C | CG | 10 | a0001c0001t0029g0017a0001c0001t0029g0018a0001c0001t0030g0019others(7): Show | 10 | HG00735.hp1 HG01109.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.42+174dupG | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr19 | 16198237 | |||||
chr19:16198260
|
C | T | 5 | a0001c0001t0024g0289a0001c0001t0024g0290a0001c0001t0083g0288others(2): Show | 5 | HG02647.hp1 HG02896.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.42+192C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/11 | chr19 | 16198260 | ||||||
chr19:16198330
|
T | C | 1 | a0001c0001t0104g0021 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.42+262T>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/11 | chr19 | 16198330 | ||||||
chr19:16198339
|
G | C | 1 | a0001c0001t0091g0022 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.42+271G>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/11 | chr19 | 16198339 | ||||||
chr19:16198350
|
G | A | 1 | a0001c0001t0167g0023 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.42+282G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/11 | chr19 | 16198350 | ||||||
chr19:16198438
|
G | A | 3 | a0001c0001t0006g0001a0001c0001t0006g0024a0001c0001t0006g0025 | 6 | HG02145.hp1 HG02976.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.42+370G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/11 | chr19 | 16198438 | ||||||
chr19:16198546
|
C | G | 1 | a0001c0001t0166g0286 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.42+478C>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/11 | chr19 | 16198546 | ||||||
chr19:16198668
|
A | G | 1 | a0001c0002t0002g0285 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.42+600A>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/11 | chr19 | 16198668 | ||||||
chr19:16198699
|
C | T | 1 | a0001c0002t0077g0284 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.42+631C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/11 | chr19 | 16198699 | ||||||
chr19:16198738
|
G | A | 1 | a0001c0002t0002g0026 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.42+670G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/11 | chr19 | 16198738 | ||||||
chr19:16198805
|
C | CT | 72 | a0001c0001t0004g0226a0001c0001t0004g0229a0001c0001t0004g0237others(69): Show | 72 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.42+746dupT | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr19 | 16198805 | |||||
chr19:16198871
|
A | T | 10 | a0001c0001t0009g0214a0001c0001t0009g0215a0001c0001t0009g0217others(7): Show | 10 | HG01361.hp1 HG02615.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.42+803A>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/11 | chr19 | 16198871 | ||||||
chr19:16198901
|
G | C | 1 | a0001c0001t0090g0027 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.42+833G>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/11 | chr19 | 16198901 | ||||||
chr19:16199039
|
C | T | 1 | a0001c0001t0032g0283 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.42+971C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/11 | chr19 | 16199039 | ||||||
chr19:16199087
|
T | C | 249 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0037others(246): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.42+1019T>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/11 | chr19 | 16199087 | ||||||
chr19:16199112
|
A | G | 71 | a0001c0001t0004g0226a0001c0001t0004g0229a0001c0001t0004g0237others(68): Show | 71 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.42+1044A>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/11 | chr19 | 16199112 | ||||||
chr19:16199427
|
G | A | 1 | a0001c0002t0002g0028 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.42+1359G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/11 | chr19 | 16199427 | ||||||
chr19:16199516
|
G | A | 1 | a0001c0002t0002g0285 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.42+1448G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/11 | chr19 | 16199516 | ||||||
chr19:16199558
|
G | C | 1 | a0001c0002t0002g0029 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.42+1490G>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/11 | chr19 | 16199558 | ||||||
chr19:16199814
|
C | T | 170 | a0001c0001t0004g0226a0001c0001t0004g0229a0001c0001t0004g0237others(167): Show | 170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.42+1746C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/11 | chr19 | 16199814 | ||||||
chr19:16200055
|
T | C | 1 | a0001c0001t0035g0030 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.42+1987T>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/11 | chr19 | 16200055 | ||||||
chr19:16200259
|
G | A | 69 | a0001c0001t0004g0226a0001c0001t0004g0229a0001c0001t0004g0237others(66): Show | 69 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.42+2191G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/11 | chr19 | 16200259 | ||||||
chr19:16200341
|
G | C | 1 | a0001c0001t0166g0286 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.42+2273G>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/11 | chr19 | 16200341 | ||||||
chr19:16200600
|
C | T | 1 | a0001c0002t0071g0179 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.42+2532C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/11 | chr19 | 16200600 | ||||||
chr19:16200648
|
G | A | 1 | a0001c0001t0163g0031 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.42+2580G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/11 | chr19 | 16200648 | ||||||
chr19:16200661
|
G | A | 5 | a0001c0001t0124g0011a0001c0001t0125g0013a0001c0001t0126g0014others(2): Show | 5 | HG02723.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.42+2593G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/11 | chr19 | 16200661 | ||||||
chr19:16201137
|
G | A | 3 | a0001c0002t0015g0088a0001c0002t0015g0089a0001c0002t0015g0090 | 3 | NA18944.hp1 NA18964.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.43-2322G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/11 | chr19 | 16201137 | ||||||
chr19:16201290
|
G | T | 1 | a0001c0002t0060g0178 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.43-2169G>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/11 | chr19 | 16201290 | ||||||
chr19:16201388
|
C | CT | 7 | a0001c0001t0003g0212a0001c0001t0003g0213a0001c0001t0095g0211others(4): Show | 7 | HG00597.hp2 HG02451.hp1 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.43-2043dupT | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr19 | 16201388 | |||||
chr19:16201388
|
CT | C | 123 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0042others(120): Show | 131 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.43-2043delT | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr19 | 16201388 | |||||
chr19:16201388
|
CTT | C | 17 | a0001c0001t0001g0037a0001c0001t0001g0040a0001c0001t0004g0226others(14): Show | 17 | HG00099.hp2 HG00558.hp2 HG00673.hp2 others(14): Show |
intron_variant | MODIFIER | c.43-2044_43-2043del others(2): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr19 | 16201388 | |||||
chr19:16201388
|
CTTTTTTT others(9): Show |
C | 2 | a0001c0001t0153g0033a0001c0001t0165g0032 | 2 | HG01884.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.43-2058_43-2043del others(16): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr19 | 16201388 | |||||
chr19:16201439
|
G | C | 173 | a0001c0001t0004g0226a0001c0001t0004g0229a0001c0001t0004g0237others(170): Show | 173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.43-2020G>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/11 | chr19 | 16201439 | ||||||
chr19:16201456
|
TGGCACAA others(4): Show |
T | 173 | a0001c0001t0004g0226a0001c0001t0004g0229a0001c0001t0004g0237others(170): Show | 173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.43-1999_43-1989del others(11): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr19 | 16201456 | |||||
chr19:16201641
|
G | A | 2 | a0001c0001t0039g0041a0001c0001t0174g0080 | 2 | HG02257.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.43-1818G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/11 | chr19 | 16201641 | ||||||
chr19:16201846
|
C | T | 1 | a0001c0001t0159g0222 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.43-1613C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/11 | chr19 | 16201846 | ||||||
chr19:16201868
|
G | A | 1 | a0001c0001t0001g0042 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.43-1591G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/11 | chr19 | 16201868 | ||||||
chr19:16201908
|
T | C | 173 | a0001c0001t0004g0226a0001c0001t0004g0229a0001c0001t0004g0237others(170): Show | 173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.43-1551T>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/11 | chr19 | 16201908 | ||||||
chr19:16201940
|
G | A | 3 | a0001c0001t0006g0001a0001c0001t0006g0024a0001c0001t0006g0025 | 6 | HG02145.hp1 HG02976.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.43-1519G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/11 | chr19 | 16201940 | ||||||
chr19:16201986
|
G | A | 2 | a0001c0001t0037g0233a0001c0001t0037g0234 | 2 | HG02615.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.43-1473G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/11 | chr19 | 16201986 | ||||||
chr19:16202041
|
G | A | 2 | a0001c0002t0056g0102a0001c0002t0073g0091 | 2 | HG01071.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.43-1418G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/11 | chr19 | 16202041 | ||||||
chr19:16202064
|
G | A | 3 | a0001c0001t0115g0224a0001c0001t0153g0033a0001c0001t0165g0032 | 3 | HG01884.hp1 HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.43-1395G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/11 | chr19 | 16202064 | ||||||
chr19:16202121
|
C | T | 1 | a0001c0001t0001g0040 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.43-1338C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/11 | chr19 | 16202121 | ||||||
chr19:16202141
|
G | A | 1 | a0001c0001t0001g0043 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.43-1318G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/11 | chr19 | 16202141 | ||||||
chr19:16202172
|
G | A | 1 | a0001c0001t0001g0044 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.43-1287G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/11 | chr19 | 16202172 | ||||||
chr19:16202249
|
A | G | 173 | a0001c0001t0004g0226a0001c0001t0004g0229a0001c0001t0004g0237others(170): Show | 173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.43-1210A>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/11 | chr19 | 16202249 | ||||||
chr19:16202311
|
C | T | 1 | a0001c0001t0001g0078 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.43-1148C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/11 | chr19 | 16202311 | ||||||
chr19:16202395
|
T | A | 1 | a0001c0002t0002g0103 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.43-1064T>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/11 | chr19 | 16202395 | ||||||
chr19:16202417
|
C | T | 1 | a0001c0002t0021g0101 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.43-1042C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/11 | chr19 | 16202417 | ||||||
chr19:16202796
|
G | T | 2 | a0001c0001t0037g0233a0001c0001t0037g0234 | 2 | HG02615.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.43-663G>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/11 | chr19 | 16202796 | ||||||
chr19:16203113
|
C | T | 99 | a0001c0002t0002g0026a0001c0002t0002g0028a0001c0002t0002g0029others(96): Show | 99 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(96): Show |
intron_variant | MODIFIER | c.43-346C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/11 | chr19 | 16203113 | ||||||
chr19:16203313
|
G | A | 1 | a0001c0001t0084g0185 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.43-146G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 1/11 | chr19 | 16203313 | ||||||
chr19:16203728
|
C | T | 3 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0014g0039 | 3 | HG02523.hp1 NA18981.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.199+113C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 2/11 | chr19 | 16203728 | ||||||
chr19:16203891
|
C | G | 5 | a0001c0001t0115g0224a0001c0001t0152g0079a0001c0001t0153g0033others(2): Show | 5 | HG01884.hp1 HG02055.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.199+276C>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 2/11 | chr19 | 16203891 | ||||||
chr19:16203966
|
A | G | 168 | a0001c0001t0004g0226a0001c0001t0004g0229a0001c0001t0004g0237others(165): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.199+351A>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 2/11 | chr19 | 16203966 | ||||||
chr19:16203997
|
C | T | 1 | a0001c0002t0047g0174 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.199+382C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 2/11 | chr19 | 16203997 | ||||||
chr19:16203998
|
G | A | 2 | a0001c0001t0039g0041a0001c0001t0174g0080 | 2 | HG02257.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.199+383G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 2/11 | chr19 | 16203998 | ||||||
chr19:16204133
|
C | A | 42 | a0001c0001t0004g0226a0001c0001t0004g0229a0001c0001t0004g0237others(39): Show | 42 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(39): Show |
intron_variant | MODIFIER | c.199+518C>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 2/11 | chr19 | 16204133 | ||||||
chr19:16204140
|
G | T | 3 | a0001c0002t0023g0172a0001c0002t0023g0177a0001c0002t0051g0173 | 3 | HG03471.hp2 HG03540.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.199+525G>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 2/11 | chr19 | 16204140 | ||||||
chr19:16204184
|
G | A | 1 | a0001c0001t0161g0045 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.199+569G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 2/11 | chr19 | 16204184 | ||||||
chr19:16204334
|
C | G | 1 | a0001c0001t0166g0286 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.199+719C>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 2/11 | chr19 | 16204334 | ||||||
chr19:16204353
|
C | T | 4 | a0001c0001t0029g0017a0001c0001t0029g0018a0001c0001t0030g0019others(1): Show | 4 | HG00735.hp1 HG01109.hp1 HG01884.hp2 others(1): Show |
intron_variant | MODIFIER | c.199+738C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 2/11 | chr19 | 16204353 | ||||||
chr19:16204412
|
C | T | 168 | a0001c0001t0004g0226a0001c0001t0004g0229a0001c0001t0004g0237others(165): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.199+797C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 2/11 | chr19 | 16204412 | ||||||
chr19:16204428
|
C | T | 1 | a0001c0002t0002g0171 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.199+813C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 2/11 | chr19 | 16204428 | ||||||
chr19:16204578
|
C | T | 5 | a0001c0001t0115g0224a0001c0001t0152g0079a0001c0001t0153g0033others(2): Show | 5 | HG01884.hp1 HG02055.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.199+963C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 2/11 | chr19 | 16204578 | ||||||
chr19:16204712
|
G | A | 99 | a0001c0002t0002g0026a0001c0002t0002g0028a0001c0002t0002g0029others(96): Show | 99 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(96): Show |
intron_variant | MODIFIER | c.199+1097G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 2/11 | chr19 | 16204712 | ||||||
chr19:16204714
|
C | A | 6 | a0001c0002t0007g0092a0001c0002t0007g0106a0001c0002t0012g0104others(3): Show | 6 | HG00738.hp2 HG01123.hp1 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.199+1099C>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 2/11 | chr19 | 16204714 | ||||||
chr19:16204833
|
C | CT | 38 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0037others(35): Show | 42 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(39): Show |
intron_variant | MODIFIER | c.199+1233dupT | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 16204833 | |||||
chr19:16204833
|
CT | C | 154 | a0001c0001t0004g0226a0001c0001t0004g0229a0001c0001t0004g0237others(151): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.199+1233delT | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 16204833 | |||||
chr19:16204894
|
C | G | 168 | a0001c0001t0004g0226a0001c0001t0004g0229a0001c0001t0004g0237others(165): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.199+1279C>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 2/11 | chr19 | 16204894 | ||||||
chr19:16204916
|
C | T | 69 | a0001c0001t0004g0226a0001c0001t0004g0229a0001c0001t0004g0237others(66): Show | 69 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.199+1301C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 2/11 | chr19 | 16204916 | ||||||
chr19:16204944
|
C | T | 14 | a0001c0001t0039g0041a0001c0001t0039g0084a0001c0001t0040g0052others(11): Show | 14 | HG01167.hp1 HG01169.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.199+1329C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 2/11 | chr19 | 16204944 | ||||||
chr19:16204950
|
C | A | 10 | a0001c0001t0009g0214a0001c0001t0009g0215a0001c0001t0009g0217others(7): Show | 10 | HG01361.hp1 HG02615.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.199+1335C>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 2/11 | chr19 | 16204950 | ||||||
chr19:16204955
|
C | CGA | 99 | a0001c0002t0002g0026a0001c0002t0002g0028a0001c0002t0002g0029others(96): Show | 99 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(96): Show |
intron_variant | MODIFIER | c.199+1342_199+1343d others(4): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 16204955 | |||||
chr19:16205122
|
C | T | 5 | a0001c0001t0115g0224a0001c0001t0152g0079a0001c0001t0153g0033others(2): Show | 5 | HG01884.hp1 HG02055.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.200-1219C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 2/11 | chr19 | 16205122 | ||||||
chr19:16205129
|
G | A | 1 | a0001c0001t0033g0264 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.200-1212G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 2/11 | chr19 | 16205129 | ||||||
chr19:16205205
|
G | A | 2 | a0001c0001t0009g0214a0001c0001t0009g0215 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.200-1136G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 2/11 | chr19 | 16205205 | ||||||
chr19:16205341
|
A | G | 1 | a0001c0002t0060g0178 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.200-1000A>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 2/11 | chr19 | 16205341 | ||||||
chr19:16205357
|
G | A | 1 | a0001c0002t0074g0109 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.200-984G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 2/11 | chr19 | 16205357 | ||||||
chr19:16205436
|
A | G | 1 | a0001c0001t0042g0016 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.200-905A>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 2/11 | chr19 | 16205436 | ||||||
chr19:16205563
|
C | A | 1 | a0001c0002t0056g0102 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.200-778C>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 2/11 | chr19 | 16205563 | ||||||
chr19:16205587
|
C | T | 1 | a0001c0001t0008g0263 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.200-754C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 2/11 | chr19 | 16205587 | ||||||
chr19:16205669
|
A | G | 2 | a0001c0001t0001g0077a0001c0001t0014g0039 | 2 | NA18981.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.200-672A>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 2/11 | chr19 | 16205669 | ||||||
chr19:16205969
|
G | A | 12 | a0001c0001t0026g0008a0001c0001t0026g0192a0001c0001t0027g0008others(9): Show | 12 | HG01934.hp1 HG02055.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.200-372G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 2/11 | chr19 | 16205969 | ||||||
chr19:16206063
|
G | A | 39 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0037others(36): Show | 43 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.200-278G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 2/11 | chr19 | 16206063 | ||||||
chr19:16206608
|
T | TG | 98 | a0001c0002t0002g0026a0001c0002t0002g0028a0001c0002t0002g0029others(95): Show | 98 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(95): Show |
intron_variant | MODIFIER | c.267+204dupG | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 16206608 | |||||
chr19:16206668
|
T | C | 10 | a0001c0001t0009g0214a0001c0001t0009g0215a0001c0001t0009g0217others(7): Show | 10 | HG01361.hp1 HG02615.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.267+260T>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 3/11 | chr19 | 16206668 | ||||||
chr19:16206965
|
G | A | 99 | a0001c0002t0002g0026a0001c0002t0002g0028a0001c0002t0002g0029others(96): Show | 99 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(96): Show |
intron_variant | MODIFIER | c.267+557G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 3/11 | chr19 | 16206965 | ||||||
chr19:16206984
|
G | A | 1 | a0001c0002t0002g0111 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.267+576G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 3/11 | chr19 | 16206984 | ||||||
chr19:16207063
|
G | A | 99 | a0001c0002t0002g0026a0001c0002t0002g0028a0001c0002t0002g0029others(96): Show | 99 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(96): Show |
intron_variant | MODIFIER | c.267+655G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 3/11 | chr19 | 16207063 | ||||||
chr19:16207143
|
G | T | 2 | a0001c0001t0039g0084a0001c0001t0175g0083 | 2 | HG02602.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.267+735G>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 3/11 | chr19 | 16207143 | ||||||
chr19:16207345
|
T | C | 1 | a0001c0001t0127g0012 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.268-674T>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 3/11 | chr19 | 16207345 | ||||||
chr19:16207435
|
G | A | 1 | a0001c0001t0163g0031 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.268-584G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 3/11 | chr19 | 16207435 | ||||||
chr19:16207470
|
G | A | 9 | a0001c0002t0007g0092a0001c0002t0007g0106a0001c0002t0011g0093others(6): Show | 9 | HG00738.hp2 HG01123.hp1 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.268-549G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 3/11 | chr19 | 16207470 | ||||||
chr19:16207522
|
G | A | 168 | a0001c0001t0004g0226a0001c0001t0004g0229a0001c0001t0004g0237others(165): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.268-497G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 3/11 | chr19 | 16207522 | ||||||
chr19:16207523
|
A | G | 69 | a0001c0001t0004g0226a0001c0001t0004g0229a0001c0001t0004g0237others(66): Show | 69 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.268-496A>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 3/11 | chr19 | 16207523 | ||||||
chr19:16207533
|
C | T | 1 | a0001c0001t0034g0050 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.268-486C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 3/11 | chr19 | 16207533 | ||||||
chr19:16207584
|
G | A | 3 | a0001c0001t0115g0224a0001c0001t0153g0033a0001c0001t0165g0032 | 3 | HG01884.hp1 HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.268-435G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 3/11 | chr19 | 16207584 | ||||||
chr19:16207610
|
C | A | 1 | a0001c0001t0091g0022 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.268-409C>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 3/11 | chr19 | 16207610 | ||||||
chr19:16207689
|
C | G | 1 | a0001c0002t0065g0167 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.268-330C>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 3/11 | chr19 | 16207689 | ||||||
chr19:16207775
|
C | T | 1 | a0001c0001t0030g0020 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.268-244C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 3/11 | chr19 | 16207775 | ||||||
chr19:16207796
|
G | A | 2 | a0001c0001t0013g0193a0001c0001t0013g0194 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.268-223G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 3/11 | chr19 | 16207796 | ||||||
chr19:16207846
|
C | G | 1 | a0001c0001t0025g0010 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.268-173C>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 3/11 | chr19 | 16207846 | ||||||
chr19:16207885
|
C | T | 1 | a0001c0001t0001g0075 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.268-134C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 3/11 | chr19 | 16207885 | ||||||
chr19:16207886
|
A | G | 169 | a0001c0001t0001g0075a0001c0001t0004g0226a0001c0001t0004g0229others(166): Show | 169 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(166): Show |
intron_variant | MODIFIER | c.268-133A>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 3/11 | chr19 | 16207886 | ||||||
chr19:16207938
|
G | A | 1 | a0001c0001t0001g0059 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.268-81G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 3/11 | chr19 | 16207938 | ||||||
chr19:16207970
|
C | T | 70 | a0001c0001t0004g0226a0001c0001t0004g0229a0001c0001t0004g0237others(67): Show | 70 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.268-49C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 3/11 | chr19 | 16207970 | ||||||
chr19:16208001
|
C | A | 12 | a0001c0001t0026g0008a0001c0001t0026g0192a0001c0001t0027g0008others(9): Show | 12 | HG01934.hp1 HG02055.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.268-18C>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 3/11 | chr19 | 16208001 | ||||||
chr19:16208334
|
G | A | 5 | a0001c0001t0115g0224a0001c0001t0152g0079a0001c0001t0153g0033others(2): Show | 5 | HG01884.hp1 HG02055.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.398+185G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 4/11 | chr19 | 16208334 | ||||||
chr19:16208516
|
C | T | 1 | a0001c0001t0001g0074 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.398+367C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 4/11 | chr19 | 16208516 | ||||||
chr19:16208691
|
G | A | 7 | a0001c0001t0033g0264a0001c0001t0033g0276a0001c0001t0141g0267others(4): Show | 7 | HG01109.hp2 HG01243.hp1 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.399-339G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 4/11 | chr19 | 16208691 | ||||||
chr19:16208732
|
C | T | 3 | a0001c0001t0033g0264a0001c0001t0033g0276a0001c0001t0144g0269 | 3 | NA18943.hp2 NA18983.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.399-298C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 4/11 | chr19 | 16208732 | ||||||
chr19:16208814
|
A | ATTGGCTT others(18): Show |
1 | a0001c0002t0005g0094 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.399-213_399-189dup others(25): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr19 | 16208814 | |||||
chr19:16208943
|
C | G | 3 | a0001c0001t0006g0001a0001c0001t0006g0024a0001c0001t0006g0025 | 6 | HG02145.hp1 HG02976.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.399-87C>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 4/11 | chr19 | 16208943 | ||||||
chr19:16209198
|
T | C | 3 | a0001c0001t0033g0264a0001c0001t0033g0276a0001c0001t0144g0269 | 3 | NA18943.hp2 NA18983.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.546+21T>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16209198 | ||||||
chr19:16209264
|
C | G | 99 | a0001c0002t0002g0026a0001c0002t0002g0028a0001c0002t0002g0029others(96): Show | 99 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(96): Show |
intron_variant | MODIFIER | c.546+87C>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16209264 | ||||||
chr19:16209340
|
T | C | 2 | a0001c0001t0142g0266a0001c0001t0143g0265 | 2 | HG01243.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.546+163T>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16209340 | ||||||
chr19:16209370
|
G | A | 1 | a0001c0001t0162g0051 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.546+193G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16209370 | ||||||
chr19:16209487
|
C | T | 1 | a0001c0002t0058g0166 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.546+310C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16209487 | ||||||
chr19:16209578
|
G | C | 1 | a0001c0003t0098g0195 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.546+401G>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16209578 | ||||||
chr19:16209619
|
GA | G | 98 | a0001c0002t0002g0026a0001c0002t0002g0028a0001c0002t0002g0029others(95): Show | 98 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(95): Show |
intron_variant | MODIFIER | c.546+454delA | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 16209619 | |||||
chr19:16209683
|
C | T | 4 | a0001c0001t0008g0260a0001c0001t0008g0261a0001c0001t0008g0262others(1): Show | 4 | NA18947.hp1 NA18951.hp2 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.546+506C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16209683 | ||||||
chr19:16209706
|
C | G | 1 | a0001c0002t0010g0165 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.546+529C>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16209706 | ||||||
chr19:16209726
|
G | C | 3 | a0001c0001t0115g0224a0001c0001t0153g0033a0001c0001t0165g0032 | 3 | HG01884.hp1 HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.546+549G>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16209726 | ||||||
chr19:16209744
|
A | AGATCATA others(39): Show |
1 | a0001c0002t0015g0088 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.546+568_546+613dup others(46): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 16209744 | |||||
chr19:16209895
|
G | A | 1 | a0001c0001t0162g0051 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.546+718G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16209895 | ||||||
chr19:16209942
|
C | T | 168 | a0001c0001t0004g0226a0001c0001t0004g0229a0001c0001t0004g0237others(165): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.546+765C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16209942 | ||||||
chr19:16209962
|
G | A | 2 | a0001c0001t0037g0233a0001c0001t0037g0234 | 2 | HG02615.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.546+785G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16209962 | ||||||
chr19:16209979
|
T | C | 168 | a0001c0001t0004g0226a0001c0001t0004g0229a0001c0001t0004g0237others(165): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.546+802T>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16209979 | ||||||
chr19:16210163
|
T | G | 1 | a0001c0002t0061g0114 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.546+986T>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16210163 | ||||||
chr19:16210173
|
T | A | 1 | a0001c0001t0167g0023 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.546+996T>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16210173 | ||||||
chr19:16210236
|
T | C | 168 | a0001c0001t0004g0226a0001c0001t0004g0229a0001c0001t0004g0237others(165): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.546+1059T>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16210236 | ||||||
chr19:16210262
|
A | G | 69 | a0001c0001t0004g0226a0001c0001t0004g0229a0001c0001t0004g0237others(66): Show | 69 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.546+1085A>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16210262 | ||||||
chr19:16210268
|
G | T | 1 | a0001c0002t0002g0164 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.546+1091G>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16210268 | ||||||
chr19:16210269
|
T | G | 1 | a0001c0002t0002g0164 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.546+1092T>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16210269 | ||||||
chr19:16210382
|
G | A | 2 | a0001c0001t0001g0060a0001c0001t0014g0061 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.546+1205G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16210382 | ||||||
chr19:16210543
|
C | T | 2 | a0001c0001t0037g0233a0001c0001t0037g0234 | 2 | HG02615.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.546+1366C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16210543 | ||||||
chr19:16211100
|
T | TG | 152 | a0001c0001t0004g0226a0001c0001t0004g0229a0001c0001t0004g0237others(149): Show | 152 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(149): Show |
intron_variant | MODIFIER | c.546+1924dupG | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 16211100 | |||||
chr19:16211101
|
G | GGT | 15 | a0001c0001t0030g0020a0001c0001t0031g0258a0001c0001t0145g0268others(12): Show | 15 | HG00735.hp1 HG01099.hp1 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.546+1924_546+1925i others(4): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16211101 | ||||||
chr19:16211101
|
G | GT | 9 | a0001c0001t0001g0043a0001c0001t0035g0049a0001c0001t0115g0224others(6): Show | 9 | HG01433.hp2 HG01884.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.546+1936dupT | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 16211101 | |||||
chr19:16211159
|
G | GAT | 294 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0037others(291): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.546+1982_546+1983i others(4): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16211159 | ||||||
chr19:16211309
|
G | A | 1 | a0001c0001t0145g0268 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.546+2132G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16211309 | ||||||
chr19:16211373
|
C | T | 4 | a0001c0001t0003g0183a0001c0001t0089g0184a0001c0001t0097g0007others(1): Show | 4 | HG01099.hp2 HG03239.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.546+2196C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16211373 | ||||||
chr19:16211556
|
A | T | 168 | a0001c0001t0004g0226a0001c0001t0004g0229a0001c0001t0004g0237others(165): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.546+2379A>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16211556 | ||||||
chr19:16211611
|
G | A | 12 | a0001c0001t0004g0226a0001c0001t0004g0237a0001c0001t0004g0239others(9): Show | 12 | HG00423.hp2 HG00438.hp2 HG00609.hp1 others(9): Show |
intron_variant | MODIFIER | c.546+2434G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16211611 | ||||||
chr19:16211614
|
G | T | 1 | a0001c0001t0163g0031 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.546+2437G>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16211614 | ||||||
chr19:16211622
|
C | T | 1 | a0001c0002t0051g0173 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.546+2445C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16211622 | ||||||
chr19:16211881
|
A | C | 2 | a0001c0001t0020g0280a0001c0001t0036g0281 | 2 | HG02647.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.546+2704A>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16211881 | ||||||
chr19:16212136
|
C | T | 10 | a0001c0001t0009g0214a0001c0001t0009g0215a0001c0001t0009g0217others(7): Show | 10 | HG01361.hp1 HG02615.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.546+2959C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16212136 | ||||||
chr19:16212248
|
T | G | 1 | a0001c0002t0068g0115 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.546+3071T>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16212248 | ||||||
chr19:16212412
|
G | A | 1 | a0001c0002t0063g0116 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.546+3235G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16212412 | ||||||
chr19:16212484
|
T | C | 1 | a0001c0001t0008g0228 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.546+3307T>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16212484 | ||||||
chr19:16212485
|
C | T | 1 | a0001c0001t0008g0228 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.546+3308C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16212485 | ||||||
chr19:16212486
|
T | G | 1 | a0001c0001t0008g0228 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.546+3309T>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16212486 | ||||||
chr19:16212515
|
C | T | 2 | a0001c0001t0003g0212a0001c0001t0003g0213 | 2 | HG03927.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.546+3338C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16212515 | ||||||
chr19:16212646
|
A | G | 3 | a0001c0001t0004g0256a0001c0001t0004g0257a0001c0001t0146g0255 | 3 | HG02015.hp1 NA18964.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.546+3469A>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16212646 | ||||||
chr19:16212653
|
G | A | 1 | a0001c0001t0166g0286 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.546+3476G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16212653 | ||||||
chr19:16212731
|
T | G | 3 | a0001c0001t0115g0224a0001c0001t0153g0033a0001c0001t0165g0032 | 3 | HG01884.hp1 HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.546+3554T>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16212731 | ||||||
chr19:16212762
|
C | T | 247 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0037others(244): Show | 255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.546+3585C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16212762 | ||||||
chr19:16212767
|
C | T | 4 | a0001c0001t0029g0017a0001c0001t0029g0018a0001c0001t0030g0019others(1): Show | 4 | HG00735.hp1 HG01109.hp1 HG01884.hp2 others(1): Show |
intron_variant | MODIFIER | c.546+3590C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16212767 | ||||||
chr19:16212782
|
C | G | 2 | a0001c0001t0152g0079a0001c0001t0167g0023 | 2 | HG02055.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.546+3605C>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16212782 | ||||||
chr19:16212855
|
CA | C | 3 | a0001c0001t0008g0228a0001c0001t0139g0275a0001c0002t0015g0088 | 3 | NA18964.hp1 NA19056.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.546+3682delA | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 16212855 | |||||
chr19:16212910
|
T | C | 168 | a0001c0001t0004g0226a0001c0001t0004g0229a0001c0001t0004g0237others(165): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.546+3733T>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16212910 | ||||||
chr19:16213126
|
T | A | 3 | a0001c0002t0023g0172a0001c0002t0023g0177a0001c0002t0051g0173 | 3 | HG03471.hp2 HG03540.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.546+3949T>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16213126 | ||||||
chr19:16213265
|
G | C | 1 | a0001c0001t0118g0282 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.546+4088G>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16213265 | ||||||
chr19:16213271
|
T | C | 168 | a0001c0001t0004g0226a0001c0001t0004g0229a0001c0001t0004g0237others(165): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.546+4094T>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16213271 | ||||||
chr19:16213352
|
CT | C | 3 | a0001c0002t0015g0088a0001c0002t0015g0089a0001c0002t0072g0168 | 3 | NA18964.hp1 NA18988.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.546+4182delT | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 16213352 | |||||
chr19:16213401
|
T | C | 168 | a0001c0001t0004g0226a0001c0001t0004g0229a0001c0001t0004g0237others(165): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.546+4224T>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16213401 | ||||||
chr19:16213428
|
A | G | 1 | a0001c0001t0166g0286 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.546+4251A>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16213428 | ||||||
chr19:16213506
|
T | C | 13 | a0001c0001t0039g0041a0001c0001t0039g0084a0001c0001t0040g0052others(10): Show | 13 | HG01167.hp1 HG01169.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.546+4329T>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16213506 | ||||||
chr19:16213603
|
T | C | 5 | a0001c0001t0124g0011a0001c0001t0125g0013a0001c0001t0126g0014others(2): Show | 5 | HG02723.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.546+4426T>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16213603 | ||||||
chr19:16213718
|
C | T | 10 | a0001c0001t0009g0214a0001c0001t0009g0215a0001c0001t0009g0217others(7): Show | 10 | HG01361.hp1 HG02615.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.546+4541C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16213718 | ||||||
chr19:16213955
|
A | T | 1 | a0001c0001t0092g0205 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.546+4778A>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16213955 | ||||||
chr19:16213959
|
T | C | 2 | a0001c0001t0008g0228a0001c0001t0032g0283 | 2 | HG02132.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.546+4782T>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16213959 | ||||||
chr19:16214044
|
T | C | 1 | a0001c0001t0029g0017 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.546+4867T>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16214044 | ||||||
chr19:16214046
|
C | T | 1 | a0001c0001t0029g0017 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.546+4869C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16214046 | ||||||
chr19:16214052
|
C | CTTT | 127 | a0001c0001t0004g0226a0001c0001t0004g0229a0001c0001t0004g0237others(124): Show | 127 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(124): Show |
intron_variant | MODIFIER | c.546+4887_546+4889d others(5): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 16214052 | |||||
chr19:16214052
|
C | CTTTT | 37 | a0001c0001t0004g0241a0001c0001t0004g0252a0001c0001t0004g0253others(34): Show | 37 | HG00423.hp2 HG00673.hp1 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.546+4886_546+4889d others(6): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 16214052 | |||||
chr19:16214052
|
C | T | 1 | a0001c0001t0029g0017 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.546+4875C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16214052 | ||||||
chr19:16214081
|
C | T | 2 | a0001c0001t0001g0043a0001c0001t0035g0049 | 2 | HG02809.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.546+4904C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16214081 | ||||||
chr19:16214178
|
A | G | 5 | a0001c0001t0024g0289a0001c0001t0024g0290a0001c0001t0083g0288others(2): Show | 5 | HG02647.hp1 HG02896.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.546+5001A>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16214178 | ||||||
chr19:16214213
|
T | A | 1 | a0001c0001t0034g0048 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.546+5036T>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16214213 | ||||||
chr19:16214293
|
G | A | 4 | a0001c0002t0005g0119a0001c0002t0005g0161a0001c0002t0055g0120others(1): Show | 4 | HG03239.hp1 HG03834.hp2 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.546+5116G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16214293 | ||||||
chr19:16214316
|
C | G | 1 | a0001c0001t0164g0293 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.546+5139C>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16214316 | ||||||
chr19:16214353
|
G | A | 1 | a0001c0001t0162g0051 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.546+5176G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16214353 | ||||||
chr19:16214356
|
C | CT | 8 | a0001c0001t0001g0073a0001c0001t0003g0204a0001c0001t0095g0211others(5): Show | 8 | HG01928.hp1 HG02486.hp2 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.546+5192dupT | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 16214356 | |||||
chr19:16214356
|
C | CTT | 146 | a0001c0001t0004g0229a0001c0001t0004g0237a0001c0001t0004g0239others(143): Show | 146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): Show |
intron_variant | MODIFIER | c.546+5191_546+5192d others(4): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 16214356 | |||||
chr19:16214356
|
C | CTTT | 17 | a0001c0001t0004g0226a0001c0001t0020g0279a0001c0001t0030g0019others(14): Show | 17 | HG00544.hp1 HG01069.hp1 HG01358.hp1 others(14): Show |
intron_variant | MODIFIER | c.546+5190_546+5192d others(5): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 16214356 | |||||
chr19:16214356
|
C | T | 1 | a0001c0002t0016g0160 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.546+5179C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16214356 | ||||||
chr19:16214512
|
C | T | 167 | a0001c0001t0004g0226a0001c0001t0004g0229a0001c0001t0004g0237others(164): Show | 167 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(164): Show |
intron_variant | MODIFIER | c.546+5335C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16214512 | ||||||
chr19:16214691
|
C | A | 174 | a0001c0001t0004g0226a0001c0001t0004g0229a0001c0001t0004g0237others(171): Show | 174 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(171): Show |
intron_variant | MODIFIER | c.546+5514C>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16214691 | ||||||
chr19:16214729
|
C | T | 1 | a0001c0001t0004g0226 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.546+5552C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16214729 | ||||||
chr19:16214744
|
C | A | 3 | a0001c0001t0115g0224a0001c0001t0153g0033a0001c0001t0165g0032 | 3 | HG01884.hp1 HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.546+5567C>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16214744 | ||||||
chr19:16214759
|
T | G | 5 | a0001c0001t0115g0224a0001c0001t0152g0079a0001c0001t0153g0033others(2): Show | 5 | HG01884.hp1 HG02055.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.546+5582T>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16214759 | ||||||
chr19:16214810
|
A | T | 3 | a0001c0001t0115g0224a0001c0001t0153g0033a0001c0001t0165g0032 | 3 | HG01884.hp1 HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.546+5633A>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16214810 | ||||||
chr19:16214910
|
G | T | 1 | a0001c0001t0166g0286 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.546+5733G>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16214910 | ||||||
chr19:16214950
|
T | C | 1 | a0001c0001t0013g0206 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.546+5773T>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16214950 | ||||||
chr19:16215053
|
A | G | 40 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0037others(37): Show | 44 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.546+5876A>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16215053 | ||||||
chr19:16215087
|
G | T | 168 | a0001c0001t0004g0226a0001c0001t0004g0229a0001c0001t0004g0237others(165): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.546+5910G>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16215087 | ||||||
chr19:16215190
|
A | G | 168 | a0001c0001t0004g0226a0001c0001t0004g0229a0001c0001t0004g0237others(165): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.546+6013A>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16215190 | ||||||
chr19:16215191
|
A | AGGCAGG | 12 | a0001c0001t0123g0259a0001c0001t0146g0255a0001c0002t0002g0135others(9): Show | 12 | HG01074.hp1 HG01074.hp2 HG01192.hp1 others(9): Show |
intron_variant | MODIFIER | c.546+6017_546+6018i others(8): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 16215191 | |||||
chr19:16215194
|
C | CAGGGGCG | 8 | a0001c0001t0149g0231a0001c0002t0002g0100a0001c0002t0002g0157others(5): Show | 8 | HG00099.hp2 HG01099.hp1 HG02165.hp1 others(5): Show |
intron_variant | MODIFIER | c.546+6017_546+6018i others(9): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16215194 | ||||||
chr19:16215194
|
C | CAGGGGCG others(1): Show |
9 | a0001c0001t0004g0256a0001c0001t0008g0260a0001c0001t0131g0236others(6): Show | 9 | HG01169.hp1 HG01433.hp2 HG03688.hp2 others(6): Show |
intron_variant | MODIFIER | c.546+6017_546+6018i others(10): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16215194 | ||||||
chr19:16215194
|
C | CAGGGGCG others(2): Show |
4 | a0001c0001t0008g0261a0001c0002t0002g0155a0001c0002t0002g0164others(1): Show | 4 | NA18971.hp2 NA19002.hp2 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.546+6017_546+6018i others(11): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16215194 | ||||||
chr19:16215194
|
C | CAGGGGCG others(3): Show |
7 | a0001c0001t0004g0241a0001c0001t0004g0257a0001c0001t0008g0262others(4): Show | 7 | HG00423.hp2 HG01361.hp2 HG02015.hp1 others(4): Show |
intron_variant | MODIFIER | c.546+6017_546+6018i others(12): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16215194 | ||||||
chr19:16215194
|
C | CAGGGGCG others(4): Show |
4 | a0001c0001t0136g0250a0001c0001t0139g0275a0001c0002t0002g0171others(1): Show | 4 | HG03710.hp1 NA18939.hp2 NA18947.hp2 others(1): Show |
intron_variant | MODIFIER | c.546+6017_546+6018i others(13): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16215194 | ||||||
chr19:16215194
|
C | CAGGGGCG others(5): Show |
1 | a0001c0002t0052g0098 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.546+6017_546+6018i others(14): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16215194 | ||||||
chr19:16215194
|
C | CAGGGGCG others(7): Show |
1 | a0001c0002t0005g0094 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.546+6017_546+6018i others(16): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16215194 | ||||||
chr19:16215194
|
C | CAGGGGCG others(6): Show |
2 | a0001c0001t0037g0233a0001c0001t0129g0232 | 2 | HG02895.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.546+6017_546+6018i others(15): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16215194 | ||||||
chr19:16215194
|
C | CAGGGGCG others(7): Show |
6 | a0001c0001t0004g0237a0001c0001t0031g0258a0001c0001t0134g0243others(3): Show | 6 | HG00609.hp1 HG01358.hp1 HG01928.hp2 others(3): Show |
intron_variant | MODIFIER | c.546+6017_546+6018i others(16): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16215194 | ||||||
chr19:16215194
|
C | CAGGGGCG others(8): Show |
7 | a0001c0001t0004g0226a0001c0001t0008g0228a0001c0001t0008g0263others(4): Show | 7 | HG01069.hp1 HG02080.hp2 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.546+6017_546+6018i others(17): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16215194 | ||||||
chr19:16215194
|
C | CAGGGGCG others(9): Show |
1 | a0001c0001t0032g0283 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.546+6017_546+6018i others(18): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16215194 | ||||||
chr19:16215194
|
C | CAGGGGCG others(10): Show |
3 | a0001c0001t0004g0239a0001c0001t0130g0225a0001c0001t0147g0240 | 3 | NA18945.hp1 NA18949.hp2 NA18997.hp2 |
intron_variant | MODIFIER | c.546+6017_546+6018i others(19): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16215194 | ||||||
chr19:16215194
|
C | CAGGGGCG others(11): Show |
1 | a0001c0001t0151g0227 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.546+6017_546+6018i others(20): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16215194 | ||||||
chr19:16215194
|
C | CAGGGGCG others(13): Show |
1 | a0001c0002t0072g0168 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.546+6017_546+6018i others(22): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16215194 | ||||||
chr19:16215194
|
C | CAGGGGCG others(14): Show |
1 | a0001c0001t0004g0253 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.546+6017_546+6018i others(23): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16215194 | ||||||
chr19:16215194
|
C | CAGGGGGC others(3): Show |
1 | a0001c0002t0069g0162 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.546+6017_546+6018i others(12): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16215194 | ||||||
chr19:16215195
|
G | A | 96 | a0001c0001t0001g0078a0001c0001t0004g0229a0001c0001t0004g0252others(93): Show | 96 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.546+6018G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16215195 | ||||||
chr19:16215200
|
C | CG | 30 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0071others(27): Show | 31 | HG00544.hp2 HG01258.hp2 HG01361.hp1 others(28): Show |
intron_variant | MODIFIER | c.546+6034dupG | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 16215200 | |||||
chr19:16215200
|
C | CGG | 20 | a0001c0001t0003g0181a0001c0001t0020g0278a0001c0001t0024g0289others(17): Show | 20 | HG00738.hp1 HG01257.hp1 HG01358.hp2 others(17): Show |
intron_variant | MODIFIER | c.546+6033_546+6034d others(4): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 16215200 | |||||
chr19:16215200
|
C | CGGG | 17 | a0001c0001t0018g0072a0001c0001t0020g0279a0001c0001t0039g0084others(14): Show | 17 | HG00140.hp1 HG00423.hp1 HG01261.hp1 others(14): Show |
intron_variant | MODIFIER | c.546+6032_546+6034d others(5): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 16215200 | |||||
chr19:16215200
|
C | G | 74 | a0001c0001t0004g0226a0001c0001t0004g0237a0001c0001t0004g0239others(71): Show | 74 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(71): Show |
intron_variant | MODIFIER | c.546+6023C>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16215200 | ||||||
chr19:16215200
|
CG | C | 32 | a0001c0001t0001g0005a0001c0001t0001g0040a0001c0001t0001g0060others(29): Show | 33 | HG00558.hp2 HG01069.hp2 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.546+6034delG | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 16215200 | |||||
chr19:16215206
|
G | A | 1 | a0001c0001t0133g0235 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.546+6029G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16215206 | ||||||
chr19:16215207
|
G | GGGGGGGG others(5): Show |
1 | a0001c0001t0004g0252 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.546+6034_546+6035i others(14): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 16215207 | |||||
chr19:16215207
|
GGGGGAGA others(7): Show |
G | 1 | a0001c0001t0133g0235 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.546+6035_546+6048d others(16): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 16215207 | |||||
chr19:16215209
|
G | GGGGGGGG others(21): Show |
1 | a0001c0001t0117g0244 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.546+6034_546+6035i others(30): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 16215209 | |||||
chr19:16215210
|
G | A | 1 | a0001c0001t0167g0023 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.546+6033G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16215210 | ||||||
chr19:16215210
|
G | GGGGGGGG others(13): Show |
1 | a0001c0001t0132g0230 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.546+6034_546+6035i others(22): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 16215210 | |||||
chr19:16215210
|
G | GGGGGGGG others(14): Show |
1 | a0001c0001t0116g0251 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.546+6034_546+6035i others(23): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 16215210 | |||||
chr19:16215210
|
GGAGAGGG others(11): Show |
G | 1 | a0001c0001t0041g0246 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.546+6035_546+6052d others(20): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 16215210 | |||||
chr19:16215211
|
GA | G | 3 | a0001c0001t0162g0051a0001c0002t0007g0092a0001c0002t0078g0108 | 3 | HG01123.hp1 HG01256.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.546+6035delA | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16215211 | ||||||
chr19:16215212
|
A | G | 153 | a0001c0001t0004g0226a0001c0001t0004g0229a0001c0001t0004g0237others(150): Show | 153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.546+6035A>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16215212 | ||||||
chr19:16215213
|
G | A | 1 | a0001c0001t0115g0224 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.546+6036G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16215213 | ||||||
chr19:16215214
|
A | G | 158 | a0001c0001t0001g0076a0001c0001t0004g0226a0001c0001t0004g0229others(155): Show | 158 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(155): Show |
intron_variant | MODIFIER | c.546+6037A>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16215214 | ||||||
chr19:16215214
|
AG | A | 6 | a0001c0001t0009g0214a0001c0001t0009g0217a0001c0001t0159g0222others(3): Show | 6 | HG01361.hp1 HG02723.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.546+6043delG | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 16215214 | |||||
chr19:16215216
|
G | GGGGGGGG others(5): Show |
1 | a0001c0001t0030g0019 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.546+6043_546+6044i others(14): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 16215216 | |||||
chr19:16215216
|
G | GGGGGGGG others(6): Show |
1 | a0001c0001t0037g0234 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.546+6043_546+6044i others(15): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 16215216 | |||||
chr19:16215216
|
G | GGGGGGGG others(9): Show |
1 | a0001c0001t0029g0017 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.546+6043_546+6044i others(18): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 16215216 | |||||
chr19:16215219
|
G | GGGGGGGG others(4): Show |
1 | a0001c0002t0016g0156 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.546+6043_546+6044i others(13): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 16215219 | |||||
chr19:16215220
|
G | A | 4 | a0001c0001t0001g0076a0001c0001t0009g0215a0001c0001t0009g0218others(1): Show | 4 | HG02523.hp1 HG02615.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.546+6043G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16215220 | ||||||
chr19:16215220
|
G | GGGGGGGG others(7): Show |
1 | a0001c0001t0042g0016 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.546+6043_546+6044i others(16): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16215220 | ||||||
chr19:16215220
|
G | GGGGGGGG others(5): Show |
1 | a0001c0002t0071g0179 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.546+6043_546+6044i others(14): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16215220 | ||||||
chr19:16215220
|
G | GGGGGGGG others(11): Show |
1 | a0001c0001t0030g0020 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.546+6043_546+6044i others(20): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16215220 | ||||||
chr19:16215220
|
G | GGGGGGGG others(9): Show |
1 | a0001c0002t0002g0103 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.546+6043_546+6044i others(18): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16215220 | ||||||
chr19:16215221
|
A | G | 31 | a0001c0001t0001g0076a0001c0001t0004g0253a0001c0001t0009g0215others(28): Show | 31 | HG00673.hp1 HG00735.hp1 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.546+6044A>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16215221 | ||||||
chr19:16215221
|
A | T | 1 | a0001c0002t0071g0179 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.546+6044A>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16215221 | ||||||
chr19:16215222
|
G | C | 1 | a0001c0002t0045g0122 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.546+6045G>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16215222 | ||||||
chr19:16215223
|
G | GGGGGGGG others(14): Show |
1 | a0001c0002t0060g0178 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.546+6050_546+6051i others(23): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 16215223 | |||||
chr19:16215233
|
A | G | 1 | a0001c0001t0041g0246 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.546+6056A>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16215233 | ||||||
chr19:16215237
|
G | GA | 3 | a0001c0001t0115g0224a0001c0001t0153g0033a0001c0001t0165g0032 | 3 | HG01884.hp1 HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.546+6061dupA | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 16215237 | |||||
chr19:16215284
|
A | C | 1 | a0001c0001t0139g0275 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.546+6107A>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16215284 | ||||||
chr19:16215333
|
T | C | 1 | a0001c0001t0029g0017 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.546+6156T>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16215333 | ||||||
chr19:16215334
|
G | T | 1 | a0001c0001t0029g0017 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.546+6157G>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16215334 | ||||||
chr19:16215335
|
C | G | 1 | a0001c0001t0029g0017 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.546+6158C>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16215335 | ||||||
chr19:16215391
|
G | C | 1 | a0001c0001t0029g0017 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.546+6214G>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16215391 | ||||||
chr19:16215392
|
C | G | 1 | a0001c0001t0029g0017 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.546+6215C>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16215392 | ||||||
chr19:16215392
|
C | T | 12 | a0001c0001t0039g0041a0001c0001t0039g0084a0001c0001t0040g0052others(9): Show | 12 | HG01167.hp1 HG01169.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.546+6215C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16215392 | ||||||
chr19:16215400
|
G | A | 99 | a0001c0002t0002g0026a0001c0002t0002g0028a0001c0002t0002g0029others(96): Show | 99 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(96): Show |
intron_variant | MODIFIER | c.546+6223G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16215400 | ||||||
chr19:16215463
|
C | CA | 25 | a0001c0001t0001g0037a0001c0001t0004g0229a0001c0001t0013g0206others(22): Show | 25 | HG00597.hp2 HG00673.hp2 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.546+6315dupA | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 16215463 | |||||
chr19:16215463
|
C | CAA | 6 | a0001c0001t0164g0293a0001c0002t0002g0028a0001c0002t0002g0164others(3): Show | 6 | HG03209.hp2 NA18947.hp2 NA18955.hp2 others(3): Show |
intron_variant | MODIFIER | c.546+6314_546+6315d others(4): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 16215463 | |||||
chr19:16215463
|
CA | C | 127 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0040others(124): Show | 135 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.546+6315delA | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 16215463 | |||||
chr19:16215463
|
CAA | C | 35 | a0001c0001t0001g0071a0001c0001t0004g0226a0001c0001t0008g0228others(32): Show | 36 | HG01069.hp1 HG01109.hp1 HG01256.hp2 others(33): Show |
intron_variant | MODIFIER | c.546+6314_546+6315d others(4): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 16215463 | |||||
chr19:16215463
|
CAAAAAAA others(1): Show |
C | 11 | a0001c0001t0004g0241a0001c0001t0009g0214a0001c0001t0009g0215others(8): Show | 11 | HG00423.hp2 HG01361.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.546+6308_546+6315d others(10): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 16215463 | |||||
chr19:16215463
|
CAAAAAAA others(7): Show |
C | 2 | a0001c0001t0037g0233a0001c0001t0037g0234 | 2 | HG02615.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.546+6302_546+6315d others(16): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 16215463 | |||||
chr19:16215467
|
A | T | 1 | a0001c0002t0074g0109 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.546+6290A>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16215467 | ||||||
chr19:16215496
|
T | TGTTTAAT others(3): Show |
1 | a0001c0001t0030g0020 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.546+6321_546+6330d others(12): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 16215496 | |||||
chr19:16215622
|
T | C | 5 | a0001c0001t0115g0224a0001c0001t0152g0079a0001c0001t0153g0033others(2): Show | 5 | HG01884.hp1 HG02055.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.546+6445T>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16215622 | ||||||
chr19:16215855
|
G | A | 7 | a0001c0001t0033g0264a0001c0001t0033g0276a0001c0001t0141g0267others(4): Show | 7 | HG01109.hp2 HG01243.hp1 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.546+6678G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16215855 | ||||||
chr19:16215869
|
G | A | 1 | a0001c0001t0162g0051 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.546+6692G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16215869 | ||||||
chr19:16216005
|
T | C | 2 | a0001c0001t0013g0193a0001c0001t0013g0194 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.546+6828T>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16216005 | ||||||
chr19:16216077
|
T | TATGATTC others(3): Show |
1 | a0001c0002t0002g0135 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.546+6902_546+6903i others(12): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 16216077 | |||||
chr19:16216080
|
A | G | 222 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0037others(219): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.546+6903A>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16216080 | ||||||
chr19:16216080
|
A | T | 1 | a0001c0001t0001g0075 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.546+6903A>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16216080 | ||||||
chr19:16216211
|
C | T | 1 | a0001c0001t0027g0191 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.546+7034C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16216211 | ||||||
chr19:16216212
|
A | G | 1 | a0001c0001t0027g0191 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.546+7035A>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16216212 | ||||||
chr19:16216220
|
C | T | 69 | a0001c0001t0004g0226a0001c0001t0004g0229a0001c0001t0004g0237others(66): Show | 69 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.546+7043C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16216220 | ||||||
chr19:16216272
|
C | A | 1 | a0001c0002t0002g0125 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.546+7095C>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16216272 | ||||||
chr19:16216348
|
G | A | 1 | a0001c0001t0100g0208 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.546+7171G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16216348 | ||||||
chr19:16216355
|
G | C | 1 | a0001c0001t0084g0185 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.546+7178G>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16216355 | ||||||
chr19:16216404
|
C | A | 1 | a0001c0001t0008g0228 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.546+7227C>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16216404 | ||||||
chr19:16216405
|
A | C | 1 | a0001c0001t0008g0228 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.546+7228A>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16216405 | ||||||
chr19:16216444
|
C | CA | 6 | a0001c0001t0037g0234a0001c0001t0139g0275a0001c0001t0162g0051others(3): Show | 6 | HG02135.hp1 HG02615.hp1 NA18943.hp1 others(3): Show |
intron_variant | MODIFIER | c.546+7281dupA | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 16216444 | |||||
chr19:16216444
|
CA | C | 8 | a0001c0001t0008g0228a0001c0001t0036g0281a0001c0001t0111g0190others(5): Show | 8 | HG01167.hp2 HG01257.hp1 HG01928.hp1 others(5): Show |
intron_variant | MODIFIER | c.546+7281delA | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 16216444 | |||||
chr19:16216478
|
A | G | 40 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0037others(37): Show | 44 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.546+7301A>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16216478 | ||||||
chr19:16216505
|
C | G | 1 | a0001c0001t0024g0290 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.546+7328C>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16216505 | ||||||
chr19:16216507
|
G | T | 1 | a0001c0001t0008g0228 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.546+7330G>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16216507 | ||||||
chr19:16216531
|
T | G | 1 | a0001c0002t0112g0151 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.546+7354T>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16216531 | ||||||
chr19:16216570
|
T | C | 167 | a0001c0001t0004g0226a0001c0001t0004g0229a0001c0001t0004g0237others(164): Show | 167 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(164): Show |
intron_variant | MODIFIER | c.546+7393T>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16216570 | ||||||
chr19:16216788
|
G | T | 1 | a0001c0001t0008g0228 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.546+7611G>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16216788 | ||||||
chr19:16216944
|
T | C | 168 | a0001c0001t0004g0226a0001c0001t0004g0229a0001c0001t0004g0237others(165): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.546+7767T>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16216944 | ||||||
chr19:16216972
|
G | T | 1 | a0001c0002t0072g0168 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.546+7795G>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16216972 | ||||||
chr19:16217051
|
G | A | 1 | a0001c0001t0159g0222 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.546+7874G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16217051 | ||||||
chr19:16217118
|
G | A | 10 | a0001c0001t0009g0214a0001c0001t0009g0215a0001c0001t0009g0217others(7): Show | 10 | HG01361.hp1 HG02615.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.546+7941G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16217118 | ||||||
chr19:16217234
|
A | C | 249 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0037others(246): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.546+8057A>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16217234 | ||||||
chr19:16217263
|
A | G | 1 | a0001c0001t0168g0221 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.546+8086A>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16217263 | ||||||
chr19:16217421
|
A | T | 1 | a0001c0001t0008g0228 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.546+8244A>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16217421 | ||||||
chr19:16217466
|
A | G | 1 | a0001c0002t0023g0172 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.546+8289A>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16217466 | ||||||
chr19:16217516
|
G | C | 1 | a0001c0002t0081g0118 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.546+8339G>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16217516 | ||||||
chr19:16217520
|
G | A | 5 | a0001c0001t0115g0224a0001c0001t0152g0079a0001c0001t0153g0033others(2): Show | 5 | HG01884.hp1 HG02055.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.546+8343G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16217520 | ||||||
chr19:16217546
|
G | A | 13 | a0001c0001t0039g0041a0001c0001t0039g0084a0001c0001t0040g0052others(10): Show | 13 | HG01167.hp1 HG01169.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.546+8369G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16217546 | ||||||
chr19:16217577
|
C | T | 69 | a0001c0001t0004g0226a0001c0001t0004g0229a0001c0001t0004g0237others(66): Show | 69 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.546+8400C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16217577 | ||||||
chr19:16217632
|
C | G | 1 | a0001c0002t0002g0164 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.546+8455C>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16217632 | ||||||
chr19:16217753
|
C | T | 44 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0037others(41): Show | 49 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(46): Show |
intron_variant | MODIFIER | c.546+8576C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16217753 | ||||||
chr19:16217871
|
C | T | 69 | a0001c0001t0004g0226a0001c0001t0004g0229a0001c0001t0004g0237others(66): Show | 69 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.547-8550C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16217871 | ||||||
chr19:16218157
|
C | T | 1 | a0001c0002t0002g0125 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.547-8264C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16218157 | ||||||
chr19:16218180
|
G | A | 69 | a0001c0001t0004g0226a0001c0001t0004g0229a0001c0001t0004g0237others(66): Show | 69 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.547-8241G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16218180 | ||||||
chr19:16218242
|
A | C | 42 | a0001c0001t0004g0226a0001c0001t0004g0229a0001c0001t0004g0237others(39): Show | 42 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(39): Show |
intron_variant | MODIFIER | c.547-8179A>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16218242 | ||||||
chr19:16218288
|
A | G | 1 | a0001c0002t0002g0103 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.547-8133A>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16218288 | ||||||
chr19:16218487
|
T | C | 173 | a0001c0001t0004g0226a0001c0001t0004g0229a0001c0001t0004g0237others(170): Show | 173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.547-7934T>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16218487 | ||||||
chr19:16218557
|
G | A | 168 | a0001c0001t0004g0226a0001c0001t0004g0229a0001c0001t0004g0237others(165): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.547-7864G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16218557 | ||||||
chr19:16218571
|
C | G | 1 | a0001c0002t0066g0112 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.547-7850C>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16218571 | ||||||
chr19:16218825
|
C | T | 1 | a0001c0002t0005g0094 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.547-7596C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16218825 | ||||||
chr19:16218826
|
T | C | 1 | a0001c0002t0005g0094 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.547-7595T>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16218826 | ||||||
chr19:16219064
|
G | GT | 72 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0037others(69): Show | 80 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(77): Show |
intron_variant | MODIFIER | c.547-7342dupT | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 16219064 | |||||
chr19:16219064
|
GT | G | 87 | a0001c0001t0004g0226a0001c0001t0004g0229a0001c0001t0004g0237others(84): Show | 87 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.547-7342delT | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 16219064 | |||||
chr19:16219068
|
T | G | 1 | a0001c0003t0098g0195 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.547-7353T>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16219068 | ||||||
chr19:16219086
|
G | T | 1 | a0001c0001t0025g0010 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.547-7335G>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16219086 | ||||||
chr19:16219126
|
A | G | 168 | a0001c0001t0004g0226a0001c0001t0004g0229a0001c0001t0004g0237others(165): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.547-7295A>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16219126 | ||||||
chr19:16219232
|
A | G | 168 | a0001c0001t0004g0226a0001c0001t0004g0229a0001c0001t0004g0237others(165): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.547-7189A>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16219232 | ||||||
chr19:16219363
|
C | A | 1 | a0001c0001t0032g0273 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.547-7058C>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16219363 | ||||||
chr19:16219397
|
TG | T | 150 | a0001c0001t0004g0226a0001c0001t0004g0229a0001c0001t0004g0237others(147): Show | 150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): Show |
intron_variant | MODIFIER | c.547-7023delG | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16219397 | ||||||
chr19:16219398
|
G | GT | 6 | a0001c0001t0001g0042a0001c0001t0001g0070a0001c0001t0003g0213others(3): Show | 6 | HG00544.hp2 HG02630.hp2 HG03669.hp1 others(3): Show |
intron_variant | MODIFIER | c.547-7007dupT | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 16219398 | |||||
chr19:16219398
|
G | T | 15 | a0001c0001t0029g0017a0001c0001t0030g0020a0001c0001t0032g0283others(12): Show | 15 | HG00735.hp1 HG01109.hp1 HG01255.hp1 others(12): Show |
intron_variant | MODIFIER | c.547-7023G>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16219398 | ||||||
chr19:16219400
|
T | G | 9 | a0001c0001t0029g0017a0001c0001t0042g0016a0001c0001t0119g0271others(6): Show | 9 | HG01109.hp1 HG01361.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.547-7021T>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16219400 | ||||||
chr19:16219401
|
T | G | 156 | a0001c0001t0004g0226a0001c0001t0004g0229a0001c0001t0004g0237others(153): Show | 156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.547-7020T>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16219401 | ||||||
chr19:16219402
|
T | G | 1 | a0001c0002t0002g0125 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.547-7019T>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16219402 | ||||||
chr19:16219406
|
T | G | 1 | a0001c0001t0001g0069 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.547-7015T>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16219406 | ||||||
chr19:16219407
|
T | C | 1 | a0001c0002t0080g0176 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.547-7014T>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16219407 | ||||||
chr19:16219428
|
G | A | 2 | a0001c0001t0001g0070a0001c0001t0001g0075 | 2 | HG03834.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.547-6993G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16219428 | ||||||
chr19:16219544
|
C | T | 69 | a0001c0001t0004g0226a0001c0001t0004g0229a0001c0001t0004g0237others(66): Show | 69 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.547-6877C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16219544 | ||||||
chr19:16219558
|
C | T | 2 | a0001c0002t0069g0162a0001c0003t0098g0195 | 2 | HG01891.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.547-6863C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16219558 | ||||||
chr19:16219607
|
A | C | 10 | a0001c0001t0009g0214a0001c0001t0009g0215a0001c0001t0009g0217others(7): Show | 10 | HG01361.hp1 HG02615.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.547-6814A>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16219607 | ||||||
chr19:16219734
|
T | C | 173 | a0001c0001t0004g0226a0001c0001t0004g0229a0001c0001t0004g0237others(170): Show | 173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.547-6687T>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16219734 | ||||||
chr19:16220005
|
G | A | 46 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0037others(43): Show | 51 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(48): Show |
intron_variant | MODIFIER | c.547-6416G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16220005 | ||||||
chr19:16220013
|
T | C | 1 | a0001c0001t0089g0184 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.547-6408T>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16220013 | ||||||
chr19:16220037
|
G | A | 168 | a0001c0001t0004g0226a0001c0001t0004g0229a0001c0001t0004g0237others(165): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.547-6384G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16220037 | ||||||
chr19:16220204
|
C | A | 1 | a0001c0001t0166g0286 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.547-6217C>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16220204 | ||||||
chr19:16220266
|
G | A | 1 | a0001c0002t0050g0117 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.547-6155G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16220266 | ||||||
chr19:16220324
|
G | A | 1 | a0001c0002t0011g0123 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.547-6097G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16220324 | ||||||
chr19:16220372
|
C | T | 1 | a0001c0001t0141g0267 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.547-6049C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16220372 | ||||||
chr19:16220375
|
CTTTTGGG others(4): Show |
C | 1 | a0001c0002t0064g0169 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.547-6040_547-6030d others(13): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 16220375 | |||||
chr19:16220383
|
G | GT | 5 | a0001c0001t0006g0025a0001c0001t0042g0016a0001c0002t0002g0175others(2): Show | 5 | HG00597.hp2 HG01928.hp1 HG02135.hp1 others(2): Show |
intron_variant | MODIFIER | c.547-6031dupT | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 16220383 | |||||
chr19:16220436
|
G | C | 1 | a0001c0001t0030g0020 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.547-5985G>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16220436 | ||||||
chr19:16220437
|
C | G | 1 | a0001c0001t0030g0020 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.547-5984C>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16220437 | ||||||
chr19:16220452
|
G | A | 1 | a0001c0001t0094g0198 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.547-5969G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16220452 | ||||||
chr19:16220542
|
C | T | 168 | a0001c0001t0004g0226a0001c0001t0004g0229a0001c0001t0004g0237others(165): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.547-5879C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16220542 | ||||||
chr19:16220633
|
T | C | 168 | a0001c0001t0004g0226a0001c0001t0004g0229a0001c0001t0004g0237others(165): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.547-5788T>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16220633 | ||||||
chr19:16220832
|
G | A | 5 | a0001c0001t0115g0224a0001c0001t0152g0079a0001c0001t0153g0033others(2): Show | 5 | HG01884.hp1 HG02055.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.547-5589G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16220832 | ||||||
chr19:16220885
|
T | C | 1 | a0001c0002t0072g0168 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.547-5536T>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16220885 | ||||||
chr19:16221085
|
G | A | 1 | a0001c0001t0039g0084 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.547-5336G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16221085 | ||||||
chr19:16221132
|
T | C | 5 | a0001c0001t0115g0224a0001c0001t0152g0079a0001c0001t0153g0033others(2): Show | 5 | HG01884.hp1 HG02055.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.547-5289T>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16221132 | ||||||
chr19:16221196
|
T | C | 173 | a0001c0001t0004g0226a0001c0001t0004g0229a0001c0001t0004g0237others(170): Show | 173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.547-5225T>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16221196 | ||||||
chr19:16221275
|
C | T | 168 | a0001c0001t0004g0226a0001c0001t0004g0229a0001c0001t0004g0237others(165): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.547-5146C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16221275 | ||||||
chr19:16221394
|
G | T | 1 | a0001c0002t0045g0122 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.547-5027G>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16221394 | ||||||
chr19:16221523
|
A | G | 168 | a0001c0001t0004g0226a0001c0001t0004g0229a0001c0001t0004g0237others(165): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.547-4898A>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16221523 | ||||||
chr19:16221683
|
C | T | 1 | a0001c0001t0155g0056 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.547-4738C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16221683 | ||||||
chr19:16221689
|
A | C | 3 | a0001c0001t0115g0224a0001c0001t0153g0033a0001c0001t0165g0032 | 3 | HG01884.hp1 HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.547-4732A>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16221689 | ||||||
chr19:16221738
|
C | T | 1 | a0001c0002t0045g0122 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.547-4683C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16221738 | ||||||
chr19:16221975
|
C | T | 1 | a0001c0001t0114g0067 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.547-4446C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16221975 | ||||||
chr19:16222188
|
TTATTATT others(2): Show |
T | 152 | a0001c0001t0004g0226a0001c0001t0004g0229a0001c0001t0004g0237others(149): Show | 152 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(149): Show |
intron_variant | MODIFIER | c.547-4224_547-4216d others(11): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 16222188 | |||||
chr19:16222197
|
C | T | 21 | a0001c0001t0029g0017a0001c0001t0029g0018a0001c0001t0030g0019others(18): Show | 21 | HG00735.hp1 HG01109.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.547-4224C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16222197 | ||||||
chr19:16222199
|
A | T | 1 | a0001c0001t0152g0079 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.547-4222A>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16222199 | ||||||
chr19:16222200
|
TTATTATT others(1): Show |
T | 5 | a0001c0002t0005g0138a0001c0002t0058g0166a0001c0002t0060g0178others(2): Show | 5 | HG01192.hp1 HG02155.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.547-4219_547-4212d others(10): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 16222200 | |||||
chr19:16222201
|
TATTATTA others(3): Show |
T | 5 | a0001c0001t0037g0233a0001c0001t0037g0234a0001c0001t0124g0011others(2): Show | 5 | HG02615.hp1 HG02895.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.547-4219_547-4210d others(12): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16222201 | ||||||
chr19:16222202
|
A | T | 1 | a0001c0001t0152g0079 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.547-4219A>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16222202 | ||||||
chr19:16222202
|
ATTATTAT others(3): Show |
A | 5 | a0001c0001t0029g0017a0001c0001t0029g0018a0001c0001t0030g0019others(2): Show | 5 | HG00735.hp1 HG01109.hp1 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.547-4216_547-4207d others(12): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 16222202 | |||||
chr19:16222205
|
A | T | 3 | a0001c0001t0115g0224a0001c0001t0152g0079a0001c0001t0167g0023 | 3 | HG02055.hp2 HG02486.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.547-4216A>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16222205 | ||||||
chr19:16222206
|
TTA | T | 5 | a0001c0001t0001g0005a0001c0001t0001g0043a0001c0001t0001g0071others(2): Show | 6 | HG01123.hp2 HG01255.hp2 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.547-4213_547-4212d others(4): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 16222206 | |||||
chr19:16222207
|
TA | T | 34 | a0001c0001t0001g0002a0001c0001t0001g0040a0001c0001t0001g0042others(31): Show | 37 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.547-4213delA | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16222207 | ||||||
chr19:16222208
|
A | AT | 14 | a0001c0001t0009g0217a0001c0001t0009g0219a0001c0001t0039g0041others(11): Show | 14 | HG01167.hp1 HG01169.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.547-4211dupT | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 16222208 | |||||
chr19:16222208
|
A | T | 13 | a0001c0001t0115g0224a0001c0001t0152g0079a0001c0001t0153g0033others(10): Show | 13 | HG00597.hp2 HG01074.hp1 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.547-4213A>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16222208 | ||||||
chr19:16222211
|
A | AT | 12 | a0001c0001t0006g0001a0001c0001t0006g0024a0001c0001t0006g0025others(9): Show | 15 | HG01361.hp1 HG02145.hp1 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.547-4196dupT | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 16222211 | |||||
chr19:16222211
|
A | T | 153 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0040others(150): Show | 157 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(154): Show |
intron_variant | MODIFIER | c.547-4210A>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16222211 | ||||||
chr19:16222214
|
T | A | 3 | a0001c0001t0003g0181a0001c0001t0036g0281a0001c0001t0104g0021 | 3 | HG00738.hp1 HG02922.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.547-4207T>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16222214 | ||||||
chr19:16222223
|
T | G | 1 | a0001c0001t0041g0246 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.547-4198T>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16222223 | ||||||
chr19:16222283
|
C | T | 5 | a0001c0001t0115g0224a0001c0001t0152g0079a0001c0001t0153g0033others(2): Show | 5 | HG01884.hp1 HG02055.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.547-4138C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16222283 | ||||||
chr19:16222379
|
TA | T | 7 | a0001c0001t0008g0228a0001c0001t0035g0049a0001c0001t0036g0281others(4): Show | 7 | HG01256.hp2 HG03130.hp2 NA18522.hp1 others(4): Show |
intron_variant | MODIFIER | c.547-4033delA | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 16222379 | |||||
chr19:16222405
|
G | A | 1 | a0001c0001t0162g0051 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.547-4016G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16222405 | ||||||
chr19:16222411
|
T | G | 168 | a0001c0001t0004g0226a0001c0001t0004g0229a0001c0001t0004g0237others(165): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.547-4010T>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16222411 | ||||||
chr19:16222559
|
C | T | 1 | a0001c0001t0035g0049 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.547-3862C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16222559 | ||||||
chr19:16222595
|
T | TTTTG | 173 | a0001c0001t0004g0226a0001c0001t0004g0229a0001c0001t0004g0237others(170): Show | 173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.547-3818_547-3815d others(6): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 16222595 | |||||
chr19:16222755
|
G | C | 1 | a0001c0001t0018g0072 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.547-3666G>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16222755 | ||||||
chr19:16222998
|
C | G | 1 | a0001c0001t0159g0222 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.547-3423C>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16222998 | ||||||
chr19:16223023
|
G | A | 1 | a0001c0001t0018g0072 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.547-3398G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16223023 | ||||||
chr19:16223109
|
T | C | 69 | a0001c0001t0004g0226a0001c0001t0004g0229a0001c0001t0004g0237others(66): Show | 69 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.547-3312T>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16223109 | ||||||
chr19:16223139
|
A | G | 1 | a0001c0002t0048g0130 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.547-3282A>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16223139 | ||||||
chr19:16223187
|
G | A | 50 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0037others(47): Show | 58 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.547-3234G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16223187 | ||||||
chr19:16223193
|
C | T | 1 | a0001c0001t0166g0286 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.547-3228C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16223193 | ||||||
chr19:16223203
|
T | G | 176 | a0001c0001t0001g0085a0001c0001t0003g0199a0001c0001t0004g0226others(173): Show | 177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.547-3218T>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16223203 | ||||||
chr19:16223213
|
G | A | 71 | a0001c0001t0003g0199a0001c0001t0004g0226a0001c0001t0004g0229others(68): Show | 71 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.547-3208G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16223213 | ||||||
chr19:16223223
|
C | A | 1 | a0001c0001t0001g0069 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.547-3198C>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16223223 | ||||||
chr19:16223272
|
G | T | 1 | a0001c0002t0057g0128 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.547-3149G>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16223272 | ||||||
chr19:16223312
|
C | G | 168 | a0001c0001t0004g0226a0001c0001t0004g0229a0001c0001t0004g0237others(165): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.547-3109C>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16223312 | ||||||
chr19:16223520
|
C | T | 1 | a0001c0002t0002g0132 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.547-2901C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16223520 | ||||||
chr19:16223589
|
G | A | 2 | a0001c0001t0037g0233a0001c0001t0037g0234 | 2 | HG02615.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.547-2832G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16223589 | ||||||
chr19:16223753
|
G | A | 1 | a0001c0002t0060g0178 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.547-2668G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16223753 | ||||||
chr19:16223791
|
C | T | 2 | a0001c0001t0085g0197a0001c0001t0087g0200 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.547-2630C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16223791 | ||||||
chr19:16223846
|
A | G | 5 | a0001c0001t0024g0289a0001c0001t0024g0290a0001c0001t0083g0288others(2): Show | 5 | HG02647.hp1 HG02896.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.547-2575A>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16223846 | ||||||
chr19:16223897
|
C | T | 1 | a0001c0001t0128g0238 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.547-2524C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16223897 | ||||||
chr19:16223944
|
A | G | 1 | a0001c0001t0008g0263 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.547-2477A>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16223944 | ||||||
chr19:16224007
|
C | T | 168 | a0001c0001t0004g0226a0001c0001t0004g0229a0001c0001t0004g0237others(165): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.547-2414C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16224007 | ||||||
chr19:16224128
|
G | A | 168 | a0001c0001t0004g0226a0001c0001t0004g0229a0001c0001t0004g0237others(165): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.547-2293G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16224128 | ||||||
chr19:16224166
|
G | A | 168 | a0001c0001t0004g0226a0001c0001t0004g0229a0001c0001t0004g0237others(165): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.547-2255G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16224166 | ||||||
chr19:16224238
|
C | T | 1 | a0001c0001t0129g0232 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.547-2183C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16224238 | ||||||
chr19:16224349
|
C | T | 69 | a0001c0001t0004g0226a0001c0001t0004g0229a0001c0001t0004g0237others(66): Show | 69 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.547-2072C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16224349 | ||||||
chr19:16224371
|
C | T | 1 | a0001c0001t0122g0274 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.547-2050C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16224371 | ||||||
chr19:16224452
|
G | A | 2 | a0001c0001t0142g0266a0001c0001t0143g0265 | 2 | HG01243.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.547-1969G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16224452 | ||||||
chr19:16224482
|
G | A | 1 | a0001c0002t0002g0111 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.547-1939G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16224482 | ||||||
chr19:16224559
|
C | T | 49 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0037others(46): Show | 57 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.547-1862C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16224559 | ||||||
chr19:16224679
|
C | T | 1 | a0001c0002t0068g0115 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.547-1742C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16224679 | ||||||
chr19:16224774
|
C | T | 1 | a0001c0001t0145g0268 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.547-1647C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16224774 | ||||||
chr19:16224796
|
C | G | 4 | a0001c0001t0034g0048a0001c0001t0034g0050a0001c0001t0035g0030others(1): Show | 5 | HG02258.hp1 HG02630.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.547-1625C>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16224796 | ||||||
chr19:16224800
|
G | A | 1 | a0001c0001t0166g0286 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.547-1621G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16224800 | ||||||
chr19:16224929
|
C | T | 168 | a0001c0001t0004g0226a0001c0001t0004g0229a0001c0001t0004g0237others(165): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.547-1492C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16224929 | ||||||
chr19:16224965
|
G | GGA | 72 | a0001c0001t0004g0226a0001c0001t0004g0229a0001c0001t0004g0237others(69): Show | 72 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.547-1441_547-1440d others(4): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 16224965 | |||||
chr19:16225031
|
C | T | 2 | a0001c0001t0037g0233a0001c0001t0037g0234 | 2 | HG02615.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.547-1390C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16225031 | ||||||
chr19:16225034
|
T | G | 1 | a0001c0001t0001g0064 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.547-1387T>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16225034 | ||||||
chr19:16225038
|
G | A | 1 | a0001c0001t0131g0236 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.547-1383G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16225038 | ||||||
chr19:16225051
|
G | A | 1 | a0001c0001t0092g0205 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.547-1370G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16225051 | ||||||
chr19:16225088
|
A | T | 168 | a0001c0001t0004g0226a0001c0001t0004g0229a0001c0001t0004g0237others(165): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.547-1333A>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16225088 | ||||||
chr19:16225383
|
A | G | 168 | a0001c0001t0004g0226a0001c0001t0004g0229a0001c0001t0004g0237others(165): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.547-1038A>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16225383 | ||||||
chr19:16225403
|
AG | A | 168 | a0001c0001t0004g0226a0001c0001t0004g0229a0001c0001t0004g0237others(165): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.547-1015delG | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 16225403 | |||||
chr19:16225419
|
C | T | 1 | a0001c0001t0003g0213 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.547-1002C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16225419 | ||||||
chr19:16225432
|
A | T | 168 | a0001c0001t0004g0226a0001c0001t0004g0229a0001c0001t0004g0237others(165): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.547-989A>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16225432 | ||||||
chr19:16225478
|
C | T | 1 | a0001c0004t0121g0249 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.547-943C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16225478 | ||||||
chr19:16225480
|
TCA | T | 7 | a0001c0001t0033g0264a0001c0001t0033g0276a0001c0001t0141g0267others(4): Show | 7 | HG01109.hp2 HG01243.hp1 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.547-939_547-938del others(2): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 16225480 | |||||
chr19:16225529
|
G | A | 2 | a0001c0001t0001g0043a0001c0001t0035g0049 | 2 | HG02809.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.547-892G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16225529 | ||||||
chr19:16225564
|
G | A | 1 | a0001c0002t0007g0092 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.547-857G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16225564 | ||||||
chr19:16225830
|
G | C | 99 | a0001c0002t0002g0026a0001c0002t0002g0028a0001c0002t0002g0029others(96): Show | 99 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(96): Show |
intron_variant | MODIFIER | c.547-591G>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16225830 | ||||||
chr19:16225891
|
G | A | 1 | a0001c0001t0031g0247 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.547-530G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16225891 | ||||||
chr19:16225900
|
G | T | 42 | a0001c0001t0004g0226a0001c0001t0004g0229a0001c0001t0004g0237others(39): Show | 42 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(39): Show |
intron_variant | MODIFIER | c.547-521G>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16225900 | ||||||
chr19:16226137
|
TA | T | 168 | a0001c0001t0004g0226a0001c0001t0004g0229a0001c0001t0004g0237others(165): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.547-283delA | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16226137 | ||||||
chr19:16226140
|
AG | A | 168 | a0001c0001t0004g0226a0001c0001t0004g0229a0001c0001t0004g0237others(165): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.547-278delG | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 16226140 | |||||
chr19:16226409
|
C | T | 1 | a0001c0001t0027g0191 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.547-12C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 5/11 | chr19 | 16226409 | ||||||
chr19:16226612
|
T | C | 173 | a0001c0001t0004g0226a0001c0001t0004g0229a0001c0001t0004g0237others(170): Show | 173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.673+65T>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 6/11 | chr19 | 16226612 | ||||||
chr19:16226745
|
T | C | 5 | a0001c0001t0124g0011a0001c0001t0125g0013a0001c0001t0126g0014others(2): Show | 5 | HG02723.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.673+198T>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 6/11 | chr19 | 16226745 | ||||||
chr19:16226777
|
C | T | 169 | a0001c0001t0003g0181a0001c0001t0004g0226a0001c0001t0004g0229others(166): Show | 169 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(166): Show |
intron_variant | MODIFIER | c.673+230C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 6/11 | chr19 | 16226777 | ||||||
chr19:16226848
|
C | T | 168 | a0001c0001t0004g0226a0001c0001t0004g0229a0001c0001t0004g0237others(165): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.673+301C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 6/11 | chr19 | 16226848 | ||||||
chr19:16226936
|
G | A | 168 | a0001c0001t0004g0226a0001c0001t0004g0229a0001c0001t0004g0237others(165): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.673+389G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 6/11 | chr19 | 16226936 | ||||||
chr19:16226970
|
G | A | 1 | a0001c0002t0055g0120 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.673+423G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 6/11 | chr19 | 16226970 | ||||||
chr19:16227237
|
C | T | 2 | a0001c0001t0037g0233a0001c0001t0037g0234 | 2 | HG02615.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.674-311C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 6/11 | chr19 | 16227237 | ||||||
chr19:16227313
|
TG | T | 99 | a0001c0002t0002g0026a0001c0002t0002g0028a0001c0002t0002g0029others(96): Show | 99 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(96): Show |
intron_variant | MODIFIER | c.674-231delG | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr19 | 16227313 | |||||
chr19:16227401
|
A | G | 1 | a0001c0002t0017g0096 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.674-147A>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 6/11 | chr19 | 16227401 | ||||||
chr19:16227463
|
C | T | 69 | a0001c0001t0004g0226a0001c0001t0004g0229a0001c0001t0004g0237others(66): Show | 69 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.674-85C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 6/11 | chr19 | 16227463 | ||||||
chr19:16227721
|
G | A | 168 | a0001c0001t0004g0226a0001c0001t0004g0229a0001c0001t0004g0237others(165): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.816+31G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 7/11 | chr19 | 16227721 | ||||||
chr19:16227884
|
C | T | 4 | a0001c0001t0029g0017a0001c0001t0029g0018a0001c0001t0030g0019others(1): Show | 4 | HG00735.hp1 HG01109.hp1 HG01884.hp2 others(1): Show |
intron_variant | MODIFIER | c.816+194C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 7/11 | chr19 | 16227884 | ||||||
chr19:16228219
|
C | T | 1 | a0001c0002t0002g0111 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.888+11C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 8/11 | chr19 | 16228219 | ||||||
chr19:16228258
|
G | A | 99 | a0001c0002t0002g0026a0001c0002t0002g0028a0001c0002t0002g0029others(96): Show | 99 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(96): Show |
intron_variant | MODIFIER | c.888+50G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 8/11 | chr19 | 16228258 | ||||||
chr19:16228336
|
A | T | 1 | a0001c0001t0162g0051 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.888+128A>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 8/11 | chr19 | 16228336 | ||||||
chr19:16228537
|
G | T | 2 | a0001c0002t0002g0171a0001c0002t0002g0175 | 2 | HG00597.hp2 NA18947.hp2 |
intron_variant | MODIFIER | c.889-233G>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 8/11 | chr19 | 16228537 | ||||||
chr19:16228547
|
C | T | 9 | a0001c0001t0009g0214a0001c0001t0009g0215a0001c0001t0009g0217others(6): Show | 9 | HG01361.hp1 HG02615.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.889-223C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 8/11 | chr19 | 16228547 | ||||||
chr19:16228620
|
G | A | 1 | a0001c0002t0066g0112 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.889-150G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 8/11 | chr19 | 16228620 | ||||||
chr19:16228751
|
G | A | 10 | a0001c0001t0026g0008a0001c0001t0026g0192a0001c0001t0027g0008others(7): Show | 10 | HG01934.hp1 HG02055.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.889-19G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 8/11 | chr19 | 16228751 | ||||||
chr19:16229063
|
A | G | 168 | a0001c0001t0004g0226a0001c0001t0004g0229a0001c0001t0004g0237others(165): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.1047+135A>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16229063 | ||||||
chr19:16229066
|
G | A | 1 | a0001c0001t0001g0042 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1047+138G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16229066 | ||||||
chr19:16229075
|
G | T | 168 | a0001c0001t0004g0226a0001c0001t0004g0229a0001c0001t0004g0237others(165): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.1047+147G>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16229075 | ||||||
chr19:16229076
|
A | T | 168 | a0001c0001t0004g0226a0001c0001t0004g0229a0001c0001t0004g0237others(165): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.1047+148A>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16229076 | ||||||
chr19:16229110
|
A | C | 1 | a0001c0001t0042g0016 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1047+182A>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16229110 | ||||||
chr19:16229114
|
G | A | 99 | a0001c0002t0002g0026a0001c0002t0002g0028a0001c0002t0002g0029others(96): Show | 99 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(96): Show |
intron_variant | MODIFIER | c.1047+186G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16229114 | ||||||
chr19:16229162
|
G | C | 1 | a0001c0001t0031g0247 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1047+234G>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16229162 | ||||||
chr19:16229319
|
A | G | 199 | a0001c0001t0001g0043a0001c0001t0004g0226a0001c0001t0004g0229others(196): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.1047+391A>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16229319 | ||||||
chr19:16229368
|
G | A | 1 | a0001c0001t0162g0051 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1047+440G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16229368 | ||||||
chr19:16229469
|
A | G | 161 | a0001c0001t0004g0226a0001c0001t0004g0229a0001c0001t0004g0237others(158): Show | 161 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(158): Show |
intron_variant | MODIFIER | c.1047+541A>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16229469 | ||||||
chr19:16229601
|
G | A | 2 | a0001c0002t0074g0109a0001c0002t0075g0121 | 2 | HG02717.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1047+673G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16229601 | ||||||
chr19:16229820
|
T | C | 1 | a0001c0001t0175g0083 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1047+892T>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16229820 | ||||||
chr19:16229873
|
G | A | 1 | a0001c0002t0043g0141 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1047+945G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16229873 | ||||||
chr19:16229877
|
C | T | 2 | a0001c0001t0040g0058a0001c0001t0176g0053 | 2 | HG03195.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1047+949C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16229877 | ||||||
chr19:16229935
|
G | A | 3 | a0001c0001t0001g0043a0001c0001t0035g0049a0001c0002t0002g0029 | 3 | HG02602.hp1 HG02809.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1047+1007G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16229935 | ||||||
chr19:16229982
|
G | T | 1 | a0001c0001t0156g0047 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1047+1054G>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16229982 | ||||||
chr19:16230027
|
T | A | 1 | a0001c0001t0032g0273 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1047+1099T>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16230027 | ||||||
chr19:16230044
|
G | A | 1 | a0001c0001t0004g0241 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1047+1116G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16230044 | ||||||
chr19:16230245
|
G | T | 49 | a0001c0002t0002g0026a0001c0002t0002g0028a0001c0002t0002g0100others(46): Show | 49 | HG00609.hp2 HG00738.hp2 HG01074.hp2 others(46): Show |
intron_variant | MODIFIER | c.1047+1317G>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16230245 | ||||||
chr19:16230404
|
C | CTT | 160 | a0001c0001t0004g0226a0001c0001t0004g0229a0001c0001t0004g0237others(157): Show | 160 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(157): Show |
intron_variant | MODIFIER | c.1047+1489_1047+149 others(6): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr19 | 16230404 | |||||
chr19:16230404
|
C | CTTT | 6 | a0001c0001t0004g0256a0001c0001t0124g0011a0001c0001t0125g0013others(3): Show | 6 | HG02723.hp2 HG02895.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1047+1488_1047+149 others(7): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr19 | 16230404 | |||||
chr19:16230404
|
CT | C | 67 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0037others(64): Show | 75 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.1047+1490delT | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr19 | 16230404 | |||||
chr19:16230404
|
CTT | C | 10 | a0001c0001t0009g0214a0001c0001t0009g0215a0001c0001t0009g0217others(7): Show | 10 | HG01361.hp1 HG02615.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.1047+1489_1047+149 others(6): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr19 | 16230404 | |||||
chr19:16230423
|
C | T | 1 | a0001c0001t0166g0286 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1047+1495C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16230423 | ||||||
chr19:16230471
|
G | A | 3 | a0001c0001t0024g0289a0001c0001t0024g0290a0001c0001t0105g0287 | 3 | HG02647.hp1 HG02896.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1047+1543G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16230471 | ||||||
chr19:16230485
|
G | C | 168 | a0001c0001t0004g0226a0001c0001t0004g0229a0001c0001t0004g0237others(165): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.1047+1557G>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16230485 | ||||||
chr19:16230521
|
G | A | 3 | a0001c0001t0115g0224a0001c0001t0153g0033a0001c0001t0165g0032 | 3 | HG01884.hp1 HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1047+1593G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16230521 | ||||||
chr19:16230828
|
C | T | 173 | a0001c0001t0004g0226a0001c0001t0004g0229a0001c0001t0004g0237others(170): Show | 173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.1047+1900C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16230828 | ||||||
chr19:16230938
|
G | A | 3 | a0001c0001t0115g0224a0001c0001t0153g0033a0001c0001t0165g0032 | 3 | HG01884.hp1 HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1047+2010G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16230938 | ||||||
chr19:16231054
|
T | C | 294 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0037others(291): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.1047+2126T>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16231054 | ||||||
chr19:16231063
|
C | T | 1 | a0001c0002t0047g0174 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1047+2135C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16231063 | ||||||
chr19:16231116
|
G | A | 2 | a0001c0001t0110g0187a0001c0002t0002g0285 | 2 | HG02451.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1047+2188G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16231116 | ||||||
chr19:16231157
|
G | A | 7 | a0001c0001t0040g0052a0001c0001t0040g0058a0001c0001t0155g0056others(4): Show | 7 | HG01167.hp1 HG01169.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.1047+2229G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16231157 | ||||||
chr19:16231218
|
G | A | 1 | a0001c0001t0166g0286 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1048-2275G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16231218 | ||||||
chr19:16231220
|
G | A | 1 | a0001c0001t0167g0023 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1048-2273G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16231220 | ||||||
chr19:16231236
|
C | T | 4 | a0001c0001t0029g0017a0001c0001t0029g0018a0001c0001t0030g0019others(1): Show | 4 | HG00735.hp1 HG01109.hp1 HG01884.hp2 others(1): Show |
intron_variant | MODIFIER | c.1048-2257C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16231236 | ||||||
chr19:16231237
|
A | G | 173 | a0001c0001t0004g0226a0001c0001t0004g0229a0001c0001t0004g0237others(170): Show | 173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.1048-2256A>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16231237 | ||||||
chr19:16231287
|
C | CA | 8 | a0001c0001t0003g0204a0001c0001t0013g0206a0001c0001t0026g0192others(5): Show | 8 | HG00735.hp1 HG01081.hp1 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.1048-2183dupA | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr19 | 16231287 | |||||
chr19:16231287
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0003g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1048-2193_1048-218 others(15): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr19 | 16231287 | |||||
chr19:16231297
|
AAAAAAAA others(9): Show |
A | 1 | a0001c0002t0010g0145 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1048-2194_1048-217 others(20): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr19 | 16231297 | |||||
chr19:16231298
|
AAAAAAAA others(8): Show |
A | 97 | a0001c0002t0002g0026a0001c0002t0002g0028a0001c0002t0002g0029others(94): Show | 97 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(94): Show |
intron_variant | MODIFIER | c.1048-2193_1048-217 others(19): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr19 | 16231298 | |||||
chr19:16231299
|
AAAAAAAA others(7): Show |
A | 1 | a0001c0002t0056g0102 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1048-2192_1048-217 others(18): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr19 | 16231299 | |||||
chr19:16231309
|
A | AC | 56 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0037others(53): Show | 61 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.1048-2184_1048-218 others(5): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16231309 | ||||||
chr19:16231309
|
A | C | 5 | a0001c0001t0014g0039a0001c0001t0014g0061a0001c0001t0019g0046others(2): Show | 5 | HG01069.hp2 HG01167.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.1048-2184A>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16231309 | ||||||
chr19:16231310
|
AC | A | 48 | a0001c0001t0004g0226a0001c0001t0004g0229a0001c0001t0004g0237others(45): Show | 48 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(45): Show |
intron_variant | MODIFIER | c.1048-2182delC | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16231310 | ||||||
chr19:16231311
|
C | A | 13 | a0001c0001t0020g0280a0001c0001t0029g0017a0001c0001t0029g0018others(10): Show | 13 | HG00558.hp1 HG00735.hp1 HG01109.hp1 others(10): Show |
intron_variant | MODIFIER | c.1048-2182C>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16231311 | ||||||
chr19:16231313
|
C | CAG | 15 | a0001c0001t0001g0065a0001c0001t0001g0070a0001c0001t0006g0001others(12): Show | 18 | HG00423.hp1 HG00735.hp2 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.1048-2172_1048-217 others(6): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr19 | 16231313 | |||||
chr19:16231313
|
C | G | 64 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0037others(61): Show | 69 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.1048-2180C>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16231313 | ||||||
chr19:16231313
|
CAG | C | 8 | a0001c0001t0033g0264a0001c0001t0033g0276a0001c0001t0124g0011others(5): Show | 8 | HG02723.hp2 HG02895.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.1048-2172_1048-217 others(6): Show |
AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr19 | 16231313 | |||||
chr19:16231315
|
G | C | 160 | a0001c0001t0004g0226a0001c0001t0004g0229a0001c0001t0004g0237others(157): Show | 160 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(157): Show |
intron_variant | MODIFIER | c.1048-2178G>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16231315 | ||||||
chr19:16231332
|
C | T | 2 | a0001c0001t0152g0079a0001c0001t0167g0023 | 2 | HG02055.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1048-2161C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16231332 | ||||||
chr19:16231333
|
A | G | 99 | a0001c0002t0002g0026a0001c0002t0002g0028a0001c0002t0002g0029others(96): Show | 99 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(96): Show |
intron_variant | MODIFIER | c.1048-2160A>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16231333 | ||||||
chr19:16231335
|
A | G | 1 | a0001c0001t0166g0286 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1048-2158A>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16231335 | ||||||
chr19:16231403
|
T | A | 1 | a0001c0001t0166g0286 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1048-2090T>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16231403 | ||||||
chr19:16231501
|
G | C | 168 | a0001c0001t0004g0226a0001c0001t0004g0229a0001c0001t0004g0237others(165): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.1048-1992G>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16231501 | ||||||
chr19:16231533
|
G | A | 67 | a0001c0001t0004g0226a0001c0001t0004g0229a0001c0001t0004g0237others(64): Show | 67 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.1048-1960G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16231533 | ||||||
chr19:16231630
|
AT | A | 168 | a0001c0001t0004g0226a0001c0001t0004g0229a0001c0001t0004g0237others(165): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.1048-1861delT | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr19 | 16231630 | |||||
chr19:16231646
|
G | T | 2 | a0001c0001t0004g0237a0001c0001t0133g0235 | 2 | HG00438.hp2 HG00609.hp1 |
intron_variant | MODIFIER | c.1048-1847G>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16231646 | ||||||
chr19:16231692
|
C | T | 99 | a0001c0002t0002g0026a0001c0002t0002g0028a0001c0002t0002g0029others(96): Show | 99 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(96): Show |
intron_variant | MODIFIER | c.1048-1801C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16231692 | ||||||
chr19:16231746
|
G | A | 2 | a0001c0001t0003g0202a0001c0001t0086g0201 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1048-1747G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16231746 | ||||||
chr19:16231781
|
T | A | 168 | a0001c0001t0004g0226a0001c0001t0004g0229a0001c0001t0004g0237others(165): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.1048-1712T>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16231781 | ||||||
chr19:16231860
|
G | A | 3 | a0001c0001t0115g0224a0001c0001t0153g0033a0001c0001t0165g0032 | 3 | HG01884.hp1 HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1048-1633G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16231860 | ||||||
chr19:16231883
|
A | G | 3 | a0001c0001t0115g0224a0001c0001t0153g0033a0001c0001t0165g0032 | 3 | HG01884.hp1 HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1048-1610A>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16231883 | ||||||
chr19:16232129
|
G | A | 1 | a0001c0001t0162g0051 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1048-1364G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16232129 | ||||||
chr19:16232282
|
G | T | 1 | a0001c0002t0005g0119 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1048-1211G>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16232282 | ||||||
chr19:16232288
|
G | T | 1 | a0001c0001t0001g0069 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1048-1205G>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16232288 | ||||||
chr19:16232307
|
C | T | 3 | a0001c0001t0115g0224a0001c0001t0153g0033a0001c0001t0165g0032 | 3 | HG01884.hp1 HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1048-1186C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16232307 | ||||||
chr19:16232401
|
G | A | 1 | a0001c0002t0012g0104 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1048-1092G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16232401 | ||||||
chr19:16232425
|
T | C | 2 | a0001c0001t0171g0034a0001c0001t0173g0054 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1048-1068T>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16232425 | ||||||
chr19:16232519
|
C | T | 4 | a0001c0001t0029g0017a0001c0001t0029g0018a0001c0001t0030g0019others(1): Show | 4 | HG00735.hp1 HG01109.hp1 HG01884.hp2 others(1): Show |
intron_variant | MODIFIER | c.1048-974C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16232519 | ||||||
chr19:16232600
|
G | A | 1 | a0001c0002t0002g0111 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1048-893G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16232600 | ||||||
chr19:16232610
|
G | A | 5 | a0001c0001t0024g0289a0001c0001t0024g0290a0001c0001t0083g0288others(2): Show | 5 | HG02647.hp1 HG02896.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1048-883G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16232610 | ||||||
chr19:16232660
|
G | A | 10 | a0001c0001t0009g0214a0001c0001t0009g0215a0001c0001t0009g0217others(7): Show | 10 | HG01361.hp1 HG02615.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.1048-833G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16232660 | ||||||
chr19:16232685
|
C | A | 1 | a0001c0002t0007g0139 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1048-808C>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16232685 | ||||||
chr19:16232755
|
G | A | 1 | a0001c0001t0113g0182 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1048-738G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16232755 | ||||||
chr19:16233003
|
G | A | 60 | a0001c0001t0004g0226a0001c0001t0004g0229a0001c0001t0004g0237others(57): Show | 60 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.1048-490G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16233003 | ||||||
chr19:16233036
|
T | A | 99 | a0001c0002t0002g0026a0001c0002t0002g0028a0001c0002t0002g0029others(96): Show | 99 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(96): Show |
intron_variant | MODIFIER | c.1048-457T>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16233036 | ||||||
chr19:16233107
|
G | A | 1 | a0001c0001t0003g0212 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1048-386G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16233107 | ||||||
chr19:16233146
|
A | G | 168 | a0001c0001t0004g0226a0001c0001t0004g0229a0001c0001t0004g0237others(165): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.1048-347A>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16233146 | ||||||
chr19:16233154
|
A | G | 6 | a0001c0001t0026g0008a0001c0001t0026g0192a0001c0001t0027g0008others(3): Show | 6 | HG02280.hp1 HG02451.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1048-339A>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16233154 | ||||||
chr19:16233169
|
T | C | 2 | a0001c0001t0116g0251a0001c0001t0132g0230 | 2 | HG00544.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.1048-324T>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16233169 | ||||||
chr19:16233268
|
C | T | 46 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0037others(43): Show | 51 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(48): Show |
intron_variant | MODIFIER | c.1048-225C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16233268 | ||||||
chr19:16233372
|
C | T | 1 | a0001c0001t0094g0198 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1048-121C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16233372 | ||||||
chr19:16233480
|
G | A | 3 | a0001c0001t0006g0001a0001c0001t0006g0024a0001c0001t0006g0025 | 6 | HG02145.hp1 HG02976.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.1048-13G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 9/11 | chr19 | 16233480 | ||||||
chr19:16233640
|
G | A | 1 | a0001c0001t0041g0246 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1173+22G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 10/11 | chr19 | 16233640 | ||||||
chr19:16233702
|
G | T | 7 | a0001c0001t0033g0264a0001c0001t0033g0276a0001c0001t0141g0267others(4): Show | 7 | HG01109.hp2 HG01243.hp1 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.1173+84G>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 10/11 | chr19 | 16233702 | ||||||
chr19:16233717
|
C | G | 170 | a0001c0001t0004g0226a0001c0001t0004g0229a0001c0001t0004g0237others(167): Show | 170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.1173+99C>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 10/11 | chr19 | 16233717 | ||||||
chr19:16233788
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A | C | 9 | a0001c0001t0009g0214a0001c0001t0009g0215a0001c0001t0009g0217others(6): Show | 9 | HG01361.hp1 HG02615.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.1173+170A>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 10/11 | chr19 | 16233788 | ||||||
chr19:16233817
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C | T | 39 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0037others(36): Show | 43 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.1173+199C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 10/11 | chr19 | 16233817 | ||||||
chr19:16233836
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A | G | 173 | a0001c0001t0004g0226a0001c0001t0004g0229a0001c0001t0004g0237others(170): Show | 173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.1173+218A>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 10/11 | chr19 | 16233836 | ||||||
chr19:16233871
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AC | A | 42 | a0001c0001t0004g0226a0001c0001t0004g0229a0001c0001t0004g0237others(39): Show | 42 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(39): Show |
intron_variant | MODIFIER | c.1173+255delC | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr19 | 16233871 | |||||
chr19:16233948
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G | A | 3 | a0001c0001t0013g0193a0001c0001t0013g0194a0001c0001t0025g0010 | 4 | HG01257.hp2 HG01258.hp1 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.1174-251G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 10/11 | chr19 | 16233948 | ||||||
chr19:16233974
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G | A | 1 | a0001c0001t0164g0293 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1174-225G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 10/11 | chr19 | 16233974 | ||||||
chr19:16234095
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A | C | 1 | a0001c0002t0060g0178 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1174-104A>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 10/11 | chr19 | 16234095 | ||||||
chr19:16234157
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C | T | 1 | a0001c0001t0110g0187 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1174-42C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 10/11 | chr19 | 16234157 | ||||||
chr19:16234282
|
A | G | 1 | a0001c0001t0041g0246 | 1 | NA19002.hp1 | splice_region_variant&intron_variant | LOW | c.1249+8A>G | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 11/11 | chr19 | 16234282 | ||||||
chr19:16234283
|
G | A | 1 | a0001c0001t0041g0246 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1249+9G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 11/11 | chr19 | 16234283 | ||||||
chr19:16234288
|
T | C | 171 | a0001c0001t0004g0226a0001c0001t0004g0229a0001c0001t0004g0237others(168): Show | 171 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(168): Show |
intron_variant | MODIFIER | c.1249+14T>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 11/11 | chr19 | 16234288 | ||||||
chr19:16234292
|
C | T | 1 | a0001c0001t0164g0293 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1249+18C>T | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 11/11 | chr19 | 16234292 | ||||||
chr19:16234298
|
G | C | 1 | a0001c0001t0037g0234 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1249+24G>C | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 11/11 | chr19 | 16234298 | ||||||
chr19:16234379
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G | A | 1 | a0001c0001t0167g0023 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1250-34G>A | AP1M1 | ENSG00000072958.9 | transcript | ENST00000291439.8 | protein_coding | 11/11 | chr19 | 16234379 |