geneid | 2166 |
---|---|
ensemblid | ENSG00000117480.16 |
hgncid | 3553 |
symbol | FAAH |
name | fatty acid amide hydrolase |
refseq_nuc | NM_001441.3 |
refseq_prot | NP_001432.2 |
ensembl_nuc | ENST00000243167.9 |
ensembl_prot | ENSP00000243167.8 |
mane_status | MANE Select |
chr | chr1 |
start | 46394317 |
end | 46413845 |
strand | + |
ver | v1.2 |
region | chr1:46394317-46413845 |
region5000 | chr1:46389317-46418845 |
regionname0 | FAAH_chr1_46394317_46413845 |
regionname5000 | FAAH_chr1_46389317_46418845 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 579 | 258 | 59 | 38 | 111 | 12 | 37 | 88 | FAAH_chr1_46389317_46418845 | FAAH | copy fasta | chr1 | 46389317 | 46418845 |
a0002 | 0/1 | 579 | 101 | 24 | 24 | 40 | 4 | 8 | 34 | FAAH_chr1_46389317_46418845 | FAAH | copy fasta | chr1 | 46389317 | 46418845 |
a0003 | 0/0 | 116 | 9 | 3 | 0 | 5 | 0 | 1 | 4 | FAAH_chr1_46389317_46418845 | FAAH | copy fasta | chr1 | 46389317 | 46418845 |
a0004 | 0/0 | 579 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | copy fasta | chr1 | 46389317 | 46418845 |
a0005 | 0/0 | 328 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | copy fasta | chr1 | 46389317 | 46418845 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 1740 | 218 | 40 | 34 | 111 | 9 | 24 | FAAH_chr1_46389317_46418845 | FAAH | copy fasta | chr1 | 46389317 | 46418845 |
c0002 | 0/0 | 1740 | 95 | 24 | 23 | 40 | 2 | 6 | FAAH_chr1_46389317_46418845 | FAAH | copy fasta | chr1 | 46389317 | 46418845 |
c0003 | 1/0 | 1740 | 38 | 17 | 4 | 0 | 3 | 13 | FAAH_chr1_46389317_46418845 | FAAH | copy fasta | chr1 | 46389317 | 46418845 |
c0004 | 0/0 | 1732 | 7 | 1 | 0 | 5 | 0 | 1 | FAAH_chr1_46389317_46418845 | FAAH | copy fasta | chr1 | 46389317 | 46418845 |
c0005 | 0/1 | 1740 | 6 | 0 | 1 | 0 | 2 | 2 | FAAH_chr1_46389317_46418845 | FAAH | copy fasta | chr1 | 46389317 | 46418845 |
c0006 | 0/0 | 1732 | 2 | 2 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | copy fasta | chr1 | 46389317 | 46418845 |
c0007 | 0/0 | 1740 | 2 | 2 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | copy fasta | chr1 | 46389317 | 46418845 |
c0008 | 0/0 | 1754 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | copy fasta | chr1 | 46389317 | 46418845 |
c0009 | 0/0 | 1740 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | copy fasta | chr1 | 46389317 | 46418845 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 303 | 361 | 87 | 61 | 151 | 16 | 44 | FAAH_chr1_46389317_46418845 | FAAH | copy fasta | chr1 | 46389317 | 46418845 |
t0002 | 0/0 | 290 | 7 | 1 | 0 | 5 | 0 | 1 | FAAH_chr1_46389317_46418845 | FAAH | copy fasta | chr1 | 46389317 | 46418845 |
t0003 | 0/0 | 303 | 1 | 0 | 0 | 0 | 0 | 1 | FAAH_chr1_46389317_46418845 | FAAH | copy fasta | chr1 | 46389317 | 46418845 |
t0004 | 0/0 | 303 | 1 | 0 | 1 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | copy fasta | chr1 | 46389317 | 46418845 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/1 | 48 | 8 | 16 | 15 | 3 | 5 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0002 | 0/0 | 48 | 1 | 8 | 34 | 2 | 3 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0003 | 0/0 | 18 | 0 | 0 | 13 | 0 | 5 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0004 | 0/0 | 17 | 1 | 4 | 5 | 4 | 3 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0005 | 0/0 | 11 | 0 | 0 | 11 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0006 | 0/0 | 10 | 0 | 6 | 1 | 2 | 1 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0007 | 0/0 | 10 | 0 | 0 | 0 | 2 | 8 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0008 | 0/0 | 7 | 0 | 0 | 6 | 0 | 1 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0009 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0010 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0011 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0013 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0014 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0015 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0019 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0021 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0030 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0033 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0056 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 1740 | 218 | 40 | 34 | 111 | 9 | 24 | FAAH_chr1_46389317_46418845 | FAAH | copy fasta | chr1 | 46389317 | 46418845 |
a0001c0003 | 1/0 | 1740 | 38 | 17 | 4 | 0 | 3 | 13 | FAAH_chr1_46389317_46418845 | FAAH | copy fasta | chr1 | 46389317 | 46418845 |
a0001c0007 | 0/0 | 1740 | 2 | 2 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | copy fasta | chr1 | 46389317 | 46418845 |
a0002c0002 | 0/0 | 1740 | 95 | 24 | 23 | 40 | 2 | 6 | FAAH_chr1_46389317_46418845 | FAAH | copy fasta | chr1 | 46389317 | 46418845 |
a0002c0005 | 0/1 | 1740 | 6 | 0 | 1 | 0 | 2 | 2 | FAAH_chr1_46389317_46418845 | FAAH | copy fasta | chr1 | 46389317 | 46418845 |
a0003c0004 | 0/0 | 1732 | 7 | 1 | 0 | 5 | 0 | 1 | FAAH_chr1_46389317_46418845 | FAAH | copy fasta | chr1 | 46389317 | 46418845 |
a0003c0006 | 0/0 | 1732 | 2 | 2 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | copy fasta | chr1 | 46389317 | 46418845 |
a0004c0009 | 0/0 | 1740 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | copy fasta | chr1 | 46389317 | 46418845 |
a0005c0008 | 0/0 | 1754 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | copy fasta | chr1 | 46389317 | 46418845 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 2042 | 217 | 40 | 33 | 111 | 9 | 24 | FAAH_chr1_46389317_46418845 | FAAH | copy fasta | chr1 | 46389317 | 46418845 |
a0001c0001t0004 | 0/0 | 2042 | 1 | 0 | 1 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | copy fasta | chr1 | 46389317 | 46418845 |
a0001c0003t0001 | 1/0 | 2042 | 37 | 17 | 4 | 0 | 3 | 12 | FAAH_chr1_46389317_46418845 | FAAH | copy fasta | chr1 | 46389317 | 46418845 |
a0001c0003t0003 | 0/0 | 2042 | 1 | 0 | 0 | 0 | 0 | 1 | FAAH_chr1_46389317_46418845 | FAAH | copy fasta | chr1 | 46389317 | 46418845 |
a0001c0007t0001 | 0/0 | 2042 | 2 | 2 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | copy fasta | chr1 | 46389317 | 46418845 |
a0002c0002t0001 | 0/0 | 2042 | 95 | 24 | 23 | 40 | 2 | 6 | FAAH_chr1_46389317_46418845 | FAAH | copy fasta | chr1 | 46389317 | 46418845 |
a0002c0005t0001 | 0/1 | 2042 | 6 | 0 | 1 | 0 | 2 | 2 | FAAH_chr1_46389317_46418845 | FAAH | copy fasta | chr1 | 46389317 | 46418845 |
a0003c0004t0002 | 0/0 | 2021 | 7 | 1 | 0 | 5 | 0 | 1 | FAAH_chr1_46389317_46418845 | FAAH | copy fasta | chr1 | 46389317 | 46418845 |
a0003c0006t0001 | 0/0 | 2034 | 2 | 2 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | copy fasta | chr1 | 46389317 | 46418845 |
a0004c0009t0001 | 0/0 | 2042 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | copy fasta | chr1 | 46389317 | 46418845 |
a0005c0008t0001 | 0/0 | 2056 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | copy fasta | chr1 | 46389317 | 46418845 |
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 | 48 | 1 | 8 | 34 | 2 | 3 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0001t0001g0003 | 0/0 | 18 | 0 | 0 | 13 | 0 | 5 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0001t0001g0004 | 0/0 | 17 | 1 | 4 | 5 | 4 | 3 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0001t0001g0006 | 0/0 | 10 | 0 | 6 | 1 | 2 | 1 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0001t0001g0008 | 0/0 | 7 | 0 | 0 | 6 | 0 | 1 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0001t0001g0009 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0001t0001g0011 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0001t0001g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0001t0001g0015 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0001t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0001t0001g0021 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0001t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0001t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0001t0001g0033 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0001t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0001t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0001t0004g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0003t0001g0007 | 0/0 | 10 | 0 | 0 | 0 | 2 | 8 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0003t0001g0010 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0003t0001g0014 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0003t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0003t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0003t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0003t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0003t0001g0056 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0003t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0003t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0003t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0003t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0003t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0003t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0003t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0003t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0003t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0003t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0003t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0003t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0003t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0003t0003g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0001c0007t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0002c0002t0001g0001 | 0/0 | 42 | 7 | 15 | 15 | 1 | 4 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0002c0002t0001g0005 | 0/0 | 11 | 0 | 0 | 11 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0002c0002t0001g0013 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0002c0002t0001g0019 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0002c0002t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0002c0002t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0002c0002t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0002c0002t0001g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0002c0002t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0002c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0002c0002t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0002c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0002c0002t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0002c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0002c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0002c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0002c0002t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0002c0002t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0002c0002t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0002c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0002c0002t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0002c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0002c0002t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0002c0002t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0002c0002t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0002c0002t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0002c0002t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0002c0002t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0002c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0002c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0002c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0002c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0002c0002t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0002c0002t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0002c0002t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0002c0002t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0002c0005t0001g0001 | 0/1 | 5 | 0 | 1 | 0 | 2 | 1 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0002c0005t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0003c0004t0002g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0003c0004t0002g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0003c0004t0002g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0003c0004t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0003c0004t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0003c0006t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0003c0006t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0004c0009t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
a0005c0008t0001g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0005 | t0001 | g0001 | EUR | GBR | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | GBR | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG00140 | hp1 | a0001 | c0003 | t0001 | g0007 | EUR | GBR | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0041 | EUR | GBR | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG00280 | hp1 | a0002 | c0005 | t0001 | g0001 | EUR | FIN | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG00323 | hp2 | a0002 | c0002 | t0001 | g0001 | EUR | FIN | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG00544 | hp2 | a0003 | c0004 | t0002 | g0018 | EAS | CHS | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | CHS | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG00609 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | CHS | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | CHS | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG00673 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | CHS | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG00733 | hp1 | a0002 | c0002 | t0001 | g0025 | AMR | PUR | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG00733 | hp2 | a0001 | c0003 | t0001 | g0014 | AMR | PUR | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG00738 | hp1 | a0002 | c0002 | t0001 | g0013 | AMR | PUR | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG00738 | hp2 | a0001 | c0003 | t0001 | g0061 | AMR | PUR | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG00741 | hp1 | a0002 | c0005 | t0001 | g0001 | AMR | PUR | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG01069 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG01069 | hp2 | a0001 | c0001 | t0004 | g0047 | AMR | PUR | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG01071 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG01071 | hp2 | a0002 | c0002 | t0001 | g0013 | AMR | PUR | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG01074 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG01099 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG01167 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG01175 | hp2 | a0002 | c0002 | t0001 | g0077 | AMR | PUR | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG01192 | hp1 | a0002 | c0002 | t0001 | g0025 | AMR | PUR | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG01243 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG01256 | hp2 | a0001 | c0003 | t0001 | g0014 | AMR | CLM | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG01261 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | CLM | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG01346 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | CLM | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | CLM | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | IBS | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG01515 | hp2 | a0002 | c0002 | t0001 | g0066 | EUR | IBS | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | IBS | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0006 | EUR | IBS | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG01884 | hp1 | a0002 | c0002 | t0001 | g0001 | AFR | ACB | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG01884 | hp2 | a0003 | c0004 | t0002 | g0137 | AFR | ACB | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG01891 | hp1 | a0001 | c0003 | t0001 | g0148 | AFR | ACB | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG01891 | hp2 | a0001 | c0003 | t0001 | g0010 | AFR | ACB | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG01928 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG01934 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG01943 | hp1 | a0002 | c0002 | t0001 | g0075 | AMR | PEL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PEL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG01975 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PEL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG01981 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PEL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG01993 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG02004 | hp1 | a0002 | c0002 | t0001 | g0073 | AMR | PEL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | KHV | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG02040 | hp1 | a0002 | c0002 | t0001 | g0019 | EAS | KHV | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG02040 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | KHV | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG02055 | hp1 | a0002 | c0002 | t0001 | g0150 | AFR | ACB | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | ACB | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | KHV | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | KHV | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | KHV | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | KHV | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | ACB | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | ACB | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG02148 | hp1 | a0002 | c0002 | t0001 | g0084 | AMR | PEL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CDX | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | CDX | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG02165 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | CDX | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG02257 | hp1 | a0001 | c0003 | t0001 | g0010 | AFR | ACB | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | ACB | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG02258 | hp1 | a0002 | c0002 | t0001 | g0013 | AFR | ACB | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | ACB | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG02280 | hp1 | a0002 | c0002 | t0001 | g0163 | AFR | ACB | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG02280 | hp2 | a0001 | c0003 | t0001 | g0112 | AFR | ACB | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG02293 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG02300 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | ACB | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | ACB | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG02523 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG02572 | hp1 | a0002 | c0002 | t0001 | g0001 | AFR | GWD | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | GWD | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG02602 | hp2 | a0001 | c0003 | t0003 | g0164 | SAS | PJL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG02615 | hp2 | a0002 | c0002 | t0001 | g0001 | AFR | GWD | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG02622 | hp1 | a0001 | c0003 | t0001 | g0139 | AFR | GWD | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG02622 | hp2 | a0002 | c0002 | t0001 | g0078 | AFR | GWD | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG02630 | hp1 | a0002 | c0002 | t0001 | g0074 | AFR | GWD | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG02630 | hp2 | a0001 | c0003 | t0001 | g0133 | AFR | GWD | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG02683 | hp1 | a0002 | c0002 | t0001 | g0001 | SAS | PJL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG02698 | hp1 | a0001 | c0003 | t0001 | g0007 | SAS | PJL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0088 | SAS | PJL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG02717 | hp1 | a0002 | c0002 | t0001 | g0022 | AFR | GWD | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG02717 | hp2 | a0001 | c0007 | t0001 | g0017 | AFR | GWD | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG02735 | hp2 | a0001 | c0003 | t0001 | g0159 | SAS | PJL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | PJL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG02738 | hp2 | a0001 | c0003 | t0001 | g0007 | SAS | PJL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | GWD | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG02818 | hp2 | a0002 | c0002 | t0001 | g0063 | AFR | GWD | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | GWD | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | GWD | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | GWD | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | GWD | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG02896 | hp1 | a0002 | c0002 | t0001 | g0069 | AFR | GWD | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG02896 | hp2 | a0001 | c0003 | t0001 | g0138 | AFR | GWD | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG02897 | hp1 | a0001 | c0003 | t0001 | g0031 | AFR | GWD | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | GWD | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG02965 | hp1 | a0001 | c0003 | t0001 | g0031 | AFR | ESN | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | ESN | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | ESN | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG03017 | hp2 | a0001 | c0003 | t0001 | g0062 | SAS | PJL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG03041 | hp1 | a0002 | c0002 | t0001 | g0068 | AFR | GWD | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG03041 | hp2 | a0001 | c0003 | t0001 | g0010 | AFR | GWD | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG03098 | hp2 | a0001 | c0003 | t0001 | g0144 | AFR | MSL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | ESN | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | ESN | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ESN | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG03139 | hp2 | a0003 | c0006 | t0001 | g0135 | AFR | ESN | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG03195 | hp1 | a0001 | c0003 | t0001 | g0143 | AFR | ESN | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | ESN | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG03209 | hp1 | a0002 | c0002 | t0001 | g0001 | AFR | MSL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG03209 | hp2 | a0002 | c0002 | t0001 | g0153 | AFR | MSL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG03225 | hp1 | a0002 | c0002 | t0001 | g0079 | AFR | MSL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | MSL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG03239 | hp1 | a0002 | c0002 | t0001 | g0064 | SAS | PJL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG03239 | hp2 | a0001 | c0003 | t0001 | g0085 | SAS | PJL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | MSL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG03453 | hp2 | a0002 | c0002 | t0001 | g0022 | AFR | MSL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | MSL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | MSL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG03490 | hp1 | a0001 | c0003 | t0001 | g0007 | SAS | PJL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG03490 | hp2 | a0002 | c0002 | t0001 | g0019 | SAS | PJL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG03492 | hp2 | a0002 | c0002 | t0001 | g0001 | SAS | PJL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG03516 | hp1 | a0003 | c0006 | t0001 | g0134 | AFR | ESN | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG03516 | hp2 | a0001 | c0003 | t0001 | g0049 | AFR | ESN | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG03540 | hp1 | a0002 | c0002 | t0001 | g0001 | AFR | GWD | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG03579 | hp1 | a0001 | c0003 | t0001 | g0010 | AFR | MSL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | MSL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG03654 | hp1 | a0002 | c0005 | t0001 | g0001 | SAS | PJL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG03654 | hp2 | a0001 | c0003 | t0001 | g0007 | SAS | PJL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG03669 | hp2 | a0002 | c0002 | t0001 | g0001 | SAS | PJL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | STU | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | STU | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG03710 | hp2 | a0001 | c0003 | t0001 | g0007 | SAS | PJL | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG03834 | hp1 | a0002 | c0005 | t0001 | g0054 | SAS | BEB | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG03834 | hp2 | a0003 | c0004 | t0002 | g0045 | SAS | BEB | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG03927 | hp1 | a0001 | c0003 | t0001 | g0007 | SAS | BEB | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG03942 | hp1 | a0001 | c0003 | t0001 | g0087 | SAS | BEB | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG03942 | hp2 | a0001 | c0003 | t0001 | g0007 | SAS | BEB | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | STU | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | STU | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0103 | SAS | STU | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0053 | SAS | STU | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG04228 | hp1 | a0002 | c0002 | t0001 | g0001 | SAS | STU | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | STU | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA18906 | hp1 | a0002 | c0002 | t0001 | g0067 | AFR | YRI | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | YRI | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA18939 | hp1 | a0002 | c0002 | t0001 | g0065 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA18947 | hp2 | a0002 | c0002 | t0001 | g0024 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA18948 | hp2 | a0002 | c0002 | t0001 | g0023 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA18950 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA18952 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA18957 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA18959 | hp1 | a0003 | c0004 | t0002 | g0018 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA18965 | hp1 | a0002 | c0002 | t0001 | g0058 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA18965 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA18967 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA18969 | hp1 | a0003 | c0004 | t0002 | g0020 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA18973 | hp2 | a0002 | c0002 | t0001 | g0080 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA18979 | hp1 | a0002 | c0002 | t0001 | g0081 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA18980 | hp1 | a0002 | c0002 | t0001 | g0082 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA18984 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA18986 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA18987 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA18991 | hp1 | a0002 | c0002 | t0001 | g0083 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA18992 | hp1 | a0002 | c0002 | t0001 | g0072 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA18994 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA18997 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA19004 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA19005 | hp2 | a0002 | c0002 | t0001 | g0070 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA19009 | hp2 | a0003 | c0004 | t0002 | g0076 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA19011 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA19012 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA19012 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | LWK | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA19030 | hp2 | a0002 | c0002 | t0001 | g0026 | AFR | LWK | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA19043 | hp1 | a0004 | c0009 | t0001 | g0147 | AFR | LWK | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA19043 | hp2 | a0001 | c0003 | t0001 | g0048 | AFR | LWK | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA19054 | hp2 | a0003 | c0004 | t0002 | g0020 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA19064 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA19065 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA19068 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA19074 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA19079 | hp1 | a0002 | c0002 | t0001 | g0055 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA19080 | hp2 | a0002 | c0002 | t0001 | g0023 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA19081 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA19085 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA19087 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA19091 | hp2 | a0002 | c0002 | t0001 | g0024 | EAS | JPT | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA19240 | hp1 | a0001 | c0007 | t0001 | g0017 | AFR | YRI | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA19240 | hp2 | a0002 | c0002 | t0001 | g0057 | AFR | YRI | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | ASW | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA20129 | hp2 | a0002 | c0002 | t0001 | g0071 | AFR | ASW | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA20752 | hp1 | a0001 | c0003 | t0001 | g0014 | EUR | TSI | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | TSI | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA20805 | hp1 | a0001 | c0003 | t0001 | g0007 | EUR | TSI | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0006 | EUR | TSI | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA20905 | hp1 | a0001 | c0003 | t0001 | g0007 | SAS | GIH | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0051 | SAS | GIH | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG01123 | hp1 | a0001 | c0003 | t0001 | g0060 | AMR | CLM | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG02486 | hp1 | a0005 | c0008 | t0001 | g0001 | AFR | ACB | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG02559 | hp2 | a0002 | c0002 | t0001 | g0026 | AFR | ACB | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | USA | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
HG06807 | hp2 | a0001 | c0003 | t0001 | g0052 | AFR | USA | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA20300 | hp1 | a0002 | c0002 | t0001 | g0001 | AFR | USA | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA20300 | hp2 | a0001 | c0003 | t0001 | g0010 | AFR | USA | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA21309 | hp1 | a0002 | c0002 | t0001 | g0001 | AFR | LWK | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | LWK | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
homoSapiens_chm13v2 | hp1 | a0002 | c0005 | t0001 | g0001 | REF | REF | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
homoSapiens_grch38 | hp1 | a0001 | c0003 | t0001 | g0056 | REF | REF | FAAH_chr1_46389317_46418845 | FAAH | chr1 | 46389317 | 46418845 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:46405089
|
C | A | 2 | a0002a0005 | 102 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(99): Show |
missense_variant | MODERATE | c.385C>A | p.Pro129Thr | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 3/15 | 417/2042 | 385/1740 | 129/579 | chr1 | 46405089 | ||
chr1:46408494
|
C | G | 1 | a0005 | 1 | HG02486.hp1 | stop_gained | HIGH | c.987C>G | p.Tyr329* | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 8/15 | 1019/2042 | 987/1740 | 329/579 | chr1 | 46408494 | ||
chr1:46408496
|
A | ACCCCACC others(7): Show |
1 | a0005 | 1 | HG02486.hp1 | frameshift_variant&stop_gained | HIGH | c.989_990insCCCCACCT others(6): Show |
p.Glu331fs | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 8/15 | 1022/2042 | 990/1740 | 330/579 | chr1 | 46408496 | ||
chr1:46408574
|
C | T | 1 | a0003 | 7 | HG00544.hp2 HG01884.hp2 HG03834.hp2 others(4): Show |
missense_variant | MODERATE | c.1067C>T | p.Ala356Val | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 8/15 | 1099/2042 | 1067/1740 | 356/579 | chr1 | 46408574 | ||
chr1:46409132
|
A | G | 1 | a0004 | 1 | NA19043.hp1 | missense_variant | MODERATE | c.1109A>G | p.His370Arg | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 9/15 | 1141/2042 | 1109/1740 | 370/579 | chr1 | 46409132 | ||
chr1:46412213
|
C | G | 1 | a0003 | 7 | HG00544.hp2 HG01884.hp2 HG03834.hp2 others(4): Show |
missense_variant | MODERATE | c.1427C>G | p.Ala476Gly | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 13/15 | 1459/2042 | 1427/1740 | 476/579 | chr1 | 46412213 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:46405702
|
C | G | 1 | a0001c0007 | 2 | HG02717.hp2 NA19240.hp1 |
synonymous_variant | LOW | c.693C>G | p.Pro231Pro | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 5/15 | 725/2042 | 693/1740 | 231/579 | chr1 | 46405702 | ||
chr1:46406041
|
G | A | 2 | a0003c0004a0003c0006 | 9 | HG00544.hp2 HG01884.hp2 HG03139.hp2 others(6): Show |
synonymous_variant | LOW | c.789G>A | p.Lys263Lys | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 6/15 | 821/2042 | 789/1740 | 263/579 | chr1 | 46406041 | ||
chr1:46406074
|
G | A | 1 | a0002c0005 | 6 | HG00099.hp1 HG00280.hp1 HG00741.hp1 others(3): Show |
synonymous_variant | LOW | c.822G>A | p.Glu274Glu | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 6/15 | 854/2042 | 822/1740 | 274/579 | chr1 | 46406074 | ||
chr1:46406314
|
T | C | 7 | a0001c0001a0001c0007a0002c0002others(4): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(328): Show |
synonymous_variant | LOW | c.897T>C | p.Cys299Cys | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 7/15 | 929/2042 | 897/1740 | 299/579 | chr1 | 46406314 | ||
chr1:46410816
|
G | C | 1 | a0003c0004 | 7 | HG00544.hp2 HG01884.hp2 HG03834.hp2 others(4): Show |
splice_region_variant&synonymous_variant | LOW | c.1278G>C | p.Leu426Leu | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 11/15 | 1310/2042 | 1278/1740 | 426/579 | chr1 | 46410816 | ||
chr1:46411612
|
T | G | 1 | a0003c0004 | 7 | HG00544.hp2 HG01884.hp2 HG03834.hp2 others(4): Show |
splice_region_variant&synonymous_variant | LOW | c.1317T>G | p.Arg439Arg | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 12/15 | 1349/2042 | 1317/1740 | 439/579 | chr1 | 46411612 | ||
chr1:46413467
|
G | A | 1 | a0003c0004 | 7 | HG00544.hp2 HG01884.hp2 HG03834.hp2 others(4): Show |
synonymous_variant | LOW | c.1632G>A | p.Gly544Gly | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 15/15 | 1664/2042 | 1632/1740 | 544/579 | chr1 | 46413467 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:46394338
|
C | G | 1 | a0001c0001t0004 | 1 | HG01069.hp2 | 5_prime_UTR_variant | MODIFIER | c.-11C>G | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/15 | 11 | chr1 | 46394338 | |||||
chr1:46394339
|
T | G | 1 | a0001c0003t0003 | 1 | HG02602.hp2 | 5_prime_UTR_variant | MODIFIER | c.-10T>G | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/15 | 10 | chr1 | 46394339 | |||||
chr1:46413589
|
A | G | 1 | a0003c0004t0002 | 7 | HG00544.hp2 HG01884.hp2 HG03834.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*14A>G | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 15/15 | 14 | chr1 | 46413589 | |||||
chr1:46413769
|
C | T | 1 | a0003c0004t0002 | 7 | HG00544.hp2 HG01884.hp2 HG03834.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*194C>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 15/15 | 194 | chr1 | 46413769 | |||||
chr1:46413771
|
TCCTGATC others(6): Show |
T | 1 | a0003c0004t0002 | 7 | HG00544.hp2 HG01884.hp2 HG03834.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*199_*211delTGATCC others(7): Show |
FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 15/15 | 199 | INFO_REALIGN_3_PRIME | chr1 | 46413771 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:46394552
|
C | T | 1 | a0001c0001t0001g0167 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.195+9C>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46394552 | ||||||
chr1:46394565
|
G | A | 14 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0016others(11): Show | 28 | HG00140.hp2 HG00544.hp1 HG00544.hp2 others(25): Show |
intron_variant | MODIFIER | c.195+22G>A | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46394565 | ||||||
chr1:46394590
|
C | A | 1 | a0001c0001t0004g0047 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.195+47C>A | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46394590 | ||||||
chr1:46394619
|
G | A | 4 | a0001c0001t0001g0016a0001c0001t0001g0038a0001c0001t0001g0039others(1): Show | 5 | HG01243.hp1 HG02145.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.195+76G>A | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46394619 | ||||||
chr1:46394750
|
T | C | 2 | a0001c0003t0001g0048a0001c0003t0001g0049 | 2 | HG03516.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.195+207T>C | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46394750 | ||||||
chr1:46394863
|
G | A | 1 | a0001c0001t0001g0050 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.195+320G>A | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46394863 | ||||||
chr1:46394938
|
G | GT | 6 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0165others(3): Show | 8 | HG00621.hp2 HG02015.hp1 HG02074.hp1 others(5): Show |
intron_variant | MODIFIER | c.195+404dupT | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 46394938 | |||||
chr1:46394938
|
GT | G | 14 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0016others(11): Show | 28 | HG00140.hp2 HG00544.hp1 HG00544.hp2 others(25): Show |
intron_variant | MODIFIER | c.195+404delT | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 46394938 | |||||
chr1:46394986
|
C | T | 3 | a0001c0001t0001g0035a0001c0001t0001g0050a0001c0001t0001g0162 | 4 | HG02145.hp2 HG02257.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.195+443C>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46394986 | ||||||
chr1:46395155
|
G | C | 14 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0016others(11): Show | 28 | HG00140.hp2 HG00544.hp1 HG00544.hp2 others(25): Show |
intron_variant | MODIFIER | c.195+612G>C | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46395155 | ||||||
chr1:46395215
|
G | T | 1 | a0001c0001t0004g0047 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.195+672G>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46395215 | ||||||
chr1:46395472
|
T | C | 1 | a0001c0001t0001g0051 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.195+929T>C | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46395472 | ||||||
chr1:46395610
|
G | T | 1 | a0001c0001t0004g0047 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.195+1067G>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46395610 | ||||||
chr1:46395634
|
A | C | 16 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0012others(13): Show | 33 | HG00140.hp2 HG00544.hp1 HG00544.hp2 others(30): Show |
intron_variant | MODIFIER | c.195+1091A>C | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46395634 | ||||||
chr1:46395986
|
G | C | 1 | a0001c0003t0001g0052 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.195+1443G>C | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46395986 | ||||||
chr1:46396035
|
G | A | 1 | a0001c0001t0001g0053 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.195+1492G>A | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46396035 | ||||||
chr1:46396235
|
A | G | 124 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(121): Show | 260 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(257): Show |
intron_variant | MODIFIER | c.195+1692A>G | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46396235 | ||||||
chr1:46396270
|
T | G | 1 | a0002c0005t0001g0054 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.195+1727T>G | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46396270 | ||||||
chr1:46396327
|
A | G | 1 | a0002c0002t0001g0084 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.195+1784A>G | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46396327 | ||||||
chr1:46396345
|
C | T | 1 | a0001c0001t0001g0160 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.195+1802C>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46396345 | ||||||
chr1:46396349
|
C | T | 1 | a0001c0001t0004g0047 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.195+1806C>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46396349 | ||||||
chr1:46396369
|
C | T | 1 | a0001c0003t0001g0159 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.195+1826C>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46396369 | ||||||
chr1:46396395
|
C | T | 1 | a0001c0001t0001g0158 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.195+1852C>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46396395 | ||||||
chr1:46396477
|
C | T | 1 | a0001c0001t0001g0034 | 2 | HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.195+1934C>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46396477 | ||||||
chr1:46396608
|
TG | T | 14 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0016others(11): Show | 28 | HG00140.hp2 HG00544.hp1 HG00544.hp2 others(25): Show |
intron_variant | MODIFIER | c.195+2066delG | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46396608 | ||||||
chr1:46396660
|
C | G | 14 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0016others(11): Show | 28 | HG00140.hp2 HG00544.hp1 HG00544.hp2 others(25): Show |
intron_variant | MODIFIER | c.195+2117C>G | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46396660 | ||||||
chr1:46396683
|
A | C | 2 | a0001c0001t0001g0156a0001c0001t0001g0157 | 2 | HG02809.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.195+2140A>C | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46396683 | ||||||
chr1:46396746
|
C | T | 4 | a0001c0001t0001g0155a0001c0001t0001g0158a0001c0003t0001g0048others(1): Show | 4 | HG02572.hp2 HG03516.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.195+2203C>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46396746 | ||||||
chr1:46396829
|
C | T | 5 | a0002c0002t0001g0005a0002c0002t0001g0080a0002c0002t0001g0081others(2): Show | 15 | HG00673.hp2 HG02040.hp2 NA18950.hp1 others(12): Show |
intron_variant | MODIFIER | c.195+2286C>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46396829 | ||||||
chr1:46396883
|
C | T | 14 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0016others(11): Show | 28 | HG00140.hp2 HG00544.hp1 HG00544.hp2 others(25): Show |
intron_variant | MODIFIER | c.195+2340C>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46396883 | ||||||
chr1:46397108
|
C | T | 13 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0016others(10): Show | 26 | HG00140.hp2 HG00544.hp1 HG00544.hp2 others(23): Show |
intron_variant | MODIFIER | c.195+2565C>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46397108 | ||||||
chr1:46397221
|
C | T | 14 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0016others(11): Show | 28 | HG00140.hp2 HG00544.hp1 HG00544.hp2 others(25): Show |
intron_variant | MODIFIER | c.195+2678C>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46397221 | ||||||
chr1:46397277
|
T | C | 1 | a0001c0007t0001g0017 | 2 | HG02717.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.195+2734T>C | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46397277 | ||||||
chr1:46397404
|
G | A | 1 | a0002c0002t0001g0055 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.195+2861G>A | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46397404 | ||||||
chr1:46397529
|
C | G | 166 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(163): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.195+2986C>G | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46397529 | ||||||
chr1:46397529
|
C | T | 2 | a0001c0001t0001g0155a0001c0001t0001g0158 | 2 | HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.195+2986C>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46397529 | ||||||
chr1:46397530
|
G | A | 7 | a0001c0001t0001g0034a0001c0001t0001g0086a0001c0003t0001g0007others(4): Show | 19 | HG00140.hp1 HG00733.hp2 HG01256.hp2 others(16): Show |
intron_variant | MODIFIER | c.195+2987G>A | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46397530 | ||||||
chr1:46397530
|
G | C | 4 | a0001c0001t0001g0016a0001c0001t0001g0038a0001c0001t0001g0039others(1): Show | 5 | HG01243.hp1 HG02145.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.195+2987G>C | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46397530 | ||||||
chr1:46397530
|
G | T | 5 | a0002c0002t0001g0005a0002c0002t0001g0080a0002c0002t0001g0081others(2): Show | 15 | HG00673.hp2 HG02040.hp2 NA18950.hp1 others(12): Show |
intron_variant | MODIFIER | c.195+2987G>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46397530 | ||||||
chr1:46397552
|
G | T | 1 | a0001c0001t0001g0154 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.195+3009G>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46397552 | ||||||
chr1:46397598
|
G | A | 42 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(39): Show | 85 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.195+3055G>A | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46397598 | ||||||
chr1:46397624
|
C | T | 1 | a0002c0002t0001g0079 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.195+3081C>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46397624 | ||||||
chr1:46397760
|
C | T | 1 | a0001c0003t0001g0049 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.195+3217C>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46397760 | ||||||
chr1:46397843
|
A | G | 17 | a0001c0001t0001g0011a0001c0001t0001g0032a0001c0001t0001g0033others(14): Show | 22 | HG00639.hp1 HG00642.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.195+3300A>G | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46397843 | ||||||
chr1:46397874
|
A | G | 1 | a0001c0001t0001g0167 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.195+3331A>G | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46397874 | ||||||
chr1:46397884
|
G | A | 1 | a0001c0001t0001g0113 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.195+3341G>A | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46397884 | ||||||
chr1:46397932
|
C | CT | 35 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0032others(32): Show | 58 | HG00140.hp1 HG00639.hp1 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.195+3408dupT | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 46397932 | |||||
chr1:46397932
|
C | CTT | 6 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0003t0001g0048others(3): Show | 6 | HG02895.hp1 HG02897.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.195+3407_195+3408d others(4): Show |
FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 46397932 | |||||
chr1:46397932
|
CT | C | 5 | a0001c0001t0001g0016a0001c0001t0001g0038a0001c0001t0001g0039others(2): Show | 7 | HG01243.hp1 HG02040.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.195+3408delT | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 46397932 | |||||
chr1:46397937
|
TTTTTTTT others(13): Show |
T | 33 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(30): Show | 63 | HG00408.hp2 HG00423.hp2 HG00673.hp1 others(60): Show |
intron_variant | MODIFIER | c.195+3395_195+3414d others(22): Show |
FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46397937 | ||||||
chr1:46398072
|
T | C | 1 | a0001c0001t0001g0145 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.195+3529T>C | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46398072 | ||||||
chr1:46398156
|
A | G | 1 | a0001c0001t0001g0157 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.195+3613A>G | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46398156 | ||||||
chr1:46398478
|
C | T | 13 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0016others(10): Show | 26 | HG00140.hp2 HG00544.hp1 HG00544.hp2 others(23): Show |
intron_variant | MODIFIER | c.196-3613C>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46398478 | ||||||
chr1:46398539
|
C | CTTTTT | 6 | a0001c0001t0001g0016a0001c0001t0001g0038a0001c0001t0001g0039others(3): Show | 8 | HG00544.hp2 HG01243.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.196-3544_196-3540d others(7): Show |
FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 46398539 | |||||
chr1:46398539
|
C | CTTTTTT | 7 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0041others(4): Show | 18 | HG00140.hp2 HG00544.hp1 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.196-3545_196-3540d others(8): Show |
FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 46398539 | |||||
chr1:46398552
|
G | A | 1 | a0002c0002t0001g0057 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.196-3539G>A | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46398552 | ||||||
chr1:46398560
|
G | T | 1 | a0003c0004t0002g0137 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.196-3531G>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46398560 | ||||||
chr1:46398582
|
G | A | 2 | a0001c0001t0001g0146a0004c0009t0001g0147 | 2 | HG03130.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.196-3509G>A | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46398582 | ||||||
chr1:46398765
|
C | T | 1 | a0001c0001t0001g0044 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.196-3326C>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46398765 | ||||||
chr1:46398819
|
G | A | 6 | a0001c0003t0001g0010a0001c0003t0001g0031a0001c0003t0001g0052others(3): Show | 11 | HG01891.hp2 HG02257.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.196-3272G>A | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46398819 | ||||||
chr1:46398839
|
G | A | 119 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(116): Show | 254 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.196-3252G>A | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46398839 | ||||||
chr1:46398856
|
A | C | 16 | a0001c0001t0001g0113a0001c0001t0001g0146a0001c0001t0001g0155others(13): Show | 21 | HG01891.hp2 HG02257.hp1 HG02280.hp2 others(18): Show |
intron_variant | MODIFIER | c.196-3235A>C | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46398856 | ||||||
chr1:46398878
|
C | CTAAACAC others(35): Show |
1 | a0001c0001t0001g0110 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.196-3212_196-3171d others(44): Show |
FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 46398878 | |||||
chr1:46398981
|
A | AT | 51 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0009others(48): Show | 92 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.196-3104dupT | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 46398981 | |||||
chr1:46398996
|
GC | G | 96 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(93): Show | 213 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(210): Show |
intron_variant | MODIFIER | c.196-3090delC | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 46398996 | |||||
chr1:46399055
|
A | G | 12 | a0001c0001t0001g0034a0001c0001t0001g0086a0001c0001t0001g0132others(9): Show | 18 | HG01891.hp2 HG01943.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.196-3036A>G | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46399055 | ||||||
chr1:46399108
|
T | G | 1 | a0001c0001t0001g0132 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.196-2983T>G | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46399108 | ||||||
chr1:46399132
|
C | T | 1 | a0001c0001t0001g0162 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.196-2959C>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46399132 | ||||||
chr1:46399321
|
C | T | 2 | a0001c0001t0001g0155a0001c0001t0001g0158 | 2 | HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.196-2770C>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46399321 | ||||||
chr1:46399332
|
G | A | 2 | a0001c0001t0001g0155a0001c0001t0001g0158 | 2 | HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.196-2759G>A | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46399332 | ||||||
chr1:46399368
|
T | C | 59 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(56): Show | 143 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.196-2723T>C | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46399368 | ||||||
chr1:46399411
|
C | T | 1 | a0002c0002t0001g0073 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.196-2680C>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46399411 | ||||||
chr1:46399487
|
T | C | 1 | a0001c0001t0001g0114 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.196-2604T>C | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46399487 | ||||||
chr1:46399522
|
G | A | 1 | a0001c0001t0001g0113 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.196-2569G>A | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46399522 | ||||||
chr1:46399549
|
G | A | 1 | a0002c0002t0001g0058 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.196-2542G>A | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46399549 | ||||||
chr1:46399584
|
T | G | 1 | a0001c0001t0001g0157 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.196-2507T>G | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46399584 | ||||||
chr1:46399714
|
A | G | 2 | a0001c0001t0001g0155a0001c0001t0001g0158 | 2 | HG02572.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.196-2377A>G | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46399714 | ||||||
chr1:46399715
|
A | G | 94 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(91): Show | 237 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.196-2376A>G | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46399715 | ||||||
chr1:46399848
|
A | T | 1 | a0001c0001t0001g0131 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.196-2243A>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46399848 | ||||||
chr1:46399877
|
C | T | 1 | a0001c0001t0001g0161 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.196-2214C>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46399877 | ||||||
chr1:46399893
|
T | C | 2 | a0001c0003t0001g0031a0001c0003t0001g0138 | 3 | HG02896.hp2 HG02897.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.196-2198T>C | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46399893 | ||||||
chr1:46399999
|
A | G | 53 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(50): Show | 133 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.196-2092A>G | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46399999 | ||||||
chr1:46400084
|
T | A | 1 | a0001c0001t0001g0165 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.196-2007T>A | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46400084 | ||||||
chr1:46400190
|
G | T | 1 | a0001c0001t0001g0158 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.196-1901G>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46400190 | ||||||
chr1:46400358
|
T | C | 7 | a0003c0004t0002g0018a0003c0004t0002g0020a0003c0004t0002g0045others(4): Show | 9 | HG00544.hp2 HG01884.hp2 HG03139.hp2 others(6): Show |
intron_variant | MODIFIER | c.196-1733T>C | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46400358 | ||||||
chr1:46400412
|
G | A | 1 | a0001c0003t0001g0085 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.196-1679G>A | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46400412 | ||||||
chr1:46400413
|
CGTGTGAC others(11): Show |
C | 7 | a0003c0004t0002g0018a0003c0004t0002g0020a0003c0004t0002g0045others(4): Show | 9 | HG00544.hp2 HG01884.hp2 HG03139.hp2 others(6): Show |
intron_variant | MODIFIER | c.196-1676_196-1659d others(20): Show |
FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 46400413 | |||||
chr1:46400587
|
G | A | 7 | a0003c0004t0002g0018a0003c0004t0002g0020a0003c0004t0002g0045others(4): Show | 9 | HG00544.hp2 HG01884.hp2 HG03139.hp2 others(6): Show |
intron_variant | MODIFIER | c.196-1504G>A | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46400587 | ||||||
chr1:46400588
|
G | T | 7 | a0003c0004t0002g0018a0003c0004t0002g0020a0003c0004t0002g0045others(4): Show | 9 | HG00544.hp2 HG01884.hp2 HG03139.hp2 others(6): Show |
intron_variant | MODIFIER | c.196-1503G>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46400588 | ||||||
chr1:46400662
|
A | G | 3 | a0003c0004t0002g0020a0003c0004t0002g0045a0003c0004t0002g0076 | 4 | HG03834.hp2 NA18969.hp1 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.196-1429A>G | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46400662 | ||||||
chr1:46400678
|
G | A | 1 | a0001c0001t0001g0095 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.196-1413G>A | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46400678 | ||||||
chr1:46400905
|
A | G | 166 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(163): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.196-1186A>G | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46400905 | ||||||
chr1:46400906
|
A | G | 1 | a0001c0001t0001g0118 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.196-1185A>G | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46400906 | ||||||
chr1:46400907
|
A | G | 1 | a0001c0001t0001g0118 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.196-1184A>G | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46400907 | ||||||
chr1:46400962
|
G | A | 1 | a0002c0002t0001g0063 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.196-1129G>A | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46400962 | ||||||
chr1:46401043
|
G | GA | 168 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(165): Show | 369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.196-1045dupA | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 46401043 | |||||
chr1:46401052
|
G | A | 1 | a0001c0001t0001g0145 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.196-1039G>A | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46401052 | ||||||
chr1:46401113
|
G | C | 1 | a0001c0001t0001g0039 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.196-978G>C | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46401113 | ||||||
chr1:46401159
|
TA | T | 7 | a0003c0004t0002g0018a0003c0004t0002g0020a0003c0004t0002g0045others(4): Show | 9 | HG00544.hp2 HG01884.hp2 HG03139.hp2 others(6): Show |
intron_variant | MODIFIER | c.196-931delA | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46401159 | ||||||
chr1:46401236
|
G | T | 1 | a0001c0001t0001g0132 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.196-855G>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46401236 | ||||||
chr1:46401300
|
C | G | 2 | a0001c0001t0001g0016a0001c0001t0001g0040 | 3 | HG02486.hp2 HG02922.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.196-791C>G | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46401300 | ||||||
chr1:46401325
|
T | C | 7 | a0003c0004t0002g0018a0003c0004t0002g0020a0003c0004t0002g0045others(4): Show | 9 | HG00544.hp2 HG01884.hp2 HG03139.hp2 others(6): Show |
intron_variant | MODIFIER | c.196-766T>C | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46401325 | ||||||
chr1:46401335
|
T | C | 48 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(45): Show | 89 | HG00408.hp2 HG00423.hp2 HG00639.hp1 others(86): Show |
intron_variant | MODIFIER | c.196-756T>C | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46401335 | ||||||
chr1:46401375
|
T | C | 7 | a0003c0004t0002g0018a0003c0004t0002g0020a0003c0004t0002g0045others(4): Show | 9 | HG00544.hp2 HG01884.hp2 HG03139.hp2 others(6): Show |
intron_variant | MODIFIER | c.196-716T>C | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46401375 | ||||||
chr1:46401759
|
T | G | 1 | a0001c0001t0001g0140 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.196-332T>G | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46401759 | ||||||
chr1:46401780
|
A | T | 1 | a0001c0001t0001g0094 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.196-311A>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46401780 | ||||||
chr1:46401797
|
G | A | 7 | a0003c0004t0002g0018a0003c0004t0002g0020a0003c0004t0002g0045others(4): Show | 9 | HG00544.hp2 HG01884.hp2 HG03139.hp2 others(6): Show |
intron_variant | MODIFIER | c.196-294G>A | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46401797 | ||||||
chr1:46401802
|
T | G | 1 | a0002c0002t0001g0064 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.196-289T>G | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46401802 | ||||||
chr1:46401860
|
A | C | 1 | a0001c0007t0001g0017 | 2 | HG02717.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.196-231A>C | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46401860 | ||||||
chr1:46401884
|
G | GA | 7 | a0001c0001t0001g0030a0001c0001t0001g0089a0001c0001t0001g0140others(4): Show | 8 | HG00642.hp2 HG01515.hp2 HG03688.hp1 others(5): Show |
intron_variant | MODIFIER | c.196-197dupA | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 46401884 | |||||
chr1:46401884
|
GA | G | 7 | a0003c0004t0002g0018a0003c0004t0002g0020a0003c0004t0002g0045others(4): Show | 9 | HG00544.hp2 HG01884.hp2 HG03139.hp2 others(6): Show |
intron_variant | MODIFIER | c.196-197delA | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 46401884 | |||||
chr1:46402009
|
C | G | 4 | a0001c0001t0001g0011a0001c0001t0001g0032a0001c0001t0001g0033others(1): Show | 9 | HG00639.hp1 HG00642.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.196-82C>G | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 1/14 | chr1 | 46402009 | ||||||
chr1:46402196
|
GTGGGAAA others(29): Show |
G | 7 | a0003c0004t0002g0018a0003c0004t0002g0020a0003c0004t0002g0045others(4): Show | 9 | HG00544.hp2 HG01884.hp2 HG03139.hp2 others(6): Show |
intron_variant | MODIFIER | c.309+30_309+65delGG others(34): Show |
FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 46402196 | |||||
chr1:46402242
|
T | TAAGGCCA others(3): Show |
4 | a0001c0001t0001g0132a0001c0001t0001g0151a0001c0001t0001g0152others(1): Show | 5 | HG02717.hp2 HG02886.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.309+49_309+58dupAA others(8): Show |
FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 46402242 | |||||
chr1:46402351
|
G | T | 1 | a0001c0001t0001g0140 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.309+147G>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 2/14 | chr1 | 46402351 | ||||||
chr1:46402352
|
T | G | 1 | a0001c0001t0001g0140 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.309+148T>G | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 2/14 | chr1 | 46402352 | ||||||
chr1:46402361
|
C | T | 1 | a0001c0001t0001g0130 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.309+157C>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 2/14 | chr1 | 46402361 | ||||||
chr1:46402395
|
G | T | 3 | a0003c0004t0002g0020a0003c0004t0002g0045a0003c0004t0002g0076 | 4 | HG03834.hp2 NA18969.hp1 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.309+191G>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 2/14 | chr1 | 46402395 | ||||||
chr1:46402520
|
C | CT | 8 | a0001c0001t0001g0146a0001c0001t0001g0149a0003c0004t0002g0018others(5): Show | 10 | HG00544.hp2 HG03130.hp1 HG03139.hp2 others(7): Show |
intron_variant | MODIFIER | c.309+325dupT | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 46402520 | |||||
chr1:46402558
|
G | T | 5 | a0001c0001t0001g0009a0001c0001t0001g0093a0001c0001t0001g0094others(2): Show | 10 | HG00423.hp2 HG02056.hp2 HG02129.hp2 others(7): Show |
intron_variant | MODIFIER | c.309+354G>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 2/14 | chr1 | 46402558 | ||||||
chr1:46402664
|
C | A | 1 | a0003c0006t0001g0134 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.309+460C>A | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 2/14 | chr1 | 46402664 | ||||||
chr1:46402694
|
A | AT | 8 | a0001c0001t0001g0043a0001c0001t0001g0092a0001c0001t0001g0096others(5): Show | 8 | HG02897.hp2 HG03669.hp1 NA18941.hp2 others(5): Show |
intron_variant | MODIFIER | c.309+506dupT | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 46402694 | |||||
chr1:46402694
|
A | T | 1 | a0001c0001t0001g0129 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.309+490A>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 2/14 | chr1 | 46402694 | ||||||
chr1:46402694
|
AT | A | 6 | a0001c0001t0001g0118a0001c0001t0001g0120a0001c0001t0001g0166others(3): Show | 6 | NA18939.hp1 NA18946.hp1 NA18979.hp1 others(3): Show |
intron_variant | MODIFIER | c.309+506delT | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 46402694 | |||||
chr1:46402695
|
T | A | 3 | a0001c0001t0001g0119a0003c0004t0002g0020a0003c0004t0002g0076 | 4 | NA18969.hp1 NA19009.hp2 NA19054.hp2 others(1): Show |
intron_variant | MODIFIER | c.309+491T>A | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 2/14 | chr1 | 46402695 | ||||||
chr1:46402696
|
T | A | 1 | a0001c0001t0001g0166 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.309+492T>A | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 2/14 | chr1 | 46402696 | ||||||
chr1:46402735
|
C | T | 2 | a0002c0002t0001g0025a0002c0002t0001g0066 | 3 | HG00733.hp1 HG01192.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.309+531C>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 2/14 | chr1 | 46402735 | ||||||
chr1:46403129
|
C | T | 2 | a0003c0006t0001g0134a0003c0006t0001g0135 | 2 | HG03139.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.309+925C>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 2/14 | chr1 | 46403129 | ||||||
chr1:46403139
|
T | C | 1 | a0001c0003t0001g0048 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.309+935T>C | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 2/14 | chr1 | 46403139 | ||||||
chr1:46403161
|
T | C | 9 | a0001c0001t0001g0146a0001c0001t0001g0149a0003c0004t0002g0018others(6): Show | 11 | HG00544.hp2 HG01884.hp2 HG03130.hp1 others(8): Show |
intron_variant | MODIFIER | c.309+957T>C | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 2/14 | chr1 | 46403161 | ||||||
chr1:46403255
|
C | T | 1 | a0001c0001t0001g0127 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.309+1051C>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 2/14 | chr1 | 46403255 | ||||||
chr1:46403455
|
G | A | 1 | a0001c0001t0001g0132 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.309+1251G>A | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 2/14 | chr1 | 46403455 | ||||||
chr1:46403730
|
C | T | 1 | a0002c0002t0001g0072 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.310-1284C>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 2/14 | chr1 | 46403730 | ||||||
chr1:46403743
|
A | G | 1 | a0001c0001t0001g0044 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.310-1271A>G | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 2/14 | chr1 | 46403743 | ||||||
chr1:46404037
|
C | A | 1 | a0003c0004t0002g0018 | 2 | HG00544.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.310-977C>A | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 2/14 | chr1 | 46404037 | ||||||
chr1:46404253
|
G | A | 4 | a0001c0001t0001g0146a0001c0001t0001g0149a0001c0003t0001g0112others(1): Show | 4 | HG02280.hp2 HG02622.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.310-761G>A | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 2/14 | chr1 | 46404253 | ||||||
chr1:46404358
|
G | A | 1 | a0001c0001t0001g0145 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.310-656G>A | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 2/14 | chr1 | 46404358 | ||||||
chr1:46404383
|
C | A | 1 | a0001c0001t0001g0090 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.310-631C>A | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 2/14 | chr1 | 46404383 | ||||||
chr1:46404520
|
A | G | 7 | a0003c0004t0002g0018a0003c0004t0002g0020a0003c0004t0002g0045others(4): Show | 9 | HG00544.hp2 HG01884.hp2 HG03139.hp2 others(6): Show |
intron_variant | MODIFIER | c.310-494A>G | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 2/14 | chr1 | 46404520 | ||||||
chr1:46404620
|
T | C | 7 | a0003c0004t0002g0018a0003c0004t0002g0020a0003c0004t0002g0045others(4): Show | 9 | HG00544.hp2 HG01884.hp2 HG03139.hp2 others(6): Show |
intron_variant | MODIFIER | c.310-394T>C | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 2/14 | chr1 | 46404620 | ||||||
chr1:46404625
|
C | T | 6 | a0001c0001t0001g0132a0001c0001t0001g0151a0001c0001t0001g0152others(3): Show | 7 | HG02572.hp2 HG02717.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.310-389C>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 2/14 | chr1 | 46404625 | ||||||
chr1:46405167
|
C | T | 1 | a0001c0003t0001g0049 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.444+19C>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 3/14 | chr1 | 46405167 | ||||||
chr1:46405187
|
C | T | 1 | a0003c0004t0002g0018 | 2 | HG00544.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.444+39C>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 3/14 | chr1 | 46405187 | ||||||
chr1:46405367
|
C | T | 3 | a0003c0004t0002g0020a0003c0004t0002g0045a0003c0004t0002g0076 | 4 | HG03834.hp2 NA18969.hp1 NA19009.hp2 others(1): Show |
splice_region_variant&intron_variant | LOW | c.445-5C>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 3/14 | chr1 | 46405367 | ||||||
chr1:46405887
|
C | T | 1 | a0001c0001t0001g0126 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.785+93C>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 5/14 | chr1 | 46405887 | ||||||
chr1:46405931
|
G | C | 2 | a0001c0001t0001g0119a0001c0001t0001g0166 | 2 | NA19003.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.786-107G>C | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 5/14 | chr1 | 46405931 | ||||||
chr1:46406203
|
G | A | 7 | a0001c0003t0001g0007a0001c0003t0001g0014a0001c0003t0001g0085others(4): Show | 18 | HG00140.hp1 HG00733.hp2 HG01256.hp2 others(15): Show |
intron_variant | MODIFIER | c.827-41G>A | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 6/14 | chr1 | 46406203 | ||||||
chr1:46406393
|
A | G | 7 | a0003c0004t0002g0018a0003c0004t0002g0020a0003c0004t0002g0045others(4): Show | 9 | HG00544.hp2 HG01884.hp2 HG03139.hp2 others(6): Show |
intron_variant | MODIFIER | c.951+25A>G | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 7/14 | chr1 | 46406393 | ||||||
chr1:46406457
|
C | T | 1 | a0001c0001t0001g0127 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.951+89C>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 7/14 | chr1 | 46406457 | ||||||
chr1:46406555
|
C | CT | 8 | a0001c0001t0001g0089a0001c0001t0001g0106a0001c0001t0001g0125others(5): Show | 9 | HG03098.hp2 NA18939.hp1 NA18947.hp2 others(6): Show |
intron_variant | MODIFIER | c.951+200dupT | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr1 | 46406555 | |||||
chr1:46406555
|
CT | C | 9 | a0001c0001t0001g0115a0001c0001t0001g0118a0003c0004t0002g0018others(6): Show | 11 | HG00544.hp2 HG01884.hp2 HG03139.hp2 others(8): Show |
intron_variant | MODIFIER | c.951+200delT | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr1 | 46406555 | |||||
chr1:46406583
|
C | CT | 8 | a0001c0001t0001g0011a0001c0001t0001g0032a0001c0001t0001g0033others(5): Show | 13 | HG00639.hp1 HG00642.hp1 HG00735.hp2 others(10): Show |
intron_variant | MODIFIER | c.951+232dupT | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr1 | 46406583 | |||||
chr1:46406583
|
CT | C | 15 | a0001c0001t0001g0006a0001c0001t0001g0041a0001c0001t0001g0042others(12): Show | 24 | HG00140.hp2 HG00544.hp1 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.951+232delT | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr1 | 46406583 | |||||
chr1:46406583
|
CTTTTTTT others(4): Show |
C | 7 | a0003c0004t0002g0018a0003c0004t0002g0020a0003c0004t0002g0045others(4): Show | 9 | HG00544.hp2 HG01884.hp2 HG03139.hp2 others(6): Show |
intron_variant | MODIFIER | c.951+222_951+232del others(11): Show |
FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr1 | 46406583 | |||||
chr1:46406584
|
T | C | 1 | a0002c0002t0001g0065 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.951+216T>C | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 7/14 | chr1 | 46406584 | ||||||
chr1:46406587
|
T | C | 1 | a0002c0002t0001g0067 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.951+219T>C | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 7/14 | chr1 | 46406587 | ||||||
chr1:46406611
|
A | C | 7 | a0003c0004t0002g0018a0003c0004t0002g0020a0003c0004t0002g0045others(4): Show | 9 | HG00544.hp2 HG01884.hp2 HG03139.hp2 others(6): Show |
intron_variant | MODIFIER | c.951+243A>C | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 7/14 | chr1 | 46406611 | ||||||
chr1:46406654
|
C | T | 7 | a0003c0004t0002g0018a0003c0004t0002g0020a0003c0004t0002g0045others(4): Show | 9 | HG00544.hp2 HG01884.hp2 HG03139.hp2 others(6): Show |
intron_variant | MODIFIER | c.951+286C>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 7/14 | chr1 | 46406654 | ||||||
chr1:46406675
|
CGGGTTCA others(12): Show |
C | 7 | a0003c0004t0002g0018a0003c0004t0002g0020a0003c0004t0002g0045others(4): Show | 9 | HG00544.hp2 HG01884.hp2 HG03139.hp2 others(6): Show |
intron_variant | MODIFIER | c.951+328_951+346del others(19): Show |
FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr1 | 46406675 | |||||
chr1:46406702
|
C | T | 1 | a0002c0002t0001g0058 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.951+334C>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 7/14 | chr1 | 46406702 | ||||||
chr1:46406726
|
C | T | 4 | a0002c0002t0001g0013a0002c0002t0001g0063a0002c0002t0001g0077others(1): Show | 6 | HG00738.hp1 HG01071.hp2 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.951+358C>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 7/14 | chr1 | 46406726 | ||||||
chr1:46406750
|
C | T | 3 | a0001c0001t0001g0091a0001c0001t0001g0104a0001c0001t0001g0105 | 3 | HG00735.hp2 HG03710.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.951+382C>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 7/14 | chr1 | 46406750 | ||||||
chr1:46406752
|
G | C | 5 | a0003c0004t0002g0018a0003c0004t0002g0020a0003c0004t0002g0045others(2): Show | 7 | HG00544.hp2 HG01884.hp2 HG03834.hp2 others(4): Show |
intron_variant | MODIFIER | c.951+384G>C | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 7/14 | chr1 | 46406752 | ||||||
chr1:46406758
|
C | T | 1 | a0001c0001t0001g0103 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.951+390C>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 7/14 | chr1 | 46406758 | ||||||
chr1:46406762
|
C | T | 5 | a0003c0004t0002g0018a0003c0004t0002g0020a0003c0004t0002g0045others(2): Show | 7 | HG00544.hp2 HG01884.hp2 HG03834.hp2 others(4): Show |
intron_variant | MODIFIER | c.951+394C>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 7/14 | chr1 | 46406762 | ||||||
chr1:46406768
|
A | AT | 5 | a0003c0004t0002g0018a0003c0004t0002g0020a0003c0004t0002g0045others(2): Show | 7 | HG00544.hp2 HG01884.hp2 HG03834.hp2 others(4): Show |
intron_variant | MODIFIER | c.951+408dupT | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr1 | 46406768 | |||||
chr1:46406784
|
TAG | T | 5 | a0003c0004t0002g0018a0003c0004t0002g0020a0003c0004t0002g0045others(2): Show | 7 | HG00544.hp2 HG01884.hp2 HG03834.hp2 others(4): Show |
intron_variant | MODIFIER | c.951+417_951+418del others(2): Show |
FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 7/14 | chr1 | 46406784 | ||||||
chr1:46406814
|
T | G | 5 | a0003c0004t0002g0018a0003c0004t0002g0020a0003c0004t0002g0045others(2): Show | 7 | HG00544.hp2 HG01884.hp2 HG03834.hp2 others(4): Show |
intron_variant | MODIFIER | c.951+446T>G | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 7/14 | chr1 | 46406814 | ||||||
chr1:46406827
|
G | C | 5 | a0003c0004t0002g0018a0003c0004t0002g0020a0003c0004t0002g0045others(2): Show | 7 | HG00544.hp2 HG01884.hp2 HG03834.hp2 others(4): Show |
intron_variant | MODIFIER | c.951+459G>C | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 7/14 | chr1 | 46406827 | ||||||
chr1:46406849
|
G | A | 5 | a0003c0004t0002g0018a0003c0004t0002g0020a0003c0004t0002g0045others(2): Show | 7 | HG00544.hp2 HG01884.hp2 HG03834.hp2 others(4): Show |
intron_variant | MODIFIER | c.951+481G>A | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 7/14 | chr1 | 46406849 | ||||||
chr1:46406852
|
C | T | 1 | a0001c0003t0001g0062 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.951+484C>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 7/14 | chr1 | 46406852 | ||||||
chr1:46406892
|
T | C | 7 | a0003c0004t0002g0018a0003c0004t0002g0020a0003c0004t0002g0045others(4): Show | 9 | HG00544.hp2 HG01884.hp2 HG03139.hp2 others(6): Show |
intron_variant | MODIFIER | c.951+524T>C | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 7/14 | chr1 | 46406892 | ||||||
chr1:46406898
|
G | A | 42 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(39): Show | 78 | HG00408.hp2 HG00423.hp2 HG00673.hp1 others(75): Show |
intron_variant | MODIFIER | c.951+530G>A | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 7/14 | chr1 | 46406898 | ||||||
chr1:46406900
|
C | A | 2 | a0001c0001t0001g0146a0001c0001t0001g0149 | 2 | HG03130.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.951+532C>A | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 7/14 | chr1 | 46406900 | ||||||
chr1:46407026
|
A | G | 42 | a0001c0001t0001g0102a0001c0001t0001g0136a0001c0001t0001g0142others(39): Show | 105 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.951+658A>G | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 7/14 | chr1 | 46407026 | ||||||
chr1:46407077
|
G | C | 1 | a0001c0001t0001g0155 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.951+709G>C | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 7/14 | chr1 | 46407077 | ||||||
chr1:46407079
|
T | C | 1 | a0001c0001t0001g0109 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.951+711T>C | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 7/14 | chr1 | 46407079 | ||||||
chr1:46407107
|
A | G | 7 | a0003c0004t0002g0018a0003c0004t0002g0020a0003c0004t0002g0045others(4): Show | 9 | HG00544.hp2 HG01884.hp2 HG03139.hp2 others(6): Show |
intron_variant | MODIFIER | c.951+739A>G | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 7/14 | chr1 | 46407107 | ||||||
chr1:46407196
|
G | T | 1 | a0001c0001t0001g0124 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.951+828G>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 7/14 | chr1 | 46407196 | ||||||
chr1:46407367
|
G | A | 10 | a0001c0001t0001g0004a0001c0001t0001g0053a0001c0001t0001g0088others(7): Show | 26 | HG00099.hp2 HG01081.hp2 HG01099.hp1 others(23): Show |
intron_variant | MODIFIER | c.951+999G>A | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 7/14 | chr1 | 46407367 | ||||||
chr1:46407403
|
G | A | 2 | a0002c0002t0001g0022a0002c0002t0001g0068 | 3 | HG02717.hp1 HG03041.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.951+1035G>A | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 7/14 | chr1 | 46407403 | ||||||
chr1:46407607
|
CTG | C | 7 | a0001c0001t0001g0156a0001c0001t0001g0157a0003c0004t0002g0018others(4): Show | 9 | HG00544.hp2 HG01884.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.952-850_952-849del others(2): Show |
FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr1 | 46407607 | |||||
chr1:46407609
|
G | C | 39 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(36): Show | 116 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.952-850G>C | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 7/14 | chr1 | 46407609 | ||||||
chr1:46407621
|
G | A | 1 | a0002c0002t0001g0023 | 2 | NA18948.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.952-838G>A | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 7/14 | chr1 | 46407621 | ||||||
chr1:46407875
|
G | A | 2 | a0003c0004t0002g0020a0003c0004t0002g0076 | 3 | NA18969.hp1 NA19009.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.952-584G>A | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 7/14 | chr1 | 46407875 | ||||||
chr1:46407925
|
G | A | 5 | a0003c0004t0002g0018a0003c0004t0002g0020a0003c0004t0002g0045others(2): Show | 7 | HG00544.hp2 HG01884.hp2 HG03834.hp2 others(4): Show |
intron_variant | MODIFIER | c.952-534G>A | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 7/14 | chr1 | 46407925 | ||||||
chr1:46407977
|
C | T | 8 | a0001c0003t0001g0010a0001c0003t0001g0031a0001c0003t0001g0052others(5): Show | 13 | HG01891.hp2 HG02257.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.952-482C>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 7/14 | chr1 | 46407977 | ||||||
chr1:46408201
|
C | G | 5 | a0003c0004t0002g0018a0003c0004t0002g0020a0003c0004t0002g0045others(2): Show | 7 | HG00544.hp2 HG01884.hp2 HG03834.hp2 others(4): Show |
intron_variant | MODIFIER | c.952-258C>G | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 7/14 | chr1 | 46408201 | ||||||
chr1:46408228
|
G | T | 5 | a0003c0004t0002g0018a0003c0004t0002g0020a0003c0004t0002g0045others(2): Show | 7 | HG00544.hp2 HG01884.hp2 HG03834.hp2 others(4): Show |
intron_variant | MODIFIER | c.952-231G>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 7/14 | chr1 | 46408228 | ||||||
chr1:46408231
|
C | T | 42 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(39): Show | 78 | HG00408.hp2 HG00423.hp2 HG00673.hp1 others(75): Show |
intron_variant | MODIFIER | c.952-228C>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 7/14 | chr1 | 46408231 | ||||||
chr1:46408388
|
C | T | 1 | a0003c0004t0002g0018 | 2 | HG00544.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.952-71C>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 7/14 | chr1 | 46408388 | ||||||
chr1:46408414
|
T | C | 5 | a0003c0004t0002g0018a0003c0004t0002g0020a0003c0004t0002g0045others(2): Show | 7 | HG00544.hp2 HG01884.hp2 HG03834.hp2 others(4): Show |
intron_variant | MODIFIER | c.952-45T>C | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 7/14 | chr1 | 46408414 | ||||||
chr1:46408641
|
C | T | 1 | a0003c0004t0002g0137 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1077+57C>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 8/14 | chr1 | 46408641 | ||||||
chr1:46408687
|
A | G | 5 | a0003c0004t0002g0018a0003c0004t0002g0020a0003c0004t0002g0045others(2): Show | 7 | HG00544.hp2 HG01884.hp2 HG03834.hp2 others(4): Show |
intron_variant | MODIFIER | c.1077+103A>G | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 8/14 | chr1 | 46408687 | ||||||
chr1:46408711
|
A | G | 102 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(99): Show | 224 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(221): Show |
intron_variant | MODIFIER | c.1077+127A>G | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 8/14 | chr1 | 46408711 | ||||||
chr1:46409346
|
A | G | 1 | a0001c0001t0001g0145 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1175+148A>G | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 9/14 | chr1 | 46409346 | ||||||
chr1:46409356
|
A | G | 2 | a0001c0001t0001g0034a0001c0001t0001g0086 | 3 | HG02895.hp2 HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1175+158A>G | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 9/14 | chr1 | 46409356 | ||||||
chr1:46409395
|
G | T | 33 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0015others(30): Show | 101 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.1175+197G>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 9/14 | chr1 | 46409395 | ||||||
chr1:46409427
|
CT | C | 46 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(43): Show | 87 | HG00408.hp2 HG00423.hp2 HG00639.hp1 others(84): Show |
intron_variant | MODIFIER | c.1175+230delT | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 9/14 | chr1 | 46409427 | ||||||
chr1:46409698
|
C | T | 3 | a0003c0004t0002g0020a0003c0004t0002g0045a0003c0004t0002g0076 | 4 | HG03834.hp2 NA18969.hp1 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.1175+500C>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 9/14 | chr1 | 46409698 | ||||||
chr1:46409699
|
A | C | 1 | a0003c0004t0002g0137 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1175+501A>C | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 9/14 | chr1 | 46409699 | ||||||
chr1:46409706
|
G | GT | 5 | a0003c0004t0002g0018a0003c0004t0002g0020a0003c0004t0002g0045others(2): Show | 7 | HG00544.hp2 HG01884.hp2 HG03834.hp2 others(4): Show |
intron_variant | MODIFIER | c.1175+509dupT | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr1 | 46409706 | |||||
chr1:46409754
|
C | A | 1 | a0002c0002t0001g0082 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1175+556C>A | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 9/14 | chr1 | 46409754 | ||||||
chr1:46409858
|
C | T | 5 | a0003c0004t0002g0018a0003c0004t0002g0020a0003c0004t0002g0045others(2): Show | 7 | HG00544.hp2 HG01884.hp2 HG03834.hp2 others(4): Show |
intron_variant | MODIFIER | c.1176-540C>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 9/14 | chr1 | 46409858 | ||||||
chr1:46409875
|
C | T | 1 | a0003c0004t0002g0018 | 2 | HG00544.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.1176-523C>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 9/14 | chr1 | 46409875 | ||||||
chr1:46409922
|
T | C | 5 | a0003c0004t0002g0018a0003c0004t0002g0020a0003c0004t0002g0045others(2): Show | 7 | HG00544.hp2 HG01884.hp2 HG03834.hp2 others(4): Show |
intron_variant | MODIFIER | c.1176-476T>C | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 9/14 | chr1 | 46409922 | ||||||
chr1:46410190
|
T | G | 1 | a0001c0001t0001g0132 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1176-208T>G | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 9/14 | chr1 | 46410190 | ||||||
chr1:46410234
|
G | A | 5 | a0003c0004t0002g0018a0003c0004t0002g0020a0003c0004t0002g0045others(2): Show | 7 | HG00544.hp2 HG01884.hp2 HG03834.hp2 others(4): Show |
intron_variant | MODIFIER | c.1176-164G>A | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 9/14 | chr1 | 46410234 | ||||||
chr1:46410261
|
G | A | 5 | a0003c0004t0002g0018a0003c0004t0002g0020a0003c0004t0002g0045others(2): Show | 7 | HG00544.hp2 HG01884.hp2 HG03834.hp2 others(4): Show |
intron_variant | MODIFIER | c.1176-137G>A | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 9/14 | chr1 | 46410261 | ||||||
chr1:46410277
|
G | A | 5 | a0001c0001t0001g0009a0001c0001t0001g0093a0001c0001t0001g0094others(2): Show | 10 | HG00423.hp2 HG02056.hp2 HG02129.hp2 others(7): Show |
intron_variant | MODIFIER | c.1176-121G>A | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 9/14 | chr1 | 46410277 | ||||||
chr1:46410511
|
G | A | 2 | a0001c0001t0001g0034a0001c0001t0001g0086 | 3 | HG02895.hp2 HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1275+14G>A | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 10/14 | chr1 | 46410511 | ||||||
chr1:46410570
|
A | G | 1 | a0001c0001t0001g0100 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1275+73A>G | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 10/14 | chr1 | 46410570 | ||||||
chr1:46410776
|
C | G | 5 | a0003c0004t0002g0018a0003c0004t0002g0020a0003c0004t0002g0045others(2): Show | 7 | HG00544.hp2 HG01884.hp2 HG03834.hp2 others(4): Show |
intron_variant | MODIFIER | c.1276-38C>G | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 10/14 | chr1 | 46410776 | ||||||
chr1:46410798
|
C | T | 1 | a0001c0001t0001g0099 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1276-16C>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 10/14 | chr1 | 46410798 | ||||||
chr1:46410857
|
A | G | 5 | a0003c0004t0002g0018a0003c0004t0002g0020a0003c0004t0002g0045others(2): Show | 7 | HG00544.hp2 HG01884.hp2 HG03834.hp2 others(4): Show |
splice_region_variant&intron_variant | LOW | c.1316+3A>G | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 11/14 | chr1 | 46410857 | ||||||
chr1:46410889
|
GCC | G | 5 | a0003c0004t0002g0018a0003c0004t0002g0020a0003c0004t0002g0045others(2): Show | 7 | HG00544.hp2 HG01884.hp2 HG03834.hp2 others(4): Show |
intron_variant | MODIFIER | c.1316+36_1316+37del others(2): Show |
FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 11/14 | chr1 | 46410889 | ||||||
chr1:46410994
|
T | C | 5 | a0003c0004t0002g0018a0003c0004t0002g0020a0003c0004t0002g0045others(2): Show | 7 | HG00544.hp2 HG01884.hp2 HG03834.hp2 others(4): Show |
intron_variant | MODIFIER | c.1316+140T>C | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 11/14 | chr1 | 46410994 | ||||||
chr1:46411080
|
G | A | 1 | a0001c0001t0001g0122 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1316+226G>A | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 11/14 | chr1 | 46411080 | ||||||
chr1:46411155
|
A | G | 5 | a0003c0004t0002g0018a0003c0004t0002g0020a0003c0004t0002g0045others(2): Show | 7 | HG00544.hp2 HG01884.hp2 HG03834.hp2 others(4): Show |
intron_variant | MODIFIER | c.1316+301A>G | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 11/14 | chr1 | 46411155 | ||||||
chr1:46411212
|
C | T | 1 | a0001c0001t0001g0098 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1316+358C>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 11/14 | chr1 | 46411212 | ||||||
chr1:46411241
|
G | T | 5 | a0003c0004t0002g0018a0003c0004t0002g0020a0003c0004t0002g0045others(2): Show | 7 | HG00544.hp2 HG01884.hp2 HG03834.hp2 others(4): Show |
intron_variant | MODIFIER | c.1317-371G>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 11/14 | chr1 | 46411241 | ||||||
chr1:46411259
|
C | T | 2 | a0001c0003t0001g0061a0001c0003t0001g0062 | 2 | HG00738.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.1317-353C>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 11/14 | chr1 | 46411259 | ||||||
chr1:46411311
|
T | C | 5 | a0003c0004t0002g0018a0003c0004t0002g0020a0003c0004t0002g0045others(2): Show | 7 | HG00544.hp2 HG01884.hp2 HG03834.hp2 others(4): Show |
intron_variant | MODIFIER | c.1317-301T>C | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 11/14 | chr1 | 46411311 | ||||||
chr1:46411379
|
G | T | 1 | a0002c0002t0001g0071 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1317-233G>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 11/14 | chr1 | 46411379 | ||||||
chr1:46411508
|
G | A | 7 | a0001c0001t0001g0006a0001c0001t0001g0041a0001c0001t0001g0042others(4): Show | 16 | HG00140.hp2 HG00544.hp1 HG00735.hp1 others(13): Show |
intron_variant | MODIFIER | c.1317-104G>A | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 11/14 | chr1 | 46411508 | ||||||
chr1:46411513
|
C | T | 3 | a0001c0001t0001g0029a0001c0001t0001g0115a0001c0001t0001g0117 | 4 | NA18946.hp2 NA18972.hp2 NA19085.hp2 others(1): Show |
intron_variant | MODIFIER | c.1317-99C>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 11/14 | chr1 | 46411513 | ||||||
chr1:46411566
|
C | T | 1 | a0003c0004t0002g0018 | 2 | HG00544.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.1317-46C>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 11/14 | chr1 | 46411566 | ||||||
chr1:46411591
|
G | A | 1 | a0001c0001t0001g0086 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1317-21G>A | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 11/14 | chr1 | 46411591 | ||||||
chr1:46411877
|
C | T | 5 | a0003c0004t0002g0018a0003c0004t0002g0020a0003c0004t0002g0045others(2): Show | 7 | HG00544.hp2 HG01884.hp2 HG03834.hp2 others(4): Show |
intron_variant | MODIFIER | c.1356+226C>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 12/14 | chr1 | 46411877 | ||||||
chr1:46411898
|
C | G | 1 | a0002c0002t0001g0070 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1357-245C>G | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 12/14 | chr1 | 46411898 | ||||||
chr1:46411916
|
G | A | 5 | a0003c0004t0002g0018a0003c0004t0002g0020a0003c0004t0002g0045others(2): Show | 7 | HG00544.hp2 HG01884.hp2 HG03834.hp2 others(4): Show |
intron_variant | MODIFIER | c.1357-227G>A | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 12/14 | chr1 | 46411916 | ||||||
chr1:46411933
|
T | C | 5 | a0003c0004t0002g0018a0003c0004t0002g0020a0003c0004t0002g0045others(2): Show | 7 | HG00544.hp2 HG01884.hp2 HG03834.hp2 others(4): Show |
intron_variant | MODIFIER | c.1357-210T>C | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 12/14 | chr1 | 46411933 | ||||||
chr1:46412074
|
C | A | 5 | a0003c0004t0002g0018a0003c0004t0002g0020a0003c0004t0002g0045others(2): Show | 7 | HG00544.hp2 HG01884.hp2 HG03834.hp2 others(4): Show |
intron_variant | MODIFIER | c.1357-69C>A | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 12/14 | chr1 | 46412074 | ||||||
chr1:46412138
|
C | T | 6 | a0001c0003t0001g0007a0001c0003t0001g0014a0001c0003t0001g0085others(3): Show | 17 | HG00140.hp1 HG00733.hp2 HG01256.hp2 others(14): Show |
splice_region_variant&intron_variant | LOW | c.1357-5C>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 12/14 | chr1 | 46412138 | ||||||
chr1:46412258
|
C | G | 1 | a0001c0001t0001g0097 | 1 | NA18979.hp2 | splice_region_variant&intron_variant | LOW | c.1465+7C>G | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 13/14 | chr1 | 46412258 | ||||||
chr1:46412351
|
C | T | 1 | a0003c0004t0002g0018 | 2 | HG00544.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.1465+100C>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 13/14 | chr1 | 46412351 | ||||||
chr1:46412388
|
C | G | 5 | a0003c0004t0002g0018a0003c0004t0002g0020a0003c0004t0002g0045others(2): Show | 7 | HG00544.hp2 HG01884.hp2 HG03834.hp2 others(4): Show |
intron_variant | MODIFIER | c.1465+137C>G | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 13/14 | chr1 | 46412388 | ||||||
chr1:46412518
|
A | C | 1 | a0001c0003t0001g0049 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1465+267A>C | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 13/14 | chr1 | 46412518 | ||||||
chr1:46412648
|
A | C | 6 | a0001c0001t0001g0132a0001c0001t0001g0151a0001c0001t0001g0152others(3): Show | 7 | HG02572.hp2 HG02717.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1465+397A>C | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 13/14 | chr1 | 46412648 | ||||||
chr1:46412667
|
T | C | 5 | a0003c0004t0002g0018a0003c0004t0002g0020a0003c0004t0002g0045others(2): Show | 7 | HG00544.hp2 HG01884.hp2 HG03834.hp2 others(4): Show |
intron_variant | MODIFIER | c.1466-408T>C | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 13/14 | chr1 | 46412667 | ||||||
chr1:46412708
|
G | A | 1 | a0001c0001t0001g0113 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1466-367G>A | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 13/14 | chr1 | 46412708 | ||||||
chr1:46412793
|
A | T | 1 | a0001c0001t0001g0027 | 2 | HG02293.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.1466-282A>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 13/14 | chr1 | 46412793 | ||||||
chr1:46412892
|
G | A | 1 | a0001c0001t0001g0132 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1466-183G>A | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 13/14 | chr1 | 46412892 | ||||||
chr1:46412979
|
GAC | G | 5 | a0003c0004t0002g0018a0003c0004t0002g0020a0003c0004t0002g0045others(2): Show | 7 | HG00544.hp2 HG01884.hp2 HG03834.hp2 others(4): Show |
intron_variant | MODIFIER | c.1466-92_1466-91del others(2): Show |
FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr1 | 46412979 | |||||
chr1:46413000
|
T | G | 1 | a0002c0002t0001g0163 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1466-75T>G | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 13/14 | chr1 | 46413000 | ||||||
chr1:46413040
|
C | T | 1 | a0001c0001t0001g0044 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1466-35C>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 13/14 | chr1 | 46413040 | ||||||
chr1:46413231
|
A | G | 5 | a0003c0004t0002g0018a0003c0004t0002g0020a0003c0004t0002g0045others(2): Show | 7 | HG00544.hp2 HG01884.hp2 HG03834.hp2 others(4): Show |
intron_variant | MODIFIER | c.1611+11A>G | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 14/14 | chr1 | 46413231 | ||||||
chr1:46413355
|
G | A | 1 | a0001c0001t0001g0123 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1612-92G>A | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 14/14 | chr1 | 46413355 | ||||||
chr1:46413355
|
G | T | 5 | a0003c0004t0002g0018a0003c0004t0002g0020a0003c0004t0002g0045others(2): Show | 7 | HG00544.hp2 HG01884.hp2 HG03834.hp2 others(4): Show |
intron_variant | MODIFIER | c.1612-92G>T | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 14/14 | chr1 | 46413355 | ||||||
chr1:46413412
|
T | C | 5 | a0003c0004t0002g0018a0003c0004t0002g0020a0003c0004t0002g0045others(2): Show | 7 | HG00544.hp2 HG01884.hp2 HG03834.hp2 others(4): Show |
intron_variant | MODIFIER | c.1612-35T>C | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 14/14 | chr1 | 46413412 | ||||||
chr1:46413423
|
T | C | 5 | a0003c0004t0002g0018a0003c0004t0002g0020a0003c0004t0002g0045others(2): Show | 7 | HG00544.hp2 HG01884.hp2 HG03834.hp2 others(4): Show |
intron_variant | MODIFIER | c.1612-24T>C | FAAH | ENSG00000117480.16 | transcript | ENST00000243167.9 | protein_coding | 14/14 | chr1 | 46413423 |