geneid | 4673 |
---|---|
ensemblid | ENSG00000187109.15 |
hgncid | 7637 |
symbol | NAP1L1 |
name | nucleosome assembly protein 1 like 1 |
refseq_nuc | NM_004537.7 |
refseq_prot | NP_004528.1 |
ensembl_nuc | ENST00000618691.5 |
ensembl_prot | ENSP00000477538.1 |
mane_status | MANE Select |
chr | chr12 |
start | 76036585 |
end | 76084685 |
strand | - |
ver | v1.2 |
region | chr12:76036585-76084685 |
region5000 | chr12:76031585-76089685 |
regionname0 | NAP1L1_chr12_76036585_76084685 |
regionname5000 | NAP1L1_chr12_76031585_76089685 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 391 | 355 | 95 | 70 | 140 | 14 | 34 | 104 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
a0002 | 0/0 | 391 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 1176 | 230 | 28 | 38 | 137 | 6 | 20 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
c0002 | 0/0 | 1176 | 93 | 61 | 16 | 3 | 5 | 8 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
c0003 | 1/0 | 1176 | 32 | 6 | 16 | 0 | 3 | 6 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
c0004 | 0/0 | 1176 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 11985 | 66 | 0 | 8 | 50 | 0 | 8 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
t0002 | 0/1 | 11986 | 45 | 4 | 12 | 17 | 5 | 6 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
t0003 | 0/0 | 11986 | 24 | 0 | 1 | 23 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
t0004 | 0/0 | 11987 | 23 | 2 | 9 | 3 | 2 | 7 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
t0005 | 1/0 | 11984 | 21 | 6 | 8 | 0 | 1 | 5 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
t0006 | 0/0 | 11986 | 16 | 2 | 7 | 6 | 1 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
t0007 | 0/0 | 11986 | 8 | 8 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
t0008 | 0/0 | 11986 | 6 | 0 | 4 | 2 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
t0009 | 0/0 | 11987 | 4 | 4 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
t0010 | 0/0 | 11984 | 4 | 0 | 1 | 0 | 2 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
t0011 | 0/0 | 11988 | 4 | 0 | 0 | 4 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
t0012 | 0/0 | 11987 | 4 | 2 | 0 | 0 | 0 | 2 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
t0013 | 0/0 | 11985 | 4 | 3 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
t0014 | 0/0 | 11974 | 4 | 4 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
t0015 | 0/0 | 11969 | 4 | 3 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
t0016 | 0/0 | 11985 | 3 | 3 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
t0017 | 0/0 | 11986 | 3 | 2 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
t0018 | 0/0 | 11983 | 3 | 0 | 3 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
t0019 | 0/0 | 11983 | 3 | 3 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
t0020 | 0/0 | 11988 | 2 | 2 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
t0021 | 0/0 | 11988 | 2 | 0 | 0 | 0 | 1 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
t0022 | 0/0 | 11986 | 2 | 2 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
t0023 | 0/0 | 11986 | 2 | 2 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
t0024 | 0/0 | 11985 | 2 | 2 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
t0025 | 0/0 | 11986 | 2 | 2 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
t0026 | 0/0 | 11985 | 2 | 0 | 2 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
t0027 | 0/0 | 11986 | 2 | 0 | 1 | 0 | 1 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
t0028 | 0/0 | 11987 | 2 | 2 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
t0029 | 0/0 | 11988 | 2 | 2 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
t0030 | 0/0 | 11986 | 2 | 2 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
t0031 | 0/0 | 11987 | 2 | 2 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
t0032 | 0/0 | 11984 | 2 | 0 | 0 | 1 | 0 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
t0033 | 0/0 | 11985 | 2 | 0 | 0 | 2 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
t0034 | 0/0 | 11986 | 2 | 0 | 0 | 2 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
t0035 | 0/0 | 11985 | 2 | 0 | 0 | 2 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
t0036 | 0/0 | 11987 | 2 | 0 | 2 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
t0037 | 0/0 | 11985 | 2 | 1 | 0 | 0 | 0 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
t0038 | 0/0 | 11986 | 2 | 2 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
t0039 | 0/0 | 11985 | 2 | 2 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
t0040 | 0/0 | 11986 | 2 | 2 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
t0041 | 0/0 | 11974 | 2 | 1 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
t0042 | 0/0 | 11986 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
t0043 | 0/0 | 11986 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
t0044 | 0/0 | 11986 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
t0045 | 0/0 | 11988 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
t0046 | 0/0 | 11968 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
t0047 | 0/0 | 11986 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
t0048 | 0/0 | 11987 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
t0049 | 0/0 | 11987 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
t0050 | 0/0 | 11987 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
t0051 | 0/0 | 11986 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
t0052 | 0/0 | 11985 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
t0053 | 0/0 | 11986 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
t0054 | 0/0 | 11987 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
t0055 | 0/0 | 11987 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
t0056 | 0/0 | 11984 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
t0057 | 0/0 | 11985 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
t0058 | 0/0 | 11984 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
t0059 | 0/0 | 11984 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
t0060 | 0/0 | 11984 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
t0061 | 0/0 | 11986 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
t0062 | 0/0 | 11984 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
t0063 | 0/0 | 11985 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
t0064 | 0/0 | 11984 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
t0065 | 0/0 | 11941 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
t0066 | 0/0 | 11985 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
t0067 | 0/0 | 11982 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
t0068 | 0/0 | 11985 | 1 | 0 | 0 | 0 | 1 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
t0069 | 0/0 | 11987 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
t0070 | 0/0 | 11986 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
t0071 | 0/0 | 11973 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
t0072 | 0/0 | 11986 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
t0073 | 0/0 | 11988 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
t0074 | 0/0 | 11972 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
t0075 | 0/0 | 11972 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
t0076 | 0/0 | 11986 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
t0077 | 0/0 | 11985 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
t0078 | 0/0 | 11985 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
t0079 | 0/0 | 11987 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
t0080 | 0/0 | 11987 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
t0081 | 0/0 | 11985 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
t0082 | 0/0 | 11986 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
t0083 | 0/0 | 11987 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
t0084 | 0/0 | 11988 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
t0085 | 0/0 | 11986 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
t0086 | 0/0 | 11987 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
t0087 | 0/0 | 11986 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
t0088 | 0/0 | 11987 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
t0089 | 0/0 | 11986 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
t0090 | 0/0 | 11987 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
t0091 | 0/0 | 11986 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
t0092 | 0/0 | 11988 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
t0093 | 0/0 | 11985 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
t0094 | 0/0 | 11985 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
t0095 | 0/0 | 11986 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
t0096 | 0/0 | 11986 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
t0097 | 0/0 | 11984 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
t0098 | 0/0 | 11985 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
t0099 | 0/0 | 11987 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
t0100 | 0/0 | 11988 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
t0101 | 0/0 | 11987 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
t0102 | 0/0 | 11985 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
t0103 | 0/0 | 11970 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
t0104 | 0/0 | 11987 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 6 | 0 | 2 | 4 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0002 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0003 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0005 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0009 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0012 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0013 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0020 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0022 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0025 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0201 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0251 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0297 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0309 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0314 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 1176 | 230 | 28 | 38 | 137 | 6 | 20 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
a0001c0002 | 0/0 | 1176 | 93 | 61 | 16 | 3 | 5 | 8 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
a0001c0003 | 1/0 | 1176 | 32 | 6 | 16 | 0 | 3 | 6 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
a0002c0004 | 0/0 | 1176 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 13160 | 66 | 0 | 8 | 50 | 0 | 8 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
a0001c0001t0002 | 0/1 | 13161 | 45 | 4 | 12 | 17 | 5 | 6 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
a0001c0001t0003 | 0/0 | 13161 | 24 | 0 | 1 | 23 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
a0001c0001t0006 | 0/0 | 13161 | 16 | 2 | 7 | 6 | 1 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
a0001c0001t0007 | 0/0 | 13161 | 8 | 8 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
a0001c0001t0008 | 0/0 | 13161 | 6 | 0 | 4 | 2 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
a0001c0001t0011 | 0/0 | 13163 | 4 | 0 | 0 | 4 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
a0001c0001t0012 | 0/0 | 13162 | 4 | 2 | 0 | 0 | 0 | 2 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
a0001c0001t0013 | 0/0 | 13160 | 4 | 3 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
a0001c0001t0030 | 0/0 | 13161 | 2 | 2 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
a0001c0001t0032 | 0/0 | 13159 | 2 | 0 | 0 | 1 | 0 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
a0001c0001t0033 | 0/0 | 13160 | 2 | 0 | 0 | 2 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
a0001c0001t0034 | 0/0 | 13161 | 2 | 0 | 0 | 2 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
a0001c0001t0035 | 0/0 | 13160 | 2 | 0 | 0 | 2 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
a0001c0001t0036 | 0/0 | 13162 | 2 | 0 | 2 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
a0001c0001t0037 | 0/0 | 13160 | 2 | 1 | 0 | 0 | 0 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
a0001c0001t0038 | 0/0 | 13161 | 2 | 2 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
a0001c0001t0042 | 0/0 | 13161 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
a0001c0001t0043 | 0/0 | 13161 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
a0001c0001t0047 | 0/0 | 13161 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
a0001c0001t0048 | 0/0 | 13162 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
a0001c0001t0049 | 0/0 | 13162 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
a0001c0001t0050 | 0/0 | 13162 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
a0001c0001t0057 | 0/0 | 13160 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
a0001c0001t0066 | 0/0 | 13160 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
a0001c0001t0069 | 0/0 | 13162 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
a0001c0001t0070 | 0/0 | 13161 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
a0001c0001t0071 | 0/0 | 13148 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
a0001c0001t0072 | 0/0 | 13161 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
a0001c0001t0074 | 0/0 | 13147 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
a0001c0001t0075 | 0/0 | 13147 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
a0001c0001t0076 | 0/0 | 13161 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
a0001c0001t0077 | 0/0 | 13160 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
a0001c0001t0078 | 0/0 | 13160 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
a0001c0001t0079 | 0/0 | 13162 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
a0001c0001t0080 | 0/0 | 13162 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
a0001c0001t0081 | 0/0 | 13160 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
a0001c0001t0082 | 0/0 | 13161 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
a0001c0001t0083 | 0/0 | 13162 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
a0001c0001t0084 | 0/0 | 13163 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
a0001c0001t0085 | 0/0 | 13161 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
a0001c0001t0086 | 0/0 | 13162 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
a0001c0001t0087 | 0/0 | 13161 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
a0001c0001t0089 | 0/0 | 13161 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
a0001c0001t0090 | 0/0 | 13162 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
a0001c0001t0091 | 0/0 | 13161 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
a0001c0001t0092 | 0/0 | 13163 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
a0001c0001t0093 | 0/0 | 13160 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
a0001c0001t0094 | 0/0 | 13160 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
a0001c0001t0095 | 0/0 | 13161 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
a0001c0001t0096 | 0/0 | 13161 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
a0001c0001t0097 | 0/0 | 13159 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
a0001c0001t0098 | 0/0 | 13160 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
a0001c0001t0101 | 0/0 | 13162 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
a0001c0002t0004 | 0/0 | 13162 | 23 | 2 | 9 | 3 | 2 | 7 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
a0001c0002t0005 | 0/0 | 13159 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
a0001c0002t0009 | 0/0 | 13162 | 4 | 4 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
a0001c0002t0014 | 0/0 | 13149 | 3 | 3 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
a0001c0002t0015 | 0/0 | 13144 | 4 | 3 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
a0001c0002t0016 | 0/0 | 13160 | 3 | 3 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
a0001c0002t0017 | 0/0 | 13161 | 3 | 2 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
a0001c0002t0019 | 0/0 | 13158 | 3 | 3 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
a0001c0002t0020 | 0/0 | 13163 | 2 | 2 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
a0001c0002t0021 | 0/0 | 13163 | 2 | 0 | 0 | 0 | 1 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
a0001c0002t0022 | 0/0 | 13161 | 2 | 2 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
a0001c0002t0023 | 0/0 | 13161 | 2 | 2 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
a0001c0002t0024 | 0/0 | 13160 | 2 | 2 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
a0001c0002t0025 | 0/0 | 13161 | 2 | 2 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
a0001c0002t0027 | 0/0 | 13161 | 2 | 0 | 1 | 0 | 1 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
a0001c0002t0028 | 0/0 | 13162 | 2 | 2 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
a0001c0002t0029 | 0/0 | 13163 | 2 | 2 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
a0001c0002t0031 | 0/0 | 13162 | 2 | 2 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
a0001c0002t0039 | 0/0 | 13160 | 2 | 2 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
a0001c0002t0040 | 0/0 | 13161 | 2 | 2 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
a0001c0002t0041 | 0/0 | 13149 | 2 | 1 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
a0001c0002t0044 | 0/0 | 13161 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
a0001c0002t0045 | 0/0 | 13163 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
a0001c0002t0046 | 0/0 | 13143 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
a0001c0002t0051 | 0/0 | 13161 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
a0001c0002t0052 | 0/0 | 13160 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
a0001c0002t0053 | 0/0 | 13161 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
a0001c0002t0054 | 0/0 | 13162 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
a0001c0002t0055 | 0/0 | 13162 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
a0001c0002t0056 | 0/0 | 13159 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
a0001c0002t0058 | 0/0 | 13159 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
a0001c0002t0061 | 0/0 | 13161 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
a0001c0002t0062 | 0/0 | 13159 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
a0001c0002t0063 | 0/0 | 13160 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
a0001c0002t0064 | 0/0 | 13159 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
a0001c0002t0065 | 0/0 | 13116 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
a0001c0002t0068 | 0/0 | 13160 | 1 | 0 | 0 | 0 | 1 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
a0001c0002t0073 | 0/0 | 13163 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
a0001c0002t0088 | 0/0 | 13162 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
a0001c0002t0099 | 0/0 | 13162 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
a0001c0002t0100 | 0/0 | 13163 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
a0001c0002t0102 | 0/0 | 13160 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
a0001c0002t0103 | 0/0 | 13145 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
a0001c0002t0104 | 0/0 | 13162 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
a0001c0003t0005 | 1/0 | 13159 | 20 | 5 | 8 | 0 | 1 | 5 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
a0001c0003t0010 | 0/0 | 13159 | 4 | 0 | 1 | 0 | 2 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
a0001c0003t0018 | 0/0 | 13158 | 3 | 0 | 3 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
a0001c0003t0026 | 0/0 | 13160 | 2 | 0 | 2 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
a0001c0003t0059 | 0/0 | 13159 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
a0001c0003t0060 | 0/0 | 13159 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
a0001c0003t0067 | 0/0 | 13157 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
a0002c0004t0014 | 0/0 | 13149 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | copy fasta | chr12 | 76031585 | 76089685 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 6 | 0 | 2 | 4 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0002g0002 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0002g0003 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0002g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0002g0012 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0002g0020 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0002g0022 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0002g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0002g0201 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0003g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0003g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0003g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0003g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0006g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0006g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0006g0009 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0006g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0006g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0006g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0006g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0006g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0006g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0006g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0006g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0006g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0006g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0007g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0007g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0007g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0007g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0007g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0007g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0007g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0008g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0008g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0008g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0008g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0008g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0008g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0011g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0011g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0011g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0011g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0012g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0012g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0012g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0012g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0013g0013 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0013g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0013g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0030g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0032g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0032g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0033g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0033g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0034g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0034g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0035g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0035g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0036g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0037g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0037g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0038g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0038g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0042g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0043g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0047g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0048g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0049g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0050g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0057g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0066g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0069g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0070g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0071g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0072g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0074g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0075g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0076g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0077g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0078g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0079g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0080g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0081g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0082g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0083g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0084g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0085g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0086g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0087g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0089g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0090g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0091g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0092g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0093g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0094g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0095g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0096g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0097g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0098g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0001t0101g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0004g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0004g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0004g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0004g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0004g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0004g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0004g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0004g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0004g0297 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0004g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0004g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0004g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0004g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0004g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0004g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0004g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0004g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0004g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0004g0314 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0004g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0004g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0004g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0004g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0005g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0009g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0009g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0009g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0014g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0014g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0015g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0015g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0015g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0016g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0016g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0016g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0017g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0017g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0017g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0019g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0019g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0019g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0020g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0020g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0021g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0021g0309 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0022g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0022g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0023g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0023g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0024g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0024g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0025g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0025g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0027g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0027g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0028g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0028g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0029g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0029g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0031g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0031g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0039g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0039g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0040g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0040g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0041g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0041g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0044g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0045g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0046g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0051g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0052g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0053g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0054g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0055g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0056g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0058g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0061g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0062g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0063g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0064g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0065g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0068g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0073g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0088g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0099g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0100g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0102g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0103g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0002t0104g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0003t0005g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0003t0005g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0003t0005g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0003t0005g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0003t0005g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0003t0005g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0003t0005g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0003t0005g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0003t0005g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0003t0005g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0003t0005g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0003t0005g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0003t0005g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0003t0005g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0003t0005g0251 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0003t0005g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0003t0005g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0003t0005g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0003t0005g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0003t0005g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0003t0010g0025 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0003t0010g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0003t0010g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0003t0018g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0003t0018g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0003t0018g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0003t0026g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0003t0026g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0003t0059g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0003t0060g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0001c0003t0067g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
a0002c0004t0014g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0002 | t0004 | g0314 | EUR | GBR | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0022 | EUR | GBR | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG00323 | hp1 | a0001 | c0001 | t0006 | g0088 | EUR | FIN | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG00323 | hp2 | a0001 | c0003 | t0005 | g0240 | EUR | FIN | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG00423 | hp1 | a0001 | c0001 | t0003 | g0124 | EAS | CHS | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | CHS | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | CHS | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0080 | EAS | CHS | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | CHS | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG00544 | hp2 | a0001 | c0001 | t0002 | g0114 | EAS | CHS | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | CHS | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG00558 | hp2 | a0001 | c0001 | t0006 | g0038 | EAS | CHS | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | CHS | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0104 | EAS | CHS | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG00642 | hp1 | a0001 | c0003 | t0010 | g0253 | AMR | PUR | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0260 | AMR | PUR | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG00733 | hp1 | a0001 | c0002 | t0104 | g0323 | AMR | PUR | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG00735 | hp1 | a0001 | c0001 | t0003 | g0091 | AMR | PUR | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG00738 | hp1 | a0001 | c0002 | t0004 | g0321 | AMR | PUR | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG00738 | hp2 | a0001 | c0003 | t0026 | g0233 | AMR | PUR | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG00741 | hp1 | a0001 | c0002 | t0004 | g0294 | AMR | PUR | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG00741 | hp2 | a0001 | c0003 | t0005 | g0232 | AMR | PUR | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01069 | hp1 | a0001 | c0002 | t0053 | g0305 | AMR | PUR | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01069 | hp2 | a0001 | c0003 | t0067 | g0255 | AMR | PUR | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01070 | hp1 | a0001 | c0001 | t0002 | g0037 | AMR | PUR | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01071 | hp2 | a0001 | c0003 | t0018 | g0256 | AMR | PUR | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01074 | hp1 | a0001 | c0003 | t0060 | g0249 | AMR | PUR | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01081 | hp1 | a0001 | c0002 | t0004 | g0306 | AMR | PUR | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01081 | hp2 | a0001 | c0002 | t0061 | g0286 | AMR | PUR | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01099 | hp1 | a0001 | c0002 | t0017 | g0315 | AMR | PUR | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01099 | hp2 | a0001 | c0001 | t0002 | g0116 | AMR | PUR | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01106 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | PUR | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01106 | hp2 | a0001 | c0001 | t0070 | g0204 | AMR | PUR | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0020 | AMR | PUR | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01109 | hp2 | a0001 | c0002 | t0041 | g0146 | AMR | PUR | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01167 | hp1 | a0001 | c0003 | t0005 | g0244 | AMR | PUR | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01167 | hp2 | a0001 | c0001 | t0002 | g0011 | AMR | PUR | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0059 | AMR | PUR | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01169 | hp2 | a0001 | c0003 | t0018 | g0243 | AMR | PUR | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01175 | hp1 | a0001 | c0003 | t0026 | g0278 | AMR | PUR | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01175 | hp2 | a0001 | c0001 | t0002 | g0181 | AMR | PUR | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01192 | hp1 | a0001 | c0003 | t0005 | g0235 | AMR | PUR | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01192 | hp2 | a0001 | c0002 | t0004 | g0288 | AMR | PUR | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01243 | hp1 | a0001 | c0001 | t0013 | g0013 | AMR | PUR | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01243 | hp2 | a0001 | c0003 | t0005 | g0254 | AMR | PUR | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01255 | hp1 | a0001 | c0001 | t0006 | g0007 | AMR | CLM | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01255 | hp2 | a0001 | c0003 | t0005 | g0234 | AMR | CLM | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01256 | hp1 | a0001 | c0001 | t0006 | g0006 | AMR | CLM | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01256 | hp2 | a0001 | c0003 | t0005 | g0246 | AMR | CLM | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01258 | hp1 | a0001 | c0001 | t0006 | g0006 | AMR | CLM | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0022 | AMR | CLM | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01261 | hp1 | a0001 | c0002 | t0015 | g0150 | AMR | CLM | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01261 | hp2 | a0001 | c0001 | t0036 | g0008 | AMR | CLM | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01358 | hp1 | a0001 | c0001 | t0036 | g0008 | AMR | CLM | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01358 | hp2 | a0001 | c0003 | t0005 | g0238 | AMR | CLM | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01361 | hp1 | a0001 | c0003 | t0018 | g0236 | AMR | CLM | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01361 | hp2 | a0001 | c0002 | t0004 | g0300 | AMR | CLM | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | CLM | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01433 | hp2 | a0001 | c0002 | t0004 | g0310 | AMR | CLM | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01515 | hp1 | a0001 | c0001 | t0002 | g0020 | EUR | IBS | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01515 | hp2 | a0001 | c0003 | t0010 | g0025 | EUR | IBS | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01516 | hp1 | a0001 | c0001 | t0002 | g0118 | EUR | IBS | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01516 | hp2 | a0001 | c0002 | t0027 | g0284 | EUR | IBS | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01517 | hp1 | a0001 | c0002 | t0068 | g0285 | EUR | IBS | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01517 | hp2 | a0001 | c0003 | t0010 | g0025 | EUR | IBS | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01884 | hp1 | a0001 | c0003 | t0005 | g0237 | AFR | ACB | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01884 | hp2 | a0001 | c0002 | t0102 | g0224 | AFR | ACB | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01891 | hp1 | a0001 | c0001 | t0007 | g0019 | AFR | ACB | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01891 | hp2 | a0001 | c0003 | t0059 | g0241 | AFR | ACB | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01928 | hp1 | a0001 | c0001 | t0006 | g0007 | AMR | PEL | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01928 | hp2 | a0001 | c0001 | t0008 | g0263 | AMR | PEL | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | PEL | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01934 | hp2 | a0001 | c0001 | t0083 | g0128 | AMR | PEL | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01975 | hp1 | a0001 | c0001 | t0006 | g0028 | AMR | PEL | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01975 | hp2 | a0001 | c0001 | t0008 | g0129 | AMR | PEL | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01978 | hp1 | a0001 | c0002 | t0004 | g0293 | AMR | PEL | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01978 | hp2 | a0001 | c0002 | t0004 | g0295 | AMR | PEL | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01981 | hp1 | a0001 | c0001 | t0006 | g0049 | AMR | PEL | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | PEL | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | KHV | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02015 | hp2 | a0001 | c0001 | t0049 | g0065 | EAS | KHV | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02040 | hp1 | a0001 | c0001 | t0078 | g0179 | EAS | KHV | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02040 | hp2 | a0001 | c0001 | t0003 | g0094 | EAS | KHV | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02055 | hp1 | a0001 | c0002 | t0063 | g0212 | AFR | ACB | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02055 | hp2 | a0001 | c0002 | t0014 | g0148 | AFR | ACB | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02056 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | KHV | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | KHV | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02074 | hp1 | a0001 | c0001 | t0006 | g0121 | EAS | KHV | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02074 | hp2 | a0001 | c0001 | t0003 | g0041 | EAS | KHV | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | KHV | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02080 | hp2 | a0001 | c0001 | t0069 | g0076 | EAS | KHV | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | KHV | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | KHV | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02129 | hp2 | a0001 | c0001 | t0006 | g0061 | EAS | KHV | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02132 | hp1 | a0001 | c0001 | t0094 | g0106 | EAS | KHV | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02145 | hp1 | a0001 | c0002 | t0103 | g0231 | AFR | ACB | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02145 | hp2 | a0001 | c0001 | t0101 | g0156 | AFR | ACB | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02148 | hp1 | a0001 | c0001 | t0006 | g0119 | AMR | PEL | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | PEL | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02155 | hp1 | a0001 | c0001 | t0095 | g0100 | EAS | CDX | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | CDX | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02165 | hp1 | a0001 | c0001 | t0032 | g0141 | EAS | CDX | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02165 | hp2 | a0001 | c0001 | t0006 | g0009 | EAS | CDX | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02257 | hp1 | a0001 | c0002 | t0023 | g0274 | AFR | ACB | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02257 | hp2 | a0001 | c0002 | t0009 | g0145 | AFR | ACB | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02258 | hp1 | a0001 | c0002 | t0020 | g0216 | AFR | ACB | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02258 | hp2 | a0001 | c0003 | t0005 | g0252 | AFR | ACB | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0265 | AMR | PEL | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02273 | hp2 | a0001 | c0002 | t0004 | g0296 | AMR | PEL | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02280 | hp1 | a0001 | c0001 | t0007 | g0161 | AFR | ACB | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02280 | hp2 | a0001 | c0002 | t0024 | g0222 | AFR | ACB | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | PEL | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02293 | hp2 | a0001 | c0001 | t0008 | g0125 | AMR | PEL | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02300 | hp1 | a0001 | c0003 | t0005 | g0250 | AMR | PEL | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02300 | hp2 | a0001 | c0001 | t0077 | g0206 | AMR | PEL | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02451 | hp1 | a0001 | c0001 | t0007 | g0154 | AFR | ACB | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02451 | hp2 | a0001 | c0001 | t0012 | g0056 | AFR | ACB | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02523 | hp1 | a0001 | c0001 | t0071 | g0077 | EAS | KHV | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02523 | hp2 | a0001 | c0001 | t0035 | g0109 | EAS | KHV | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02572 | hp1 | a0001 | c0001 | t0013 | g0013 | AFR | GWD | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02572 | hp2 | a0001 | c0002 | t0031 | g0280 | AFR | GWD | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02602 | hp1 | a0001 | c0002 | t0004 | g0304 | SAS | PJL | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02602 | hp2 | a0001 | c0003 | t0005 | g0245 | SAS | PJL | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02615 | hp1 | a0001 | c0002 | t0024 | g0223 | AFR | GWD | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02615 | hp2 | a0001 | c0001 | t0007 | g0158 | AFR | GWD | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02622 | hp1 | a0001 | c0002 | t0073 | g0281 | AFR | GWD | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02622 | hp2 | a0001 | c0002 | t0039 | g0151 | AFR | GWD | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02630 | hp1 | a0001 | c0001 | t0085 | g0082 | AFR | GWD | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02630 | hp2 | a0001 | c0002 | t0028 | g0143 | AFR | GWD | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02647 | hp1 | a0001 | c0001 | t0038 | g0070 | AFR | GWD | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02647 | hp2 | a0001 | c0002 | t0004 | g0320 | AFR | GWD | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | PJL | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02698 | hp2 | a0001 | c0001 | t0037 | g0057 | SAS | PJL | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02717 | hp1 | a0001 | c0002 | t0025 | g0283 | AFR | GWD | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02717 | hp2 | a0002 | c0004 | t0014 | g0147 | AFR | GWD | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02723 | hp1 | a0001 | c0002 | t0005 | g0259 | AFR | GWD | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02723 | hp2 | a0001 | c0002 | t0029 | g0135 | AFR | GWD | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02809 | hp1 | a0001 | c0002 | t0019 | g0138 | AFR | GWD | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02809 | hp2 | a0001 | c0001 | t0007 | g0157 | AFR | GWD | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02818 | hp1 | a0001 | c0001 | t0002 | g0060 | AFR | GWD | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02818 | hp2 | a0001 | c0001 | t0057 | g0083 | AFR | GWD | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02886 | hp1 | a0001 | c0002 | t0016 | g0276 | AFR | GWD | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02886 | hp2 | a0001 | c0002 | t0019 | g0139 | AFR | GWD | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02895 | hp1 | a0001 | c0002 | t0025 | g0282 | AFR | GWD | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02895 | hp2 | a0001 | c0002 | t0056 | g0275 | AFR | GWD | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02896 | hp1 | a0001 | c0001 | t0007 | g0133 | AFR | GWD | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02896 | hp2 | a0001 | c0002 | t0052 | g0319 | AFR | GWD | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02897 | hp1 | a0001 | c0002 | t0022 | g0317 | AFR | GWD | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02897 | hp2 | a0001 | c0002 | t0064 | g0225 | AFR | GWD | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02922 | hp1 | a0001 | c0002 | t0017 | g0301 | AFR | ESN | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02922 | hp2 | a0001 | c0002 | t0065 | g0291 | AFR | ESN | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02965 | hp1 | a0001 | c0001 | t0037 | g0071 | AFR | ESN | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02965 | hp2 | a0001 | c0001 | t0007 | g0019 | AFR | ESN | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02970 | hp1 | a0001 | c0003 | t0005 | g0239 | AFR | ESN | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02970 | hp2 | a0001 | c0001 | t0007 | g0155 | AFR | ESN | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02976 | hp1 | a0001 | c0002 | t0088 | g0134 | AFR | ESN | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02976 | hp2 | a0001 | c0002 | t0040 | g0208 | AFR | ESN | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG03017 | hp1 | a0001 | c0003 | t0005 | g0248 | SAS | PJL | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0066 | SAS | PJL | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG03041 | hp1 | a0001 | c0002 | t0009 | g0016 | AFR | GWD | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG03041 | hp2 | a0001 | c0001 | t0002 | g0045 | AFR | GWD | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG03098 | hp1 | a0001 | c0002 | t0046 | g0218 | AFR | MSL | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG03098 | hp2 | a0001 | c0002 | t0004 | g0312 | AFR | MSL | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG03130 | hp1 | a0001 | c0001 | t0030 | g0010 | AFR | ESN | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG03130 | hp2 | a0001 | c0002 | t0014 | g0017 | AFR | ESN | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG03139 | hp1 | a0001 | c0002 | t0015 | g0018 | AFR | ESN | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG03139 | hp2 | a0001 | c0002 | t0040 | g0153 | AFR | ESN | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG03195 | hp1 | a0001 | c0002 | t0016 | g0227 | AFR | ESN | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG03195 | hp2 | a0001 | c0002 | t0051 | g0221 | AFR | ESN | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG03209 | hp1 | a0001 | c0002 | t0039 | g0152 | AFR | MSL | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG03209 | hp2 | a0001 | c0002 | t0009 | g0016 | AFR | MSL | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG03225 | hp1 | a0001 | c0002 | t0015 | g0018 | AFR | MSL | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG03225 | hp2 | a0001 | c0001 | t0013 | g0084 | AFR | MSL | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG03239 | hp1 | a0001 | c0001 | t0093 | g0043 | SAS | PJL | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG03239 | hp2 | a0001 | c0003 | t0005 | g0242 | SAS | PJL | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG03453 | hp1 | a0001 | c0001 | t0030 | g0010 | AFR | MSL | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG03453 | hp2 | a0001 | c0002 | t0055 | g0287 | AFR | MSL | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG03486 | hp1 | a0001 | c0002 | t0031 | g0272 | AFR | MSL | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG03486 | hp2 | a0001 | c0002 | t0099 | g0210 | AFR | MSL | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0261 | SAS | PJL | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG03490 | hp2 | a0001 | c0001 | t0066 | g0307 | SAS | PJL | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG03491 | hp1 | a0001 | c0002 | t0004 | g0290 | SAS | PJL | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG03491 | hp2 | a0001 | c0001 | t0032 | g0027 | SAS | PJL | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG03540 | hp1 | a0001 | c0002 | t0045 | g0215 | AFR | GWD | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG03540 | hp2 | a0001 | c0001 | t0013 | g0081 | AFR | GWD | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG03654 | hp1 | a0001 | c0002 | t0004 | g0289 | SAS | PJL | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0166 | SAS | PJL | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG03704 | hp1 | a0001 | c0002 | t0021 | g0299 | SAS | PJL | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0012 | SAS | PJL | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG03710 | hp2 | a0001 | c0002 | t0004 | g0316 | SAS | PJL | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0267 | SAS | BEB | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG03831 | hp2 | a0001 | c0003 | t0005 | g0247 | SAS | BEB | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG03834 | hp1 | a0001 | c0002 | t0004 | g0302 | SAS | BEB | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | BEB | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG03927 | hp1 | a0001 | c0003 | t0010 | g0277 | SAS | BEB | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG03927 | hp2 | a0001 | c0002 | t0004 | g0308 | SAS | BEB | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG04115 | hp1 | a0001 | c0001 | t0012 | g0029 | SAS | STU | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG04115 | hp2 | a0001 | c0001 | t0012 | g0031 | SAS | STU | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0044 | SAS | BEB | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0169 | SAS | BEB | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG04199 | hp1 | a0001 | c0003 | t0005 | g0279 | SAS | STU | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG04199 | hp2 | a0001 | c0002 | t0004 | g0322 | SAS | STU | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0073 | SAS | STU | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | STU | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18522 | hp1 | a0001 | c0002 | t0015 | g0149 | AFR | YRI | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18522 | hp2 | a0001 | c0002 | t0028 | g0142 | AFR | YRI | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | CHB | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | CHB | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18747 | hp1 | a0001 | c0001 | t0047 | g0053 | EAS | CHB | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | CHB | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18906 | hp1 | a0001 | c0001 | t0002 | g0086 | AFR | YRI | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18906 | hp2 | a0001 | c0002 | t0023 | g0273 | AFR | YRI | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18939 | hp2 | a0001 | c0001 | t0098 | g0097 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18941 | hp1 | a0001 | c0001 | t0091 | g0099 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18944 | hp1 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18948 | hp1 | a0001 | c0001 | t0081 | g0193 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18948 | hp2 | a0001 | c0001 | t0011 | g0034 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18949 | hp2 | a0001 | c0001 | t0003 | g0089 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18951 | hp2 | a0001 | c0001 | t0003 | g0113 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18954 | hp2 | a0001 | c0001 | t0097 | g0052 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18956 | hp2 | a0001 | c0001 | t0096 | g0090 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18957 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18957 | hp2 | a0001 | c0001 | t0087 | g0103 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18962 | hp1 | a0001 | c0001 | t0035 | g0110 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18962 | hp2 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18963 | hp2 | a0001 | c0001 | t0089 | g0095 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18965 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18969 | hp1 | a0001 | c0001 | t0079 | g0033 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18971 | hp1 | a0001 | c0001 | t0086 | g0122 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18972 | hp1 | a0001 | c0001 | t0003 | g0112 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18972 | hp2 | a0001 | c0001 | t0080 | g0194 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18974 | hp1 | a0001 | c0001 | t0003 | g0107 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18975 | hp2 | a0001 | c0001 | t0003 | g0111 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18977 | hp1 | a0001 | c0001 | t0090 | g0067 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18977 | hp2 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18979 | hp1 | a0001 | c0001 | t0072 | g0126 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18979 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18980 | hp1 | a0001 | c0002 | t0004 | g0292 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18981 | hp1 | a0001 | c0001 | t0050 | g0192 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18981 | hp2 | a0001 | c0001 | t0092 | g0093 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18982 | hp1 | a0001 | c0001 | t0003 | g0123 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18982 | hp2 | a0001 | c0001 | t0006 | g0046 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18983 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18988 | hp1 | a0001 | c0001 | t0008 | g0268 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18988 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18991 | hp1 | a0001 | c0001 | t0033 | g0064 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18991 | hp2 | a0001 | c0001 | t0011 | g0117 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18992 | hp1 | a0001 | c0001 | t0003 | g0096 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18993 | hp1 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18993 | hp2 | a0001 | c0001 | t0003 | g0085 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18998 | hp1 | a0001 | c0001 | t0011 | g0036 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18999 | hp1 | a0001 | c0002 | t0004 | g0313 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA19001 | hp2 | a0001 | c0002 | t0004 | g0311 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA19002 | hp1 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA19002 | hp2 | a0001 | c0001 | t0034 | g0185 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA19003 | hp1 | a0001 | c0001 | t0084 | g0035 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA19004 | hp1 | a0001 | c0001 | t0003 | g0102 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA19005 | hp2 | a0001 | c0001 | t0011 | g0032 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA19006 | hp1 | a0001 | c0001 | t0048 | g0062 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA19006 | hp2 | a0001 | c0001 | t0075 | g0200 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA19007 | hp1 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA19009 | hp2 | a0001 | c0001 | t0003 | g0092 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA19010 | hp1 | a0001 | c0001 | t0003 | g0105 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA19011 | hp1 | a0001 | c0001 | t0082 | g0072 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA19011 | hp2 | a0001 | c0001 | t0074 | g0163 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA19012 | hp1 | a0001 | c0001 | t0006 | g0048 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA19030 | hp1 | a0001 | c0002 | t0009 | g0229 | AFR | LWK | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA19030 | hp2 | a0001 | c0002 | t0022 | g0318 | AFR | LWK | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA19043 | hp1 | a0001 | c0002 | t0058 | g0144 | AFR | LWK | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA19043 | hp2 | a0001 | c0001 | t0038 | g0058 | AFR | LWK | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA19054 | hp1 | a0001 | c0001 | t0033 | g0075 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA19057 | hp2 | a0001 | c0001 | t0008 | g0266 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA19060 | hp1 | a0001 | c0001 | t0043 | g0030 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA19065 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA19065 | hp2 | a0001 | c0001 | t0034 | g0197 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA19074 | hp2 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA19079 | hp2 | a0001 | c0001 | t0003 | g0115 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA19083 | hp1 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA19085 | hp1 | a0001 | c0001 | t0003 | g0101 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA19087 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA19090 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA19240 | hp1 | a0001 | c0002 | t0020 | g0217 | AFR | YRI | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA19240 | hp2 | a0001 | c0002 | t0054 | g0298 | AFR | YRI | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA20129 | hp1 | a0001 | c0001 | t0006 | g0050 | AFR | ASW | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA20129 | hp2 | a0001 | c0003 | t0005 | g0258 | AFR | ASW | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0069 | EUR | TSI | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA20752 | hp2 | a0001 | c0002 | t0004 | g0297 | EUR | TSI | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0131 | EUR | TSI | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA20805 | hp2 | a0001 | c0002 | t0021 | g0309 | EUR | TSI | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0209 | SAS | GIH | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0063 | SAS | GIH | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01123 | hp1 | a0001 | c0001 | t0008 | g0127 | AMR | CLM | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG01123 | hp2 | a0001 | c0002 | t0027 | g0220 | AMR | CLM | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02109 | hp1 | a0001 | c0002 | t0100 | g0160 | AFR | ACB | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02109 | hp2 | a0001 | c0002 | t0044 | g0219 | AFR | ACB | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02486 | hp1 | a0001 | c0002 | t0062 | g0228 | AFR | ACB | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02486 | hp2 | a0001 | c0002 | t0029 | g0136 | AFR | ACB | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02559 | hp1 | a0001 | c0002 | t0019 | g0137 | AFR | ACB | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG02559 | hp2 | a0001 | c0002 | t0014 | g0017 | AFR | ACB | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG03471 | hp1 | a0001 | c0002 | t0041 | g0230 | AFR | MSL | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG03471 | hp2 | a0001 | c0001 | t0002 | g0087 | AFR | MSL | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG06807 | hp1 | a0001 | c0003 | t0005 | g0257 | AFR | USA | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
HG06807 | hp2 | a0001 | c0001 | t0012 | g0039 | AFR | USA | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18955 | hp1 | a0001 | c0001 | t0076 | g0079 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA20300 | hp1 | a0001 | c0001 | t0006 | g0009 | AFR | USA | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA20300 | hp2 | a0001 | c0002 | t0016 | g0226 | AFR | USA | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA21309 | hp1 | a0001 | c0001 | t0042 | g0199 | AFR | LWK | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
NA21309 | hp2 | a0001 | c0002 | t0017 | g0303 | AFR | LWK | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0201 | REF | REF | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
homoSapiens_grch38 | hp1 | a0001 | c0003 | t0005 | g0251 | REF | REF | NAP1L1_chr12_76031585_76089685 | NAP1L1 | chr12 | 76031585 | 76089685 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:76060272
|
T | C | 1 | a0002 | 1 | HG02717.hp2 | missense_variant | MODERATE | c.214A>G | p.Arg72Gly | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 5/15 | 353/13159 | 214/1176 | 72/391 | chr12 | 76060272 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:76056120
|
T | C | 3 | a0001c0001a0001c0002a0002c0004 | 324 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(321): Show |
synonymous_variant | LOW | c.471A>G | p.Lys157Lys | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 7/15 | 610/13159 | 471/1176 | 157/391 | chr12 | 76056120 | ||
chr12:76060186
|
G | A | 1 | a0001c0001 | 230 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(227): Show |
synonymous_variant | LOW | c.300C>T | p.His100His | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 5/15 | 439/13159 | 300/1176 | 100/391 | chr12 | 76060186 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:76036610
|
CATA | C | 2 | a0001c0002t0015a0001c0002t0103 | 5 | HG01261.hp1 HG02145.hp1 HG03139.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*11816_*11818delTA others(1): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 11816 | chr12 | 76036610 | |||||
chr12:76036612
|
T | C | 1 | a0001c0001t0085 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*11817A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 11817 | chr12 | 76036612 | |||||
chr12:76036728
|
G | A | 1 | a0001c0002t0024 | 2 | HG02280.hp2 HG02615.hp1 |
3_prime_UTR_variant | MODIFIER | c.*11701C>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 11701 | chr12 | 76036728 | |||||
chr12:76036734
|
G | A | 65 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(62): Show | 254 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(251): Show |
3_prime_UTR_variant | MODIFIER | c.*11695C>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 11695 | chr12 | 76036734 | |||||
chr12:76036918
|
C | CA | 17 | a0001c0001t0034a0001c0001t0076a0001c0001t0086others(14): Show | 26 | HG01261.hp1 HG01891.hp2 HG02109.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*11510dupT | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 11510 | chr12 | 76036918 | |||||
chr12:76036941
|
G | A | 1 | a0001c0001t0077 | 1 | HG02300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11488C>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 11488 | chr12 | 76036941 | |||||
chr12:76036981
|
T | C | 4 | a0001c0002t0014a0001c0002t0028a0001c0002t0041others(1): Show | 8 | HG01109.hp2 HG02055.hp2 HG02559.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*11448A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 11448 | chr12 | 76036981 | |||||
chr12:76037016
|
C | G | 1 | a0001c0003t0060 | 1 | HG01074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*11413G>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 11413 | chr12 | 76037016 | |||||
chr12:76037236
|
T | C | 1 | a0001c0001t0091 | 1 | NA18941.hp1 | 3_prime_UTR_variant | MODIFIER | c.*11193A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 11193 | chr12 | 76037236 | |||||
chr12:76037285
|
A | G | 1 | a0001c0002t0009 | 4 | HG02257.hp2 HG03041.hp1 HG03209.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*11144T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 11144 | chr12 | 76037285 | |||||
chr12:76037358
|
T | C | 55 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(52): Show | 232 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(229): Show |
3_prime_UTR_variant | MODIFIER | c.*11071A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 11071 | chr12 | 76037358 | |||||
chr12:76037572
|
C | T | 8 | a0001c0002t0009a0001c0002t0014a0001c0002t0028others(5): Show | 17 | HG01109.hp2 HG02055.hp2 HG02257.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*10857G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 10857 | chr12 | 76037572 | |||||
chr12:76037585
|
GACAA | G | 1 | a0001c0002t0019 | 3 | HG02559.hp1 HG02809.hp1 HG02886.hp2 |
3_prime_UTR_variant | MODIFIER | c.*10840_*10843delTT others(2): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 10840 | chr12 | 76037585 | |||||
chr12:76037848
|
G | A | 1 | a0001c0002t0009 | 4 | HG02257.hp2 HG03041.hp1 HG03209.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*10581C>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 10581 | chr12 | 76037848 | |||||
chr12:76037879
|
T | C | 1 | a0001c0001t0078 | 1 | HG02040.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10550A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 10550 | chr12 | 76037879 | |||||
chr12:76038053
|
G | C | 1 | a0001c0002t0061 | 1 | HG01081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*10376C>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 10376 | chr12 | 76038053 | |||||
chr12:76038062
|
G | C | 1 | a0001c0002t0045 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10367C>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 10367 | chr12 | 76038062 | |||||
chr12:76038148
|
T | C | 2 | a0001c0001t0047a0001c0001t0049 | 2 | HG02015.hp2 NA18747.hp1 |
3_prime_UTR_variant | MODIFIER | c.*10281A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 10281 | chr12 | 76038148 | |||||
chr12:76038322
|
T | G | 1 | a0001c0002t0046 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10107A>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 10107 | chr12 | 76038322 | |||||
chr12:76038594
|
A | G | 1 | a0001c0001t0089 | 1 | NA18963.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9835T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 9835 | chr12 | 76038594 | |||||
chr12:76038726
|
A | T | 1 | a0001c0003t0010 | 4 | HG00642.hp1 HG01515.hp2 HG01517.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*9703T>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 9703 | chr12 | 76038726 | |||||
chr12:76038932
|
T | C | 1 | a0001c0002t0019 | 3 | HG02559.hp1 HG02809.hp1 HG02886.hp2 |
3_prime_UTR_variant | MODIFIER | c.*9497A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 9497 | chr12 | 76038932 | |||||
chr12:76039021
|
G | A | 3 | a0001c0001t0011a0001c0001t0079a0001c0001t0084 | 6 | NA18948.hp2 NA18969.hp1 NA18991.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*9408C>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 9408 | chr12 | 76039021 | |||||
chr12:76039052
|
G | C | 4 | a0001c0002t0025a0001c0002t0027a0001c0002t0061others(1): Show | 6 | HG01081.hp2 HG01123.hp2 HG01516.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*9377C>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 9377 | chr12 | 76039052 | |||||
chr12:76039199
|
T | C | 1 | a0001c0002t0055 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9230A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 9230 | chr12 | 76039199 | |||||
chr12:76039350
|
A | C | 2 | a0001c0002t0015a0001c0002t0103 | 5 | HG01261.hp1 HG02145.hp1 HG03139.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*9079T>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 9079 | chr12 | 76039350 | |||||
chr12:76039441
|
C | T | 10 | a0001c0002t0009a0001c0002t0014a0001c0002t0020others(7): Show | 20 | HG01109.hp2 HG02055.hp2 HG02257.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*8988G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 8988 | chr12 | 76039441 | |||||
chr12:76039456
|
T | C | 16 | a0001c0001t0001a0001c0001t0008a0001c0001t0032others(13): Show | 89 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(86): Show |
3_prime_UTR_variant | MODIFIER | c.*8973A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 8973 | chr12 | 76039456 | |||||
chr12:76039922
|
G | A | 1 | a0001c0001t0101 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8507C>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 8507 | chr12 | 76039922 | |||||
chr12:76040068
|
T | C | 2 | a0001c0002t0015a0001c0002t0103 | 5 | HG01261.hp1 HG02145.hp1 HG03139.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*8361A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 8361 | chr12 | 76040068 | |||||
chr12:76040110
|
T | G | 1 | a0001c0002t0019 | 3 | HG02559.hp1 HG02809.hp1 HG02886.hp2 |
3_prime_UTR_variant | MODIFIER | c.*8319A>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 8319 | chr12 | 76040110 | |||||
chr12:76040347
|
T | C | 10 | a0001c0002t0009a0001c0002t0014a0001c0002t0020others(7): Show | 20 | HG01109.hp2 HG02055.hp2 HG02257.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*8082A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 8082 | chr12 | 76040347 | |||||
chr12:76040369
|
A | G | 2 | a0001c0002t0015a0001c0002t0103 | 5 | HG01261.hp1 HG02145.hp1 HG03139.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*8060T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 8060 | chr12 | 76040369 | |||||
chr12:76040518
|
T | TAC | 4 | a0001c0001t0011a0001c0001t0079a0001c0001t0080others(1): Show | 7 | NA18948.hp2 NA18969.hp1 NA18972.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*7909_*7910dupGT | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 7910 | chr12 | 76040518 | |||||
chr12:76040518
|
TAC | T | 2 | a0001c0002t0015a0001c0002t0103 | 5 | HG01261.hp1 HG02145.hp1 HG03139.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*7909_*7910delGT | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 7909 | chr12 | 76040518 | |||||
chr12:76040584
|
CGGCTCAC others(37): Show |
C | 1 | a0001c0002t0065 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7801_*7844delCACA others(40): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 7801 | chr12 | 76040584 | |||||
chr12:76040710
|
C | T | 3 | a0001c0002t0044a0001c0002t0046a0001c0002t0102 | 3 | HG01884.hp2 HG02109.hp2 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7719G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 7719 | chr12 | 76040710 | |||||
chr12:76041461
|
A | G | 1 | a0001c0002t0051 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6968T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 6968 | chr12 | 76041461 | |||||
chr12:76041541
|
C | G | 1 | a0001c0001t0084 | 1 | NA19003.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6888G>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 6888 | chr12 | 76041541 | |||||
chr12:76041631
|
T | C | 1 | a0001c0002t0058 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6798A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 6798 | chr12 | 76041631 | |||||
chr12:76041651
|
G | A | 2 | a0001c0002t0009a0001c0002t0039 | 6 | HG02257.hp2 HG02622.hp2 HG03041.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*6778C>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 6778 | chr12 | 76041651 | |||||
chr12:76041678
|
T | TA | 4 | a0001c0002t0025a0001c0002t0027a0001c0002t0061others(1): Show | 6 | HG01081.hp2 HG01123.hp2 HG01516.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*6750dupT | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 6750 | chr12 | 76041678 | |||||
chr12:76041694
|
C | A | 4 | a0001c0002t0025a0001c0002t0027a0001c0002t0061others(1): Show | 6 | HG01081.hp2 HG01123.hp2 HG01516.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*6735G>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 6735 | chr12 | 76041694 | |||||
chr12:76041793
|
T | C | 1 | a0001c0002t0019 | 3 | HG02559.hp1 HG02809.hp1 HG02886.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6636A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 6636 | chr12 | 76041793 | |||||
chr12:76041801
|
C | T | 1 | a0001c0002t0025 | 2 | HG02717.hp1 HG02895.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6628G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 6628 | chr12 | 76041801 | |||||
chr12:76041895
|
A | G | 1 | a0001c0001t0074 | 1 | NA19011.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6534T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 6534 | chr12 | 76041895 | |||||
chr12:76041912
|
C | T | 1 | a0001c0002t0054 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6517G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 6517 | chr12 | 76041912 | |||||
chr12:76041929
|
G | C | 1 | a0001c0002t0019 | 3 | HG02559.hp1 HG02809.hp1 HG02886.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6500C>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 6500 | chr12 | 76041929 | |||||
chr12:76041959
|
G | A | 1 | a0001c0001t0081 | 1 | NA18948.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6470C>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 6470 | chr12 | 76041959 | |||||
chr12:76041980
|
A | T | 1 | a0001c0002t0019 | 3 | HG02559.hp1 HG02809.hp1 HG02886.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6449T>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 6449 | chr12 | 76041980 | |||||
chr12:76042054
|
A | AT | 10 | a0001c0001t0036a0001c0001t0083a0001c0001t0101others(7): Show | 17 | HG00642.hp1 HG01261.hp2 HG01358.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*6374dupA | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 6374 | chr12 | 76042054 | |||||
chr12:76042313
|
T | G | 3 | a0001c0002t0014a0001c0002t0041a0002c0004t0014 | 6 | HG01109.hp2 HG02055.hp2 HG02559.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*6116A>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 6116 | chr12 | 76042313 | |||||
chr12:76042405
|
TAAAGACA others(6): Show |
T | 2 | a0001c0001t0074a0001c0001t0075 | 2 | NA19006.hp2 NA19011.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6011_*6023delGGGT others(9): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 6011 | chr12 | 76042405 | |||||
chr12:76042413
|
C | G | 2 | a0001c0002t0015a0001c0002t0103 | 5 | HG01261.hp1 HG02145.hp1 HG03139.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*6016G>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 6016 | chr12 | 76042413 | |||||
chr12:76042509
|
G | A | 1 | a0001c0002t0051 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5920C>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 5920 | chr12 | 76042509 | |||||
chr12:76042602
|
T | C | 1 | a0001c0002t0058 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5827A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 5827 | chr12 | 76042602 | |||||
chr12:76042734
|
T | C | 1 | a0001c0002t0019 | 3 | HG02559.hp1 HG02809.hp1 HG02886.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5695A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 5695 | chr12 | 76042734 | |||||
chr12:76043031
|
T | A | 3 | a0001c0002t0022a0001c0002t0052a0001c0002t0065 | 4 | HG02896.hp2 HG02897.hp1 HG02922.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5398A>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 5398 | chr12 | 76043031 | |||||
chr12:76043065
|
T | A | 1 | a0001c0001t0087 | 1 | NA18957.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5364A>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 5364 | chr12 | 76043065 | |||||
chr12:76043098
|
C | T | 2 | a0001c0002t0056a0001c0002t0064 | 2 | HG02895.hp2 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5331G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 5331 | chr12 | 76043098 | |||||
chr12:76043127
|
T | C | 2 | a0001c0002t0056a0001c0002t0064 | 2 | HG02895.hp2 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5302A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 5302 | chr12 | 76043127 | |||||
chr12:76043153
|
T | C | 1 | a0001c0002t0019 | 3 | HG02559.hp1 HG02809.hp1 HG02886.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5276A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 5276 | chr12 | 76043153 | |||||
chr12:76043301
|
G | A | 2 | a0001c0002t0029a0001c0002t0088 | 3 | HG02486.hp2 HG02723.hp2 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5128C>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 5128 | chr12 | 76043301 | |||||
chr12:76043358
|
T | G | 9 | a0001c0001t0003a0001c0001t0035a0001c0001t0043others(6): Show | 33 | HG00423.hp1 HG00735.hp1 HG02040.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*5071A>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 5071 | chr12 | 76043358 | |||||
chr12:76043385
|
C | T | 3 | a0001c0002t0014a0001c0002t0041a0002c0004t0014 | 6 | HG01109.hp2 HG02055.hp2 HG02559.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*5044G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 5044 | chr12 | 76043385 | |||||
chr12:76043395
|
C | T | 1 | a0001c0001t0082 | 1 | NA19011.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5034G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 5034 | chr12 | 76043395 | |||||
chr12:76043477
|
G | GA | 54 | a0001c0001t0002a0001c0001t0003a0001c0001t0006others(51): Show | 175 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(172): Show |
3_prime_UTR_variant | MODIFIER | c.*4951dupT | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 4951 | chr12 | 76043477 | |||||
chr12:76043477
|
G | GAA | 13 | a0001c0001t0012a0001c0001t0066a0001c0001t0092others(10): Show | 42 | HG00140.hp1 HG00733.hp1 HG00738.hp1 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*4950_*4951dupTT | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 4951 | chr12 | 76043477 | |||||
chr12:76043477
|
GA | G | 6 | a0001c0001t0032a0001c0002t0056a0001c0003t0010others(3): Show | 12 | HG00642.hp1 HG01069.hp2 HG01071.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*4951delT | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 4951 | chr12 | 76043477 | |||||
chr12:76043536
|
A | G | 4 | a0001c0001t0007a0001c0001t0101a0001c0002t0015others(1): Show | 14 | HG01261.hp1 HG01891.hp1 HG02145.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*4893T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 4893 | chr12 | 76043536 | |||||
chr12:76043839
|
T | G | 1 | a0001c0002t0062 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4590A>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 4590 | chr12 | 76043839 | |||||
chr12:76043911
|
G | C | 3 | a0001c0001t0006a0001c0001t0036a0001c0001t0093 | 19 | HG00323.hp1 HG00558.hp2 HG01255.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*4518C>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 4518 | chr12 | 76043911 | |||||
chr12:76043937
|
C | G | 1 | a0001c0002t0065 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4492G>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 4492 | chr12 | 76043937 | |||||
chr12:76043993
|
G | A | 66 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(63): Show | 257 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(254): Show |
3_prime_UTR_variant | MODIFIER | c.*4436C>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 4436 | chr12 | 76043993 | |||||
chr12:76044040
|
TTTTGAGA others(9): Show |
T | 1 | a0001c0002t0046 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4373_*4388delGTGC others(12): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 4373 | chr12 | 76044040 | |||||
chr12:76044225
|
C | T | 5 | a0001c0001t0007a0001c0001t0042a0001c0001t0101others(2): Show | 15 | HG01261.hp1 HG01891.hp1 HG02145.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*4204G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 4204 | chr12 | 76044225 | |||||
chr12:76044481
|
T | C | 2 | a0001c0001t0037a0001c0001t0038 | 4 | HG02647.hp1 HG02698.hp2 HG02965.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3948A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 3948 | chr12 | 76044481 | |||||
chr12:76044483
|
T | C | 3 | a0001c0002t0014a0001c0002t0041a0002c0004t0014 | 6 | HG01109.hp2 HG02055.hp2 HG02559.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3946A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 3946 | chr12 | 76044483 | |||||
chr12:76045085
|
T | A | 2 | a0001c0001t0094a0001c0001t0095 | 2 | HG02132.hp1 HG02155.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3344A>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 3344 | chr12 | 76045085 | |||||
chr12:76045201
|
A | G | 1 | a0001c0001t0072 | 1 | NA18979.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3228T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 3228 | chr12 | 76045201 | |||||
chr12:76045369
|
G | A | 5 | a0001c0001t0007a0001c0001t0042a0001c0001t0101others(2): Show | 15 | HG01261.hp1 HG01891.hp1 HG02145.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*3060C>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 3060 | chr12 | 76045369 | |||||
chr12:76045471
|
A | G | 1 | a0001c0001t0070 | 1 | HG01106.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2958T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 2958 | chr12 | 76045471 | |||||
chr12:76045604
|
C | T | 1 | a0001c0002t0058 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2825G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 2825 | chr12 | 76045604 | |||||
chr12:76045682
|
C | A | 1 | a0001c0002t0102 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2747G>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 2747 | chr12 | 76045682 | |||||
chr12:76045698
|
T | C | 2 | a0001c0002t0009a0001c0002t0039 | 6 | HG02257.hp2 HG02622.hp2 HG03041.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2731A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 2731 | chr12 | 76045698 | |||||
chr12:76045724
|
C | T | 1 | a0001c0001t0030 | 2 | HG03130.hp1 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2705G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 2705 | chr12 | 76045724 | |||||
chr12:76045879
|
A | G | 71 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(68): Show | 264 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(261): Show |
3_prime_UTR_variant | MODIFIER | c.*2550T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 2550 | chr12 | 76045879 | |||||
chr12:76045941
|
TCAGAATA others(6): Show |
T | 6 | a0001c0001t0071a0001c0002t0014a0001c0002t0015others(3): Show | 12 | HG01109.hp2 HG01261.hp1 HG02055.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2475_*2487delGGTT others(9): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 2475 | chr12 | 76045941 | |||||
chr12:76045954
|
C | T | 82 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(79): Show | 295 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(292): Show |
3_prime_UTR_variant | MODIFIER | c.*2475G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 2475 | chr12 | 76045954 | |||||
chr12:76046206
|
A | T | 1 | a0001c0001t0070 | 1 | HG01106.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2223T>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 2223 | chr12 | 76046206 | |||||
chr12:76046275
|
A | T | 1 | a0001c0002t0044 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2154T>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 2154 | chr12 | 76046275 | |||||
chr12:76046429
|
T | C | 1 | a0001c0002t0019 | 3 | HG02559.hp1 HG02809.hp1 HG02886.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2000A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 2000 | chr12 | 76046429 | |||||
chr12:76046740
|
T | C | 1 | a0001c0002t0063 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1689A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 1689 | chr12 | 76046740 | |||||
chr12:76046762
|
C | T | 3 | a0001c0002t0016a0001c0002t0056a0001c0002t0064 | 5 | HG02886.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1667G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 1667 | chr12 | 76046762 | |||||
chr12:76046842
|
A | T | 1 | a0001c0002t0028 | 2 | HG02630.hp2 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1587T>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 1587 | chr12 | 76046842 | |||||
chr12:76046868
|
T | A | 1 | a0001c0001t0096 | 1 | NA18956.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1561A>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 1561 | chr12 | 76046868 | |||||
chr12:76047162
|
T | C | 1 | a0001c0002t0019 | 3 | HG02559.hp1 HG02809.hp1 HG02886.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1267A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 1267 | chr12 | 76047162 | |||||
chr12:76047371
|
A | AT | 15 | a0001c0002t0004a0001c0002t0020a0001c0002t0021others(12): Show | 42 | HG00140.hp1 HG00733.hp1 HG00738.hp1 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*1057dupA | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 1057 | chr12 | 76047371 | |||||
chr12:76047371
|
AT | A | 6 | a0001c0001t0066a0001c0002t0046a0001c0002t0064others(3): Show | 6 | HG01069.hp2 HG01517.hp1 HG02897.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1057delA | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 1057 | chr12 | 76047371 | |||||
chr12:76047374
|
T | TTA | 6 | a0001c0001t0069a0001c0002t0014a0001c0002t0028others(3): Show | 11 | HG01109.hp2 HG02055.hp2 HG02080.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1054_*1055insTA | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 1054 | chr12 | 76047374 | |||||
chr12:76047375
|
T | TA | 59 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(56): Show | 243 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(240): Show |
3_prime_UTR_variant | MODIFIER | c.*1053_*1054insT | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 1053 | chr12 | 76047375 | |||||
chr12:76047376
|
T | A | 3 | a0001c0001t0013a0001c0001t0097a0001c0001t0098 | 6 | HG01243.hp1 HG02572.hp1 HG03225.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1053A>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 1053 | chr12 | 76047376 | |||||
chr12:76047379
|
T | A | 1 | a0001c0002t0041 | 2 | HG01109.hp2 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1050A>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 1050 | chr12 | 76047379 | |||||
chr12:76047380
|
T | A | 1 | a0001c0002t0009 | 4 | HG02257.hp2 HG03041.hp1 HG03209.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1049A>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 1049 | chr12 | 76047380 | |||||
chr12:76047388
|
T | A | 5 | a0001c0001t0007a0001c0001t0101a0001c0002t0040others(2): Show | 13 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1041A>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 1041 | chr12 | 76047388 | |||||
chr12:76047427
|
C | CT | 10 | a0001c0001t0047a0001c0001t0048a0001c0001t0049others(7): Show | 15 | HG02015.hp2 HG02109.hp2 HG02257.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1001dupA | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 1001 | chr12 | 76047427 | |||||
chr12:76047632
|
A | G | 1 | a0001c0002t0009 | 4 | HG02257.hp2 HG03041.hp1 HG03209.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*797T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 797 | chr12 | 76047632 | |||||
chr12:76047673
|
T | C | 1 | a0001c0002t0102 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*756A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 756 | chr12 | 76047673 | |||||
chr12:76047808
|
C | T | 1 | a0001c0001t0043 | 1 | NA19060.hp1 | 3_prime_UTR_variant | MODIFIER | c.*621G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 621 | chr12 | 76047808 | |||||
chr12:76048031
|
A | G | 1 | a0001c0001t0042 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*398T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 398 | chr12 | 76048031 | |||||
chr12:76048133
|
T | A | 5 | a0001c0002t0014a0001c0002t0015a0001c0002t0041others(2): Show | 11 | HG01109.hp2 HG01261.hp1 HG02055.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*296A>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 15/15 | 296 | chr12 | 76048133 | |||||
chr12:76084660
|
G | A | 1 | a0001c0002t0104 | 1 | HG00733.hp1 | 5_prime_UTR_variant | MODIFIER | c.-114C>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/15 | 10441 | chr12 | 76084660 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:76048619
|
T | C | 1 | a0001c0001t0057g0083 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1141-155A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 14/14 | chr12 | 76048619 | ||||||
chr12:76049110
|
C | CT | 3 | a0001c0002t0019g0137a0001c0002t0019g0138a0001c0002t0019g0139 | 3 | HG02559.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1140+89dupA | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 14/14 | chr12 | 76049110 | ||||||
chr12:76049127
|
T | C | 81 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0021others(78): Show | 93 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.1140+73A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 14/14 | chr12 | 76049127 | ||||||
chr12:76049137
|
A | G | 3 | a0001c0002t0019g0137a0001c0002t0019g0138a0001c0002t0019g0139 | 3 | HG02559.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1140+63T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 14/14 | chr12 | 76049137 | ||||||
chr12:76049406
|
A | G | 1 | a0001c0002t0046g0218 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1090-156T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 13/14 | chr12 | 76049406 | ||||||
chr12:76049476
|
C | T | 1 | a0001c0002t0028g0142 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1090-226G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 13/14 | chr12 | 76049476 | ||||||
chr12:76049676
|
C | T | 3 | a0001c0002t0044g0219a0001c0002t0046g0218a0001c0002t0102g0224 | 3 | HG01884.hp2 HG02109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1089+80G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 13/14 | chr12 | 76049676 | ||||||
chr12:76049687
|
A | G | 6 | a0001c0002t0025g0282a0001c0002t0025g0283a0001c0002t0027g0220others(3): Show | 6 | HG01081.hp2 HG01123.hp2 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.1089+69T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 13/14 | chr12 | 76049687 | ||||||
chr12:76049712
|
T | C | 1 | a0001c0001t0043g0030 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1089+44A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 13/14 | chr12 | 76049712 | ||||||
chr12:76049804
|
G | C | 3 | a0001c0001t0001g0262a0001c0001t0001g0264a0001c0001t0008g0266 | 3 | NA18971.hp2 NA19054.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.1060-19C>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 12/14 | chr12 | 76049804 | ||||||
chr12:76049813
|
T | C | 1 | a0001c0001t0070g0204 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1060-28A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 12/14 | chr12 | 76049813 | ||||||
chr12:76049910
|
G | T | 3 | a0001c0002t0022g0317a0001c0002t0022g0318a0001c0002t0052g0319 | 3 | HG02896.hp2 HG02897.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1060-125C>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 12/14 | chr12 | 76049910 | ||||||
chr12:76049997
|
G | A | 1 | a0001c0001t0002g0114 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1060-212C>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 12/14 | chr12 | 76049997 | ||||||
chr12:76050103
|
G | A | 3 | a0001c0002t0031g0272a0001c0002t0031g0280a0001c0002t0073g0281 | 3 | HG02572.hp2 HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1060-318C>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 12/14 | chr12 | 76050103 | ||||||
chr12:76050106
|
G | A | 1 | a0001c0002t0021g0309 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1060-321C>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 12/14 | chr12 | 76050106 | ||||||
chr12:76050237
|
C | T | 3 | a0001c0002t0019g0137a0001c0002t0019g0138a0001c0002t0019g0139 | 3 | HG02559.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1059+294G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 12/14 | chr12 | 76050237 | ||||||
chr12:76050272
|
T | C | 5 | a0001c0002t0009g0016a0001c0002t0009g0145a0001c0002t0009g0229others(2): Show | 6 | HG02257.hp2 HG02622.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1059+259A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 12/14 | chr12 | 76050272 | ||||||
chr12:76050351
|
A | G | 75 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0021others(72): Show | 87 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.1059+180T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 12/14 | chr12 | 76050351 | ||||||
chr12:76050436
|
A | G | 3 | a0001c0002t0019g0137a0001c0002t0019g0138a0001c0002t0019g0139 | 3 | HG02559.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1059+95T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 12/14 | chr12 | 76050436 | ||||||
chr12:76050730
|
G | A | 200 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0021others(197): Show | 229 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(226): Show |
intron_variant | MODIFIER | c.937-77C>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 11/14 | chr12 | 76050730 | ||||||
chr12:76050753
|
A | G | 1 | a0001c0002t0062g0228 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.937-100T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 11/14 | chr12 | 76050753 | ||||||
chr12:76050802
|
C | T | 1 | a0001c0001t0037g0071 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.937-149G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 11/14 | chr12 | 76050802 | ||||||
chr12:76050905
|
G | A | 1 | a0001c0001t0006g0061 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.937-252C>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 11/14 | chr12 | 76050905 | ||||||
chr12:76051002
|
G | GA | 48 | a0001c0001t0001g0169a0001c0001t0001g0174a0001c0001t0003g0041others(45): Show | 48 | HG00140.hp1 HG00733.hp1 HG00738.hp1 others(45): Show |
intron_variant | MODIFIER | c.937-350dupT | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 11/14 | chr12 | 76051002 | ||||||
chr12:76051002
|
G | GAA | 17 | a0001c0002t0004g0312a0001c0002t0009g0016a0001c0002t0009g0145others(14): Show | 19 | HG01109.hp2 HG02257.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.937-351_937-350dup others(2): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 11/14 | chr12 | 76051002 | ||||||
chr12:76051030
|
T | C | 4 | a0001c0001t0001g0021a0001c0001t0001g0177a0001c0001t0074g0163others(1): Show | 5 | NA18955.hp2 NA18999.hp2 NA19006.hp2 others(2): Show |
intron_variant | MODIFIER | c.937-377A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 11/14 | chr12 | 76051030 | ||||||
chr12:76051330
|
T | A | 1 | a0001c0001t0002g0054 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.937-677A>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 11/14 | chr12 | 76051330 | ||||||
chr12:76051330
|
T | TA | 111 | a0001c0001t0001g0166a0001c0001t0002g0002a0001c0001t0002g0003others(108): Show | 127 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.937-678dupT | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 11/14 | chr12 | 76051330 | ||||||
chr12:76051341
|
A | C | 1 | a0001c0002t0051g0221 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.937-688T>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 11/14 | chr12 | 76051341 | ||||||
chr12:76051617
|
C | T | 1 | a0001c0001t0002g0020 | 2 | HG01109.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.937-964G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 11/14 | chr12 | 76051617 | ||||||
chr12:76051633
|
G | A | 1 | a0001c0001t0001g0271 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.937-980C>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 11/14 | chr12 | 76051633 | ||||||
chr12:76051634
|
G | C | 1 | a0001c0001t0001g0271 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.937-981C>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 11/14 | chr12 | 76051634 | ||||||
chr12:76051637
|
C | T | 204 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0021others(201): Show | 233 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(230): Show |
intron_variant | MODIFIER | c.937-984G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 11/14 | chr12 | 76051637 | ||||||
chr12:76051826
|
C | T | 1 | a0001c0002t0065g0291 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.937-1173G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 11/14 | chr12 | 76051826 | ||||||
chr12:76052024
|
T | A | 1 | a0001c0002t0004g0320 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.936+1067A>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 11/14 | chr12 | 76052024 | ||||||
chr12:76052266
|
C | A | 6 | a0001c0002t0020g0216a0001c0002t0020g0217a0001c0002t0029g0135others(3): Show | 6 | HG02258.hp1 HG02486.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.936+825G>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 11/14 | chr12 | 76052266 | ||||||
chr12:76052270
|
A | C | 1 | a0001c0001t0008g0268 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.936+821T>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 11/14 | chr12 | 76052270 | ||||||
chr12:76052276
|
C | T | 5 | a0001c0002t0014g0017a0001c0002t0014g0148a0001c0002t0041g0146others(2): Show | 6 | HG01109.hp2 HG02055.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.936+815G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 11/14 | chr12 | 76052276 | ||||||
chr12:76052312
|
A | G | 3 | a0001c0002t0019g0137a0001c0002t0019g0138a0001c0002t0019g0139 | 3 | HG02559.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.936+779T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 11/14 | chr12 | 76052312 | ||||||
chr12:76052315
|
T | C | 49 | a0001c0001t0066g0307a0001c0002t0004g0288a0001c0002t0004g0289others(46): Show | 50 | HG00140.hp1 HG00733.hp1 HG00738.hp1 others(47): Show |
intron_variant | MODIFIER | c.936+776A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 11/14 | chr12 | 76052315 | ||||||
chr12:76052528
|
T | G | 204 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0021others(201): Show | 233 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(230): Show |
intron_variant | MODIFIER | c.936+563A>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 11/14 | chr12 | 76052528 | ||||||
chr12:76052712
|
T | C | 1 | a0001c0002t0004g0316 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.936+379A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 11/14 | chr12 | 76052712 | ||||||
chr12:76053144
|
A | G | 6 | a0001c0002t0025g0282a0001c0002t0025g0283a0001c0002t0027g0220others(3): Show | 6 | HG01081.hp2 HG01123.hp2 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.917-34T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 10/14 | chr12 | 76053144 | ||||||
chr12:76053575
|
T | A | 1 | a0001c0001t0008g0263 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.770+195A>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 9/14 | chr12 | 76053575 | ||||||
chr12:76053610
|
G | C | 38 | a0001c0001t0066g0307a0001c0002t0004g0288a0001c0002t0004g0289others(35): Show | 38 | HG00140.hp1 HG00733.hp1 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.770+160C>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 9/14 | chr12 | 76053610 | ||||||
chr12:76053731
|
A | T | 1 | a0001c0001t0002g0037 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.770+39T>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 9/14 | chr12 | 76053731 | ||||||
chr12:76053733
|
A | T | 1 | a0001c0001t0002g0037 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.770+37T>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 9/14 | chr12 | 76053733 | ||||||
chr12:76053734
|
A | T | 1 | a0001c0001t0002g0037 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.770+36T>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 9/14 | chr12 | 76053734 | ||||||
chr12:76053736
|
A | C | 1 | a0001c0001t0002g0037 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.770+34T>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 9/14 | chr12 | 76053736 | ||||||
chr12:76053737
|
A | T | 1 | a0001c0001t0002g0037 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.770+33T>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 9/14 | chr12 | 76053737 | ||||||
chr12:76053740
|
A | C | 1 | a0001c0001t0002g0037 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.770+30T>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 9/14 | chr12 | 76053740 | ||||||
chr12:76054012
|
A | T | 1 | a0001c0003t0005g0240 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.631-103T>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 8/14 | chr12 | 76054012 | ||||||
chr12:76054012
|
AT | A | 275 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0021others(272): Show | 307 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(304): Show |
intron_variant | MODIFIER | c.631-104delA | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 8/14 | chr12 | 76054012 | ||||||
chr12:76054111
|
C | G | 1 | a0001c0002t0023g0273 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.631-202G>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 8/14 | chr12 | 76054111 | ||||||
chr12:76054144
|
G | A | 1 | a0001c0002t0058g0144 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.631-235C>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 8/14 | chr12 | 76054144 | ||||||
chr12:76054180
|
C | T | 1 | a0001c0001t0002g0118 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.631-271G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 8/14 | chr12 | 76054180 | ||||||
chr12:76054277
|
ACCTCGG | A | 75 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0021others(72): Show | 87 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.631-374_631-369del others(6): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 8/14 | chr12 | 76054277 | ||||||
chr12:76054305
|
C | T | 2 | a0001c0002t0019g0138a0001c0002t0019g0139 | 2 | HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.631-396G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 8/14 | chr12 | 76054305 | ||||||
chr12:76054804
|
T | A | 204 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0021others(201): Show | 233 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(230): Show |
intron_variant | MODIFIER | c.630+215A>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 8/14 | chr12 | 76054804 | ||||||
chr12:76054912
|
A | G | 1 | a0001c0001t0001g0270 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.630+107T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 8/14 | chr12 | 76054912 | ||||||
chr12:76055003
|
T | C | 5 | a0001c0002t0009g0016a0001c0002t0009g0145a0001c0002t0009g0229others(2): Show | 6 | HG02257.hp2 HG02622.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.630+16A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 8/14 | chr12 | 76055003 | ||||||
chr12:76055433
|
G | A | 2 | a0001c0002t0016g0226a0001c0002t0016g0276 | 2 | HG02886.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.559-343C>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 7/14 | chr12 | 76055433 | ||||||
chr12:76055727
|
G | C | 1 | a0001c0001t0006g0050 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.558+306C>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 7/14 | chr12 | 76055727 | ||||||
chr12:76055817
|
T | C | 1 | a0001c0002t0023g0274 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.558+216A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 7/14 | chr12 | 76055817 | ||||||
chr12:76056240
|
AAGCACAG others(2): Show |
A | 4 | a0001c0002t0015g0018a0001c0002t0015g0149a0001c0002t0015g0150others(1): Show | 5 | HG01261.hp1 HG02145.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.430-88_430-80delGA others(7): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76056240 | ||||||
chr12:76056356
|
A | G | 5 | a0001c0002t0009g0016a0001c0002t0009g0145a0001c0002t0009g0229others(2): Show | 6 | HG02257.hp2 HG02622.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.430-195T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76056356 | ||||||
chr12:76056378
|
T | C | 1 | a0001c0002t0102g0224 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.430-217A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76056378 | ||||||
chr12:76056398
|
T | TA | 15 | a0001c0001t0003g0101a0001c0001t0003g0102a0001c0002t0014g0017others(12): Show | 16 | HG01109.hp2 HG02055.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.430-238dupT | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76056398 | ||||||
chr12:76056398
|
T | TAA | 5 | a0001c0002t0009g0016a0001c0002t0009g0145a0001c0002t0009g0229others(2): Show | 6 | HG02257.hp2 HG02622.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.430-239_430-238dup others(2): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76056398 | ||||||
chr12:76056652
|
A | G | 1 | a0001c0002t0046g0218 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.430-491T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76056652 | ||||||
chr12:76057079
|
T | C | 2 | a0001c0001t0047g0053a0001c0001t0049g0065 | 2 | HG02015.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.430-918A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76057079 | ||||||
chr12:76057636
|
T | C | 6 | a0001c0002t0020g0216a0001c0002t0020g0217a0001c0002t0029g0135others(3): Show | 6 | HG02258.hp1 HG02486.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.430-1475A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76057636 | ||||||
chr12:76057657
|
AAT | A | 8 | a0001c0002t0020g0216a0001c0002t0020g0217a0001c0002t0028g0142others(5): Show | 8 | HG02258.hp1 HG02486.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.430-1498_430-1497d others(4): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76057657 | ||||||
chr12:76057688
|
G | C | 1 | a0001c0001t0001g0175 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.430-1527C>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76057688 | ||||||
chr12:76057867
|
C | T | 1 | a0001c0001t0036g0008 | 2 | HG01261.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.430-1706G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76057867 | ||||||
chr12:76057916
|
T | C | 240 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0021others(237): Show | 269 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(266): Show |
intron_variant | MODIFIER | c.430-1755A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76057916 | ||||||
chr12:76057919
|
G | C | 6 | a0001c0002t0020g0216a0001c0002t0020g0217a0001c0002t0029g0135others(3): Show | 6 | HG02258.hp1 HG02486.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.430-1758C>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76057919 | ||||||
chr12:76057986
|
A | G | 1 | a0001c0001t0001g0271 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.429+1812T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76057986 | ||||||
chr12:76058095
|
G | A | 6 | a0001c0002t0020g0216a0001c0002t0020g0217a0001c0002t0029g0135others(3): Show | 6 | HG02258.hp1 HG02486.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.429+1703C>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76058095 | ||||||
chr12:76058150
|
T | C | 1 | a0001c0001t0001g0169 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.429+1648A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76058150 | ||||||
chr12:76058159
|
C | A | 3 | a0001c0002t0009g0016a0001c0002t0009g0145a0001c0002t0009g0229 | 4 | HG02257.hp2 HG03041.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.429+1639G>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76058159 | ||||||
chr12:76058166
|
T | C | 5 | a0001c0001t0013g0013a0001c0001t0013g0081a0001c0001t0013g0084others(2): Show | 6 | HG01243.hp1 HG02572.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.429+1632A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76058166 | ||||||
chr12:76058191
|
C | CTTCA | 6 | a0001c0001t0003g0094a0001c0002t0015g0018a0001c0002t0015g0149others(3): Show | 7 | HG01261.hp1 HG02040.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.429+1606_429+1607i others(6): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76058191 | ||||||
chr12:76058191
|
C | CTTCATAT others(3): Show |
5 | a0001c0002t0019g0137a0001c0002t0019g0138a0001c0002t0019g0139others(2): Show | 5 | HG02559.hp1 HG02622.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.429+1606_429+1607i others(12): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76058191 | ||||||
chr12:76058191
|
C | CTTCATAT others(11): Show |
1 | a0001c0001t0007g0157 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.429+1606_429+1607i others(20): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76058191 | ||||||
chr12:76058191
|
C | CTTCATAT others(15): Show |
2 | a0001c0001t0007g0161a0001c0001t0042g0199 | 2 | HG02280.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.429+1606_429+1607i others(24): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76058191 | ||||||
chr12:76058191
|
C | CTTCATAT others(17): Show |
1 | a0001c0001t0007g0019 | 2 | HG01891.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.429+1606_429+1607i others(26): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76058191 | ||||||
chr12:76058191
|
C | CTTCATAT others(19): Show |
2 | a0001c0001t0007g0133a0001c0001t0007g0154 | 2 | HG02451.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.429+1606_429+1607i others(28): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76058191 | ||||||
chr12:76058191
|
C | CTTCATAT others(23): Show |
1 | a0001c0001t0101g0156 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.429+1606_429+1607i others(32): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76058191 | ||||||
chr12:76058191
|
C | CTTCATAT others(35): Show |
1 | a0001c0001t0007g0158 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.429+1606_429+1607i others(44): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76058191 | ||||||
chr12:76058192
|
T | TTC | 7 | a0001c0001t0002g0098a0001c0001t0003g0014a0001c0001t0035g0109others(4): Show | 8 | HG02258.hp1 HG02523.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.429+1605_429+1606i others(4): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76058192 | ||||||
chr12:76058193
|
A | T | 202 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0021others(199): Show | 231 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(228): Show |
intron_variant | MODIFIER | c.429+1605T>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76058193 | ||||||
chr12:76058194
|
C | CAT | 4 | a0001c0002t0004g0294a0001c0002t0004g0310a0001c0002t0025g0282others(1): Show | 4 | HG00741.hp1 HG01433.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.429+1602_429+1603d others(4): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76058194 | ||||||
chr12:76058194
|
C | CATAT | 4 | a0001c0002t0004g0312a0001c0002t0027g0284a0001c0002t0061g0286others(1): Show | 4 | HG01081.hp2 HG01516.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.429+1600_429+1603d others(6): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76058194 | ||||||
chr12:76058194
|
C | CATATATA others(1): Show |
4 | a0001c0002t0024g0223a0001c0002t0027g0220a0001c0002t0044g0219others(1): Show | 4 | HG01123.hp2 HG02109.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.429+1596_429+1603d others(10): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76058194 | ||||||
chr12:76058194
|
C | CATATATA others(3): Show |
1 | a0001c0002t0024g0222 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.429+1594_429+1603d others(12): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76058194 | ||||||
chr12:76058194
|
C | CATATATA others(11): Show |
1 | a0001c0002t0021g0309 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.429+1586_429+1603d others(20): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76058194 | ||||||
chr12:76058194
|
C | CATATATA others(13): Show |
1 | a0001c0002t0065g0291 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.429+1584_429+1603d others(22): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76058194 | ||||||
chr12:76058194
|
C | T | 26 | a0001c0001t0002g0098a0001c0001t0003g0014a0001c0001t0003g0094others(23): Show | 29 | HG01261.hp1 HG01891.hp1 HG02040.hp2 others(26): Show |
intron_variant | MODIFIER | c.429+1604G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76058194 | ||||||
chr12:76058194
|
CAT | C | 67 | a0001c0001t0002g0045a0001c0001t0002g0047a0001c0001t0002g0104others(64): Show | 74 | HG00558.hp2 HG00597.hp2 HG00735.hp1 others(71): Show |
intron_variant | MODIFIER | c.429+1602_429+1603d others(4): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76058194 | ||||||
chr12:76058194
|
CATAT | C | 44 | a0001c0001t0002g0060a0001c0001t0030g0010a0001c0001t0037g0057others(41): Show | 46 | HG00323.hp2 HG00642.hp1 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.429+1600_429+1603d others(6): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76058194 | ||||||
chr12:76058194
|
CATATAT | C | 44 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0011others(41): Show | 51 | HG00438.hp2 HG00544.hp2 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.429+1598_429+1603d others(8): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76058194 | ||||||
chr12:76058194
|
CATATATA others(7): Show |
C | 84 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0021others(81): Show | 96 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.429+1590_429+1603d others(16): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76058194 | ||||||
chr12:76058284
|
A | G | 3 | a0001c0002t0019g0137a0001c0002t0019g0138a0001c0002t0019g0139 | 3 | HG02559.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.429+1514T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76058284 | ||||||
chr12:76058311
|
T | C | 22 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0037others(19): Show | 24 | HG00544.hp2 HG01070.hp1 HG01099.hp2 others(21): Show |
intron_variant | MODIFIER | c.429+1487A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76058311 | ||||||
chr12:76058387
|
C | CT | 10 | a0001c0002t0004g0316a0001c0002t0014g0017a0001c0002t0014g0148others(7): Show | 11 | HG01109.hp2 HG01175.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.429+1410dupA | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76058387 | ||||||
chr12:76058387
|
CT | C | 112 | a0001c0001t0001g0176a0001c0001t0002g0002a0001c0001t0002g0003others(109): Show | 128 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.429+1410delA | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76058387 | ||||||
chr12:76058543
|
C | T | 9 | a0001c0003t0005g0242a0001c0003t0005g0245a0001c0003t0010g0025others(6): Show | 10 | HG00642.hp1 HG01069.hp2 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.429+1255G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76058543 | ||||||
chr12:76058699
|
CTTTT | C | 3 | a0001c0002t0019g0137a0001c0002t0019g0138a0001c0002t0019g0139 | 3 | HG02559.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.429+1095_429+1098d others(6): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76058699 | ||||||
chr12:76058724
|
A | T | 1 | a0001c0001t0012g0029 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.429+1074T>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76058724 | ||||||
chr12:76058810
|
C | G | 203 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0021others(200): Show | 232 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(229): Show |
intron_variant | MODIFIER | c.429+988G>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76058810 | ||||||
chr12:76058818
|
A | T | 1 | a0001c0001t0012g0029 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.429+980T>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76058818 | ||||||
chr12:76058864
|
T | C | 1 | a0001c0001t0001g0186 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.429+934A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76058864 | ||||||
chr12:76059008
|
A | G | 18 | a0001c0002t0009g0016a0001c0002t0009g0145a0001c0002t0009g0229others(15): Show | 20 | HG01109.hp2 HG02055.hp2 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.429+790T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76059008 | ||||||
chr12:76059026
|
C | T | 1 | a0001c0002t0062g0228 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.429+772G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76059026 | ||||||
chr12:76059136
|
A | G | 2 | a0001c0002t0027g0284a0001c0002t0068g0285 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.429+662T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76059136 | ||||||
chr12:76059258
|
T | C | 3 | a0001c0002t0019g0137a0001c0002t0019g0138a0001c0002t0019g0139 | 3 | HG02559.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.429+540A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76059258 | ||||||
chr12:76059522
|
T | C | 111 | a0001c0001t0001g0165a0001c0001t0002g0002a0001c0001t0002g0003others(108): Show | 127 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.429+276A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76059522 | ||||||
chr12:76059647
|
T | C | 1 | a0001c0001t0001g0214 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.429+151A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76059647 | ||||||
chr12:76059656
|
G | A | 1 | a0001c0002t0004g0295 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.429+142C>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76059656 | ||||||
chr12:76059668
|
C | T | 2 | a0001c0002t0004g0316a0001c0002t0021g0299 | 2 | HG03704.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.429+130G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 6/14 | chr12 | 76059668 | ||||||
chr12:76060057
|
T | C | 3 | a0001c0002t0019g0137a0001c0002t0019g0138a0001c0002t0019g0139 | 3 | HG02559.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.348+81A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 5/14 | chr12 | 76060057 | ||||||
chr12:76060081
|
G | A | 275 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0021others(272): Show | 307 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(304): Show |
intron_variant | MODIFIER | c.348+57C>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 5/14 | chr12 | 76060081 | ||||||
chr12:76060093
|
C | T | 203 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0021others(200): Show | 232 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(229): Show |
intron_variant | MODIFIER | c.348+45G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 5/14 | chr12 | 76060093 | ||||||
chr12:76060117
|
CAAAGTAG others(3): Show |
C | 3 | a0001c0002t0004g0288a0001c0002t0004g0312a0001c0002t0054g0298 | 3 | HG01192.hp2 HG03098.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.348+11_348+20delCT others(8): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 5/14 | chr12 | 76060117 | ||||||
chr12:76060461
|
C | T | 1 | a0001c0002t0029g0135 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.207-182G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76060461 | ||||||
chr12:76060582
|
T | C | 9 | a0001c0002t0016g0226a0001c0002t0016g0227a0001c0002t0016g0276others(6): Show | 9 | HG02109.hp1 HG02886.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.207-303A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76060582 | ||||||
chr12:76060668
|
A | G | 228 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0021others(225): Show | 260 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(257): Show |
intron_variant | MODIFIER | c.207-389T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76060668 | ||||||
chr12:76060826
|
C | T | 9 | a0001c0003t0005g0234a0001c0003t0005g0235a0001c0003t0005g0238others(6): Show | 9 | HG00323.hp2 HG00738.hp2 HG01167.hp1 others(6): Show |
intron_variant | MODIFIER | c.207-547G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76060826 | ||||||
chr12:76060939
|
A | T | 10 | a0001c0002t0009g0016a0001c0002t0009g0145a0001c0002t0009g0229others(7): Show | 11 | HG02257.hp2 HG02486.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.207-660T>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76060939 | ||||||
chr12:76060980
|
C | A | 5 | a0001c0002t0028g0142a0001c0002t0028g0143a0001c0002t0029g0135others(2): Show | 5 | HG02486.hp2 HG02630.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.207-701G>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76060980 | ||||||
chr12:76061032
|
G | C | 9 | a0001c0002t0014g0017a0001c0002t0014g0148a0001c0002t0015g0018others(6): Show | 11 | HG01109.hp2 HG01261.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.207-753C>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76061032 | ||||||
chr12:76061076
|
C | G | 1 | a0001c0001t0001g0177 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.207-797G>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76061076 | ||||||
chr12:76061103
|
A | G | 3 | a0001c0002t0022g0317a0001c0002t0022g0318a0001c0002t0052g0319 | 3 | HG02896.hp2 HG02897.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.207-824T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76061103 | ||||||
chr12:76061234
|
T | G | 1 | a0001c0002t0058g0144 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.207-955A>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76061234 | ||||||
chr12:76061313
|
T | C | 9 | a0001c0002t0014g0017a0001c0002t0014g0148a0001c0002t0015g0018others(6): Show | 11 | HG01109.hp2 HG01261.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.207-1034A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76061313 | ||||||
chr12:76061377
|
G | A | 1 | a0001c0001t0003g0091 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.207-1098C>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76061377 | ||||||
chr12:76061487
|
C | T | 1 | a0001c0001t0002g0059 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.207-1208G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76061487 | ||||||
chr12:76061640
|
A | C | 1 | a0001c0001t0085g0082 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.207-1361T>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76061640 | ||||||
chr12:76061822
|
T | C | 6 | a0001c0002t0020g0216a0001c0002t0020g0217a0001c0002t0029g0135others(3): Show | 6 | HG02258.hp1 HG02486.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.207-1543A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76061822 | ||||||
chr12:76061934
|
T | C | 275 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0021others(272): Show | 307 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(304): Show |
intron_variant | MODIFIER | c.207-1655A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76061934 | ||||||
chr12:76062037
|
C | T | 229 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0021others(226): Show | 261 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(258): Show |
intron_variant | MODIFIER | c.207-1758G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76062037 | ||||||
chr12:76062155
|
G | A | 1 | a0001c0002t0004g0322 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.207-1876C>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76062155 | ||||||
chr12:76062176
|
G | A | 1 | a0001c0002t0044g0219 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.207-1897C>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76062176 | ||||||
chr12:76062228
|
C | G | 3 | a0001c0002t0019g0137a0001c0002t0019g0138a0001c0002t0019g0139 | 3 | HG02559.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.207-1949G>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76062228 | ||||||
chr12:76062341
|
C | T | 3 | a0001c0002t0009g0016a0001c0002t0009g0145a0001c0002t0009g0229 | 4 | HG02257.hp2 HG03041.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.207-2062G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76062341 | ||||||
chr12:76062412
|
T | C | 1 | a0001c0001t0003g0089 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.207-2133A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76062412 | ||||||
chr12:76062447
|
G | A | 1 | a0001c0001t0002g0074 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.207-2168C>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76062447 | ||||||
chr12:76062777
|
C | T | 1 | a0001c0001t0008g0263 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.207-2498G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76062777 | ||||||
chr12:76062936
|
G | GA | 3 | a0001c0002t0019g0137a0001c0002t0019g0138a0001c0002t0019g0139 | 3 | HG02559.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.207-2658dupT | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76062936 | ||||||
chr12:76062994
|
T | C | 9 | a0001c0002t0014g0017a0001c0002t0014g0148a0001c0002t0015g0018others(6): Show | 11 | HG01109.hp2 HG01261.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.207-2715A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76062994 | ||||||
chr12:76063006
|
A | G | 4 | a0001c0002t0027g0220a0001c0002t0027g0284a0001c0002t0061g0286others(1): Show | 4 | HG01081.hp2 HG01123.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.207-2727T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76063006 | ||||||
chr12:76063067
|
A | G | 2 | a0001c0002t0023g0273a0001c0002t0023g0274 | 2 | HG02257.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.207-2788T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76063067 | ||||||
chr12:76063076
|
A | G | 6 | a0001c0002t0020g0216a0001c0002t0020g0217a0001c0002t0029g0135others(3): Show | 6 | HG02258.hp1 HG02486.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.207-2797T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76063076 | ||||||
chr12:76063342
|
A | G | 9 | a0001c0002t0014g0017a0001c0002t0014g0148a0001c0002t0015g0018others(6): Show | 11 | HG01109.hp2 HG01261.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.207-3063T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76063342 | ||||||
chr12:76063421
|
A | C | 1 | a0001c0001t0013g0084 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.207-3142T>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76063421 | ||||||
chr12:76063538
|
C | G | 1 | a0001c0001t0002g0098 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.207-3259G>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76063538 | ||||||
chr12:76063588
|
G | A | 1 | a0001c0001t0078g0179 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.207-3309C>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76063588 | ||||||
chr12:76063712
|
A | G | 3 | a0001c0002t0019g0137a0001c0002t0019g0138a0001c0002t0019g0139 | 3 | HG02559.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.207-3433T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76063712 | ||||||
chr12:76063824
|
T | A | 13 | a0001c0001t0007g0019a0001c0001t0007g0133a0001c0001t0007g0154others(10): Show | 14 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.207-3545A>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76063824 | ||||||
chr12:76063861
|
G | C | 1 | a0001c0002t0065g0291 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.206+3510C>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76063861 | ||||||
chr12:76063880
|
T | TAAA | 7 | a0001c0002t0014g0017a0001c0002t0014g0148a0001c0002t0015g0018others(4): Show | 9 | HG01109.hp2 HG01261.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.206+3490_206+3491i others(5): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76063880 | ||||||
chr12:76063881
|
T | A | 9 | a0001c0002t0014g0017a0001c0002t0014g0148a0001c0002t0015g0018others(6): Show | 11 | HG01109.hp2 HG01261.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.206+3490A>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76063881 | ||||||
chr12:76063881
|
T | TA | 35 | a0001c0001t0001g0026a0001c0001t0001g0159a0001c0001t0001g0162others(32): Show | 35 | HG00738.hp1 HG01069.hp1 HG01361.hp2 others(32): Show |
intron_variant | MODIFIER | c.206+3489dupT | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76063881 | ||||||
chr12:76063881
|
T | TAA | 92 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0021others(89): Show | 105 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.206+3488_206+3489d others(4): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76063881 | ||||||
chr12:76063881
|
TAAAA | T | 11 | a0001c0002t0009g0016a0001c0002t0009g0145a0001c0002t0009g0229others(8): Show | 12 | HG02257.hp2 HG02258.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.206+3486_206+3489d others(6): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76063881 | ||||||
chr12:76063881
|
TAAAAAAA others(2): Show |
T | 109 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0011others(106): Show | 125 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.206+3481_206+3489d others(11): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76063881 | ||||||
chr12:76064031
|
G | A | 3 | a0001c0002t0019g0137a0001c0002t0019g0138a0001c0002t0019g0139 | 3 | HG02559.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.206+3340C>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76064031 | ||||||
chr12:76064194
|
C | T | 1 | a0001c0002t0029g0136 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.206+3177G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76064194 | ||||||
chr12:76064443
|
T | A | 1 | a0001c0001t0001g0169 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.206+2928A>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76064443 | ||||||
chr12:76064926
|
G | A | 3 | a0001c0002t0019g0137a0001c0002t0019g0138a0001c0002t0019g0139 | 3 | HG02559.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.206+2445C>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76064926 | ||||||
chr12:76065065
|
A | G | 1 | a0001c0002t0004g0304 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.206+2306T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76065065 | ||||||
chr12:76065093
|
A | G | 1 | a0001c0002t0088g0134 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.206+2278T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76065093 | ||||||
chr12:76065106
|
T | C | 1 | a0001c0001t0001g0195 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.206+2265A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76065106 | ||||||
chr12:76065124
|
T | C | 1 | a0001c0001t0006g0121 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.206+2247A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76065124 | ||||||
chr12:76065303
|
G | T | 3 | a0001c0002t0029g0135a0001c0002t0029g0136a0001c0002t0088g0134 | 3 | HG02486.hp2 HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.206+2068C>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76065303 | ||||||
chr12:76065345
|
A | C | 2 | a0001c0002t0024g0222a0001c0002t0024g0223 | 2 | HG02280.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.206+2026T>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76065345 | ||||||
chr12:76065363
|
A | G | 2 | a0001c0002t0004g0304a0001c0002t0004g0308 | 2 | HG02602.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.206+2008T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76065363 | ||||||
chr12:76065467
|
T | C | 1 | a0001c0002t0062g0228 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.206+1904A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76065467 | ||||||
chr12:76065532
|
TA | T | 313 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0021others(310): Show | 345 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(342): Show |
intron_variant | MODIFIER | c.206+1838delT | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76065532 | ||||||
chr12:76065546
|
A | G | 1 | a0001c0002t0004g0290 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.206+1825T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76065546 | ||||||
chr12:76066053
|
TA | T | 6 | a0001c0002t0019g0137a0001c0002t0019g0138a0001c0002t0019g0139others(3): Show | 6 | HG01069.hp2 HG02559.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.206+1317delT | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76066053 | ||||||
chr12:76066097
|
AAAAT | A | 3 | a0001c0002t0024g0223a0001c0002t0027g0220a0001c0003t0060g0249 | 3 | HG01074.hp1 HG01123.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.206+1270_206+1273d others(6): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76066097 | ||||||
chr12:76066097
|
AAAATAAA others(1): Show |
A | 19 | a0001c0002t0025g0282a0001c0002t0025g0283a0001c0002t0044g0219others(16): Show | 19 | HG00323.hp2 HG00738.hp2 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.206+1266_206+1273d others(10): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76066097 | ||||||
chr12:76066097
|
AAAATAAA others(5): Show |
A | 4 | a0001c0002t0027g0284a0001c0002t0058g0144a0001c0002t0063g0212others(1): Show | 4 | HG01516.hp2 HG01517.hp1 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.206+1262_206+1273d others(14): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76066097 | ||||||
chr12:76066121
|
TAAATAAA others(13): Show |
T | 1 | a0001c0002t0029g0135 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.206+1230_206+1249d others(22): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76066121 | ||||||
chr12:76066125
|
TAAATAAA others(9): Show |
T | 10 | a0001c0001t0001g0196a0001c0002t0016g0227a0001c0002t0019g0137others(7): Show | 10 | HG02258.hp1 HG02486.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.206+1230_206+1245d others(18): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76066125 | ||||||
chr12:76066125
|
TAAATAAA others(13): Show |
T | 1 | a0001c0001t0003g0107 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.206+1226_206+1245d others(22): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76066125 | ||||||
chr12:76066129
|
TAAATAAA others(5): Show |
T | 13 | a0001c0001t0007g0133a0001c0002t0004g0310a0001c0002t0014g0017others(10): Show | 14 | HG00733.hp1 HG01109.hp2 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.206+1230_206+1241d others(14): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76066129 | ||||||
chr12:76066129
|
TAAATAAA others(9): Show |
T | 75 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0021others(72): Show | 85 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.206+1226_206+1241d others(18): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76066129 | ||||||
chr12:76066133
|
T | C | 1 | a0001c0003t0005g0248 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.206+1238A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76066133 | ||||||
chr12:76066133
|
TAAATAAA others(1): Show |
T | 11 | a0001c0002t0005g0259a0001c0002t0016g0226a0001c0002t0016g0276others(8): Show | 11 | HG01175.hp1 HG01358.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.206+1230_206+1237d others(10): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76066133 | ||||||
chr12:76066133
|
TAAATAAA others(5): Show |
T | 137 | a0001c0001t0001g0173a0001c0001t0001g0175a0001c0001t0001g0271others(134): Show | 156 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(153): Show |
intron_variant | MODIFIER | c.206+1226_206+1237d others(14): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76066133 | ||||||
chr12:76066137
|
T | C | 5 | a0001c0002t0024g0222a0001c0002t0024g0223a0001c0003t0005g0246others(2): Show | 5 | HG01256.hp2 HG01891.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.206+1234A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76066137 | ||||||
chr12:76066137
|
TAAAC | T | 5 | a0001c0002t0004g0321a0001c0002t0004g0322a0001c0002t0017g0315others(2): Show | 5 | HG00738.hp1 HG01099.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.206+1230_206+1233d others(6): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76066137 | ||||||
chr12:76066137
|
TAAACAAA others(1): Show |
T | 30 | a0001c0001t0002g0022a0001c0001t0002g0069a0001c0001t0002g0181others(27): Show | 31 | HG00140.hp2 HG00741.hp1 HG01106.hp2 others(28): Show |
intron_variant | MODIFIER | c.206+1226_206+1233d others(10): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76066137 | ||||||
chr12:76066141
|
C | T | 2 | a0001c0001t0002g0020a0001c0003t0005g0258 | 3 | HG01109.hp1 HG01515.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.206+1230G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76066141 | ||||||
chr12:76066145
|
C | T | 3 | a0001c0002t0004g0321a0001c0002t0004g0322a0001c0002t0017g0315 | 3 | HG00738.hp1 HG01099.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.206+1226G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76066145 | ||||||
chr12:76066202
|
C | T | 3 | a0001c0002t0009g0016a0001c0002t0009g0145a0001c0002t0009g0229 | 4 | HG02257.hp2 HG03041.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.206+1169G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76066202 | ||||||
chr12:76066215
|
C | A | 1 | a0001c0001t0001g0180 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.206+1156G>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76066215 | ||||||
chr12:76066396
|
G | T | 1 | a0001c0001t0002g0047 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.206+975C>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76066396 | ||||||
chr12:76066452
|
A | G | 1 | a0001c0002t0004g0308 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.206+919T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76066452 | ||||||
chr12:76066527
|
C | T | 15 | a0001c0002t0009g0016a0001c0002t0009g0145a0001c0002t0009g0229others(12): Show | 17 | HG01109.hp2 HG02055.hp2 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.206+844G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76066527 | ||||||
chr12:76066605
|
C | T | 3 | a0001c0002t0019g0137a0001c0002t0019g0138a0001c0002t0019g0139 | 3 | HG02559.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.206+766G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76066605 | ||||||
chr12:76066692
|
A | G | 1 | a0001c0001t0002g0045 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.206+679T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76066692 | ||||||
chr12:76066834
|
G | A | 1 | a0001c0002t0065g0291 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.206+537C>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76066834 | ||||||
chr12:76066841
|
G | C | 1 | a0001c0001t0001g0168 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.206+530C>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76066841 | ||||||
chr12:76066912
|
G | A | 1 | a0001c0001t0002g0069 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.206+459C>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76066912 | ||||||
chr12:76066987
|
G | C | 204 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0021others(201): Show | 233 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(230): Show |
intron_variant | MODIFIER | c.206+384C>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76066987 | ||||||
chr12:76067000
|
CAA | C | 4 | a0001c0002t0015g0018a0001c0002t0015g0149a0001c0002t0015g0150others(1): Show | 5 | HG01261.hp1 HG02145.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.206+369_206+370del others(2): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76067000 | ||||||
chr12:76067153
|
C | T | 226 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0021others(223): Show | 258 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(255): Show |
intron_variant | MODIFIER | c.206+218G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76067153 | ||||||
chr12:76067259
|
A | C | 1 | a0001c0001t0013g0081 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.206+112T>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76067259 | ||||||
chr12:76067266
|
A | G | 36 | a0001c0001t0066g0307a0001c0002t0004g0288a0001c0002t0004g0289others(33): Show | 36 | HG00140.hp1 HG00733.hp1 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.206+105T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76067266 | ||||||
chr12:76067319
|
G | T | 10 | a0001c0002t0014g0017a0001c0002t0014g0148a0001c0002t0028g0142others(7): Show | 11 | HG01109.hp2 HG02055.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.206+52C>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76067319 | ||||||
chr12:76067357
|
T | C | 207 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0021others(204): Show | 236 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(233): Show |
intron_variant | MODIFIER | c.206+14A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76067357 | ||||||
chr12:76067365
|
C | T | 266 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0021others(263): Show | 298 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(295): Show |
splice_region_variant&intron_variant | LOW | c.206+6G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 4/14 | chr12 | 76067365 | ||||||
chr12:76067477
|
T | TA | 113 | a0001c0001t0001g0173a0001c0001t0002g0002a0001c0001t0002g0003others(110): Show | 129 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(126): Show |
splice_region_variant&intron_variant | LOW | c.104-5dupT | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 3/14 | chr12 | 76067477 | ||||||
chr12:76067574
|
T | G | 1 | a0001c0001t0008g0125 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.104-101A>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 3/14 | chr12 | 76067574 | ||||||
chr12:76067604
|
C | T | 1 | a0001c0001t0002g0066 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.104-131G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 3/14 | chr12 | 76067604 | ||||||
chr12:76067826
|
G | T | 1 | a0001c0002t0004g0290 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.104-353C>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 3/14 | chr12 | 76067826 | ||||||
chr12:76067934
|
T | C | 1 | a0001c0002t0046g0218 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.104-461A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 3/14 | chr12 | 76067934 | ||||||
chr12:76068095
|
T | G | 1 | a0001c0001t0087g0103 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.104-622A>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 3/14 | chr12 | 76068095 | ||||||
chr12:76068152
|
C | T | 1 | a0001c0002t0004g0302 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.104-679G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 3/14 | chr12 | 76068152 | ||||||
chr12:76068352
|
C | T | 1 | a0001c0001t0042g0199 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.103+557G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 3/14 | chr12 | 76068352 | ||||||
chr12:76068410
|
C | T | 1 | a0001c0001t0001g0164 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.103+499G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 3/14 | chr12 | 76068410 | ||||||
chr12:76068641
|
G | A | 2 | a0001c0001t0002g0054a0001c0001t0002g0068 | 2 | NA18957.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.103+268C>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 3/14 | chr12 | 76068641 | ||||||
chr12:76068722
|
C | A | 1 | a0001c0001t0001g0169 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.103+187G>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 3/14 | chr12 | 76068722 | ||||||
chr12:76068728
|
C | T | 1 | a0001c0001t0007g0133 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.103+181G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 3/14 | chr12 | 76068728 | ||||||
chr12:76068729
|
G | A | 3 | a0001c0002t0019g0137a0001c0002t0019g0138a0001c0002t0019g0139 | 3 | HG02559.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.103+180C>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 3/14 | chr12 | 76068729 | ||||||
chr12:76068735
|
T | TAC | 36 | a0001c0001t0001g0130a0001c0001t0001g0189a0001c0001t0001g0190others(33): Show | 36 | HG00140.hp1 HG00323.hp2 HG00597.hp1 others(33): Show |
intron_variant | MODIFIER | c.103+172_103+173dup others(2): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 3/14 | chr12 | 76068735 | ||||||
chr12:76068735
|
T | TACAC | 41 | a0001c0001t0001g0162a0001c0001t0001g0164a0001c0001t0001g0165others(38): Show | 44 | HG00140.hp2 HG00741.hp1 HG01099.hp1 others(41): Show |
intron_variant | MODIFIER | c.103+170_103+173dup others(4): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 3/14 | chr12 | 76068735 | ||||||
chr12:76068735
|
T | TACACAC | 66 | a0001c0001t0001g0005a0001c0001t0001g0023a0001c0001t0001g0026others(63): Show | 77 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.103+168_103+173dup others(6): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 3/14 | chr12 | 76068735 | ||||||
chr12:76068735
|
T | TACACACA others(1): Show |
44 | a0001c0001t0001g0024a0001c0001t0001g0140a0001c0001t0001g0166others(41): Show | 48 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.103+166_103+173dup others(8): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 3/14 | chr12 | 76068735 | ||||||
chr12:76068735
|
T | TACACACA others(3): Show |
29 | a0001c0001t0001g0001a0001c0001t0001g0184a0001c0001t0001g0186others(26): Show | 35 | HG00544.hp2 HG00733.hp2 HG01074.hp2 others(32): Show |
intron_variant | MODIFIER | c.103+164_103+173dup others(10): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 3/14 | chr12 | 76068735 | ||||||
chr12:76068735
|
T | TACACACA others(5): Show |
19 | a0001c0001t0001g0187a0001c0001t0001g0198a0001c0001t0002g0012others(16): Show | 21 | HG00544.hp1 HG00558.hp2 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.103+162_103+173dup others(12): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 3/14 | chr12 | 76068735 | ||||||
chr12:76068735
|
T | TACACACA others(7): Show |
15 | a0001c0001t0001g0132a0001c0001t0001g0188a0001c0001t0001g0202others(12): Show | 17 | HG01069.hp1 HG01081.hp1 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.103+160_103+173dup others(14): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 3/14 | chr12 | 76068735 | ||||||
chr12:76068735
|
T | TACACACA others(9): Show |
6 | a0001c0001t0006g0050a0001c0001t0006g0088a0001c0001t0093g0043others(3): Show | 7 | HG00323.hp1 HG01081.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.103+158_103+173dup others(16): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 3/14 | chr12 | 76068735 | ||||||
chr12:76068735
|
T | TACACACA others(11): Show |
1 | a0001c0002t0039g0152 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.103+156_103+173dup others(18): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 3/14 | chr12 | 76068735 | ||||||
chr12:76068735
|
T | TACACACA others(13): Show |
2 | a0001c0001t0002g0069a0001c0002t0009g0145 | 2 | HG02257.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.103+154_103+173dup others(20): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 3/14 | chr12 | 76068735 | ||||||
chr12:76068735
|
T | TACACACA others(19): Show |
1 | a0001c0002t0029g0136 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.103+148_103+173dup others(26): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 3/14 | chr12 | 76068735 | ||||||
chr12:76068735
|
TAC | T | 6 | a0001c0001t0001g0176a0001c0002t0024g0222a0001c0002t0065g0291others(3): Show | 6 | HG00738.hp2 HG01884.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.103+172_103+173del others(2): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 3/14 | chr12 | 76068735 | ||||||
chr12:76068735
|
TACAC | T | 7 | a0001c0001t0037g0057a0001c0002t0004g0289a0001c0002t0063g0212others(4): Show | 7 | HG00741.hp2 HG01074.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.103+170_103+173del others(4): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 3/14 | chr12 | 76068735 | ||||||
chr12:76068735
|
TACACACA others(3): Show |
T | 2 | a0001c0001t0002g0086a0001c0001t0002g0087 | 2 | HG03471.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.103+164_103+173del others(10): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 3/14 | chr12 | 76068735 | ||||||
chr12:76068735
|
TACACACA others(5): Show |
T | 2 | a0001c0002t0028g0142a0001c0002t0028g0143 | 2 | HG02630.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.103+162_103+173del others(12): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 3/14 | chr12 | 76068735 | ||||||
chr12:76068735
|
TACACACA others(9): Show |
T | 5 | a0001c0002t0014g0017a0001c0002t0014g0148a0001c0002t0041g0146others(2): Show | 6 | HG01109.hp2 HG02055.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.103+158_103+173del others(16): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 3/14 | chr12 | 76068735 | ||||||
chr12:76068735
|
TACACACA others(13): Show |
T | 2 | a0001c0001t0037g0071a0001c0001t0038g0070 | 2 | HG02647.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.103+154_103+173del others(20): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 3/14 | chr12 | 76068735 | ||||||
chr12:76068777
|
C | T | 1 | a0001c0002t0004g0320 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.103+132G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 3/14 | chr12 | 76068777 | ||||||
chr12:76068780
|
T | A | 5 | a0001c0002t0009g0016a0001c0002t0009g0145a0001c0002t0009g0229others(2): Show | 6 | HG02257.hp2 HG02622.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.103+129A>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 3/14 | chr12 | 76068780 | ||||||
chr12:76068832
|
T | C | 204 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0021others(201): Show | 233 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(230): Show |
intron_variant | MODIFIER | c.103+77A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 3/14 | chr12 | 76068832 | ||||||
chr12:76069062
|
TA | T | 3 | a0001c0002t0019g0137a0001c0002t0019g0138a0001c0002t0019g0139 | 3 | HG02559.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.18-69delT | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 2/14 | chr12 | 76069062 | ||||||
chr12:76069289
|
A | G | 1 | a0001c0001t0001g0175 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.18-295T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 2/14 | chr12 | 76069289 | ||||||
chr12:76069361
|
T | C | 2 | a0001c0001t0074g0163a0001c0001t0075g0200 | 2 | NA19006.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.18-367A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 2/14 | chr12 | 76069361 | ||||||
chr12:76069444
|
G | C | 1 | a0001c0002t0102g0224 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.18-450C>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 2/14 | chr12 | 76069444 | ||||||
chr12:76069695
|
C | T | 1 | a0001c0002t0004g0300 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.18-701G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 2/14 | chr12 | 76069695 | ||||||
chr12:76069824
|
TA | T | 7 | a0001c0001t0006g0006a0001c0002t0015g0018a0001c0002t0015g0149others(4): Show | 9 | HG01169.hp2 HG01256.hp1 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.18-831delT | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 2/14 | chr12 | 76069824 | ||||||
chr12:76070054
|
G | GA | 6 | a0001c0002t0025g0282a0001c0002t0025g0283a0001c0002t0027g0220others(3): Show | 6 | HG01081.hp2 HG01123.hp2 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.18-1061dupT | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 2/14 | chr12 | 76070054 | ||||||
chr12:76070122
|
CT | C | 205 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0021others(202): Show | 235 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(232): Show |
intron_variant | MODIFIER | c.18-1129delA | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 2/14 | chr12 | 76070122 | ||||||
chr12:76070122
|
CTT | C | 17 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0026others(14): Show | 19 | HG00438.hp1 HG00558.hp1 HG00597.hp1 others(16): Show |
intron_variant | MODIFIER | c.18-1130_18-1129del others(2): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 2/14 | chr12 | 76070122 | ||||||
chr12:76070134
|
T | G | 9 | a0001c0001t0007g0019a0001c0001t0007g0133a0001c0001t0007g0154others(6): Show | 10 | HG01891.hp1 HG02145.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.18-1140A>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 2/14 | chr12 | 76070134 | ||||||
chr12:76070196
|
C | G | 1 | a0001c0001t0001g0174 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.18-1202G>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 2/14 | chr12 | 76070196 | ||||||
chr12:76070214
|
C | G | 1 | a0001c0002t0046g0218 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.18-1220G>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 2/14 | chr12 | 76070214 | ||||||
chr12:76070269
|
T | C | 1 | a0001c0001t0006g0121 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.18-1275A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 2/14 | chr12 | 76070269 | ||||||
chr12:76070288
|
A | G | 3 | a0001c0002t0019g0137a0001c0002t0019g0138a0001c0002t0019g0139 | 3 | HG02559.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.18-1294T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 2/14 | chr12 | 76070288 | ||||||
chr12:76070370
|
A | T | 1 | a0001c0001t0002g0086 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.18-1376T>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 2/14 | chr12 | 76070370 | ||||||
chr12:76070431
|
A | C | 1 | a0001c0002t0004g0314 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.18-1437T>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 2/14 | chr12 | 76070431 | ||||||
chr12:76070520
|
T | C | 1 | a0001c0001t0035g0109 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.18-1526A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 2/14 | chr12 | 76070520 | ||||||
chr12:76070827
|
T | C | 81 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0021others(78): Show | 93 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.18-1833A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 2/14 | chr12 | 76070827 | ||||||
chr12:76070857
|
A | G | 268 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0021others(265): Show | 300 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(297): Show |
intron_variant | MODIFIER | c.18-1863T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 2/14 | chr12 | 76070857 | ||||||
chr12:76070982
|
T | C | 3 | a0001c0002t0019g0137a0001c0002t0019g0138a0001c0002t0019g0139 | 3 | HG02559.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.18-1988A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 2/14 | chr12 | 76070982 | ||||||
chr12:76070991
|
A | G | 7 | a0001c0002t0020g0216a0001c0002t0020g0217a0001c0002t0044g0219others(4): Show | 7 | HG01884.hp2 HG02109.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.18-1997T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 2/14 | chr12 | 76070991 | ||||||
chr12:76071153
|
A | T | 1 | a0001c0001t0012g0039 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.18-2159T>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 2/14 | chr12 | 76071153 | ||||||
chr12:76071267
|
A | G | 5 | a0001c0002t0020g0216a0001c0002t0020g0217a0001c0002t0044g0219others(2): Show | 5 | HG02109.hp2 HG02258.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.18-2273T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 2/14 | chr12 | 76071267 | ||||||
chr12:76071465
|
G | C | 110 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0011others(107): Show | 126 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(123): Show |
intron_variant | MODIFIER | c.18-2471C>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 2/14 | chr12 | 76071465 | ||||||
chr12:76071784
|
G | A | 3 | a0001c0002t0029g0135a0001c0002t0029g0136a0001c0002t0088g0134 | 3 | HG02486.hp2 HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.17+2419C>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 2/14 | chr12 | 76071784 | ||||||
chr12:76071960
|
GA | G | 283 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0021others(280): Show | 315 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(312): Show |
intron_variant | MODIFIER | c.17+2242delT | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 2/14 | chr12 | 76071960 | ||||||
chr12:76071974
|
T | A | 3 | a0001c0003t0005g0237a0001c0003t0005g0239a0001c0003t0005g0254 | 3 | HG01243.hp2 HG01884.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.17+2229A>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 2/14 | chr12 | 76071974 | ||||||
chr12:76072206
|
A | G | 3 | a0001c0002t0019g0137a0001c0002t0019g0138a0001c0002t0019g0139 | 3 | HG02559.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.17+1997T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 2/14 | chr12 | 76072206 | ||||||
chr12:76072231
|
A | G | 1 | a0001c0001t0002g0040 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.17+1972T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 2/14 | chr12 | 76072231 | ||||||
chr12:76072282
|
CAAG | C | 4 | a0001c0003t0005g0232a0001c0003t0005g0247a0001c0003t0005g0250others(1): Show | 4 | HG00741.hp2 HG01074.hp1 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.17+1918_17+1920del others(3): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 2/14 | chr12 | 76072282 | ||||||
chr12:76072300
|
T | TA | 10 | a0001c0002t0004g0292a0001c0002t0022g0317a0001c0002t0022g0318others(7): Show | 10 | HG01081.hp2 HG01123.hp2 HG01516.hp2 others(7): Show |
intron_variant | MODIFIER | c.17+1902dupT | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 2/14 | chr12 | 76072300 | ||||||
chr12:76072316
|
C | A | 9 | a0001c0002t0014g0017a0001c0002t0014g0148a0001c0002t0015g0018others(6): Show | 11 | HG01109.hp2 HG01261.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.17+1887G>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 2/14 | chr12 | 76072316 | ||||||
chr12:76072450
|
G | A | 222 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0021others(219): Show | 254 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(251): Show |
intron_variant | MODIFIER | c.17+1753C>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 2/14 | chr12 | 76072450 | ||||||
chr12:76072535
|
A | C | 5 | a0001c0002t0014g0017a0001c0002t0014g0148a0001c0002t0041g0146others(2): Show | 6 | HG01109.hp2 HG02055.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.17+1668T>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 2/14 | chr12 | 76072535 | ||||||
chr12:76072680
|
G | A | 1 | a0001c0001t0066g0307 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.17+1523C>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 2/14 | chr12 | 76072680 | ||||||
chr12:76072853
|
G | A | 5 | a0001c0001t0034g0197a0001c0002t0015g0018a0001c0002t0015g0149others(2): Show | 6 | HG01261.hp1 HG02145.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.17+1350C>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 2/14 | chr12 | 76072853 | ||||||
chr12:76072903
|
C | A | 1 | a0001c0001t0001g0198 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.17+1300G>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 2/14 | chr12 | 76072903 | ||||||
chr12:76072923
|
G | A | 5 | a0001c0002t0009g0016a0001c0002t0009g0145a0001c0002t0009g0229others(2): Show | 6 | HG02257.hp2 HG02622.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.17+1280C>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 2/14 | chr12 | 76072923 | ||||||
chr12:76073013
|
G | T | 2 | a0001c0001t0003g0092a0001c0001t0092g0093 | 2 | NA18981.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.17+1190C>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 2/14 | chr12 | 76073013 | ||||||
chr12:76073079
|
C | G | 1 | a0001c0002t0022g0318 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.17+1124G>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 2/14 | chr12 | 76073079 | ||||||
chr12:76073136
|
A | G | 1 | a0001c0002t0039g0151 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.17+1067T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 2/14 | chr12 | 76073136 | ||||||
chr12:76073146
|
T | A | 40 | a0001c0001t0066g0307a0001c0002t0004g0288a0001c0002t0004g0289others(37): Show | 40 | HG00140.hp1 HG00733.hp1 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.17+1057A>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 2/14 | chr12 | 76073146 | ||||||
chr12:76073158
|
T | G | 1 | a0001c0001t0070g0204 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.17+1045A>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 2/14 | chr12 | 76073158 | ||||||
chr12:76073485
|
C | T | 3 | a0001c0001t0001g0171a0001c0001t0001g0172a0001c0001t0001g0173 | 3 | HG02056.hp2 HG02129.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.17+718G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 2/14 | chr12 | 76073485 | ||||||
chr12:76073501
|
CT | C | 261 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0021others(258): Show | 293 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(290): Show |
intron_variant | MODIFIER | c.17+701delA | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 2/14 | chr12 | 76073501 | ||||||
chr12:76073562
|
T | A | 2 | a0001c0001t0076g0079a0001c0001t0097g0052 | 2 | NA18954.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.17+641A>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 2/14 | chr12 | 76073562 | ||||||
chr12:76073734
|
C | T | 3 | a0001c0002t0019g0137a0001c0002t0019g0138a0001c0002t0019g0139 | 3 | HG02559.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.17+469G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 2/14 | chr12 | 76073734 | ||||||
chr12:76073830
|
A | C | 2 | a0001c0001t0074g0163a0001c0001t0075g0200 | 2 | NA19006.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.17+373T>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 2/14 | chr12 | 76073830 | ||||||
chr12:76074010
|
A | T | 4 | a0001c0002t0027g0220a0001c0002t0027g0284a0001c0002t0061g0286others(1): Show | 4 | HG01081.hp2 HG01123.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.17+193T>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 2/14 | chr12 | 76074010 | ||||||
chr12:76074058
|
T | G | 2 | a0001c0002t0028g0142a0001c0002t0028g0143 | 2 | HG02630.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.17+145A>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 2/14 | chr12 | 76074058 | ||||||
chr12:76074129
|
T | C | 3 | a0001c0002t0022g0317a0001c0002t0022g0318a0001c0002t0052g0319 | 3 | HG02896.hp2 HG02897.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.17+74A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 2/14 | chr12 | 76074129 | ||||||
chr12:76074327
|
A | G | 3 | a0001c0002t0019g0137a0001c0002t0019g0138a0001c0002t0019g0139 | 3 | HG02559.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-20-88T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76074327 | ||||||
chr12:76074407
|
A | G | 3 | a0001c0002t0019g0137a0001c0002t0019g0138a0001c0002t0019g0139 | 3 | HG02559.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-20-168T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76074407 | ||||||
chr12:76074784
|
T | G | 1 | a0001c0002t0023g0274 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-20-545A>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76074784 | ||||||
chr12:76074794
|
G | A | 3 | a0001c0002t0019g0137a0001c0002t0019g0138a0001c0002t0019g0139 | 3 | HG02559.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-20-555C>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76074794 | ||||||
chr12:76074810
|
C | T | 3 | a0001c0002t0019g0137a0001c0002t0019g0138a0001c0002t0019g0139 | 3 | HG02559.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-20-571G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76074810 | ||||||
chr12:76075068
|
G | A | 18 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0051others(15): Show | 22 | HG00438.hp2 HG00735.hp2 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.-20-829C>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76075068 | ||||||
chr12:76075269
|
G | A | 40 | a0001c0001t0066g0307a0001c0002t0004g0288a0001c0002t0004g0289others(37): Show | 40 | HG00140.hp1 HG00733.hp1 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.-20-1030C>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76075269 | ||||||
chr12:76075330
|
T | A | 1 | a0001c0001t0002g0080 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-20-1091A>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76075330 | ||||||
chr12:76075345
|
T | C | 2 | a0001c0001t0003g0112a0001c0001t0035g0110 | 2 | NA18962.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.-20-1106A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76075345 | ||||||
chr12:76075396
|
G | A | 1 | a0001c0002t0065g0291 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-20-1157C>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76075396 | ||||||
chr12:76075413
|
C | T | 5 | a0001c0002t0009g0016a0001c0002t0009g0145a0001c0002t0009g0229others(2): Show | 6 | HG02257.hp2 HG02622.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.-20-1174G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76075413 | ||||||
chr12:76075454
|
C | T | 1 | a0001c0002t0051g0221 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-20-1215G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76075454 | ||||||
chr12:76075611
|
GA | G | 3 | a0001c0002t0019g0137a0001c0002t0019g0138a0001c0002t0019g0139 | 3 | HG02559.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-20-1373delT | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76075611 | ||||||
chr12:76075734
|
G | A | 3 | a0001c0002t0019g0137a0001c0002t0019g0138a0001c0002t0019g0139 | 3 | HG02559.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-20-1495C>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76075734 | ||||||
chr12:76075775
|
G | T | 2 | a0001c0002t0028g0142a0001c0002t0028g0143 | 2 | HG02630.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-20-1536C>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76075775 | ||||||
chr12:76075788
|
C | T | 1 | a0001c0002t0029g0136 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-20-1549G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76075788 | ||||||
chr12:76075848
|
T | C | 1 | a0001c0002t0051g0221 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-20-1609A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76075848 | ||||||
chr12:76075892
|
C | T | 1 | a0001c0001t0001g0170 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-20-1653G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76075892 | ||||||
chr12:76075944
|
G | A | 5 | a0001c0001t0013g0013a0001c0001t0013g0081a0001c0001t0013g0084others(2): Show | 6 | HG01243.hp1 HG02572.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-20-1705C>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76075944 | ||||||
chr12:76075953
|
C | A | 1 | a0001c0001t0001g0205 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-20-1714G>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76075953 | ||||||
chr12:76076064
|
C | T | 1 | a0001c0002t0044g0219 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-20-1825G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76076064 | ||||||
chr12:76076181
|
C | T | 1 | a0001c0002t0004g0310 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-20-1942G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76076181 | ||||||
chr12:76076496
|
G | T | 3 | a0001c0002t0029g0135a0001c0002t0029g0136a0001c0002t0088g0134 | 3 | HG02486.hp2 HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-20-2257C>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76076496 | ||||||
chr12:76076544
|
A | G | 1 | a0001c0002t0044g0219 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-20-2305T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76076544 | ||||||
chr12:76076547
|
GAAATATA others(3): Show |
G | 1 | a0001c0002t0025g0282 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-20-2318_-20-2309d others(12): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76076547 | ||||||
chr12:76076547
|
GAAATATA others(11): Show |
G | 1 | a0001c0001t0002g0042 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.-20-2326_-20-2309d others(20): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76076547 | ||||||
chr12:76076549
|
A | AAT | 9 | a0001c0002t0004g0296a0001c0002t0004g0312a0001c0002t0019g0138others(6): Show | 9 | HG00741.hp2 HG01074.hp1 HG02273.hp2 others(6): Show |
intron_variant | MODIFIER | c.-20-2312_-20-2311d others(4): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76076549 | ||||||
chr12:76076549
|
A | AATAT | 5 | a0001c0002t0004g0289a0001c0002t0019g0137a0001c0003t0005g0247others(2): Show | 5 | HG02559.hp1 HG02717.hp2 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.-20-2314_-20-2311d others(6): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76076549 | ||||||
chr12:76076549
|
A | AATATATA others(1): Show |
5 | a0001c0002t0004g0302a0001c0002t0028g0142a0001c0002t0028g0143others(2): Show | 5 | HG01256.hp2 HG01884.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.-20-2318_-20-2311d others(10): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76076549 | ||||||
chr12:76076549
|
A | AATATATA others(3): Show |
4 | a0001c0002t0004g0288a0001c0003t0005g0244a0001c0003t0005g0245others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.-20-2320_-20-2311d others(12): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76076549 | ||||||
chr12:76076549
|
A | AATATATA others(5): Show |
5 | a0001c0002t0004g0311a0001c0002t0017g0301a0001c0003t0005g0242others(2): Show | 5 | HG01891.hp2 HG02922.hp1 HG03239.hp2 others(2): Show |
intron_variant | MODIFIER | c.-20-2322_-20-2311d others(14): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76076549 | ||||||
chr12:76076549
|
A | AATATATA others(7): Show |
3 | a0001c0002t0004g0320a0001c0003t0005g0240a0001c0003t0005g0257 | 3 | HG00323.hp2 HG02647.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-20-2324_-20-2311d others(16): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76076549 | ||||||
chr12:76076549
|
A | AATATATA others(9): Show |
4 | a0001c0002t0004g0300a0001c0003t0005g0238a0001c0003t0005g0239others(1): Show | 4 | HG01175.hp1 HG01358.hp2 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.-20-2326_-20-2311d others(18): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76076549 | ||||||
chr12:76076549
|
A | AATATATA others(11): Show |
6 | a0001c0002t0004g0292a0001c0002t0004g0314a0001c0002t0004g0322others(3): Show | 6 | HG00140.hp1 HG01884.hp1 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.-20-2328_-20-2311d others(20): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76076549 | ||||||
chr12:76076549
|
A | AATATATA others(13): Show |
5 | a0001c0002t0004g0316a0001c0002t0004g0321a0001c0003t0005g0235others(2): Show | 6 | HG00738.hp1 HG01192.hp1 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.-20-2330_-20-2311d others(22): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76076549 | ||||||
chr12:76076549
|
A | AATATATA others(15): Show |
1 | a0001c0003t0005g0234 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-20-2332_-20-2311d others(24): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76076549 | ||||||
chr12:76076549
|
A | AATATATA others(17): Show |
2 | a0001c0002t0004g0297a0001c0003t0010g0277 | 2 | HG03927.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.-20-2334_-20-2311d others(26): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76076549 | ||||||
chr12:76076549
|
A | AATATATA others(21): Show |
1 | a0001c0003t0026g0233 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-20-2338_-20-2311d others(30): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76076549 | ||||||
chr12:76076549
|
AAT | A | 4 | a0001c0001t0066g0307a0001c0002t0024g0222a0001c0002t0041g0230others(1): Show | 4 | HG02280.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-20-2312_-20-2311d others(4): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76076549 | ||||||
chr12:76076549
|
AATAT | A | 7 | a0001c0002t0004g0308a0001c0002t0009g0016a0001c0002t0009g0145others(4): Show | 8 | HG01109.hp2 HG02109.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.-20-2314_-20-2311d others(6): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76076549 | ||||||
chr12:76076549
|
AATATATA others(1): Show |
A | 7 | a0001c0002t0016g0226a0001c0002t0016g0227a0001c0002t0016g0276others(4): Show | 7 | HG00642.hp1 HG01243.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.-20-2318_-20-2311d others(10): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76076549 | ||||||
chr12:76076549
|
AATATATA others(3): Show |
A | 2 | a0001c0002t0040g0153a0001c0002t0046g0218 | 2 | HG03098.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-20-2320_-20-2311d others(12): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76076549 | ||||||
chr12:76076549
|
AATATATA others(5): Show |
A | 5 | a0001c0002t0025g0283a0001c0002t0027g0220a0001c0002t0027g0284others(2): Show | 5 | HG01081.hp2 HG01123.hp2 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.-20-2322_-20-2311d others(14): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76076549 | ||||||
chr12:76076549
|
AATATATA others(7): Show |
A | 11 | a0001c0001t0001g0130a0001c0001t0001g0262a0001c0001t0007g0019others(8): Show | 12 | HG01891.hp1 HG01928.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.-20-2324_-20-2311d others(16): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76076549 | ||||||
chr12:76076549
|
AATATATA others(9): Show |
A | 20 | a0001c0001t0001g0260a0001c0001t0001g0264a0001c0001t0001g0265others(17): Show | 20 | HG00323.hp1 HG00642.hp2 HG00741.hp1 others(17): Show |
intron_variant | MODIFIER | c.-20-2326_-20-2311d others(18): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76076549 | ||||||
chr12:76076549
|
AATATATA others(11): Show |
A | 27 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0166others(24): Show | 28 | HG01261.hp1 HG01516.hp1 HG02145.hp1 others(25): Show |
intron_variant | MODIFIER | c.-20-2328_-20-2311d others(20): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76076549 | ||||||
chr12:76076549
|
AATATATA others(13): Show |
A | 166 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0021others(163): Show | 194 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(191): Show |
intron_variant | MODIFIER | c.-20-2330_-20-2311d others(22): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76076549 | ||||||
chr12:76076549
|
AATATATA others(15): Show |
A | 1 | a0001c0001t0001g0270 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-20-2332_-20-2311d others(24): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76076549 | ||||||
chr12:76076549
|
AATATATA others(19): Show |
A | 1 | a0001c0002t0051g0221 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-20-2336_-20-2311d others(28): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76076549 | ||||||
chr12:76076549
|
AATATATA others(21): Show |
A | 3 | a0001c0002t0005g0259a0001c0002t0023g0273a0001c0002t0023g0274 | 3 | HG02257.hp1 HG02723.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-20-2338_-20-2311d others(30): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76076549 | ||||||
chr12:76076549
|
AATATATA others(23): Show |
A | 4 | a0001c0002t0004g0310a0001c0002t0104g0323a0001c0003t0018g0256others(1): Show | 4 | HG00733.hp1 HG01069.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.-20-2340_-20-2311d others(32): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76076549 | ||||||
chr12:76076590
|
A | C | 2 | a0001c0002t0009g0016a0001c0002t0009g0145 | 3 | HG02257.hp2 HG03041.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-20-2351T>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76076590 | ||||||
chr12:76076592
|
A | ATATATAT others(9): Show |
1 | a0001c0002t0017g0315 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-20-2354_-20-2353i others(18): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76076592 | ||||||
chr12:76076592
|
A | C | 4 | a0001c0002t0015g0018a0001c0002t0015g0149a0001c0002t0015g0150others(1): Show | 5 | HG01261.hp1 HG02145.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.-20-2353T>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76076592 | ||||||
chr12:76076618
|
T | A | 1 | a0001c0001t0086g0122 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-20-2379A>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76076618 | ||||||
chr12:76076826
|
C | T | 3 | a0001c0002t0022g0317a0001c0002t0022g0318a0001c0002t0052g0319 | 3 | HG02896.hp2 HG02897.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-20-2587G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76076826 | ||||||
chr12:76077254
|
T | G | 1 | a0001c0002t0019g0139 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-20-3015A>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76077254 | ||||||
chr12:76077658
|
C | T | 1 | a0001c0002t0063g0212 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-20-3419G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76077658 | ||||||
chr12:76077929
|
G | A | 3 | a0001c0002t0019g0137a0001c0002t0019g0138a0001c0002t0019g0139 | 3 | HG02559.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-20-3690C>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76077929 | ||||||
chr12:76077980
|
C | CA | 147 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0021others(144): Show | 168 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(165): Show |
intron_variant | MODIFIER | c.-20-3742dupT | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76077980 | ||||||
chr12:76077980
|
C | CAA | 74 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0001g0261others(71): Show | 84 | HG00438.hp2 HG00544.hp2 HG00735.hp2 others(81): Show |
intron_variant | MODIFIER | c.-20-3743_-20-3742d others(4): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76077980 | ||||||
chr12:76077980
|
C | CAAA | 6 | a0001c0001t0001g0205a0001c0001t0003g0085a0001c0001t0008g0129others(3): Show | 6 | HG01975.hp2 HG02015.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.-20-3744_-20-3742d others(5): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76077980 | ||||||
chr12:76077980
|
CA | C | 5 | a0001c0002t0004g0296a0001c0002t0009g0016a0001c0002t0009g0145others(2): Show | 6 | HG02257.hp2 HG02273.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-20-3742delT | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76077980 | ||||||
chr12:76077981
|
A | G | 1 | a0001c0002t0044g0219 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-20-3742T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76077981 | ||||||
chr12:76078000
|
A | G | 11 | a0001c0002t0009g0016a0001c0002t0009g0145a0001c0002t0009g0229others(8): Show | 12 | HG02257.hp2 HG02258.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.-20-3761T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76078000 | ||||||
chr12:76078003
|
G | A | 279 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0021others(276): Show | 311 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(308): Show |
intron_variant | MODIFIER | c.-20-3764C>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76078003 | ||||||
chr12:76078025
|
G | GT | 5 | a0001c0002t0009g0016a0001c0002t0009g0145a0001c0002t0009g0229others(2): Show | 6 | HG02257.hp2 HG02622.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.-20-3787dupA | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76078025 | ||||||
chr12:76078028
|
T | C | 2 | a0001c0001t0002g0086a0001c0001t0002g0087 | 2 | HG03471.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-20-3789A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76078028 | ||||||
chr12:76078177
|
A | C | 5 | a0001c0002t0020g0216a0001c0002t0020g0217a0001c0002t0028g0142others(2): Show | 5 | HG02258.hp1 HG02630.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.-20-3938T>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76078177 | ||||||
chr12:76078324
|
T | C | 2 | a0001c0002t0028g0142a0001c0002t0028g0143 | 2 | HG02630.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-20-4085A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76078324 | ||||||
chr12:76078392
|
G | A | 1 | a0001c0001t0077g0206 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-20-4153C>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76078392 | ||||||
chr12:76078603
|
G | A | 1 | a0001c0002t0023g0274 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-20-4364C>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76078603 | ||||||
chr12:76078662
|
T | C | 1 | a0001c0002t0004g0314 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-20-4423A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76078662 | ||||||
chr12:76078753
|
T | C | 1 | a0001c0001t0006g0088 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-20-4514A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76078753 | ||||||
chr12:76078798
|
G | A | 2 | a0001c0002t0004g0321a0001c0002t0004g0322 | 2 | HG00738.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.-20-4559C>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76078798 | ||||||
chr12:76078813
|
G | C | 1 | a0001c0001t0001g0207 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.-20-4574C>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76078813 | ||||||
chr12:76078836
|
A | G | 3 | a0001c0002t0019g0137a0001c0002t0019g0138a0001c0002t0019g0139 | 3 | HG02559.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-20-4597T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76078836 | ||||||
chr12:76078910
|
C | T | 1 | a0001c0001t0002g0020 | 2 | HG01109.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.-20-4671G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76078910 | ||||||
chr12:76078958
|
A | T | 1 | a0001c0001t0003g0123 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-20-4719T>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76078958 | ||||||
chr12:76078982
|
C | CAT | 5 | a0001c0001t0002g0118a0001c0001t0003g0089a0001c0001t0003g0091others(2): Show | 5 | HG00735.hp1 HG01516.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.-20-4745_-20-4744d others(4): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76078982 | ||||||
chr12:76078994
|
T | C | 3 | a0001c0002t0005g0259a0001c0002t0039g0151a0001c0002t0039g0152 | 3 | HG02622.hp2 HG02723.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-20-4755A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76078994 | ||||||
chr12:76078994
|
T | TAC | 13 | a0001c0002t0019g0137a0001c0002t0019g0138a0001c0002t0019g0139others(10): Show | 13 | HG01109.hp2 HG02258.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.-20-4757_-20-4756d others(4): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76078994 | ||||||
chr12:76078994
|
T | TACAC | 7 | a0001c0002t0014g0017a0001c0002t0014g0148a0001c0002t0027g0220others(4): Show | 8 | HG01081.hp2 HG01123.hp2 HG01516.hp2 others(5): Show |
intron_variant | MODIFIER | c.-20-4759_-20-4756d others(6): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76078994 | ||||||
chr12:76078996
|
C | T | 197 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0021others(194): Show | 226 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(223): Show |
intron_variant | MODIFIER | c.-20-4757G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76078996 | ||||||
chr12:76079014
|
T | C | 1 | a0001c0002t0102g0224 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-20-4775A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76079014 | ||||||
chr12:76079144
|
A | G | 3 | a0001c0002t0019g0137a0001c0002t0019g0138a0001c0002t0019g0139 | 3 | HG02559.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-20-4905T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76079144 | ||||||
chr12:76079215
|
A | C | 13 | a0001c0002t0014g0017a0001c0002t0014g0148a0001c0002t0020g0216others(10): Show | 14 | HG01109.hp2 HG02055.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.-20-4976T>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76079215 | ||||||
chr12:76079241
|
T | C | 3 | a0001c0002t0009g0016a0001c0002t0009g0145a0001c0002t0009g0229 | 4 | HG02257.hp2 HG03041.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-20-5002A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76079241 | ||||||
chr12:76079249
|
T | C | 1 | a0001c0002t0041g0230 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-20-5010A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76079249 | ||||||
chr12:76079305
|
C | T | 3 | a0001c0002t0019g0137a0001c0002t0019g0138a0001c0002t0019g0139 | 3 | HG02559.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-20-5066G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76079305 | ||||||
chr12:76079494
|
T | C | 40 | a0001c0001t0002g0040a0001c0001t0002g0098a0001c0001t0002g0104others(37): Show | 44 | HG00423.hp1 HG00597.hp2 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.-21+5073A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76079494 | ||||||
chr12:76079684
|
A | AT | 55 | a0001c0001t0001g0159a0001c0001t0001g0213a0001c0001t0001g0260others(52): Show | 56 | HG00140.hp1 HG00558.hp2 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.-21+4882dupA | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76079684 | ||||||
chr12:76079684
|
A | ATT | 6 | a0001c0002t0004g0293a0001c0002t0004g0294a0001c0002t0004g0295others(3): Show | 6 | HG00741.hp1 HG01978.hp1 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.-21+4881_-21+4882d others(4): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76079684 | ||||||
chr12:76079941
|
A | C | 275 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0021others(272): Show | 307 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(304): Show |
intron_variant | MODIFIER | c.-21+4626T>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76079941 | ||||||
chr12:76080050
|
G | A | 1 | a0001c0001t0001g0211 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.-21+4517C>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76080050 | ||||||
chr12:76080077
|
T | C | 1 | a0001c0002t0004g0316 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-21+4490A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76080077 | ||||||
chr12:76080106
|
A | G | 2 | a0001c0002t0044g0219a0001c0002t0046g0218 | 2 | HG02109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-21+4461T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76080106 | ||||||
chr12:76080158
|
A | G | 229 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0021others(226): Show | 261 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(258): Show |
intron_variant | MODIFIER | c.-21+4409T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76080158 | ||||||
chr12:76080248
|
T | C | 1 | a0001c0002t0103g0231 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-21+4319A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76080248 | ||||||
chr12:76080540
|
C | G | 1 | a0001c0002t0045g0215 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-21+4027G>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76080540 | ||||||
chr12:76080678
|
G | A | 1 | a0001c0002t0063g0212 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-21+3889C>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76080678 | ||||||
chr12:76080832
|
CAT | C | 3 | a0001c0002t0019g0137a0001c0002t0019g0138a0001c0002t0019g0139 | 3 | HG02559.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-21+3733_-21+3734d others(4): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76080832 | ||||||
chr12:76080976
|
T | C | 229 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0021others(226): Show | 261 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(258): Show |
intron_variant | MODIFIER | c.-21+3591A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76080976 | ||||||
chr12:76081035
|
C | G | 204 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0021others(201): Show | 233 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(230): Show |
intron_variant | MODIFIER | c.-21+3532G>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76081035 | ||||||
chr12:76081078
|
C | CT | 262 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0021others(259): Show | 292 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(289): Show |
intron_variant | MODIFIER | c.-21+3488dupA | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76081078 | ||||||
chr12:76081078
|
C | CTT | 19 | a0001c0002t0004g0292a0001c0002t0009g0016a0001c0002t0009g0145others(16): Show | 21 | HG01109.hp2 HG02055.hp2 HG02257.hp2 others(18): Show |
intron_variant | MODIFIER | c.-21+3487_-21+3488d others(4): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76081078 | ||||||
chr12:76081082
|
T | TC | 3 | a0001c0002t0031g0272a0001c0002t0031g0280a0001c0002t0073g0281 | 3 | HG02572.hp2 HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-21+3484_-21+3485i others(3): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76081082 | ||||||
chr12:76081115
|
T | C | 204 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0021others(201): Show | 233 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(230): Show |
intron_variant | MODIFIER | c.-21+3452A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76081115 | ||||||
chr12:76081209
|
A | G | 204 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0021others(201): Show | 233 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(230): Show |
intron_variant | MODIFIER | c.-21+3358T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76081209 | ||||||
chr12:76081232
|
G | C | 1 | a0001c0001t0003g0115 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.-21+3335C>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76081232 | ||||||
chr12:76081244
|
G | C | 1 | a0001c0001t0001g0026 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-21+3323C>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76081244 | ||||||
chr12:76081307
|
TAAGTA | T | 1 | a0001c0001t0002g0002 | 3 | HG00735.hp2 HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-21+3255_-21+3259d others(7): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76081307 | ||||||
chr12:76081313
|
A | T | 1 | a0001c0001t0002g0037 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.-21+3254T>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76081313 | ||||||
chr12:76081475
|
C | T | 1 | a0001c0002t0040g0153 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-21+3092G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76081475 | ||||||
chr12:76081509
|
A | G | 3 | a0001c0002t0019g0137a0001c0002t0019g0138a0001c0002t0019g0139 | 3 | HG02559.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-21+3058T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76081509 | ||||||
chr12:76081654
|
G | C | 1 | a0001c0001t0001g0213 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-21+2913C>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76081654 | ||||||
chr12:76081656
|
A | T | 1 | a0001c0001t0001g0213 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-21+2911T>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76081656 | ||||||
chr12:76081685
|
A | T | 6 | a0001c0001t0011g0032a0001c0001t0011g0034a0001c0001t0011g0036others(3): Show | 6 | NA18948.hp2 NA18969.hp1 NA18991.hp2 others(3): Show |
intron_variant | MODIFIER | c.-21+2882T>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76081685 | ||||||
chr12:76081738
|
T | A | 1 | a0001c0001t0001g0213 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-21+2829A>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76081738 | ||||||
chr12:76081780
|
T | G | 1 | a0001c0001t0001g0213 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-21+2787A>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76081780 | ||||||
chr12:76081797
|
T | C | 1 | a0001c0001t0001g0213 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-21+2770A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76081797 | ||||||
chr12:76081807
|
T | C | 1 | a0001c0001t0001g0213 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-21+2760A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76081807 | ||||||
chr12:76081809
|
T | C | 1 | a0001c0001t0001g0213 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-21+2758A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76081809 | ||||||
chr12:76081810
|
G | C | 1 | a0001c0001t0001g0213 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-21+2757C>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76081810 | ||||||
chr12:76081811
|
C | A | 1 | a0001c0001t0001g0213 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-21+2756G>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76081811 | ||||||
chr12:76081814
|
A | T | 1 | a0001c0001t0001g0213 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-21+2753T>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76081814 | ||||||
chr12:76081817
|
A | C | 1 | a0001c0001t0001g0213 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-21+2750T>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76081817 | ||||||
chr12:76081818
|
A | C | 1 | a0001c0001t0001g0213 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-21+2749T>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76081818 | ||||||
chr12:76081820
|
T | C | 1 | a0001c0001t0001g0213 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-21+2747A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76081820 | ||||||
chr12:76081825
|
T | C | 1 | a0001c0001t0001g0213 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-21+2742A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76081825 | ||||||
chr12:76081828
|
A | C | 1 | a0001c0001t0001g0213 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-21+2739T>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76081828 | ||||||
chr12:76081829
|
T | A | 1 | a0001c0001t0001g0213 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-21+2738A>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76081829 | ||||||
chr12:76081830
|
G | A | 1 | a0001c0001t0001g0213 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-21+2737C>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76081830 | ||||||
chr12:76081837
|
G | T | 1 | a0001c0001t0001g0213 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-21+2730C>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76081837 | ||||||
chr12:76081840
|
T | A | 1 | a0001c0001t0001g0213 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-21+2727A>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76081840 | ||||||
chr12:76081970
|
C | A | 33 | a0001c0001t0066g0307a0001c0002t0004g0288a0001c0002t0004g0289others(30): Show | 33 | HG00140.hp1 HG00733.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.-21+2597G>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76081970 | ||||||
chr12:76082004
|
T | C | 6 | a0001c0001t0001g0214a0001c0001t0008g0125a0001c0001t0008g0127others(3): Show | 6 | HG01123.hp1 HG01934.hp2 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.-21+2563A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76082004 | ||||||
chr12:76082051
|
C | CAAGT | 3 | a0001c0002t0019g0137a0001c0002t0019g0138a0001c0002t0019g0139 | 3 | HG02559.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-21+2515_-21+2516i others(6): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76082051 | ||||||
chr12:76082272
|
G | C | 5 | a0001c0002t0009g0016a0001c0002t0009g0145a0001c0002t0009g0229others(2): Show | 6 | HG02257.hp2 HG02622.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.-21+2295C>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76082272 | ||||||
chr12:76082349
|
T | C | 9 | a0001c0002t0014g0017a0001c0002t0014g0148a0001c0002t0015g0018others(6): Show | 11 | HG01109.hp2 HG01261.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.-21+2218A>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76082349 | ||||||
chr12:76082391
|
G | A | 1 | a0001c0002t0029g0136 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-21+2176C>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76082391 | ||||||
chr12:76082642
|
A | G | 1 | a0001c0001t0012g0031 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-21+1925T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76082642 | ||||||
chr12:76082822
|
A | G | 1 | a0001c0001t0043g0030 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-21+1745T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76082822 | ||||||
chr12:76082857
|
A | C | 208 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0021others(205): Show | 237 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(234): Show |
intron_variant | MODIFIER | c.-21+1710T>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76082857 | ||||||
chr12:76083176
|
A | G | 291 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0021others(288): Show | 323 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(320): Show |
intron_variant | MODIFIER | c.-21+1391T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76083176 | ||||||
chr12:76083299
|
G | T | 2 | a0001c0001t0002g0116a0001c0001t0012g0029 | 2 | HG01099.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.-21+1268C>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76083299 | ||||||
chr12:76083356
|
A | T | 2 | a0001c0002t0039g0151a0001c0002t0039g0152 | 2 | HG02622.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-21+1211T>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76083356 | ||||||
chr12:76083471
|
T | TTC | 29 | a0001c0001t0066g0307a0001c0002t0004g0292a0001c0002t0004g0293others(26): Show | 29 | HG00140.hp1 HG00733.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.-21+1095_-21+1096i others(4): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76083471 | ||||||
chr12:76083472
|
C | T | 2 | a0001c0002t0004g0288a0001c0002t0055g0287 | 2 | HG01192.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-21+1095G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76083472 | ||||||
chr12:76083473
|
C | A | 29 | a0001c0001t0066g0307a0001c0002t0004g0292a0001c0002t0004g0293others(26): Show | 29 | HG00140.hp1 HG00733.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.-21+1094G>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76083473 | ||||||
chr12:76083473
|
C | CA | 26 | a0001c0001t0001g0130a0001c0001t0001g0132a0001c0001t0001g0260others(23): Show | 26 | HG00423.hp2 HG00642.hp2 HG01175.hp1 others(23): Show |
intron_variant | MODIFIER | c.-21+1093dupT | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76083473 | ||||||
chr12:76083473
|
C | CAA | 7 | a0001c0002t0025g0282a0001c0002t0025g0283a0001c0002t0027g0284others(4): Show | 7 | HG01081.hp2 HG01516.hp2 HG01517.hp1 others(4): Show |
intron_variant | MODIFIER | c.-21+1092_-21+1093d others(4): Show |
NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76083473 | ||||||
chr12:76083473
|
CA | C | 120 | a0001c0001t0001g0140a0001c0001t0002g0002a0001c0001t0002g0003others(117): Show | 139 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(136): Show |
intron_variant | MODIFIER | c.-21+1093delT | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76083473 | ||||||
chr12:76083553
|
G | C | 37 | a0001c0001t0066g0307a0001c0002t0004g0288a0001c0002t0004g0289others(34): Show | 37 | HG00140.hp1 HG00733.hp1 HG00738.hp1 others(34): Show |
intron_variant | MODIFIER | c.-21+1014C>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76083553 | ||||||
chr12:76083581
|
G | T | 3 | a0001c0002t0019g0137a0001c0002t0019g0138a0001c0002t0019g0139 | 3 | HG02559.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-21+986C>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76083581 | ||||||
chr12:76083616
|
A | G | 3 | a0001c0002t0029g0135a0001c0002t0029g0136a0001c0002t0088g0134 | 3 | HG02486.hp2 HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-21+951T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76083616 | ||||||
chr12:76083766
|
A | G | 1 | a0001c0001t0007g0133 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-21+801T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76083766 | ||||||
chr12:76083938
|
C | T | 1 | a0001c0001t0001g0132 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-21+629G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76083938 | ||||||
chr12:76083947
|
C | G | 1 | a0001c0001t0006g0028 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-21+620G>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76083947 | ||||||
chr12:76083995
|
G | A | 1 | a0001c0001t0002g0131 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-21+572C>T | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76083995 | ||||||
chr12:76084161
|
A | C | 117 | a0001c0001t0001g0130a0001c0001t0002g0002a0001c0001t0002g0003others(114): Show | 133 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(130): Show |
intron_variant | MODIFIER | c.-21+406T>G | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76084161 | ||||||
chr12:76084262
|
T | G | 2 | a0001c0002t0004g0321a0001c0002t0004g0322 | 2 | HG00738.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.-21+305A>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76084262 | ||||||
chr12:76084379
|
C | T | 1 | a0001c0001t0032g0027 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-21+188G>A | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76084379 | ||||||
chr12:76084433
|
A | G | 1 | a0001c0001t0001g0026 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-21+134T>C | NAP1L1 | ENSG00000187109.15 | transcript | ENST00000618691.5 | protein_coding | 1/14 | chr12 | 76084433 |